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Mental disorders as risk factors: assessing the evidence for the Global Burden of Disease Study



Mental disorders are associated with a considerable burden of disease as well as being risk factors for other health outcomes. The new Global Burden of Disease (GBD) Study will make estimates for both the disability and mortality directly associated with mental disorders, as well as the burden attributable to other health outcomes. Herein we discuss the process by which health outcomes in which mental disorders are risk factors are selected for inclusion in the GBD Study. We make suggestions for future research to strengthen the body of evidence for mental disorders as risk factors.


We identified a list of potential associations between mental disorders and subsequent health outcomes based on a review of the literature and consultation with mental health experts. A two-stage filter was applied to identify mental disorders and health outcomes that meet the criteria for inclusion in the GBD Study. Major limitations in the current literature are discussed and illustrated with examples identified during our review.

Results and discussion

Only two associations are included in the new GBD Study. These associations are the increased risk of ischemic heart disease with major depression and mental disorders as a risk factor for suicide. There is evidence that mental disorders are independent risk factors for cardiovascular disease (CVD), type 2 diabetes and injuries. However, these associations were unable to be included because of insufficient data. The most common reasons for exclusion were inconsistent identification of 'cases', uncertain validity of health outcomes, lack of generalizability, insufficient control for confounding factors and lack of evidence for temporality.


CVD, type 2 diabetes and injury are important public health policy areas. Prospective community studies of outcomes in patients with mental disorders are required, and their design must address a range of confounding factors.

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New Global Burden of Disease (GBD) Study estimates due for release in 2012 aim to reflect the impact of morbidity and mortality for all diseases, injuries and risk factors, including mental disorders [1]. Although disorder-specific morbidity and mortality are needed for GBD estimates and to guide health policy in the provision of treatment services, quantifying the additional burden due to health outcomes for which those disorders are risk factors provides an additional evidence base for developing preventative health policy [2]. The Comparative Risk Assessment (CRA) component within the GBD Study will be used to evaluate the impact of risk factors on public health within a unified framework [2].

Risk factors are defined within the CRA as exposures that increase the probability of disease or injury [3]. Considered in the CRA are risk factors likely to be among the leading causes of disease burden at a global or regional level [2]. Other inclusion criteria require that risk factors be sufficiently well-defined, such that population distribution can be quantified and should comprise those for whom the exposure is modifiable [2]. CRA requirements specify that data should be available to quantify the risk of health outcomes for given exposures and sufficient strength of evidence for causality based on collective scientific knowledge [2].

In considering strength of evidence for risk factors in health outcomes, the Bradford-Hill criteria are widely accepted as a guide for assessing the evidence base [4, 5]. The Bradford-Hill criteria describe the best evidence as that which demonstrates the strength and consistency of the relationship, the specificity of the risk factor and outcome, a temporal sequence in which the risk precedes the outcome, and experimental evidence such as the effect of preventative action [4].

Although previous GBD studies included outcomes for illicit drug use and alcohol use [6], the current GBD Study is the first in which other mental disorders are considered as independent risk factors for other health outcomes. A growing body of literature reports links between mental disorders and other health conditions. Higher rates of morbidity and mortality have been reported in psychiatric patients for decades. Longitudinal studies have demonstrated links between mental disorders and cardiovascular disease [7], metabolic disease [8] and injury [9].

Our aim in this paper was not to present the results of a series of systematic reviews of the strength of evidence for health outcomes. To review the evidence comprehensively, each potential outcome for mental disorders deserves in-depth discussion beyond the scope of this paper. Rather, this paper describes the process by which health outcomes were selected for inclusion in the GBD 2010 Study. We identify the most common reasons that potential outcomes were not included and provide suggestions for future research. The GBD CRA component for illicit drug use and alcohol use is outside the scope of this paper and will be reported separately by the groups undertaking that work.


