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Remembering the forgotten non-communicable diseases
BMC Medicinevolume 12, Article number: 200 (2014)
The forthcoming post-Millennium Development Goals era will bring about new challenges in global health. Low- and middle-income countries will have to contend with a dual burden of infectious and non-communicable diseases (NCDs). Some of these NCDs, such as neoplasms, COPD, cardiovascular diseases and diabetes, cause much health loss worldwide and are already widely recognised as doing so. However, 55% of the global NCD burden arises from other NCDs, which tend to be ignored in terms of premature mortality and quality of life reduction. Here, experts in some of these `forgotten NCDs' review the clinical impact of these diseases along with the consequences of their ignoring their medical importance, and discuss ways in which they can be given higher global health priority in order to decrease the growing burden of disease and disability.
Alan D. Lopez (Figure 1).
In an era of considerable interest in global health, in part motivated by the Millennium Development Goals, but also inspired by demonstrable success with disease control strategies for child survival, donors, countries and the broader global development community are increasingly asking: what's next? Certainly, the unfinished agenda of substantially reducing the six million child deaths that still occur each year must remain a focus of global health and development efforts. However, there is now increasing recognition of the imperative not only to keep babies alive until adolescence, but of keeping adolescents alive, and healthy, into old age. Seeing global health priorities as an `either/or' dichotomy is becoming increasingly irrelevant, and uncommon. There is much reference made to the `double burden' or, more correctly, the `triple burden' (including injuries) that low- and middle-income countries are facing. But are we, the global health community, adapting our knowledge base, preventive practices, health care reform and whole-of-government strategies more broadly to cope with what are already the leading causes of health loss, namely non-communicable diseases (NCDs)? Are we doing enough to reduce the significant, but largely ignored, toll that injuries cause throughout the developing world?
Large global descriptive studies of the leading causes of health loss in populations, such as the ongoing Global Burden of Disease Study  provide comparable assessments, albeit with substantial and unacceptable uncertainty, of the epidemiological transition that is occurring virtually everywhere in the developing world. They are also able to track the very modest progress that is being made in reducing premature death and disability from injuries, including suicide, homicide and collective violence. Indeed, over 10% of health loss worldwide currently arises from injuries, no different to what it was two decades ago. Meanwhile, the fraction of the global burden of disease and injury due to NCDs, including mental and behavioural disorders, increased from 57% to 65%. In other words, two out of every three years of healthy life lost on the planet are attributable to NCDs. This is not the future; it is the reality of global health today, and it is likely to gather pace.
While demographic factors have contributed substantially to this growth, disease risk has not fallen as rapidly as for leading communicable diseases. There is a very real prospect of rates from major vascular diseases, chronic obstructive pulmonary disease (COPD) and cancers rising in men throughout the developing world during our lifetime as the full effects of their massive uptake of smoking some decades ago begin to be seen . This may well be compounded by the large increases in overweight and obesity that have occurred since the early 1980s, firstly in developed countries, and more recently in many developing populations, leading to substantial increases in disease burden from diabetes . Understandably, much research and many resources worldwide have been invested in understanding the epidemiology of these conditions in order to guide treatment and preventive programs. But, just like the policy focus of the past few decades on child survival, with comparatively little attention to health loss and premature death among adults, one might also ask whether too little attention has been given in global health debates to other NCDs that, for one reason or another, might justifiably deserve more?
So what are these `forgotten NCDs' and why do they matter? Just as the creation of the concept (and terminology) of `neglected tropical diseases (NTDs)' has led to much greater recognition, research support and programmatic response, including from institutions such as the Gates Foundation and the World Health Organisation, might a more strategic focus on neglected NCDs engender a similar global response, and is it warranted? The evidence would suggest it is. While neoplasms, COPD, cardiovascular diseases and diabetes cause much health loss worldwide, more of the global NCD burden (55%) arises from other NCDs. These include a diverse set of causes and conditions, but among the more important are musculoskeletal disorders, especially low back and neck pain, depression, substance use disorders, cirrhosis of the liver, chronic kidney disease, asthma, various digestive diseases including peptic ulcer, anxiety disorders, congenital anomalies and haemoglobinopathies. Unlike the `big four' NCDs, many of these conditions cause more health loss through chronic disability rather than premature death; arguably, preventing chronic disability ought to be an important goal of any health system (Figure 2).
The collection of comments in this Medicine for Global Health forum article is a timely reminder that improving population health requires a focus not only on what is important and well-studied, but on what is important and hitherto largely overlooked. Levin and Tonelli point to the urgent need to improve the integration of research across the biomedical and clinical sciences with health systems and population-based studies to enhance policy and patient outcomes for chronic kidney disease. Peter Burney reminds us that the disease burden from asthma is not declining very much at all, and that health services, particularly in poor countries, are ill-equipped to manage the case load, compounded by a poor supply of affordable medicines. Liver cirrhosis, long neglected as a global health priority, is another condition where the etiology is well understood, but as Jürgen Rehm points out, policy responses have been disappointing, particularly in reducing alcohol consumption, a leading risk factor for the disease. More broadly, alcohol and drug use disorders are causing an increasing share of health loss in many populations, quite apart from the social pathologies associated with their use. As Volkow and Koob argue in their article, a more effective response will require a serious rethink of how health care services are provided, with greater emphasis on screening and improved case management.
One of the principal consequences of population aging, namely an increase in dementia, is often at the forefront of policy discussions about the key implications of social, economic and health trends, but there is considerable uncertainty about appropriate policy responses, in part because the condition is not well understood. As Ferri argues, that is changing, with recent evidence emphasizing the importance of primary prevention to reduce this growing disease burden. The lack of visibility for sickle cell disease, as Williams points out, is in part due to poor data, in part due to the fact it is concentrated in the world's poor, yet the condition accounts for over one-third of the disease burden from haemoglobinopathies. Even gout, though a relatively minor cause of disease burden, is an example of a severely disabling condition that ought, with current knowledge, be better managed and more readily preventable, as detailed in the article by Singh.
Collectively, this reminds us that, unlike the acute, and largely treatable nature of communicable diseases, NCDs are complex, diverse, and manifest their impact on population health in different ways. Mitigating their impact will require a more strategic, comprehensive and balanced approach to NCD research, treatment and prevention, beyond what has been the practice for the past half century or so, giving greater emphasis to those conditions that are major causes of health loss, and which hitherto have been largely ignored as global health priorities. So, what might public health research focus on to accelerate the recognition of neglected NCDs as a global health priority? In my view, four pillars of research and knowledge translation are critical to that endeavour:
rapidly reduce ignorance and uncertainty about the true disease burden from these conditions by cost-effectively and strategically improving cause of death and disability data collection systems;
improve knowledge about the most cost-effective strategies to reduce disease burden in different populations, and about the most appropriate and affordable approaches to financing treatment and prevention;
improve knowledge and understanding of established interventions for controlling the impact of the more important forgotten NCDs in health care debates, and promote targeted research on promising intervention options where this is lacking; and
raise the profile of major forgotten NCDs in national and global health fora by developing policy relevant forecasts of likely health, economic and social costs of continuing to ignore them.
We should not continue to ignore or forget these NCDs. The examples reported here suggest the need for an organized, committed and urgent response by the global health community to reducing their disease burden everywhere.
Sickle cell disease: a neglected non-communicable disease of growing global importance
Thomas N Williams (Figure 3).
Few NCDs could be more neglected than sickle cell disease (SCD) : despite the fact that, with early detection and an inexpensive package of basic care, the majority of those born with the condition can expect to lead a good quality of life into late adulthood, most patients with SCD are born in resource-limited settings (RLS) where the vast majority continue to die undiagnosed in early childhood ,. SCD is a haemoglobinopathy, which results from the pathological effects of Haemoglobin S (HbS), an abnormal form of adult haemoglobin (HbA) that results from a mutation (βs) in the HBB gene . Most subjects with SCD are βs homozygotes (sickle cell anaemia; SCA), but the condition can also result from the co-inheritance of the βs mutation with a range of other HBB mutations, of which the most common are those that result in HbC and the β-thalassaemias . Despite recent promising developments, including its recognition by both the UN  and the WHO  as a disease of major and growing importance, for the most part SCD remains virtually invisible on the global health agenda. In common with many neglected NCDs, to a large extent this can be attributed to three interrelated issues: the fact that its greatest burden falls on the world's poorest communities, the lack of reliable data and inadequate political will.
