- Research article
- Open Access
The comorbidity burden of type 2 diabetes mellitus: patterns, clusters and predictions from a large English primary care cohort
BMC Medicine volume 17, Article number: 145 (2019)
- The Correction to this article has been published in BMC Medicine 2020 18:22
The presence of additional chronic conditions has a significant impact on the treatment and management of type 2 diabetes (T2DM). Little is known about the patterns of comorbidities in this population. The aims of this study are to quantify comorbidity patterns in people with T2DM, to estimate the prevalence of six chronic conditions in 2027 and to identify clusters of similar conditions.
We used the Clinical Practice Research Datalink (CPRD) linked with the Index of Multiple Deprivation (IMD) data to identify patients diagnosed with T2DM between 2007 and 2017. 102,394 people met the study inclusion criteria. We calculated the crude and age-standardised prevalence of 18 chronic conditions present at and after the T2DM diagnosis. We analysed longitudinally the 6 most common conditions and forecasted their prevalence in 2027 using linear regression. We used agglomerative hierarchical clustering to identify comorbidity clusters. These analyses were repeated on subgroups stratified by gender and deprivation.
More people living in the most deprived areas had ≥ 1 comorbidities present at the time of diagnosis (72% of females; 64% of males) compared to the most affluent areas (67% of females; 59% of males). Depression prevalence increased in all strata and was more common in the most deprived areas. Depression was predicted to affect 33% of females and 15% of males diagnosed with T2DM in 2027. Moderate clustering tendencies were observed, with concordant conditions grouped together and some variations between groups of different demographics.
Comorbidities are common in this population, and high between-patient variability in comorbidity patterns emphasises the need for patient-centred healthcare. Mental health is a growing concern, and there is a need for interventions that target both physical and mental health in this population.
The prevalence of type 2 diabetes (T2DM) is increasing in the UK and internationally. Diabetes (all types) is estimated to affect 1 in 11 adults aged 20 to 79 years, or 415 million adults globally . In 2016, it was the seventh leading cause of death worldwide with an estimated 1.6 million deaths directly caused by diabetes . In the UK over 90% of diabetes cases are type 2 diabetes , with most individuals having at least one other chronic condition . Diabetes-related healthcare outcomes, treatment options, care needs and associated cost are complicated by the presence of comorbidities—chronic conditions existing in addition to T2DM.
Due to similar risk factors, such as obesity, endothelial dysfunction, vascular inflammation and dyslipidaemia , people with T2DM have higher risks of cardiovascular complications , end-stage renal disease  and hypertension . However, individuals with T2DM have also been found to have higher risks of depression , thyroid gland diseases  and chronic obstructive pulmonary disease (COPD) . People with multiple chronic conditions report a number of barriers to self-care such as physical limitations, lack of knowledge, financial constraints, logistics of obtaining care and the need for social and emotional support . The specific combination of comorbidities in diabetes (type 1 and 2) patients has been found to impact their ability to prioritise and manage the disease . Patients with conditions considered unrelated to diabetes may need additional support in making decisions about care priorities and self-management activities . While the presence of diabetes-“concordant” conditions (i.e. sharing the same management goals), tends to be positively associated with quality of care , certain “discordant” comorbidities, like depression and arthritis, impact on treatment options, posing barriers to lifestyle changes and self-care behaviours recommended for diabetes management [14,15,16].
The specific combinations of conditions present dictate the needs of patients, management priorities and the associated demand on healthcare services . A better understanding of the nature, prevalence and patterns of comorbidities in T2DM patients may provide key insights for managing patients with multiple conditions in primary care and facilitate a more patient-centred approach in risk assessment and more appropriate and tailored therapeutic interventions. Understanding and forecasting the prevalence of specific comorbidities can inform policy-makers in planning and structuring health services to meet the future demands of the population.
In this study, we explored the comorbidities’ patterns occurring in patients with T2DM over time, as seen in English primary care. We quantified the prevalence of 18, highly prevalent and well-recorded physical and mental health conditions and compared the patterns in subgroups of patients stratified by gender, age and socioeconomic deprivation. Focusing on an incidental cohort of patients with T2DM, we explored the patterns in comorbidity occurrence at the time of T2DM diagnosis and after 2, 5and 9 years of follow-up.