We reviewed the current literature for data on the strength of evidence for mental disorders as risk factors for other health outcomes. Mental disorders included in the GBD 2010 Study are anxiety disorders, depressive disorders (major depression and dysthymia), bipolar disorder, schizophrenia, eating disorders, autistic spectrum disorders, conduct disorder and attention-deficit/hyperactivity disorder (ADHD). Patients with these disorders are defined as those meeting the diagnostic criteria for either the ICD-10 Classification of Mental and Behavioural Disorders: Diagnostic Criteria for Research (ICD-10) classification system [10] or the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition-Text Revision (DSM-IV-TR) [11]. The disorders should not be substance-induced or due to a general medical condition, as these are covered under other categories within the GBD 2010 Study.

Potential health outcomes were identified using a consultative heuristic approach. Good-quality, peer-reviewed evaluations of the literature were initially sought. A review by Prince and colleagues [12] provided the basis for subsequent investigation. Outcome-specific reviews were then identified to examine the breadth of data available to determine the strength of the evidence. We consulted mental health epidemiologists and clinicians with a special interest in the field, and their suggestions were included. The Mental Disorders and Illicit Drug Use Expert Group was then invited to provide feedback on the proposed outcomes and to contribute additional suggestions.

A two-stage filter was then applied to identify those associations that met criteria for inclusion based on the parameters of the GBD 2010 Study and the specific requirements for risk factors and outcomes of the CRA project. The outcomes were first filtered by the GBD Study requirement that the resulting health condition must fall within the study classifications of disease and injury. The second filter focused on the CRA requirements. These criteria included clear definition of risks and outcomes and sufficient strength of evidence for an independent association guided by the Bradford-Hill criteria. GBD Study estimates aim to reflect loss of health. The methodology excludes 'out of skin' elements of functioning, such as participation restrictions which, though important, are beyond the scope of what is captured by disability-adjusted life years [13, 14]. Therefore, outcomes such as social consequences are beyond the scope of this study.


A number of good-quality reviews of health outcomes for patients with mental disorders were identified [79, 12, 15]. These reviews informed the initial list of health outcomes. Six health outcomes were considered after application of the first filter (Table 1). Examples of associations that did not meet GBD Study criteria were those with non-health-related outcomes, such as increased risk of unemployment arising from depression [16].

Table 1 Health outcomes for mental disorders considered for inclusion in the Comparative Risk Assessment component within the Global Burden of Disease study*

After applying the second filter, sufficient evidence was identified to include attributable burden for two health outcomes: suicide and ischemic heart disease [17]. A report of data identified for major depression, schizophrenia, bipolar disorder, anxiety disorders and anorexia nervosa as risk factors for suicide is currently in preparation and will be submitted for peer review (unpublished data: A. Ferrari). Given that only two conditions were included in the CRA component of the GBD 2010 Study, a reasonable question is why the attributable burden of other health outcomes is not reflected in the estimates. To illustrate the nature of the limitations in the current literature, examples are provided for associations that are likely to have a substantial impact on the global burden of disease.


The most significant factors that limited inclusion of studies and ultimately prevented inclusion of other health outcomes in the new GBD Study estimates are (1) risk factor case identification, (2) health outcome case identification, (3) generalizability, (4) confounding factors and (5) temporality.

Risk factor case identification

To attribute the proportionate burden of a condition, both risks and outcomes must be clearly defined [18]. For inclusion in the GBD CRA component, mental disorders considered as risk factors must meet the DSM-IV-TR or ICD-10 diagnostic criteria, which require a threshold level of symptomatology and, in some cases, impairment. The current strength of evidence for disorders such as anxiety disorders and childhood behavioural disorders as risk factors is hampered by the lack of consistency in the definitions used to determine the presence of these disorders.