Because the carrier state for SCD (sickle cell trait; HbAS) is associated with a strong survival advantage in malaria-endemic areas, the global burden of SCD is also aligned to that of malaria . As a consequence, the vast majority of children with SCD are born in resource-limited settings (RLS) (particularly sub-Saharan Africa) where routine data are least reliable (Figure 4). With few exceptions, diagnostic facilities are poor, early life screening is non-existent and official statistics on health-facility usage and cause of death are sketchy within the RLS in which the prevalence of SCD is highest. The net result is illustrated by the most recent Global Burden of Disease (GBD) Survey , a touchstone for policy-makers worldwide, in which causes of death were estimated from vital registration, verbal autopsy (VA), mortality surveillance, censuses, surveys, hospitals, and police and mortuary records. Few reliable data regarding the contribution of SCD to the mortality burden can be derived from any of these sources, exemplified by the fact that before 2012, no specific questions nor any specific diagnostic codes for SCD were included in the standard WHO VA tools . As a result the study grossly under-estimated global SCD-related deaths for 2010 at 28,600 (16,800-40,900) , a figure that should almost certainly be 4-6 times higher .
Because official statistics are so poor, even basic parameters such as the global number of affected births and SCD-specific morbidity and mortality can only be measured using indirect approaches. For example, we recently used a geostatistical model that combined data on HbAS frequencies, overall birth rates and population densities to estimate birth rates for SCA (which accounts for approximately 70% of SCD) by country, concluding that globally 312,000 (294,000 - 330,000) children were born with SCA in 2010, half being born in just three countries: Nigeria, the Democratic Republic of Congo and India  (Figure 4). Similarly, by analyzing population data on the age-specific prevalence of SCA, an indirect measure of the loss through death of subjects with this condition, we recently concluded that current under-5 mortality among children born with SCA in Africa lies between 50% and 90% . As for mortality, the importance of SCD as a cause of global morbidity has been consistently under-estimated through lack of data. Nevertheless, despite this caveat the numbers remain impressive, with estimates from the most recent GBD Survey of 5,641,000 (4,244,000-7,246,000) disability adjusted life years lost  and 2,954,000 (1,957,000-4,240,000) years lived with disability .
These global figures for morbidity and mortality should be considered in the context of data from the North, where in recent years, many countries have adopted universal screening for SCD and where most now provide comprehensive care for affected individuals. As a result, mortality is now rare among children born with SCD in Europe, the USA and the Caribbean where the majority of affected children can expect to live a relatively normal life into their 40s and 50s -. Providing such services is within reach in many RLS: successful pilot studies of newborn screening have been conducted in several African countries  and, in comparison to diseases of higher priority (such as HIV, TB and malaria), the provision of basic care in specialist clinics is not expensive . If widely implemented, such approaches could save the lives of almost ten million children worldwide between now and 2050 .
So how can SCD be brought `out of the shadows'  of its current status as a virtually invisible NCD? Perhaps most importantly, we need better data, without which it will remain difficult to persuade ministries of health, policy makers, funders and the pharmaceutical industry to devote appropriate resources to the condition. One essential component is better data on the birth frequencies and survival of children with SCD at the micro-epidemiological level, potentially through investigations using large-scale sample sets collected for other reasons, such as national surveys of micronutrient status, HIV or malaria prevalence. Similarly, the implementation of early-life screening would be made considerably simpler with the development of rapid tests that would circumvent the lack of quality-assured diagnostic laboratories and the logistics of returning results to patients. Better data will lead to better advocacy for SCD at every level: from education in schools and colleges, through to groups of affected patients, the media, celebrities, politicians, funders and health agencies internationally.
TNW is funded by a Senior Fellowship from the Wellcome Trust (091758). TNW thanks Dr Frederic B Piel for contributing Figure 4.
Chronic kidney disease as a global health burden: the need to integrate research and health policy
Chronic kidney disease (CKD) is increasingly acknowledged as a global public health problem, affecting 1 in 10 adults in most jurisdictions . CKD serves as a multiplier of risk in all populations and has a complex interface with other conditions (such as diabetes and cardiovascular disease). The prevalence of risk factors for CKD such as low birth-weight, obesity and hypertension is increasing, and when superimposed on environmental and genetic influences may serve to amplify the rising incidence of CKD over time. In addition, there are specific conditions (such as pregnancy, pre-eclampsia, and acute kidney injury); and specific environments (such as tropical regions, areas of poor sanitation) that may promote or attenuate the progression of CKD .
The Lancet publication of the Global Burden of Disease Study 2010 (GBD 2010) serves as important milestone in understanding of population health and disease in this century . The publication highlights the value and power of data to improve our understanding of health, its determinants, and the impact of strategies aimed at addressing specific health issues. Global changes in the incidence and prevalence of key NCDs will continue to impact the incidence of CKD. Further, CKD may influence global metrics of health such as years lived with disability (YLD), given the burden faced by both non-dialysis and dialysis CKD populations . In the GBD 2010 report, deaths due to diabetes increased by 20%, and due to chronic kidney disease by 15% between 1990 and 2010, so that both rose in the `league tables' of causes of death (15 to 9, and 27 to 18 respectively). This change in the relative burden of communicable and non-communicable diseases as drivers of mortality in most countries parallels the profound increase in the `lifestyle' driven risk factors . CKD now ranks 39 globally as a cause of YLD, while diabetes and ischemic heart disease rank 9 and 21 respectively. All of the conditions display regional variability, but note the YLDs due to CKD have increased by 20% since the 1990 report.
As infant mortality and mortality from communicable diseases are reduced in the developing world, the disability from NCDs will increase. Some of that disability will be driven by CKD and all of its consequences. Identifying and implementing proven strategies to address risk factors such as hypertension, obesity, and high salt intake will help to reduce the burden of CKD - as demonstrated in some parts of the world such as Asia .
Estimates of the economic burden of CKD vary depending on whether dialysis and transplant therapies are included or excluded. Regardless, it is clear that CKD is a key driver of the high costs associated with NCDs. One report, using provincial data in a Canadian province, described that of a cohort of patients with diabetes, cardiovascular disease and CKD, in various combinations: 18% of hospital costs were attributable to those with CKD either in isolation or combined with either DM or CVD. Thus of this high risk group comprising 7.5% of the total cluster, an annual $ 189M was spent. This study excluded those on dialysis or with transplants, and so is an underestimate of the entire burden . Others have estimated that while the end stage renal disease population (those on dialysis or transplantation) make up less than 1% of the total adult population, they consume up to 5% of national health care budgets .
The study and practice of nephrology has changed substantially over the last 50 years. Initially nephrology was a specialty characterized by detailed study of kidney physiology, but has evolved in parallel with availability of dialysis and kidney transplantation - which are no longer experimental treatments, but life-saving therapies that benefit hundreds of thousands of people worldwide. Advances in diagnostics, research and more integrated approaches to care have established CKD as a preventable and treatable chronic disease, with multiple co-morbidities that are directly and indirectly related to CKD. CKD has a dramatic impact on patients and their families - who must live with uncertainty, depression, and the symptoms of kidney disease. Since CKD is a global problem, different health systems, political environments and infrastructure have led to varied strategies and priorities around the world. As an international nephrology community, we recognize that sharing key discoveries, best practices and methodologies is the way forward.
Interventions such as certain drugs, exercise, combined specialty clinics and engagement of primary care and patients, have been studied and shown to improve patient outcomes. Administrative databases are used to understand the impact of CKD on health care systems and generate population-based estimates of disease burden. An increasing number of investigator-initiated randomized trials have begun to address fundamental questions about how best to care for CKD patients - how to prevent or delay kidney failure, when to commence dialysis treatment, how best to treat glomerulonephritis and to prevent rejection of transplanted kidneys. As in other medical researchers, kidney scientists are increasingly interested in new translational approaches to drug development, which may lead to the discovery of novel compounds.
A comprehensive investigative framework that includes four pillars of research (biomedical sciences, clinical research, health systems studies and population research) is the key to improving the outcomes for patients with CKD. The nephrology community has built on this framework to integrate clinical care and health policy with the CKD research agenda. There are multiple examples of teams where clinicians, investigators and administrators work together to improve understanding of the burden in different environments. As an example, there are provincial, national and international specific initiatives whereby researchers, administrators and clinicians collaboratively used data to inform decision making and track outcomes (for example, -). The CKD PC (Chronic Kidney Disease Prognosis Consortium) has established a rich resource, comprising over one million people with CKD in various stages . The data is collated from interventional trials, large cohort studies and administrative data sets, and as such covers the spectrum of CKD from high risk populations to established CKD populations. Through robust analysis of data, this international group of researchers has established estimates for the prognosis of major events, such cardiovascular disease, hospitalizations, infections, mortality and progression to end stage kidney disease; and recently provided evidence to support a new end point in clinical trials . The latter will facilitate testing of interventions.