The Clinical Practice Research Datalink (CPRD) is a database of anonymised electronic, primary health records. In January 2017, the CPRD held data on nearly 17 million active and historical patients registered with 714 general practices across the UK. It contains information on diagnoses, referrals, tests and therapy records, which are mainly recorded using Read clinical codes. Additional data is available for a subset of English practices (nearly 75% of English practices; 58% of all UK CPRD practices) which consented to participate in the CPRD linkage scheme and provided patient-level information. To obtain information on social deprivation at the level of the patient’s postcode, we used the linked information on the quintiles from the 2015 Index of Multiple Deprivation (IMD) measure, which aggregates data on income, employment, health and disability, education and training, barriers to housing and services, crime and living environment.
People registered with a general practice in England meeting CPRD data quality standards and with the first T2DM Read code recorded at any point between 1 April 2007 and 31 March 2017 were included. The inclusion criteria for this study were as follows: patient registered with a CPRD practice for at least 365 days before T2DM diagnosis, aged 35 years and older and no recorded diagnostic code for type-1 diabetes mellitus. In the UK, T2DM has been incentivised since 2004 through a national pay-for-performance scheme, the Quality and Outcomes Framework (QOF), along with another 20 clinical domains approximately, resulting in uniformity in Read code usage and recording. The index date was defined as the date of first recorded code for T2DM and the follow-up as the time between the index date and the earliest of date of death, transfer out of practice date and last date of data collection from the practice or the end of study period (31 March 2017). The lists of codes used to establish the presence of each comorbidity were downloaded from clinicalcodes.org and CPRD@Cambridge websites.
We selected the following 18 conditions: coronary heart disease (CHD), chronic kidney disease (CKD), atrial fibrillation, stroke, hypertension, heart failure, peripheral vascular disease (PVD), rheumatoid arthritis, cancer, osteoporosis, depression, asthma, chronic obstructive pulmonary disease (COPD), dementia, severe mental illness (SMI), epilepsy, hypothyroidism and learning disability. The reporting of these conditions is financially incentivised under the QOF, and consequently, they are well-recorded in the CPRD. The presence of asthma, epilepsy and depression was determined using Read codes and prescription data, since these can be acute or resolvable. Each condition was considered to be present at the index date if it satisfied the definition criteria at the time of the T2DM diagnosis (Additional file 1: Table S1). Each condition was considered to be present during the follow-up period if it satisfied the definition criteria at the index date or at any time during the follow-up.
First, we used the sample in terms of the total number of comorbidities present at the index date and after 1 year, 5 years and 9 years of follow-up. We examined the total number of comorbidities present at and after the index date, stratified by gender and social deprivation quintiles. Age-standardised prevalence was calculated using the direct age standardisation to the 2013 European Standard Population using 5-year age bands up to 95+ years old. Differences between means of categorical variables were tested using 2-sample t tests.
We calculated the age-standardised prevalence of each condition, stratified by gender, for patients from the least and most deprived areas. We also calculated the crude and age-standardised co-prevalence of each pair of comorbidities for the whole sample and stratified by gender, deprivation (least and most deprived areas) and age (using 35–54-, 55–74- and 75+-year-old age bands).
We longitudinally calculated the prevalence of each comorbidity present at the time of the T2DM diagnosis in the incidental cohort of patients with T2DM, for financial years (April to March) 2007/2008 to 2016/2017. To forecast the proportion of people diagnosed with T2DM in the next 10 years that will also have a particular comorbidity present at the time of diagnosis, we used linear regression on log-transformed, age-standardised prevalence. For clarity of results, we present the patterns for the six most prevalent conditions as the prevalence of remaining conditions remained relatively low and stable over the study period.
Lastly, we selected patients with two or more comorbidities present at the index date and used agglomerative hierarchical clustering to identify groups of similar conditions. Similarity was assessed using the tetrachoric correlation coefficient. Tetrachoric correlation estimates what the correlation for two binary variables would be if they were measured on a continuous scale. We used Ward’s linkage method to group conditions. At each linkage step, Ward’s method finds a pair of clusters that leads to a minimum increase in total within-cluster variance after merging. To avoid chaining (low prevalence comorbidities being sequentially linked to existing clusters), we excluded conditions with prevalence in a given group below 3%. Cluster analysis was stratified by gender, age bands (35 to 54 years, 55 to 74 years and ≥ 75 years old) and deprivation using the least and most deprived quintiles. We present the results for the whole sample. Stratified results are available in Additional file 1: Figure S12–S18. To assess the progression in clustering patterns, we performed the cluster analysis for conditions present at the time of T2DM diagnosis and those present at 2, 5 and 9 years after. We plotted the results in dendrograms and identified clusters using visual analysis. Dendrograms visually represent the clustering. The heights at which conditions fuse together correspond to their similarity. The earlier the branches merge, the more similar the groups of conditions are. The clustering structure was measured using the agglomerative coefficient, with values closer to zero suggesting tight clustering of objects and values closer to one suggesting less well-formed clusters. Due to differences in sample sizes, agglomerative coefficients should not be compared across groups. We used R version 3.4.2 for the analysis and data preparation.