Inconsistent definitions

In our review, we found that the definitions used when mental disorders were considered as risk factors varied considerably. The most common issue identified was the use of broad definitions, such as the use of 'anxiety' but its' being unclear with regard to whether this term referred to an anxiety disorder that met diagnostic criteria. Some studies tend to describe anxiety as being present on the basis of dimensional scales. These scales (for example, brief symptom checklists, lists of personality traits or measures of psychological distress) can be administered quickly and demonstrate good sensitivity. However, their low specificity [19] results in the inclusion of cases of anxiety that do not reach the threshold for a diagnosis. The issue is highlighted by a meta-analytic review of 21 studies exploring anxiety constructs and incident CHD and cardiac mortality [7]. Only two studies that reported a significant association defined 'anxiety' according to DSM-IV-TR and/or ICD-10 diagnostic criteria [7]. Whilst acknowledging that symptoms of mental disorders occur along a continuum, a threshold must be employed to derive comparable estimates of attributable burden. The question whether psychological distress and anxiety symptoms increase the risk for CHD is valid, but it does not directly allow for estimation of the extent to which one disorder (in this case, an anxiety disorder) is a risk factor for another disorder (CHD).

Incomplete identification of cases

Cross-sectional studies rely on retrospective data collection to establish patients' mental health history. These studies need to be interpreted with caution, as the accuracy of recall of symptoms of mental disorders is unreliable [20]. To illustrate, clinically defined ADHD requires the onset of symptoms and impairment before age seven years [11]. Based on recall, the onset for externalizing disorders such as ADHD, conduct disorder (CD) and oppositional defiant disorder (ODD) is generally estimated to be later than actual onset [21], resulting in potential misclassification of cases as noncases. Higher rates of accidental injury are reported for people with behavioural disorders such as ADHD [22, 23]; however, recall bias increases the chance that cases of ADHD are treated as noncases. In trying to quantify the increased risk due to mental disorders, variably defined 'cases' limit the ability to infer a consistent relationship because the characteristics of people with the risk factor are likely to be inconsistent between studies.

Health outcome case identification

The CRA framework requires that attributable burden be associated with a specific health condition [2]. A number of proposed outcomes could not be included because of the reliability of studies on self-reported measures (for example, type 2 diabetes) or on outcomes not specific to a health condition, such as vehicular accidents.

Health outcomes that cannot be verified

Biomedical measures are rarely collected in community-based studies, relying instead on self-report of health outcomes. The accuracy of self-report measures depends on the community rate of diagnosis and participants' recall and knowledge. Chronic diseases such as type 2 diabetes are particularly difficult to identify on the basis of survey data. In developed countries, almost 50% of type 2 diabetes cases are undiagnosed [24]. In a sample of patients with clinically diagnosed diabetes, only two of three patients self-reported the presence of diabetes [25]. Systematic underreporting of the outcome may underestimate or obscure the association between risk and outcome.

Outcomes that cannot be mapped to a health condition

An additional issue related to outcomes is the reporting of events (for example, vehicle collisions) rather than the health implication of the event (for example, injuries). For example, two meta-analytic reviews found strong evidence for an association between ADHD and negative driving injury outcomes, including poor performance on simulators, traffic violations and motor vehicle collisions [9, 26]. A causal pathway is plausible, considering that common ADHD characteristics include inattention, distractibility, impulsiveness and slow processing ability [9]. However, the usability of findings is limited in the attribution of disease burden because of the lack of information regarding specific health outcomes.

Generalizability of the sample

Prospective longitudinal studies of outcomes in representative community cases of mental disorders are lacking, especially for severe mental disorders such as bipolar disorders and schizophrenia. As estimates of attributable burden in the GBD CRA component are applied at the population level, studies with samples not sufficiently representative of the general population could not be included. For example, a number of well-conducted studies examining bipolar disorder [2729] and schizophrenic disorders [27] as risk factors for chronic disease focused on clinical samples. Hospitalized patients have more complex psychopathology and psychological-physical comorbidity that lead to greater risk of negative health outcomes. The degree of association may be overestimated if only severe cases are included.

Clinical samples are subject to a number of biases which may not be controlled for. Clinically ascertained samples are likely to have received treatment, with treatment rates generally being lower in community samples. Because of their use of health services, psychiatric patients with independent risk factors for physical disorders (for example, hypertension) are more likely to have these risk factors recognized and treated compared to community cases. Such sources of systemic bias hamper interpretation of studies based on clinical samples. This limits the generalizability of the risk for health outcomes at the population level.