Awareness of CKD in the global health arena will depend on continued efforts of the clinical and research communities. The research agenda for nephrology remains multifaceted: the support for basic science discoveries is essential to uncover novel targets and mechanisms to foster drug or therapeutic developments. Scaling up existing administrative, research and clinical databases (some of which have large bio-banking platforms) will optimize the design of clinical trials, and allow clinicians to target the highest risk individuals. New methods for setting research priorities, including the perspectives of administrators, health policy makers, patients and their families, along with practicing clinicians, remains critical. We need new studies that inform evidence-based public policy and assess how best to allocate scarce resources to optimize health outcomes. Finally, there is an increasing emphasis on evaluating the best methods for translation of research findings into practice, so that the science reliably benefits the patients.
CKD will continue to be a major public health problem for the foreseeable future, and the most rapid growth in disease burden will be in developing countries. To achieve a meaningful reduction in death and disability due to CKD, the global kidney research agenda must encompass and integrate basic, clinical, health outcome, and population health perspectives. The international nephrology community is committed to this engagement of patients, healthcare administrators and policymakers in the research agenda. The recognition of CKD as important in the global health and NCD agendas will improve our ability to continue progress and sustain focus on improving patient outcomes - across the continuum of kidney disease and its major risk factors.
Gout: an Old disease with New windows of opportunities
Jasvinder A. Singh (Figure 7).
Gout, a common inflammatory arthritis in adults caused by elevated levels of uric acid in the blood that lead to joint inflammation and other manifestations such as kidney stones, is a major public health burden worldwide . Recognized in 2640 B.C., and later described by Hippocrates as `the unwalkable disease', gout is one of the oldest known diseases. It is also a forgotten disease. However, in terms of its impact on patients, high prevalence, well-known pathophysiology and biochemical abnormality, and availability of cheap, affordable treatments, it's clearly a missed opportunity in medicine.
In the course of several diseases such as diabetes, cancer, rheumatoid arthritis and others, there is a single window of opportunity, where interventions in early disease can prevent future complications. In comparison, gout has several windows of opportunities throughout the disease course and amongst various aspects of the disease. The incidence and prevalence of gout seems to be increasing according to several epidemiological studies. The Rochester Epidemiology project (REP) showed a similar increase in the incidence of gout from 0.045% in 1977-1978 to 0.061% in 1995-1996 . A study in a health maintenance organization showed an almost doubling of prevalence of gout and/or hyperuricemia from 2% in 1990 to 4% in 1999 . A study based on National Health and Nutrition Survey (NHANES) also found that the prevalence of self-reported physician-diagnosis of gout increased from 2.7% in 1988-1994 to 3.9% in 2007-08 . Many of these opportunities may be missed, leading to an increased burden of gout in the face of neglected prospects for diagnosis and treatment.
First, physicians and patients need to update their knowledge regarding the dietary and lifestyle risk factors for gout in order to take advantage of these windows of opportunities. New information from well-designed epidemiological studies is available, which update our knowledge of the disease (based on clinical anecdotes) and confirm or refute previous prevalent beliefs about gout. Higher intake of meats, seafood, alcohol (in particular beer) and sugar-sweetened soft drinks (including fruit juices and sodas) increase the risk of gout, while low fat dairy products, Vitamin C supplements and coffee decrease the risk of gout (Figure 8). Importantly, purine-rich vegetables and nuts do not increase the risk of incident gout . A higher intake of purine-rich foods from animal sources (meats etc.) and alcohol increases the risk of gout flares ,. Since environmental factors play a big role in the risk of gout as well as risk of gout flares, they should be one of the main foci of gout management. Our recent work with patients shows that they are interested in discussing these options with their providers as part of their gout management ,. Physicians can counsel patients during their regular follow-up regarding strategies to prevent gout and in those with gout, ways to decrease the risk and suffering from gout flares. Therefore, this is one key area of opportunity for both physicians and patients.
Second is the challenge of correctly diagnosing gout. Gout manifests as intermittent monarticular acute arthritis in the early years/phase of the disease and as chronic polyarthritis with intermittent flares in the later years. Tophi and renal stones may accompany arthritis. The rates of joint fluid aspirate-proven diagnosis of gout are low. Given the common involvement of great toe and other lower extremity joints in two other common conditions, osteoarthritis and pseudogout, a presumptive diagnosis of gout based on a history of big toe pain and a borderline high or higher than normal range serum urate level is problematic (Figure 8). Documentation of additional clinical features of acute synovitis, radiographic signs of overhanging margin and punched-out erosions typical of gout, and close attention to looking for features of other differential diagnoses (osteoarthritis, pseudogout and rheumatoid arthritis), will often help in a correct diagnosis of gout. The 1977 American Rheumatism Association (ARA) preliminary criteria for classification of acute gouty arthritis are also commonly used for a clinical diagnosis of gout, but are inadequate for in-office diagnosis in about 21% of cases . Attempts should always be made to aspirate joint/bursa/tophus and confirm the diagnosis, since documentation of urate crystals in synovial fluid confirms gout as a single test and the treatment for gout is often life-long.
Third is the challenge of optimal control of serum urate. Urate-lowering therapy (ULT), including allopurinol and uricosurics are generic, affordable and the most commonly used drugs; febuxostat, a new ULT, is also available but is more expensive. ULT helps to lower serum urate levels, a central biochemical abnormality in gout. Current guidelines recommend achieving target serum urate of <6 mg/dl , which is achieved by at most 33% of patients -. This is a meaningful disease target since it is associated with improved clinical outcomes such as reduction in gout flares, regression of tophi and lower health care costs (Figure 8) -. Achievement of this serum urate target frequently requires titration of allopurinol dose, sometimes up to 900 mg/day , rather than a monotonic 300 mg/day dose . Physicians aiming to help gout patients avoid flares and improve function to reap the full benefits of treatment need to monitor serum urate after starting ULT and follow a treat-to-target approach. We believe that it is possible to achieve disease remission in many gout patients with this approach. This is a paradigm shift in gout treatment that is likely to improve patient outcomes. A patient-physician collaborative approach is essential for this to succeed.
We have summarized briefly a few opportunities for improving care and outcomes of gout, for which there are several additional opportunities for interventions not mentioned here. We are at the brink of new treatment options for gout, a better understanding of its impact on cardiovascular and renal disease, and better management with existing pharmacological and non-pharmacological treatment approaches. This is an exciting era in which we know ever more about this ancient disease.
JAS is supported by grants from the Agency for Health Quality and Research Center for Education and Research on Therapeutics (AHRQ CERTs) U19 HS021110, National Institute of Arthritis, Musculoskeletal and Skin Diseases (NIAMS) P50 AR060772 and U34 AR062891, National Institute of Aging (NIA) U01 AG018947, National Cancer Institute (NCI) U10 CA149950, and research contract CE-1304-6631 from the Patient Centered Outcomes Research Institute (PCORI). JAS is also supported by the resources and the use of facilities at the VA Medical Center at Birmingham, Alabama, USA. The funding sources (National Institutes of Health and others) had no role in study conception, protocol development, data analyses, manuscript preparation or decision to submit.
Asthma: a challenge for health care providers
Peter G. J. Burney (Figure 9).
Asthma is generally defined as a reversible obstruction of the airway and is one of the most common chronic conditions. Since the 1980s the term has come increasingly to signify any wheezy illness that responds to bronchodilators. Compared with other chronic lung diseases it starts much younger and because the mortality is relatively low and the disease tends to persist, it maintains a high prevalence in the population.
Asthma is generally divided into allergic and non-allergic. The relation of asthma to allergic sensitisation is complicated. Both sensitisation and atopic diseases such as asthma run in families, but they are not inherited in the same way ,. In childhood, asthma associated with allergies is more persistent and tends to be more severe. In adulthood `non-allergic' asthma tends to be more severe. In childhood allergies are less common in low income countries, as are the atopic conditions associated with allergies, but non-allergic wheeze is equally common in countries at all economic levels . The prevalence of allergic sensitisation has been increasing over the long term , though more recent changes in the prevalence of atopic conditions such as asthma have been more variable among children .
The International Study of Asthma and Allergies in Childhood (ISAAC) Study was the largest global survey of the prevalence of asthma, rhinitis and eczema involving almost 2,000,000 children in 105 countries. This study has shown very wide variations in the prevalence of wheezy illness, with very high rates in the English speaking countries and Latin America and wide variations even across single continents such as Europe, where rates fall from high levels in the northwest to low levels in the southeast . The prevalence of more severe disease has a different distribution, however, with a far higher proportion of cases being recorded as severe in sub-Saharan Africa in particular .
Information on adults is more sparse and comes from the European Community Respiratory Health Survey (ECRHS) and the World Health Survey . Although mean prevalence is least common in middle-income countries, the maximum prevalence recorded in the poorest countries is below the maximum prevalence in middle or high income countries. Sampling decisions need to inform the interpretation of all these studies. For instance, in low income countries there has been a consistent finding that asthma is less common in rural areas - and over sampling of urban populations may therefore inflate overall estimates in low income countries.