We identified 102,394 people with incident T2DM during the study period, who met the study inclusion criteria. A flow chart of the data cleaning process is available in Additional file 1: Figure S1. The median (LQ, 25th centile; UQ, 75th centile) follow-up was 4.9 years (LQ, 2.8; UQ, 7.3). Over half of the sample (56.3%) was male with an average (mean ± standard deviation) age at diagnosis of 60.3 (± 12.5) (Table 1). On average, women were diagnosed at an older age (63.7 ± 13.6, p < 0.001) and had more comorbidities at the time of T2DM diagnosis compared to males (1.6 ± 1.4 vs 1.2 ± 1.2, p < 0.001). People from the most deprived areas were diagnosed with T2DM at a younger age, compared to those from the most affluent areas (59.3 ± 13 vs 63.9 ± 12.8, p < 0.001). The age-standardised prevalence of one or more comorbid conditions was 33.3% (95% confidence interval: 32.5%; 34.1%) for the least deprived areas and 32.7% (31.7%; 33.3%) for the most deprived areas (Fig. 1). For four or more comorbid conditions, the age-standardised prevalence was 2.9% (2.7%; 3.1%) in the most affluent areas and 4.4% (4.1%; 4.7%) in the most deprived areas. In all subgroups (by sex and deprivation), the proportion of people with zero comorbidities decreased during the follow-up period (Fig. 1).
Hypertension was the most common condition among all patients, with higher prevalence among females than males (42.8% [42.3–43.3%] vs 45.8% [45%; 46.4%]) (Fig. 2, crude prevalence Additional file 1: Figure S2). In females, the second most prevalent condition was depression, with higher prevalence in females from the most deprived areas (20.2% [19.3%; 21.1%]), than from most affluent areas (15.6% [14.7%; 16.5%]). In males, the second most prevalent condition was CHD with higher prevalence among males from the most deprived areas (13.6% [12.9%; 14.3%]), than from the most affluent areas (10.8% [10.3%; 11.3%]). During follow-up, the prevalence of depression and asthma decreased in all groups whereas the prevalence of all other conditions’ increased (prevalence rates for SMI, dementia, epilepsy and learning disability was too low to make meaningful comparisons) (Additional file 1: Figure S3). Hypertension and CKD had the highest age-standardised co-prevalence rate among all patients, at 12.1% at the time of T2DM diagnosis and 15.4%, 17.8% and 21.5% after 2, 5 and 9 years from the T2DM diagnosis (Additional file 1: Figure S4–S11).
Our longitudinal analysis showed a steady decrease in the prevalence of hypertension and relatively stable prevalence rates for CHD, CKD, stroke and atrial fibrillation (Fig. 3). The prevalence of depression increased during the study period for all analysed groups. In females, the age-standardised prevalence rate of depression increased from 15.9% (95% CI 14.8%; 17.0%) in 2007 to 21.5% (19.7%; 20.8%) in 2015 and 18.8% (16.8%; 20.8%) in 2016. In males, the age-standardised prevalence rate of depression increased from 7.0% (3.4%; 7.6%) in 2007 to 10.4% (9.1%; 11.7%) in 2016. If the current trend continues, depression can affect over a third of females diagnosed with T2DM by 2026 (age-standardised prevalence, 30.7% [23.9%; 39.4%]) and over 15% (13.2%; 18.9%) of males. The prevalence of depression increased from 9.8% (8.5%; 11.1%) in 2007 to 14.9% (11.3%; 16.5%) in 2016 in the most affluent areas. In the most deprived areas, it increased13.4% (12.0%; 14.8%) in 2007 to 17.7% (15.3%; 19.6%) in 2015 and to 14.1% (11.5%; 16.7%) in 2016. If current trend continues, depression is predicted to affect 17.9% (11.7%; 27.5%) of people in the most affluent and 21% (15.9%; 29.5%) of people from the most deprived areas by 2026.