Confounding factors

An important issue in establishing the strength of evidence is whether the association persists after adjustment for confounding factors. A confounder is a variable that can cause or prevent the outcome and is also associated with the risk factor [30]. This may lead to a false-positive that erroneously suggests a causal relationship between the dependent variable and the outcome. Type 2 diabetes and CHD are examples of outcomes for which we found the strength of the evidence was further limited because of inability to control for multiple risk factors.

Causal pathways of chronic disease and injury are generally multifactorial. For example, the INTERHEART Study identified nine potentially modifiable risk factors for acute myocardial infarction, including lipid abnormality, hypertension, diabetes, abdominal obesity, consumption of fruits and vegetables, smoking, alcohol intake, physical activity and psychosocial factors [31]. Mental disorders are independently associated with many of these risk factors [32]. To clarify the relationship between mental disorders and CHD, analyses need to control for potentially confounding effects, given the network of factors involved in the development of CHD.

Adjustment for comorbidity

A review of the literature [7] found that the majority of studies that examined anxiety disorders and CHD controlled for smoking and physiological factors, yet only two studies reported adjustment for depressive symptoms and none adjusted for the impact of other comorbid mental disorders. Anxiety disorders frequently co-occur with other mental disorders, such as mood disorders and substance abuse [33], which may have a synergistic effect on the development of chronic health conditions [34].

The confounding factors that can be considered in a study vary considerably, due in part to limitations such as cost and burden on respondents. Moreover, insufficient numbers of patients meeting the criteria for the confounder, such as comorbid mental disorders, reduce researchers' capacity to detect an effect. For example, a long-term prospective study of the risk of CHD in community cases of anxiety disorder found that a significant association remained after controlling for a range of confounders [32], but the investigators were unable to control for comorbid depression. The reason for this was that the low number patients with comorbid depression and anxiety prevented adjustment for potentially additive effects of this comorbidity (personal correspondence{ I. Janszky, 2011 }).

Effects of treatment

Treatment of a mental disorder affects the course of the disorder and also introduces the risk of iatrogenic outcomes, such as glucose intolerance or atherosclerosis. Reliable data on treatment regimen, including medications, are rarely captured or controlled for in community studies. Researchers in prospective studies of depression and CVD, for example, either do not collect treatment data [35] or collect incomplete information [36].

Treatment may increase the risk of negative health outcomes in some cases or may provide a protective effect in others. Antipsychotic medications have a well-known potential to increase the risk of obesity and abnormal glucose metabolism [15]. Observational studies of women have found that antidepressant use is associated with an increased risk of sudden cardiac death [37] and stroke [38]. Conversely, it has been postulated that the reduction in the duration of psychopathology and symptom severity due to treatment may reduce the risk for chronic physical disease. A potential mechanism suggested by animal studies is that antidepressants may inhibit the expression of proinflammatory cytokines implicated in the progression of CVD [39]. To clarify the multidirectional impact of treatment on health outcomes, researchers need to consider the interactions between treatment type, symptom severity and potential comorbidities.

Environmental factors

The current literature suggests a strong link between childhood psychopathology, such as autistic disorders and behavioural disorders, and increased risks for accidental and self-inflicted injuries [4042]. However, inclusion for CRA is hindered by unrepresentative sampling (registry data or small sample sizes) and lack of data on potential comorbid and environmental risk factors. Common comorbid conditions, including epilepsy and intellectual disability [43], and environmental factors, such as the family context and unsafe physical environments [42], may inflate the risk of injury. Obtaining objective data on family and physical environments is difficult and is rarely collected when children with injuries present for treatment.


Determining temporality and establishing which condition precedes the other constitute the greatest areas of contention in establishing an argument for mental disorders as a risk factor. Temporality of onset is subject to bias arising from self-report of onset and from the use of routinely collected clinical data. Prospective cohort studies, whilst still subject to some degree of bias, produce the best empirical evidence for temporality in risk factor associations.