Asthma is not a common cause of death and age-standardised death rates fell by 42% between 1990 and 2010 from 9.0 to 5.2 per 100,000. However, the global number of deaths fell only 9% from 380,000 to 346,000 between 1990 and 2010 . The slower rate of decline in total deaths represents the aging of the population. Mortality from asthma increases markedly with age and with age some patients with asthma experience a marked decline in lung function . This will lead to an increasing problem for an ageing population whatever changes in prevalence occur. The burden associated with asthma is therefore likely to increase both because of continuing urbanisation in the poorer countries and because of the ageing of the population everywhere.
Currently there is wide variation in the relative impact of asthma on mortality. Although asthma ranks as only the 42nd most common cause of death globally, it is much more highly ranked in Oceania (13th), South East Asia (25th), South Asia (26th) and North Africa and the Middle East (30th) than in Southern and Andean (65th and 62nd) Latin America and Western Europe (60th).
Because asthma often has an early onset and is persistent throughout life, it is a relatively important cause of disability adjusted life years lost (DALYs), ranking 28th globally among the causes of DALYs but 8th in Oceania, 15th in Australasia and Tropical Latin America, 18th is South East Asia and 19th in the Caribbean .
The chronic nature of asthma requires continuous care and reliable access to affordable medications. These conditions have been set out by the Global Initiative for Asthma (GINA)  together with the need to prevent exacerbations with the use, in the first instance, of inhaled corticosteroids. However the costs and availability of inhaled steroids are very variable and there is a tendency for these to cost more in low income countries . This leads to poor management and reliance on emergency rooms to provide care, a wasteful and less effective method of managing the condition. In a survey of treatment failures seen in emergency rooms in 11 countries, patients with inadequate insurance and those without a consistent source of continuing medical care were less likely to be on the recommended dose of inhaled steroids. In addition, those without adequate steroid use were more likely to have lost work because of asthma in the recent past , demonstrating the high cost to patients and their families of inappropriate care.
Asthma is a common condition that causes considerable morbidity and with increasing age leads to a disease that is more difficult to manage, along with increasing mortality. Although it is mostly not difficult to manage, along with other chronic conditions it requires continuous care, which traditional health services are not designed to provide. Currently the problem of inadequate health services is compounded by a poor supply of over-priced medications. These problems are shared by other chronic conditions and have common solutions including the provision of continuous long-term care and reliable access to affordable, high-quality medication.
Liver cirrhosis - time for addressing a neglected non-communicable chronic disease
Jürgen Rehm (Figure 10).
Liver cirrhosis is an abnormal condition with irreversible scarring as a result of continuous and long-term liver damage, which is primarily caused by excessive alcohol consumption, hepatitis, and non-alcoholic steatohepatitis. It is among the top 15 causes of death globally and, in 2012, was estimated to have caused more than 1,000,000 deaths and more than 36,000,000 years of lives lost to either premature death or disability.
Global death rates due to liver cirrhosis seem to have been quite stable over the years: the World Health Organization (WHO) estimated and predicted 14.5 deaths per 100,000 for the years 2000 and 2030, respectively, with almost no variation for years in between ,. However, when standardized rates are considered, liver cirrhosis deaths are predicted to decrease.
There are several factors that may become important to explain trends for liver cirrhosis. A downward trend in high income countries may be predicted to be linked to improved clinical practices leading to lower case fatality rates ,, although there is not much evidence on this, and, to give just one example, historically, case fatality rates have not shown any improvement over the time period between 1968 and 1999 in England . An upward trend may be linked to increases in alcohol consumption in low- and mid-income countries as they increase their economic wealth . In terms of burden of disease, most DALYs were derived from years of life lost to mortality, that is, due to the high case fatality. However, as indicated above, this may constitute an underestimate for high-income countries due to the lower case fatality and thus higher duration of living with disability.
While the overall prevalence of liver cirrhosis mortality and burden of disease seems stable, there are huge variations by gender, age and regions , and they seem to be caused by preventable risk factors. Men have considerably higher rates of liver cirrhosis morality and burden of disease, globally more than twofold the rates of women, and highest in the men between 50 and 69 years of age. The only exception for the higher prevalence of liver cirrhosis mortality and burden is the Eastern Mediterranean region, where women have slightly higher rates; this region also has by far the lowest alcohol consumption , which is the main risk factor for liver cirrhosis.
Figure 11 gives an overview of the burden of disease of liver cirrhosis for the year 2012 in DALYs by WHO region, and the role of alcohol in causing this disease (data based on ,). As indicated above, alcohol consumption is globally the most important risk factor for liver cirrhosis, responsible for about half of the global burden (50%; men: 53%; women: 44%; ); other main global risk factors are hepatitis B and C, and obesity ,. Europe, especially the Eastern European region, has the highest rate of liver cirrhosis, with alcohol consumption a large factor (63%). For low- and mid-income countries, hepatitis-induced liver cirrhosis is relatively more important, with the relative impact differential between high income and other countries being largest for hepatitis B ,.
The role of alcohol consumption in causing and worsening the course of liver cirrhosis has been evident on the individual level  and on the aggregate level in comparisons between countries , or in analyses over time . It is important to understand that alcohol consumption increases the risk of mortality for all kinds of liver cirrhosis, independent of the original aetiology (3), and thus abstinence is the major goal in most guidelines for treatment of liver cirrhosis.
Intervention studies show that a reduction of alcohol consumption via policy interventions resulted in a marked reduction of liver cirrhosis (for example in Russia ,). Although liver cirrhosis is a chronic disease, interventions have immediate effects, as not only shown by the Russian experiences cited above, but also for instance by the impact of the German seizures of alcohol on French mortality rates during World War II, or the impact of prohibition in the US ,,). It may take up to 20 years, however, before all of the effects of interventions can be seen .
A sizable portion of liver cirrhosis mortality could be reduced in the first year after implementing effective interventions to reduce alcohol, such as higher taxation, decreased availability, advertisement and marketing bans or brief interventions and treatment ,, especially among heavy drinkers ,. The effect is more pronounced for heavy drinkers because the risk curve for mortality is exponential; that is, relatively more mortality can be avoided for the same amount of reduction in average drinking for heavy drinkers compared to light or moderate drinkers ,. Such interventions would not only reduce liver cirrhosis rates but also other causes of mortality such as other non-communicable diseases (cancers, hypertensive heart disease, stroke, pancreatitis) or injuries ,,,. Given this situation, and given the fact that there are proven effective interventions to reduce alcohol consumption, we see no reason why global liver cirrhosis rates should continue to be as high as they are now.
I would like to thank Drs. Gretchen Stevens, Michael Livingstone and Robin Room, who provided important information for this article.
Substance use disorders: implications for global health
Substance use disorders (SUD) associated with legal substances are two of the three leading contributing factors for global burden of disease and injury (DALYs for tobacco: 6.3%; for alcohol: 5.5%)  and those associated with illicit substances are within the top twenty factors (DALYs 0.8%) . The past 20 years has seen an increase in the contribution of SUD to the global burden of disease, mostly from alcohol (32%) and illicit drugs (57%) . Moreover, the global burden of disease attributable to SUD is likely to be underestimated particularly for illicit substances due to incomplete epidemiological data on estimates of impactful and preventable outcomes (i.e. injuries, violence and mental health problems) . Thus, SUV prevention and treatment would have a major impact in improving public health globally.
The recent endorsement by the United Nations Office on Drugs and Crime (UNODC) of addiction as a brain disease and the recommendation that it should be treated as a medical and public health issue rather than a criminal justice and or moral issue highlights the role that the healthcare system can play in the prevention and treatment of SUD . The conceptualization of addiction as a brain disease reflects in part findings from brain imaging studies and preclinical research that have identified the brain circuits that are disrupted by drugs (legal and illegal) and how their disruption impairs the addicted individual's ability to control his/her behaviour . Moreover, excessive drug and alcohol use in adolescence impairs executive function and increases the vulnerability to SUDs in adulthood. Clinical studies have also shown that SUD can be prevented and treated, and like other chronic diseases requires continuity of care . Because all countries have health care infrastructure, it is recommended that these healthcare systems integrate treatment of SUD within the system norms. Drug associated health consequences are still some of the main preventable causes of disability and the healthcare system can play a crucial role in their prevention and treatment. This recommendation provides a platform that is relevant and available to countries with different levels of economic development.