The hierarchical cluster analysis showed conditions being grouped into two main clusters: the first composed of atrial fibrillation, heart failure, PVD, CHD, cancer, stroke, hypertension and CKD and the second composed of depression, SMI, COPD, asthma, hypothyroidism, rheumatoid arthritis and osteoporosis (Fig. 4). This pattern was similar in all analysed groups with cancer being included in the first cluster for males, people from the most deprived areas, people age 35 to 74 and 75 and over (Additional file 1: Figure S12–S18). However, cancer was linked with cluster two in females, people from the least deprived areas and people age 55–74. Moderate clustering tendencies have been observed for conditions present at the time of T2DM diagnosis with the agglomerative coefficient around 0.45 with some variations between groups.
We showed important changes in the comorbidity patterns in a large real-world cohort of people living with T2DM, using data from the UK primary care. Our findings are relevant to patients, clinicians and policy-makers and can inform on the healthcare needs and how best to prioritise and deliver care for people with T2DM. We identified alarming levels and trends of depression prevalence, which we estimated will continue to grow over the next decade. This could have major consequences for how to offer these patients integrated care. Health systems will have to respond to a growing need for diagnosis and management of mental health problems among people with T2DM, underpinned with established links between depression and poor glycaemic control , treatment adherence , diabetes complications  and mortality . The differences in comorbidity patterns observed in groups stratified by gender and social deprivation highlight the need to address the present and increasing health inequalities, particularly with higher prevalence of comorbidities in patients from more deprived areas.
Strengths and limitations of the study
To the best of our knowledge, this is the largest study of comorbidities in patients with T2DM in England. The quality of the data is very high for our study period, primarily due to data recording in line with the QOF and the financial incentives offered to UK primary care for the management of chronic and other conditions such as T2DM.
However, the study has limitations. First, due to the low prevalence of some conditions in general and in specific groups, some comorbidities were excluded from the cluster analysis for all or some strata. However, all conditions were included in the frequency analysis which provides a starting point for the analysis of grouping patterns of specific conditions. Second, we selected only 18 conditions for which recording quality was high, but patients may have additional comorbidities impacting on their disease management and quality of life. Third, some of these comorbidities, like CKD and CHD, are closely linked to T2DM, to the extent of them being considered its complications. However, the majority of patients with these conditions do not have T2DM, while the characterisation of these conditions is immaterial to our analyses. Fourth, to identify patients with depression, we used an algorithm analysing prescriptions as well as diagnostic codes. We were unable to discriminate uses of antidepressants for other conditions such as obsessive-compulsive or bipolar disorders; therefore, patients with other mental health conditions might have been incorporated into the depression group. Fifth, the predictions of future prevalence rates were obtained from linear regression models, which are dependent on certain assumptions such as the linearity of the trend. Sixth, some of the conditions we modelled may be present but undiagnosed in our cohort. Seventh, for the hierarchical clustering, each comorbidity is necessarily considered into a single cluster, which may not be the case . Last, some diagnostic criteria were also changed during the study period, for example, the diagnostic criteria for hypertension. Therefore, the average number of comorbidities calculated in our sample is likely to be underestimated both due to the finite set of conditions we used and to non-diagnosis in practice.
Comparison with existing literature
We found that almost 75% of patients had at least one additional comorbidity at the time of T2DM diagnosis and 44% had at least two comorbidities. Prevalence of multiple conditions in addition to T2DM was lower than that reported in some clinical trials (90%)  or studies using administrative data (91.4%)  (84.6%)  but higher than in others (44%) . However, our population was younger than in some studies, and we analysed a large but not exhaustive list of conditions. As expected, the burden of comorbidity increased with age, however, contrary to previous research [4, 8], which found a higher age-standardised prevalence of coexisting comorbidities in males or no gender difference, we found that the burden was higher in females. This reflects the pattern in the general population which shows that females tend to have more comorbid conditions than males . This difference may relate to the surveillance bias with females being more likely to visit a general practitioner and therefore have a recorded diagnosis of comorbidity. In addition, previous studies tend to focus on conditions regarded as diabetes-concordant such as cardiovascular diseases and CKD . Females with T2DM were found to have a lower probability of these having conditions and a higher prevalence of depression, which we included in our study . The presence of mental health problems may have a significant impact on the ability of the patient to manage their condition, progression of T2DM [8, 16, 18]. Our findings of the high and increasing prevalence of depression in patients with T2DM imply that the inclusion of mental health conditions is essential in studies of comorbidities in this population. We found that the prevalence of all conditions except asthma and depression increased after diagnosis of T2DM. The fall in the prevalence of treated asthma during the follow-up may be related to the correlation between metformin use and decrease in asthma exacerbation . Knowing that T2DM is highly correlated with obesity, as is asthma  and depression , it may be that patients after being diagnosed with T2DM work towards lowering their BMI, and therefore, both conditions may be resolved.