Clinical data

Bias can arise from medical records, which document the diagnosis and the start of treatment more accurately than the onset of the disorder. Symptoms of mental disorders and chronic physical health conditions are often present for some time prior to clinical diagnosis. For example, studies based on data linkage of medical records have reported higher rates of type 2 diabetes in people diagnosed with a mental disorder [27, 44]. When the diagnosis of either a mental disorder or diabetes precedes the other, the one diagnosed first may be a risk factor for the other. However, temporal pathways are complicated by the lag time between the onset of the disorder and diagnosis. The high rate of undiagnosed diabetes [24] and the delay between symptom onset and diagnosis of mental disorders confounds temporality.

Recall bias

Because of recall bias, inaccurate estimates of the occurrence of disorders can arise from retrospectively collected survey data. For instance, brain injury can induce neurobehavioral changes. However, the subsequent effects can be delayed, as the more significant damage tends to ensue from a series of interrelated processes that affect the central nervous system [45]. If the injury leads to cognitive or behavioural changes, incorrect recall of the onset of occurrence might lead to the assumption that childhood disorders are a risk factor rather than an outcome.

Future directions for research

Recommendations for future research required to address gaps in the current body of evidence can be generically applied across the majority of risk factors and related health outcomes. Prospective studies of representative community samples using clear and consistent definitions of the mental disorder and outcome are essential to providing evidence for risk. Confounding factors need to be considered, including identifying and controlling for comorbid physical and mental disorders. Specific recommendations are summarized in Table 2.

Table 2 Suggested directions for future research


Whilst preliminary evidence suggests that mental disorders are linked to a range of poor health outcomes, further research is needed to confirm the strength of these relationships. The criteria discussed in this paper may be useful in the design of future studies. CVD, diabetes and accidental injury are major areas of concern for public health policy. If mental disorders are indeed shown to be independent risk factors for these outcomes, accurate diagnosis and treatment of mental disorders may lead to a reduction in the global burden of important health outcomes. As more consistent and compelling evidence becomes available, it is anticipated that these health outcomes will be considered for inclusion in future burden-of-disease studies.


  1. Murray CJL, Lopez AD, Black R, Mathers CD, Shibuya K, Ezzati M, Salomon JA, Michaud CM, Walker N, Vos T: Global Burden of Disease 2005: call for collaborators. Lancet. 2007, 370: 109-110. 10.1016/S0140-6736(07)61064-2.

    Article  PubMed  Google Scholar 

  2. Ezzati M, Vander Hoorn S, Lopez AD, Danaei G, Rodgers A, Mathers CD, Murray CJL: Comparative quantification of mortality and burden of disease attributable to selected risk factors. The Global Burden of Disease and Risk Factors. Edited by: Lopez AD, Mathers CD, Ezzati M, Jamison DT, Murray CJL. 2006, Washington, DC: IBRD/The World Bank and Oxford University Press

    Google Scholar 

  3. Lopez AD, Mathers CD, Ezzati M, Jamison DT, Murray CJL, (Eds): The Global Burden of Disease and Risk Factors. 2006, Washington, DC: IBRD/The World Bank and Oxford University Press

    Google Scholar 

  4. Bradford Hill A: The environment and disease: association or causation?. Proc R Soc Med. 1965, 58: 293-300.

    Google Scholar 

  5. Phillips CV, Goodman KJ: The missed lessons of Sir Austin Bradford Hill. Epidemiol Perspect Innov. 2004, 1: 3-10.1186/1742-5573-1-3.

    Article  PubMed  PubMed Central  Google Scholar 

  6. Murray CJL, Lopez AD: Global mortality, disability, and the contribution of risk factors: Global Burden of Disease Study. Lancet. 1997, 349: 1436-1442. 10.1016/S0140-6736(96)07495-8.

    Article  CAS  PubMed  Google Scholar 

  7. Roest AM, Martens EJ: Anxiety and risk of incident coronary heart disease: a meta-analysis. J Am Coll Cardiol. 2010, 56: 38-46. 10.1016/j.jacc.2010.03.034.