Health care systems can participate at all levels in the severity range of SUD, starting from its prevention to serving as a referral for specialized care for the most severe cases. Health care systems can also maximize the opportunity to integrate the care for the health problems associated with SUD. Of particular importance is the management of mental illnesses, since they are frequently co-morbid with SUD, and inappropriate management of either condition exacerbates the other. Similarly, integrated care is fundamental for the treatment of infectious diseases such as HIV and HCV for which substance abusers are at higher risk and for which compliance with medical treatment of the infectious disease requires parallel treatment of the SUD. In addition, SUD is the main underlying cause of vehicle accidents. Therefore, integrated care will also facilitate addressing this factor, for if untreated the alcoholic or drug abuser will continue to contribute to repeated incidents. Moreover, in these times of increasing health care costs and burden, treating SUD's would translate into significant savings in the need to treat the secondary health costs of SUD.
The challenges in implementing healthcare involvement in SUD management are complex and will vary among countries on the basis of their economic resources, cultural norms, drug availability and policies towards criminalization and legalization of drugs. This is further compounded by rapid changes in the use of drugs across the world, such as movements towards legalization of marijuana, recent access to electronic drug delivery devices, rapid dissemination of new synthetic drugs and the increased abuse of prescription medications. The opportunities that the healthcare system offers towards the control of SUD highlight the urgent need for educating health care providers in the screening and management of SUD and the need to allocate the resources necessary for its implementation.
Placing dementia in the NCDs prevention strategies
Cleusa P. Ferri (Figure 14).
Dementia is a syndrome that usually involves with loss of memory, reasoning, and other cognitive functions progressively impairing an individual's everyday functioning. The main risk factor for dementia is age, with prevalence roughly doubling every 5 years over the age of 65. Older people are likely to have multiple health conditions. Dementia however, has a disproportionate impact on independent living, being a major cause of disability and dependence , among older people. With the rapid ageing of the population worldwide, the number of people with dementia is predicted to rise. It is estimated that in 2010 there were 35.6 million people with dementia, and predictions based on population ageing show that this figure is likely to double every 20 years, reaching 115.4 million by 2050 . Most people with dementia already live in low- and middle-income countries (LMIC) and these same estimates predict that by 2050 more than 70% of people with dementia will be living in these countries .
It has been estimated that the total worldwide cost of dementia was US$604 billion in 2010 . While most of these costs are concentrated in high income countries, where the costs are divided roughly equally between formal (hospital and social) and informal (family) care settings, in low- and middle-income countries, informal care costs account for the vast majority of total costs , with the burden concentrated on families and informal carers. Formal costs are likely to increase in these countries, not only due to the increasing numbers of people with dementia in the future, but also because of a shift in the balance between informal and formal care as the health care sectors develops in LMIC.
Future estimates are mostly based on population ageing and include the assumption that age-specific prevalence will be stable over time. However, some recent studies have suggested that over the past 20 to 30 years there has been a decline in the predicted burden of dementia in high-income countries -. In the UK, for example, a recent study  indicates a reduction in dementia prevalence of around 20% over a 20-year period (from 1989-1994 to 2008-11). These reductions suggest that predicted dementia cases were perhaps avoided or delayed by changes in the risk factors for dementia at earlier ages, suggesting that these risks are modifiable and dementia, to some extent, can be prevented or, at least, the risk reduced at particular ages.
One possible explanation for the reduction in dementia is the change in cardiovascular diseases and risk factors. There is growing evidence supporting a strong and likely causal association between cardiovascular disease (CVD) and its risk factors, and dementia . Therefore, the changes seen regarding the reduction in dementia prevalence are likely partially due to improvements in service provision and disease management of CVD, and also to changes in behaviour, with around half of the reduction in morbidity and mortality thought to be accounted for by primary prevention. However, current models to estimate the impact of preventive strategies on future vascular diseases do not consider the impact on dementia. Some non-communicable diseases (NCDs), such as cardiovascular diseases, are risk factors for dementia and many risk and protective factors for dementia are the same as those for other NCDs . However, most countries' policies and prevention strategies for NCDs do not include the prevention, or reduction of risk, of dementia, despite some recent initiatives .
In low-, middle- and high-income countries, dementia can be seen as part of normal ageing. Although dementia is indeed common in the oldest age groups, it is not an inevitable consequence of long lifespans. Increasing awareness of dementia in society as whole, from patients to policy/decision makers, can contribute not only to decreasing stigma and increasing community solidarity, but also to improving the capacity of existing services with evidence based approaches that can meet the needs of older people and those with dementia. It is important to note that awareness campaigns need to be carried out with great care in order to avoid raising expectations that cannot be met, and avoid leading to unintended consequences, such as increased stigma and fear, through use of dramatic imagery and language.
Dementia costs to individuals, families and society as a whole will grow as the number of people with dementia increases, and this will have an even greater impact on LMIC, which have fewer resources and where population ageing is happening faster than in rich countries. Dementia should be on the public health agenda of each country, with careful consideration given to each country's demographic and sociocultural context, including their own stage of the unfolding demographic and health transitions. The impact of change to risk factor profiles in countries is difficult to predict. However, models looking at the relative impact of primary prevention in comparison to approaches focused more on secondary prevention suggest that up-stream primary prevention is likely to be the cheapest and most efficient way to decrease the burden of dementia for future generations -, reducing the need for costly screening and treatment regimens for established disease. It is important to strengthen the evidence on the effectiveness of dementia prevention programmes, including their timescales, and also to ensure that dementia takes its place in NCD policies and prevention strategies.
Conflict of interest
Cleusa Ferri has been named as a local principal investigator in an upcoming trial sponsored by Merck.
Murray CJ, Ezzati M, Flaxman AD, Lim S, Lozano R, Michaud C, Naghavi M, Salomon JA, Shibuya K, Vos T, Wikler D, Lopez AD: GBD 2010: design, definitions, and metrics. Lancet. 2012, 380: 2063-2066. 10.1016/S0140-6736(12)61899-6.
Peto R, Lopez AD: The future worldwide health effects of current smoking patterns. Tobacco and Public Health: Science and Policy. Edited by: Boyle P, Gray N, Henningfield J, Safrin J, Zatonski W. 2004, Oxford University Press, Oxford, 281-286.
Murray CJ, Lopez AD: Measuring the global burden of disease. N Engl J Med. 2013, 369: 448-457. 10.1056/NEJMra1201534.
Grosse SD OI, Atrash HK, Amendah D, Piel FB, Williams TN: Sickle cell disease in Africa: a neglected cause of early child mortality. Am J Prev Med. 2011, 41 (6 Suppl 4): S398-405. 10.1016/j.amepre.2011.09.013.
Rees DC, Williams TN, Gladwin MT: Sickle-cell disease. Lancet. 2010, 376: 2018-2031. 10.1016/S0140-6736(10)61029-X.
United Nations press office. Press conference on raising awareness of sickle-cell anaemia: , [http://www.un.org/News/briefings/docs/2009/090619_Anaemia.doc.htm]
World Health Organization Regional Office for Africa: Sickle-cell disease: a strategy for the WHO African Region. Report of the Regional Director. AFR/RC60/8. 2010.
Piel FB, Patil AP, Howes RE, Nyangiri OA, Gething PW, Williams TN, Weatherall DJ, Hay SI: Global distribution of the sickle cell gene and geographical confirmation of the malaria hypothesis.Nat Commun 2010, 1:104..
Lim SS, Vos T, Flaxman AD, Danaei G, Shibuya K, Adair-Rohani H, Amann M, Anderson HR, Andrews KG, Aryee M, Atkinson C, Bacchus LJ, Bahalim AN, Balakrishnan K, Balmes J, Barker-Collo S, Baxter A, Bell ML, Blore JD, Blyth F, Bonner C, Borges G, Bourne R, Boussinesq M, Brauer M, Brooks P, Bruce NG, Brunekreef B, Bryan-Hancock C, Bucello C, et al: A comparative risk assessment of burden of disease and injury attributable to 67 risk factors and risk factor clusters in 21 regions, 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet. 2012, 380: 2224-2260. 10.1016/S0140-6736(12)61766-8.
Ndila C, Bauni E, Nyirongo V, Mochamah G, Makazi A, Kosgei P, Nyutu G, Macharia A, Kapesa S, Byass P, Williams TN: Verbal autopsy as a tool for identifying children dying of sickle cell disease: a validation study conducted in Kilifi district, Kenya.BMC Med 2014, 12:65..
Piel FB, Hay SI, Gupta S, Weatherall DJ, Williams TN: Global burden of sickle cell anaemia in children under five, 2010-2050: modelling based on demographics, excess mortality, and interventions.Plos Med 2013, 10:e1001484..
Piel FB, Patil AP, Howes RE, Nyangiri OA, Gething PW, Dewi M, Temperley WH, Williams TN, Weatherall DJ, Hay SI: Global epidemiology of sickle haemoglobin in neonates: a contemporary geostatistical model-based map and population estimates. Lancet. 2013, 381 (9861): 142-151. 10.1016/S0140-6736(12)61229-X.