We observed a higher burden of comorbidity among people from the most deprived than the most affluent areas. Differences were also observed in the prevalence of specific conditions, notably higher prevalence of depression, CHD, asthma and COPD among people from the most deprived areas. This is consistent with other studies and may be explained by the higher prevalence of risk factors such as smoking, obesity and alcohol consumption [30, 31].
We found a very large increase in the prevalence of T2DM-comorbid depression, which is expected to rise over the next 10 years. The rising prevalence of depression and the large gender gap has also been observed for the general population . There is an ongoing discussion over whether antidepressants are overprescribed [33, 34] which could explain the rise in depression observed in our analysis. Furthermore, the data may represent rises in conditions other than depression such as chronic pain for which antidepressants can be prescribed . Although this discussion is inconclusive, the rise in antidepressant use in patients with T2DM should be a concern, with some evidence proposing that some antidepressants may be an independent risk factor for T2DM , suggesting that both conditions share similar risk factors. More research is needed to provide further insight into the increase in depression and antidepressants use in patients with T2DM. Nevertheless, people with both T2DM and depression may require tailored approaches of treatment for both conditions as depression was found to impair patients’ ability to manage their diabetes .
The observed and predicted stable or decreasing prevalence of comorbidities other than depression at the time of T2DM diagnosis may reflect the increase in the proportion of people diagnosed at a relatively early age . This could mean that people are diagnosed with T2DM before they develop other comorbidities.
Our hierarchical clustering analysis showed that conditions regarded as diabetes-concordant (stroke, atrial fibrillation, CKD, CHD, hypertension, PVD and heart failure) tend to group together in all analysed groups. Cancer has been linked with different condition groups, depending on the analysed stratum. This may be due to the fact that we grouped all types of cancer into one condition. However, specific types of cancer may be more prevalent in different groups and be linked with the conditions sharing common risk factors. At the time of the T2DM diagnosis, the clusters seem to follow an expected pattern with lung diseases (asthma and COPD), mental health conditions (depression and SMI) and vascular conditions (PVD, CHD, stroke, atrial fibrillation and heart failure) grouped together. However, the grouping becomes more complex after the diagnosis with conditions needing different treatment and management likely to occur together. These complexities highlight the need for patient-centred approach. Furthermore, greater emphasis is needed on preventative actions and constant monitoring for conditions not closely related to the ones already experienced by the patient.
Most people with T2DM have at least one other condition that can influence the self-management of diabetes and its progression. We found a high prevalence of T2DM-concordant conditions such as hypertension, CHD and CKD as well as T2DM-discordant conditions such as COPD and depression. The complexity of needs, specific to the patients’ comorbidities patterns as well as socio-economic situation, has to be considered when developing and providing comprehensive and precise care for people with T2DM. With the growing prevalence of T2DM , these complexities have to be taken into account when planning future care services, particularly given the higher cost of treating people with multiple conditions  and the lead times for developing appropriately skilled multi-disciplinary care teams. Further research is needed to identify the best course of action for treating people with multiple conditions, as recent research shows that existing interventions are not particularly effective for improving quality of life [40, 41].
Our analysis shows that cardiovascular conditions may become less prevalent among people with T2DM; however, clinicians will have to identify and manage the rising burden of comorbid mental health problems. Currently, services targeting people with T2DM are geared towards cardiovascular conditions. The growing burden of mental health conditions will require the restructuring of the services and workforce planning.