    Article  PubMed  Google Scholar 

  8. Knol MJ, Twisk JW, Beekman AT, Heine RJ, Snoek FJ, Pouwer F: Depression as a risk factor for the onset of type 2 diabetes mellitus: a meta-analysis. Diabetologia. 2006, 49: 837-845. 10.1007/s00125-006-0159-x.

    Article  CAS  PubMed  Google Scholar 

  9. Jerome L, Segal A, Habinski L: What we know about ADHD and driving risk: a literature review, meta-analysis and critique. J Can Acad Child Adolesc Psychiatry. 2006, 15: 105-125.

    Article  PubMed  PubMed Central  Google Scholar 

  10. World Health Organisation (WHO): The ICD-10 Classification of Mental and Behavioural Disorders: Diagnostic Criteria for Research. 1993, Geneva: WHO

    Google Scholar 

  11. American Psychiatric Association: Diagnostic and Statistical Manual of Mental Disorders (DSM-IV-TR). 2000, Washington, DC: American Psychiatric Association, Text Revision, 4

    Google Scholar 

  12. Prince M, Patel V, Saxena S, Maj M, Maselko J, Phillips MR, Rahman A: No health without mental health. Lancet. 2007, 370: 859-877. 10.1016/S0140-6736(07)61238-0.

    Article  PubMed  Google Scholar 

  13. Murray CJL: Quantifying the burden of disease: the technical basis for disability-adjusted life years. Bull World Health Organ. 1994, 72: 429-445.

    CAS  PubMed  PubMed Central  Google Scholar 

  14. Salomon JA, Murray CJ, Ustun B, Chatterji S: Health state valuations in summary measures of population health. Health Systems Performance Assessment: Debates, Methods and Empiricism. Edited by: Murray CJ, Evans DB. 2003, Geneva: World Health Organisation

    Google Scholar 

  15. Holt RI, Bushe C, Citrome L: Diabetes and schizophrenia 2005: are we any closer to understanding the link?. J Psychopharmacol. 2005, 19: 56-65. 10.1177/0269881105058379.

    Article  PubMed  Google Scholar 

  16. Lerner D, Adler DA, Chang H, Lapitsky L, Hood MY, Perissinotto C, Reed J, McLaughlin TJ, Berndt ER, Rogers WH: Unemployment, job retention, and productivity loss among employees with depression. Psychiatr Serv. 2004, 55: 1371-1378. 10.1176/

    Article  PubMed  PubMed Central  Google Scholar 

  17. Charlson FJ, Stapelberg NJC, Baxter AJ, Whiteford HA: Should global burden of disease estimates include depression as a risk factor for coronary heart disease?. BMC Med. 2011, 9: 47-10.1186/1741-7015-9-47.

    Article  PubMed  PubMed Central  Google Scholar 

  18. Global Burden of Diseases: The Global Burden of Diseases Study Operations Manual. 2009, Harvard University Initiative for Global Health, the Institute for Health Metrics and Evaluation at the University of Washington, the Johns Hopkins University, the University of Queensland, and the World Health Organization, []

    Google Scholar 

  19. Hoyer J, Becker ES, Neumer S, Soeder U, Margraf J: Screening for anxiety in an epidemiological sample: predictive accuracy of questionnaires. J Anxiety Disorders. 2002, 16: 113-134. 10.1016/S0887-6185(01)00094-9.

    Article  Google Scholar 

  20. Moffitt TE, Caspi A, Taylor AJ, Kokaua J, Milne BJ, Polanczyk G, Poulton R: How common are common mental disorders? Evidence that lifetime prevalence rates are doubled by prospective versus retrospective ascertainment. Psychol Med. 2010, 40: 899-909. 10.1017/S0033291709991036.

    Article  CAS  PubMed  Google Scholar 

  21. Todd RD, Huang H, Henderson CA: Poor utility of the age of onset criterion for DSM-IV attention deficit/hyperactivity disorder: recommendations for DSM-V and ICD-11. J Child Psychol Psychiatry. 2008, 49: 942-949. 10.1111/j.1469-7610.2008.01892.x.