Murray CJ, Vos T, Lozano R, Naghavi M, Flaxman AD, Michaud C, Ezzati M, Shibuya K, Salomon JA, Abdalla S, Aboyans V, Abraham J, Ackerman I, Aggarwal R, Ahn SY, Ali MK, Alvarado M, Anderson HR, Anderson LM, Andrews KG, Atkinson C, Baddour LM, Bahalim AN, Barker-Collo S, Barrero LH, Bartels DH, Basanez MG, Baxter A, Bell ML, Benjamin EJ, et al: Disability-adjusted life years (DALYs) for 291 diseases and injuries in 21 regions, 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet. 2012, 380: 2197-2223. 10.1016/S0140-6736(12)61689-4.
Vos T, Flaxman AD, Naghavi M, Lozano R, Michaud C, Ezzati M, Shibuya K, Salomon JA, Abdalla S, Aboyans V, Abraham J, Ackerman I, Aggarwal R, Ahn SY, Ali MK, Alvarado M, Anderson HR, Anderson LM, Andrews KG, Atkinson C, Baddour LM, Bahalim AN, Barker-Collo S, Barrero LH, Bartels DH, Basanez MG, Baxter A, Bell ML, Benjamin EJ, Bennett D, et al: Years lived with disability (YLDs) for 1160 sequelae of 289 diseases and injuries 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet. 2012, 380: 2163-2196. 10.1016/S0140-6736(12)61729-2.
Telfer P, Coen P, Chakravorty S, Wilkey O, Evans J, Newell H, Smalling B, Amos R, Stephens A, Rogers D, Kirkham F: Clinical outcomes in children with sickle cell disease living in England: a neonatal cohort in East London. Haematologica. 2007, 92: 905-912. 10.3324/haematol.10937.
Quinn CT, Rogers ZR, McCavit TL, Buchanan GR: Improved survival of children and adolescents with sickle cell disease. Blood. 2010, 115: 3447-3452. 10.1182/blood-2009-07-233700.
Wierenga KJ, Hambleton IR, Lewis NA: Survival estimates for patients with homozygous sickle-cell disease in Jamaica: a clinic-based population study. Lancet. 2001, 357: 680-683. 10.1016/S0140-6736(00)04132-5.
Ware RE: Is sickle cell anemia a neglected tropical disease?PLoS Negl Trop Dis 2013, 7:e2120..
Amendah DD, Mukamah G, Komba A, Ndila C, Williams TN: Routine paediatric sickle cell disease (SCD) outpatient care in a rural Kenyan hospital: utilization and costs.PLoS One 2013, 8:e61130..
Coresh J, Selvin E, Stevens LA, Manzi J, Kusek JW, Eggers P, Van Lente F, Levey AS: Prevalence of chronic kidney disease in the United States. JAMA. 2007, 298: 2038-2047. 10.1001/jama.298.17.2038.
Jha V, Garcia-Garcia G, Iseki K, Li Z, Naicker S, Plattner B, Saran R, Wang AY, Yang CW: Chronic kidney disease: global dimension and perspectives. Lancet. 2013, 382: 260-272. 10.1016/S0140-6736(13)60687-X.
Lozano R, Naghavi M, Foreman K, Lim S, Shibuya K, Aboyans V, Abraham J, Adair T, Aggarwal R, Ahn SY, Alvarado M, Anderson HR, Anderson LM, Andrews KG, Atkinson C, Baddour LM, Barker-Collo S, Bartels DH, Bell ML, Benjamin EJ, Bennett D, Bhalla K, Bikbov B, Bin Abdulhak A, Birbeck G, Blyth F, Bolliger I, Boufous S, Bucello C, Burch M, et al: Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet. 2012, 380: 2095-2128. 10.1016/S0140-6736(12)61728-0.
Levin A, Chaudhry MR, Djurdjev O, Beaulieu M, Komenda P: Diabetes, kidney disease and cardiovascular disease patients. Assessing care of complex patients using outpatient testing and visits: additional metrics by which to evaluate health care system functioning. Nephrol Dial Transplant. 2009, 24: 2714-2720. 10.1093/ndt/gfp180.
Manns BJ, Mendelssohn DC, Taub KJ: The economics of end-stage renal disease care in Canada: incentives and impact on delivery of care. Int J Health Care Finance Econ. 2007, 7: 149-169. 10.1007/s10754-007-9022-y.
Alberta Kidney Disease Network:., [www.AKDN.info]
The BC Renal Agency:., [www.bcrenalagency.ca]
Advancing Kidney Care and Research in Canada: Available at: ., [http://www.cann-net.ca/]
Matsushita K, Ballew SH, Astor BC, Jong PE, Gansevoort RT, Hemmelgarn BR, Levey AS, Levin A, Wen CP, Woodward M, Coresh J: Cohort profile: the Chronic Kidney Disease Prognosis Consortium. Int J Epidemiol. 2013, 42: 1660-1668. 10.1093/ije/dys173.
Coresh J, Turin TC, Matsushita K, Sang Y, Ballew SH, Appel LJ, Arima H, Chadban SJ, Cirillo M, Djurdjev O, Green JA, Heine GH, Inker LA, Irie F, Ishani A, Ix JH, Kovesdy CP, Marks A, Ohkubo T, Shalev V, Shankar A, Wen CP, de Jong PE, Iseki K, Stengel B, Gansevoort RT, Levey AS, Consortium CKDP: Decline in estimated glomerular filtration rate and subsequent risk of end-stage renal disease and mortality. JAMA. 2014, 311: 2518-2531. 10.1001/jama.2014.6634.
Smith E, Hoy D, Cross M, Merriman TR, Vos T, Buchbinder R, Woolf A, March L: The global burden of gout: estimates from the Global Burden of Disease 2010 study.Ann Rheum Dis 2014,.
Arromdee E, Michet CJ, Crowson CS, O'Fallon WM, Gabriel SE: Epidemiology of gout: is the incidence rising?. J Rheumatol. 2002, 29: 2403-2406.
Wallace KL, Riedel AA, Joseph-Ridge N, Wortmann R: Increasing prevalence of gout and hyperuricemia over 10 years among older adults in a managed care population. J Rheumatol. 2004, 31: 1582-1587.
Zhu Y, Pandya BJ, Choi HK: Prevalence of gout and hyperuricemia in the US general population: the National Health and Nutrition Examination Survey 2007-2008. Arthritis Rheum. 2011, 63: 3136-3141. 10.1002/art.30520.
Choi HK: A prescription for lifestyle change in patients with hyperuricemia and gout. Curr Opin Rheumatol. 2010, 22: 165-172. 10.1097/BOR.0b013e328335ef38.
Zhang Y, Chen C, Choi H, Chaisson C, Hunter D, Niu J, Neogi T: Purine-rich foods intake and recurrent gout attacks. Ann Rheum Dis. 2012, 71: 1448-1453. 10.1136/annrheumdis-2011-201215.
Zhang Y, Woods R, Chaisson CE, Neogi T, Niu J, McAlindon TE, Hunter D: Alcohol consumption as a trigger of recurrent gout attacks.Am J Med 2006, 119:800. e813-808..
Singh JA: Research priorities in gout: the patient perspective. J Rheumatol. 2014, 41: 615-616. 10.3899/jrheum.131258.
Singh JA: The Impact of Gout on Patient's Lives and Differences by Gender and Race: A Patient Perspective.Arthritis Res Ther 2014,.
Malik A, Schumacher HR, Dinnella JE, Clayburne GM: Clinical diagnostic criteria for gout: comparison with the gold standard of synovial fluid crystal analysis. J Clin Rheumatol. 2009, 15: 22-24. 10.1097/RHU.0b013e3181945b79.
Khanna D, Fitzgerald JD, Khanna PP, Bae S, Singh MK, Neogi T, Pillinger MH, Merill J, Lee S, Prakash S, Kaldas M, Gogia M, Perez-Ruiz F, Taylor W, Liote F, Choi H, Singh JA, Dalbeth N, Kaplan S, Niyyar V, Jones D, Yarows SA, Roessler B, Kerr G, King C, Levy G, Furst DE, Edwards NL, Mandell B, Schumacher HR, et al: 2012 American College of Rheumatology guidelines for management of gout. Part 1: systematic nonpharmacologic and pharmacologic therapeutic approaches to hyperuricemia. Arthritis Care Res. 2012, 64: 1431-1446. 10.1002/acr.21772.
Dalbeth N, House ME, Horne A, Petrie KJ, McQueen FM, Taylor WJ: Prescription and dosing of urate-lowering therapy, rather than patient behaviours, are the key modifiable factors associated with targeting serum urate in gout.BMC Musculoskelet Disord 2012, 13:174..