The cluster analysis showed that certain diseases are more likely to occur together; however, the specific grouping depends on the time after T2DM diagnosis. Further research could explore how individual patients experience the progression from no comorbidities to groups of conditions affecting different parts of the body and needing complex treatments.
Availability of data and materials
The data that support the findings of this study are available from the UK CPRD, but restrictions apply to the availability of these data, which were used under licence for the current study, and so are not publicly available. The data are, however, available from the authors upon reasonable request and with permission of the UK CPRD.
Coronary heart disease
Chronic kidney disease
Chronic obstructive pulmonary disease
Clinical Practice Research Datalink
Index of Multiple Deprivation
Peripheral vascular disease
Quality and Outcomes Framework
Severe mental illness
Type 2 diabetes
International Diabetes Federation. IDF Diabetes Atlas Eighth Edition 2017: International Diabetes Federation; 2017. https://doi.org/10.1016/j.diabres.2009.10.007.
Global Health Estimates. Disease burden by cause, age, sex, by country and by region, 2000–2016. Geneva: World Health Organization; 2016.
Holman N, Young B, Gadsby R. Current prevalence of type 1 and type 2 diabetes in adults and children in the UK. Diabet Med. 2015;32(9):1119–20. https://doi.org/10.1111/dme.12791 [cited 2018 Sep 26].
Iglay K, Hannachi H, Joseph Howie P, Xu J, Li X, Engel SS, et al. Prevalence and co-prevalence of comorbidities among patients with type 2 diabetes mellitus. Curr Med Res Opin. 2016;32(7):1243–52. https://doi.org/10.1185/03007995.2016.1168291 [cited 2017 Dec 19].
Petrie JR, Guzik TJ, Touyz RM. Diabetes, hypertension, and cardiovascular disease: clinical insights and vascular mechanisms. Can J Cardiol. 2018;34(5):575–84. https://doi.org/10.1016/j.cjca.2017.12.005 [cited 2019 May 21].
The Emerging Risk Factors Collaboration, Sarwar N, Gao P, SRK S, Gobin R, Kaptoge S, et al. Diabetes mellitus, fasting blood glucose concentration, and risk of vascular disease: a collaborative meta-analysis of 102 prospective studies. Lancet. 2010;375(9733):2215–22. https://doi.org/10.1016/S0140-6736(10)60484-9 [cited 2018 Aug 31].
United States Renal Data System. International comparisons. In: United States Renal Data System. 2014 USRDS annual data report: epidemiology of kidney disease in the United States. Bethesda: National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases; 2014.
Waeber B, Feihl F, Ruilope L. Diabetes and hypertension. Blood Press. 2001;10(5–6):311–21. https://doi.org/10.1080/080370501753400610.
de Groot M, Anderson R, Freedland KE, Clouse RE, Lustman PJ. Association of depression and diabetes complications: a meta-analysis. Psychosom Med. 2001;63(4):619–30. https://doi.org/10.1097/00006842-200107000-00015.
Vondra K, Vrbikova J, Dvorakova K. Thyroid gland diseases in adult patients with diabetes mellitus. Minerva Endocrinol. 2005;30(4):217–36.
Feary JR, Rodrigues LC, Smith CJ, Hubbard RB, Gibson JE. Prevalence of major comorbidities in subjects with COPD and incidence of myocardial infarction and stroke: a comprehensive analysis using data from primary care. Thorax. 2010;65(11):956–62. https://doi.org/10.1136/thx.2009.128082 [cited 2018 Aug 31].
Bayliss EA, Steiner JF, Fernald DH, Crane LA, Main DS. Descriptions of barriers to self-care by persons with comorbid chronic diseases. Ann Fam Med [Internet] 2003;1(1):15–21. https://doi.org/10.1370/AFM.4 [cited 2018 Aug 31]
Kerr EA, Heisler M, Krein SL, Kabeto M, Langa KM, Weir D, et al. Beyond comorbidity counts: how do comorbidity type and severity influence diabetes patients’ treatment priorities and self-management? J Gen Intern Med. 2007;22(12):1635–40. https://doi.org/10.1007/s11606-007-0313-2 [cited 2018 Jan 3].
Ricci-Cabello I, Stevens S, Kontopantelis E, Dalton ARH, Griffiths RI, Campbell JL, et al. Impact of the prevalence of concordant and discordant conditions on the quality of diabetes care in family practices in England. Ann Fam Med. 2015;13(6):514–22. https://doi.org/10.1370/afm.1848 [cited 2018 Jan 3].