    Article  PubMed  Google Scholar 

  22. Redelmeier DA, Chan WK, Lu H: Road trauma in teenage male youth with childhood disruptive behavior disorders: a population based analysis. PLoS Med. 2010, 7: e1000369-10.1371/journal.pmed.1000369.

    Article  PubMed  PubMed Central  Google Scholar 

  23. Kessler RC, Lane M, Stang PE, Van Brunt DL: The prevalence and workplace costs of adult attention deficit hyperactivity disorder in a large manufacturing firm. Psychol Med. 2009, 39: 137-147. 10.1017/S0033291708003309.

    Article  CAS  PubMed  Google Scholar 

  24. Shaw JE, Chisholm DJ: Epidemiology and prevention of type 2 diabetes and the metabolic syndrome. Med J Aust. 2003, 179: 379-383.

    PubMed  Google Scholar 

  25. Okura Y, Urban LH, Mahoney DW, Jacobsen SJ, Rodeheffer RJ: Agreement between self-report questionnaires and medical record data was substantial for diabetes, hypertension, myocardial infarction and stroke but not for heart failure. J Clin Epidemiol. 2004, 57: 1096-1103. 10.1016/j.jclinepi.2004.04.005.

    Article  PubMed  Google Scholar 

  26. Truls V: Impairments, Diseases, Age and Their Relative Risks of Accident Involvement: Results From Meta-Analysis. (Contract GMA1/2000/27043 SI2.319837, Report R1.1, version 2). 2003, Vienna: Impaired Motorists, Methods of Roadside Testing and Assessment for Licensing (IMMORTAL)

    Google Scholar 

  27. Regenold WT, Thapar RK, Marano C, Gavirneni S, Kondapavuluru PV: Increased prevalence of type 2 diabetes mellitus among psychiatric patients with bipolar I affective and schizoaffective disorders independent of psychotropic drug use. J Affect Disord. 2002, 70: 19-26. 10.1016/S0165-0327(01)00456-6.

    Article  PubMed  Google Scholar 

  28. Lin HC, Tsai SY, Lee HC: Increased risk of developing stroke among patients with bipolar disorder after an acute mood episode: a six-year follow-up study. J Affect Disord. 2007, 100: 49-54. 10.1016/j.jad.2006.09.016.

    Article  PubMed  Google Scholar 

  29. Lin HC, Tsai SY, Lee HC: No higher risk of myocardial infarction among bipolar patients in a 6-year follow-up of acute mood episodes. Psychosom Med. 2008, 70: 73-76.

    Article  PubMed  Google Scholar 

  30. Last JM: A Dictionary of Epidemiology. 1995, New York: Oxford University Press

    Google Scholar 

  31. Yusuf S, Hawken S, Ôunpuu S, Dans T, Avezum A, Lanas F, McQueen M, Budaj A, Pais P, Varigos J, Lisheng L: Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study. Lancet. 2004, 364: 937-952. 10.1016/S0140-6736(04)17018-9.

    Article  PubMed  Google Scholar 

  32. Janszky I, Ahnve S, Lundberg I, Hemmingsson T: Early-onset depression, anxiety and risk of subsequent coronary heart disease: 37-year follow-up of 49,321 young Swedish men. J Am Coll Cardiol. 2010, 56: 31-37. 10.1016/j.jacc.2010.03.033.

    Article  PubMed  Google Scholar 

  33. Scott KM, McGee MA, Oakley-Browne MA, Wells JE: Mental disorder comorbidity in Te Rau Hinengaro: The New Zealand Mental Health Survey. Aust N Z J Psychiatry. 2006, 40: 875-881. 10.1080/j.1440-1614.2006.01906.x.

    Article  PubMed  Google Scholar 

  34. Suls J, Bunde J: Anger, anxiety, and depression as risk factors for cardiovascular disease: the problems and implications of overlapping affective dispositions. Psychol Bull. 2005, 131: 260-300.