Sarawate CA, Patel PA, Schumacher HR, Yang W, Brewer KK, Bakst AW: Serum urate levels and gout flares: analysis from managed care data. J Clin Rheumatol. 2006, 12: 61-65. 10.1097/01.rhu.0000209882.50228.9f.
Singh JA, Hodges JS, Asch SM: Opportunities for improving medication use and monitoring in gout. Ann Rheum Dis. 2009, 68: 1265-1270. 10.1136/ard.2008.092619.
Becker MA, Schumacher HR, MacDonald PA, Lloyd E, Lademacher C: Clinical efficacy and safety of successful longterm urate lowering with febuxostat or allopurinol in subjects with gout. J Rheumatol. 2009, 36: 1273-1282. 10.3899/jrheum.080814.
Halpern R, Fuldeore MJ, Mody RR, Patel PA, Mikuls TR: The effect of serum urate on gout flares and their associated costs: an administrative claims analysis. J Clin Rheumatol. 2009, 15: 3-7. 10.1097/RHU.0b013e3181945d2c.
Shoji A, Yamanaka H, Kamatani N: A retrospective study of the relationship between serum urate level and recurrent attacks of gouty arthritis: evidence for reduction of recurrent gouty arthritis with antihyperuricemic therapy. Arthritis Rheum. 2004, 51: 321-325. 10.1002/art.20405.
Product Information. Zylorim™ (Allopurinol) tablets:., [http://www.aspenpharma.com.au/product_info/pi/PI_Zyloprim.pdf]
Stamp LK, O'Donnell JL, Zhang M, James J, Frampton C, Barclay ML, Chapman PT: Using allopurinol above the dose based on creatinine clearance is effective and safe in patients with chronic gout, including those with renal impairment. Arthritis Rheum. 2011, 63: 412-421. 10.1002/art.30119.
Longo G, Strinati R, Poli F, Fumi F: Genetic factors in nonspecific bronchial hyperreactivity. An epidemiologic study. Am J Dis Child. 1987, 141: 331-334. 10.1001/archpedi.1987.04460030109037.
Sibbald B: T-WM: Factors influencing the prevalence of asthma among first degree relatives of extrinsic and intrinsic asthmatics. Thorax. 1979, 34: 332-337. 10.1136/thx.34.3.332.
Weinmayr G, Weiland SK, Bjorksten B, Brunekreef B, Buchele G, Cookson WO, Garcia-Marcos L, Gotua M, Gratziou C, van Hage M, von Mutius E, Riikjarv MA, Rzehak P, Stein RT, Strachan DP, Tsanakas J, Wickens K, Wong GW, Group IPTS: Atopic sensitization and the international variation of asthma symptom prevalence in children. Am J Respir Crit Care Med. 2007, 176: 565-574. 10.1164/rccm.200607-994OC.
Law MMJ, Wald N, Luczynska C, Burney P: Changes in atopy over a quarter of a century, based on cross sectional data at three time periods. BMJ. 2005, 330: 1187-1188. 10.1136/bmj.38435.582975.AE.
Asher MI, Montefort S, Bjorksten B, Lai CK, Strachan DP, Weiland SK, Williams H, Group IPTS: Worldwide time trends in the prevalence of symptoms of asthma, allergic rhinoconjunctivitis, and eczema in childhood: ISAAC Phases One and Three repeat multicountry cross-sectional surveys. Lancet. 2006, 368: 733-743. 10.1016/S0140-6736(06)69283-0.
Asher MI, Pattemore PK, Harrison AC, Mitchell EA, Rea HH, Stewart AW, Woolcock AJ: International comparison of the prevalence of asthma symptoms and bronchial hyperresponsiveness. Am Rev Respir Dis. 1988, 138: 524-529. 10.1164/ajrccm/138.3.524.
Lai CK, Beasley R, Crane J, Foliaki S, Shah J, Weiland S: Global variation in the prevalence and severity of asthma symptoms: phase three of the International Study of Asthma and Allergies in Childhood (ISAAC). Thorax. 2009, 64: 476-483. 10.1136/thx.2008.106609.
Sembajwe G, Cifuentes M, Tak SW, Kriebel D, Gore R, Punnett L: National income, self-reported wheezing and asthma diagnosis from the World Health Survey. Eur Respir J. 2010, 35: 279-286. 10.1183/09031936.00027509.
Van Niekerk CH, Weinberg EG, Shore SC, Heese HV, Van Schalkwyk J: Prevalence of asthma: a comparative study of urban and rural Xhosa children. Clin Allergy. 1979, 9: 319-314. 10.1111/j.1365-2222.1979.tb02489.x.
Keeley DJ, Neill P, Gallivan S: Comparison of the prevalence of reversible airways obstruction in rural and urban Zimbabwean children. Thorax. 1991, 46: 549-553. 10.1136/thx.46.8.549.
Calvert J, Burney P: Ascaris, atopy, and exercise-induced bronchoconstriction in rural and urban South African children. J Allergy Clin Immunol. 2010, 125: 100-105. 10.1016/j.jaci.2009.09.010. e101-105
Obaseki D, Potts J, Joos G, Baelum J, Haahtela T, Ahlstrom M, Matricardi P, Kramer U, Gjomarkaj M, Fokkens W, Makowska J, Todo-Bom A, Toren K, Janson C, Dahlen SE, Forsberg B, Jarvis D, Howarth P, Brozek G, Minov J, Bachert C, Burney P: The relation of airway obstruction to asthma, chronic rhinosinusitis and age: results from a population survey of adults. Allergy. 2014, 69: 1205-1214. 10.1111/all.12447.
Asthma GGIf: Available at:. Accessed 6/20, 2014., [http://www.ginasthma.org/]
Ait-Khaled NED, Bissell K, Billo NE: Access to inhaled corticosteroids is key to improving quality of care for asthma in developing countries. Allergy. 2007, 62: 230-236. 10.1111/j.1398-9995.2007.01326.x.
Burney P, Potts J, Ait-Khaled N, Sepulveda RM, Zidouni N, Benali R, Jerray M, Musa OA, El-Sony A, Behbehani N, El-Sharif N, Mohammad Y, Khouri A, Paralija B, Eiser N, Fitzgerald M, Abu-Laban R: A multinational study of treatment failures in asthma management. Int J Tuberc Lung Dis. 2008, 12: 13-18.
WHO causes of death 2000 - 2011:., [http://www.who.int/healthinfo/global_burden_disease/estimates_regional/en/]
WHO projections for 2015 and 2030:., [http://www.who.int/healthinfo/global_burden_disease/projections/en/]
Talwalkar JA, Kamath PS: Influence of recent advances in medical management on clinical outcomes of cirrhosis. Mayo Clin Proc. 2005, 80: 1501-1508. 10.4065/80.11.1501.
Liang W, Chikritzhs T, Pascal R, Binns CW: Mortality rate of alcoholic liver disease and risk of hospitalization for alcoholic liver cirrhosis, alcoholic hepatitis and alcoholic liver failure in Australia between 1993 and 2005. Intern Med. 2011, 41: 34-41. 10.1111/j.1445-5994.2010.02279.x.
Roberts SE, Goldacre MJ, Yeates D: Trends in mortality after hospital admission for liver cirrhosis in an English population from 1968 to 1999. Gut. 2005, 54: 1615-1621. 10.1136/gut.2004.058636.
Schmidt LA, Mäkelä P, Rehm J, Room R: Alcohol: equity and social determinants. Equity, Social Determinants and Public Health Programmes. Edited by: Blas E, Kurup AS. 2010, World Health Organization, Geneva, Switzerland, 11-29.
Rehm J, Samokhvalov AV, Shield KD: Global burden of alcoholic liver diseases. J Hepatol. 2013, 59: 160-168. 10.1016/j.jhep.2013.03.007.
Global status report on alcohol and health. 2014, World Health Organization, Geneva, Switzerland
Rehm J, Taylor B, Mohapatra S, Irving H, Baliunas D, Patra J, Roerecke M: Alcohol as a risk factor for liver cirrhosis - a systematic review and meta-analysis. Drug Alcohol Rev. 2010, 29: 437-445. 10.1111/j.1465-3362.2009.00153.x.
Vernon G, Baranova A, Younossi ZM: Systematic review: the epidemiology and natural history of non-alcoholic fatty liver disease and non-alcoholic steatohepatitis in adults. Aliment Pharmacol Ther. 2011, 34: 274-285. 10.1111/j.1365-2036.2011.04724.x.
Perz JF, Armstrong GL, Farrington LA, Hutin YJF, Bell BP: The contributions of hepatitis B virus and hepatitis C virus infections to cirrhosis and primary liver cancer worldwide.J Hepatol 2006, 45:.