Ciechanowski PS, Katon WJ, Russo JE. Depression and diabetes: impact of depressive symptoms on adherence, function, and costs. Arch Intern Med. 2000;160(21):3278–85.
Krein SL, Heisler M, Piette JD, Makki F, Kerr EA. The effect of chronic pain on diabetes patients’ self-management. Diabetes Care. 2005;28(1):65–70.
The Academy of Medical Sciences. Multimorbidity: a priority for global health research. London: The Academy of Medical Sciences; 2018.
Lustman PJ, Anderson RJ, Freedland KE, de Groot M, Carney RM, Clouse RE. Depression and poor glycemic control: a meta-analytic review of the literature. Diabetes Care. 2000;23(7):934–42.
Ciechanowski PS, Katon WJ, Russo JE, Hirsch IB. The relationship of depressive symptoms to symptom reporting, self-care and glucose control in diabetes. Gen Hosp Psychiatry. 25(4):246–52.
Katon WJ, Rutter C, Simon G, Lin EHB, Ludman E, Ciechanowski P, et al. The association of comorbid depression with mortality in patients with type 2 diabetes. Diabetes Care. 2005;28(11):2668–72.
Prados-Torres A, Poblador-Plou B, Calderón-Larrañaga A, Gimeno-Feliu LA, González-Rubio F, Poncel-Falcó A, et al. Multimorbidity patterns in primary care: interactions among chronic diseases using factor analysis. Gagnier JJ, editor. PLoS One 2012;7(2):e32190. https://doi.org/10.1371/journal.pone.0032190 [cited 2019 May 23]
Teljeur C, Smith SM, Paul G, Kelly A, O’Dowd T. Multimorbidity in a cohort of patients with type 2 diabetes. Eur J Gen Pract. 2013;19(1):17–22. https://doi.org/10.3109/13814788.2012.714768 [cited 2018 Feb 14].
Alonso-Morán E, Orueta JF, Fraile Esteban JI, Arteagoitia Axpe JM, Marqués González ML, Toro Polanco N, et al. The prevalence of diabetes-related complications and multimorbidity in the population with type 2 diabetes mellitus in the Basque Country. BMC Public Health. 2014;14:1059. https://doi.org/10.1186/1471-2458-14-1059 [cited 2018 Feb 14].
Luijks H, Schermer T, Bor H, van Weel C, Lagro-Janssen T, Biermans M, et al. Prevalence and incidence density rates of chronic comorbidity in type 2 diabetes patients: an exploratory cohort study. BMC Med. 2012;10(1):128. https://doi.org/10.1186/1741-7015-10-128 [cited 2018 Feb 28].
Struijs JN, Baan CA, Schellevis FG, Westert GP, van den Bos GAM. Comorbidity in patients with diabetes mellitus: impact on medical health care utilization. BMC Health Serv Res. 2006;6:84. https://doi.org/10.1186/1472-6963-6-84 [cited 2018 Feb 28].
Violan C, Foguet-Boreu Q, Flores-Mateo G, Salisbury C, Blom J, Freitag M, et al. Prevalence, determinants and patterns of multimorbidity in primary care: a systematic review of observational studies. PLoS One. 2014;9(7). https://doi.org/10.1371/journal.pone.0102149 [cited 2018 Jul 9].
Forno E. Asthma in adults with diabetes: treat their diabetes with metformin, improve their asthma? Respirology. 2016;21(7):1144–5. https://doi.org/10.1111/resp.12869 [cited 2019 Jun 13].
Hjellvik V, Tverdal A, Furu K. Body mass index as predictor for asthma: a cohort study of 118,723 males and females. Eur Respir J. 2010;35(6):1235–42. https://doi.org/10.1183/09031936.00192408 [cited 2019 Jun 13].
Moussa OM, Ardissino M, Kulatilake P, Priyantha FA, Muttoni E, Darzi A, et al. Effect of body mass index on depression in a UK cohort of 363 037 obese patients: A longitudinal analysis of transition. 2019. https://doi.org/10.1111/cob.12305 [cited 2019 May 22].
Lorant V, Deliège D, Eaton W, Robert A, Philippot P, Ansseau M. Socioeconomic inequalities in depression: a meta-analysis. Am J Epidemiol. 2003;157(2):98–112. https://doi.org/10.1093/aje/kwf182 [cited 2018 Sep 18].