    Article  PubMed  Google Scholar 

  35. Ramasubbu R, Patten SB: Effect of depression on stroke morbidity and mortality. Can J Psychiatry. 2003, 48: 250-257.

    PubMed  Google Scholar 

  36. Larson SL, Owens PL, Ford D, Eaton W: Depressive disorder, dysthymia, and risk of stroke: thirteen-year follow-up from the Baltimore Epidemiologic Catchment Area Study. Stroke. 2001, 32: 1979-1983. 10.1161/hs0901.094623.

    Article  CAS  PubMed  Google Scholar 

  37. Whang W, Kubzansky LD, Kawachi I, Rexrode KM, Kroenke CH, Glynn RJ, Garan H, Albert CM: Depression and risk of sudden cardiac death and coronary heart disease in women: results from the Nurses' Health Study. J Am Coll Cardiol. 2009, 53: 950-958. 10.1016/j.jacc.2008.10.060.

    Article  PubMed  PubMed Central  Google Scholar 

  38. Smoller JW, Allison M, Cochrane BB, Curb JD, Perlis RH, Robinson JG, Rosal MC, Wenger NK, Wassertheil-Smoller S: Antidepressant use and risk of incident cardiovascular morbidity and mortality among postmenopausal women in the Women's Health Initiative study. Arch Intern Med. 2009, 169: 2128-2139. 10.1001/archinternmed.2009.436.

    Article  PubMed  Google Scholar 

  39. Castanon N, Leonard BE, Neveu PJ, Yirmiya R: Effects of antidepressants on cytokine production and actions. Brain Behav Immun. 2002, 16: 569-574. 10.1016/S0889-1591(02)00008-9.

    Article  CAS  PubMed  Google Scholar 

  40. Baghdadli A, Pascal C, Grisi S, Aussilloux C: Risk factors for self-injurious behaviours among 222 young children with autistic disorders. J Intellect Disabil Res. 2003, 47: 622-627. 10.1046/j.1365-2788.2003.00507.x.

    Article  CAS  PubMed  Google Scholar 

  41. Lee LC, Harrington RA, Chang JJ, Connors SL: Increased risk of injury in children with developmental disabilities. Res Dev Disabil. 2008, 29: 247-255. 10.1016/j.ridd.2007.05.002.

    Article  PubMed  Google Scholar 

  42. Rowe R, Maughan B, Goodman R: Childhood psychiatric disorder and unintentional injury: findings from a national cohort study. J Pediatr Psychol. 2004, 29: 119-130. 10.1093/jpepsy/jsh015.

    Article  PubMed  Google Scholar 

  43. Sherrard J, Tonge BJ, Ozanne-Smith J: Injury risk in young people with intellectual disability. J Intellect Disabil Res. 2002, 46: 6-16.

    Article  CAS  PubMed  Google Scholar 

  44. Brown LC, Majumdar SR, Newman SC, Johnson JA: History of depression increases risk of type 2 diabetes in younger adults. Diabetes Care. 2005, 28: 1063-1067. 10.2337/diacare.28.5.1063.

    Article  PubMed  Google Scholar 

  45. Dennis M: Developmental plasticity in children: the role of biological risk, development, time, and reserve. J Commun Disord. 2000, 33: 321-332. 10.1016/S0021-9924(00)00028-9.

    Article  CAS  PubMed  Google Scholar 

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AB made a substantial contribution to the conception and design of the paper, played a principal role in drafting the article and revising it critically for important intellectual content, performed the final critical editing and approved the version of the manuscript to be published. FC and AS made substantial contributions to the acquisition and interpretation of data, played an important role in drafting the manuscript and revising it critically for important intellectual content, performed the final critical editing and approved the version of the manuscript to be published. HW played an important role in drafting the article, revised it critically for important intellectual content, performed final critical editing and approved the version of the manuscript to be published. All authors read and approved the final manuscript.

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Baxter, A.J., Charlson, F.J., Somerville, A.J. et al. Mental disorders as risk factors: assessing the evidence for the Global Burden of Disease Study. BMC Med 9, 134 (2011).

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