Zatonski W, Sulkowska U, Manczuk M, Rehm J, Lowenfels AB, La Vecchia C: Liver cirrhosis mortality in Europe, with special attention to central and eastern Europe. Eur Addict Res. 2010, 16: 193-201. 10.1159/000317248.
Ye Y, Kerr WC: Alcohol and liver cirrhosis mortality in the United States: comparison of methods for the analyses of time-seriespanel data models. Alcohol Clin Exp Res. 2011, 35: 108-115. 10.1111/j.1530-0277.2010.01327.x.
Leon DA, Chenet L, Shkolnikov V, Zakharov S, Shapiro J, Rakhmanova G, Vassin S, McKee M: Huge variation in Russian mortality rates 1984-1994: artefact, alcohol, or what?. Lancet. 1997, 350: 383-388. 10.1016/S0140-6736(97)03360-6.
Pridemore WA, Chamlin MB, Kaylen MT, Andreev E: The effects of the, Russian alcohol policy on alcohol-related mortality: an interrupted time series analysis. Alcohol Clin Exp Res. 2006, 2014: 257-266.
Fillmore KM, Roizen R, Farrell M, Kerr W, Lemmens P: Wartime Paris, cirrhosis mortality, and the ceteris paribus assumption. J Stud Alcohol. 2002, 63: 436-446.
Dills AK, Miron JA: Alcohol prohibition and Cirrhosis. Am L & Econ Rev. 2004, 6: 285-318. 10.1093/aler/ahh003.
Holmes J, Meier PS, Booth A, Guo Y, Brennan A: The temporal relationship between per capita alcohol consumption and harm: a systematic review of time lag specifications in aggregate time series analyses. Drug Alcohol Depend. 2012, 123: 7-14. 10.1016/j.drugalcdep.2011.12.005.
Babor T, Caetano R, Casswell S, Edwards G, Giesbrecht N, Graham K, Grube J, Gruenewald P, Hill L, Holder H, Homel R, Livingston M, Österberg E, Rehm J, Room R, Rossow I: Alcohol: No ordinary commodity. Research and public policy. 2nd edition. 2010, Oxford University Press, Oxford and London
Rehm J, Shield KD, Rehm MX, Gmel G, Frick U: Modelling the impact of alcohol dependence on mortality burden and the effect of available treatment interventions in the European Union. Eur Neuropsychopharmacol. 2013, 23: 89-97. 10.1016/j.euroneuro.2012.08.001.
Rehm J, Roerecke M: Reduction of drinking in problem drinkers and all-cause mortality. Alcohol Alcohol. 2013, 48: 509-513. 10.1093/alcalc/agt021.
Nutt DJ, Rehm J: Doing it by numbers: a simple approach to reducing the harms of alcohol. J Psychopharmacol. 2014, 28: 3-7. 10.1177/0269881113512038.
Degenhardt LWH, Ferrari AJ, Baxter AJ, Charlson FJ, Hall WD, Freedman G, Burstein R, Johns N, Engell RE, Flaxman A, Murray CJ, Vos T: Global burden of disease attributable to illicit drug use and dependence: findings from the Global Burden of Disease Study 2010. Lancet. 2013, 382: 1564-1574. 10.1016/S0140-6736(13)61530-5.
United Nations Office on Drugs and Crime:[http://www.unodc.org/unodc/en/commissions/CND/session/57_Session_2014/CND-57-Session_HLS-Statements.htm]
Volkow ND, Wang GJ, Fowler JS, Tomasi D: Addiction circuitry in the human brain. Annu Rev Pharmacol Toxicol. 2012, 52: 321-336. 10.1146/annurev-pharmtox-010611-134625.
Amato LDM, Vecchi S, Ali R, Farrell M, Faggiano F, Foxcroft D, Ling W, Minozzi S, Chengzheng Z: Cochrane systematic reviews in the field of addiction: what's there and what should be. Drug Alcohol Depend. 2011, 113: 96-103. 10.1016/j.drugalcdep.2010.08.003.
Sousa RM, Ferri CP, Acosta D, Albanese E, Guerra M, Huang Y, Jacob KS, Jotheeswaran AT, Rodriguez JJ, Pichardo GR, Rodriguez MC, Salas A, Sosa AL, Williams J, Zuniga T, Prince M: Contribution of chronic diseases to disability in elderly people in countries with low and middle incomes: a 10/66 Dementia Research Group population-based survey. Lancet. 2009, 374: 1821-1830. 10.1016/S0140-6736(09)61829-8.
Sousa RMFC, Acosta D, Guerra M, Huang Y, Jacob K, Jotheeswaran A, Hernandez MA, Liu Z, Pichardo GR, Rodriguez JJ, Salas A, Sosa AL, Williams J, Zuniga T, Prince M: The contribution of chronic diseases to the prevalence of dependence among older people in Latin America, China and India: a 10/66 Dementia Research Group population-based survey.BMC Geriatr 2010, 10..
Prince M, Bryce R, Albanese E, Wimo A, Ribeiro W, Ferri CP: The global prevalence of dementia: a systematic review and metaanalysis. Alzheimers Dement. 2013, 9: 63-75. 10.1016/j.jalz.2012.11.007. e62
Wimo A, Jonsson L, Bond J, Prince M, Winblad B: Alzheimer Disease I: the worldwide economic impact of dementia 2010. Alzheimers Dement. 2013, 9: 1-11. 10.1016/j.jalz.2012.11.006. e13
Rocca WA, Petersen RC, Knopman DS, Hebert LE, Evans DA, Hall KS, Gao S, Unverzagt FW, Langa KM, Larson EB, White LR: Trends in the incidence and prevalence of Alzheimer's disease, dementia, and cognitive impairment in the United States. Alzheimers Dement. 2011, 7: 80-93. 10.1016/j.jalz.2010.11.002.
Matthews FE, Arthur A, Barnes LE, Bond J, Jagger C, Robinson L, Brayne C: A two-decade comparison of prevalence of dementia in individuals aged 65 years and older from three geographical areas of England: results of the Cognitive Function and Ageing Study I and II. Lancet. 2013, 382: 1405-1412. 10.1016/S0140-6736(13)61570-6.
Qiu C, von Strauss E, Backman L, Winblad B, Fratiglioni L: Twenty-year changes in dementia occurrence suggest decreasing incidence in central Stockholm, Sweden. Neurology. 2013, 80: 1888-1894. 10.1212/WNL.0b013e318292a2f9.
Schrijvers EM, Verhaaren BF, Koudstaal PJ, Hofman A, Ikram MA, Breteler MM: Is dementia incidence declining?: Trends in dementia incidence since 1990 in the Rotterdam Study. Neurology. 2012, 78: 1456-1463. 10.1212/WNL.0b013e3182553be6.
Stampfer MJ: Cardiovascular disease and Alzheimer's disease: common links. J Intern Med. 2006, 260: 211-223. 10.1111/j.1365-2796.2006.01687.x.
Lincoln P, Fenton K, Alessi C, Prince M, Brayne C, Wortmann M, Patel K, Deanfield J, Mwatsama M: The Blackfriars Consensus on brain health and dementia. Lancet. 2014, 383: 1805-1806. 10.1016/S0140-6736(14)60758-3.
Jagger C, Matthews R, Lindesay J, Robinson T, Croft P, Brayne C: The effect of dementia trends and treatments on longevity and disability: a simulation model based on the MRC Cognitive Function and Ageing Study (MRC CFAS). Age Ageing. 2009, 38: 319-325. 10.1093/ageing/afp016. discussion 251
Barnes DE, Yaffe K: The projected effect of risk factor reduction on Alzheimer's disease prevalence. Lancet Neurol. 2011, 10: 819-828. 10.1016/S1474-4422(11)70072-2.
Norton SMF, Barnes DE, Yaffe K, Brayne C: Potential for primary prevention of Alzheimer's disease: an analysis of population-based data. Lancet Neurol. 2014, 13: 788-794. 10.1016/S1474-4422(14)70136-X.
The author declares he has no competing interests.
The author declares he has no competing interests.
The authors declare they have no competing interests.
JAS has received research grants from Takeda and Savient and consultant fees from Savient, Takeda, Regeneron and Allergan. JAS is a member of the executive of OMERACT, an organization that develops outcome measures in rheumatology and receives arms-length funding from 36 companies; a member of the American College of Rheumatology's Guidelines Subcommittee of the Quality of Care Committee; and a member of the Veterans Affairs Rheumatology Field Advisory Committee.
PGJB has acted as a Consultant to Novartis through Imperial Consultants.
The author declares he has no competing interests.
The authors declare they have no competing interests.
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About this article
- Global health
- Non-communicable diseases
- Sickle cell disease
- Chronic kidney disease
- Substance abuse
- Liver cirrhosis