Floud S, Balkwill A, Moser K, Reeves GK, Green J, Beral V, et al. The role of health-related behavioural factors in accounting for inequalities in coronary heart disease risk by education and area deprivation: prospective study of 1.2 million UK women. BMC Med. 2016;14(1):145. https://doi.org/10.1186/s12916-016-0687-2 [cited 2018 Sep 18].
Randall C, Corp A, Self A. Measuring national well-being: life in the UK. London: Office for National Statistics; 2014.
Spence D. Are antidepressants overprescribed? Yes. BMJ. 2013;346:f191. https://doi.org/10.1136/bmj.f191 [cited 2019 May 22].
Reid IC. Are antidepressants overprescribed? No. BMJ. 2013;346:f190. https://doi.org/10.1136/bmj.f190 [cited 2019 May 22].
BMA. Chronic pain : supporting safer prescribing of analgesics. London: British Medical Association; 2017.
Barnard K, Peveler RC, Holt RIG. Antidepressant medication as a risk factor for type 2 diabetes and impaired glucose regulation. Diabetes Care. 2013;36(10):3337–45. https://doi.org/10.2337/DC13-0560 [cited 2019 May 22].
Holden SE, Barnett AH, Peters JR, Jenkins-Jones S, Poole CD, Morgan CL, et al. The incidence of type 2 diabetes in the United Kingdom from 1991 to 2010. Diabetes, Obes Metab. 2013;15(9):844–52. https://doi.org/10.1111/dom.12123 [cited 2019 May 22].
Zghebi SS, Steinke DT, Carr MJ, Rutter MK, Emsley RA, Ashcroft DM. Examining trends in type 2 diabetes incidence, prevalence and mortality in the UK between 2004 and 2014. Diabetes Obes Metab. 2017;19(11):1537–45. https://doi.org/10.1111/dom.12964 [cited 2017 Dec 20].
Brilleman SL, Purdy S, Salisbury C, Windmeijer F, Gravelle H, Hollinghurst S. Implications of comorbidity for primary care costs in the UK: a retrospective observational study. Br J Gen Pract. 2013;63(609):e274–82. https://doi.org/10.3399/bjgp13X665242 [cited 2017 Nov 13].
Salisbury C, Man M-S, Bower P, Guthrie B, Chaplin K, Gaunt DM, et al. Management of multimorbidity using a patient-centred care model: a pragmatic cluster-randomised trial of the 3D approach. Lancet. 2018. https://doi.org/10.1016/S0140-6736(18)31308-4 [cited 2018 Jul 4].
Boult C, Leff B, Boyd CM, Wolff JL, Marsteller JA, Frick KD, et al. A matched-pair cluster-randomized trial of guided care for high-risk older patients. J Gen Intern Med. 2013;28(5):612–21. https://doi.org/10.1007/s11606-012-2287-y [cited 2018 Jul 4].
This study was funded by the National Institute for Health Research (NIHR) School for Primary Care Research (SPCR), under the title “Quantifying severity of chronic conditions in English Primary Care using the Clinical Practice Research Datalink” (project no. 331 and 353). This paper presents independent research funded by the National Institute for Health Research (NIHR). The study funders had no role in the study design, data collection, analysis or interpretation, in the writing of the paper or in the decision to submit the paper for publication. CDM is funded by a National Institute for Health Research (NIHR) Research Professorship (NIHR-RP- 2014-04- 026), the NIHR Collaborations for Leadership in Applied Health Research and Care West Midlands and the NIHR School for Primary Care Research.
Ethics approval and consent to participate
The CPRD’s Independent Scientific Advisory Committee (ISAC) approved this study protocol (protocol number: 18_097).
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DMA has received grant funding from Abbvie and the Leo Foundation. MKR has received educational grant support from MSD and Novo Nordisk, has modest stock ownership in GSK and has consulted for Roche. Remaining authors have no competing interests to declare.
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Nowakowska, M., Zghebi, S.S., Ashcroft, D.M. et al. The comorbidity burden of type 2 diabetes mellitus: patterns, clusters and predictions from a large English primary care cohort. BMC Med 17, 145 (2019). https://doi.org/10.1186/s12916-019-1373-y
- Type 2 diabetes mellitus
- Primary care