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      Temporal trends in the prevalence and incidence of depression and the interplay of comorbidities in patients with young- and usual-onset type 2 diabetes from the USA and the UK

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          Abstract

          Aims/hypothesis

          We aimed to investigate the prevalence and incidence of depression, and the interplay of cardiometabolic comorbidities, in the differentiation of depression risk between young-onset diabetes (diagnosis at age <40 years) and usual-onset diabetes (diagnosis at age ≥40 years).

          Methods

          Using electronic medical records from the UK and USA, retrospective cohorts of adults with incident type 2 diabetes diagnosed between 2006 and 2017 were examined. Trends in the prevalence and incidence of depression, and risk of developing depression, in participants with young-onset type 2 diabetes compared with usual-onset type 2 diabetes were assessed separately by sex and comorbidity status.

          Results

          In total 230,932/1,143,122 people with type 2 diabetes from the UK/USA (mean age 58/60 years, proportion of men 57%/46%) were examined. The prevalence of depression in the UK/USA increased from 29% (95% CI 28, 30)/22% (95% CI 21, 23) in 2006 to 43% (95% CI 42, 44)/29% (95% CI 28, 29) in 2017, with the prevalence being similar across all age groups. A similar increasing trend was observed for incidence rates. In the UK, compared with people aged ≥50 years with or without comorbidity, 18–39-year-old men and women had 23–57% and 20–55% significantly higher risks of depression, respectively. In the USA, compared with those aged ≥60 years with or without comorbidity, 18–39-year-old men and women had 5–17% and 8–37% significantly higher risks of depression, respectively.

          Conclusions/interpretation

          Depression risk has been increasing in people with incident type 2 diabetes in the UK and USA, particularly among those with young-onset type 2 diabetes, irrespective of other comorbidities. This suggests that proactive mental health assessment from the time of type 2 diabetes diagnosis in primary care is essential for effective clinical management of people with type 2 diabetes.

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          Supplementary Information

          The online version contains peer-reviewed and unedited supplementary material available at 10.1007/s00125-022-05764-9.

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          Most cited references33

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          Type 2 diabetes in adolescents and young adults

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            Generalisability of The Health Improvement Network (THIN) database: demographics, chronic disease prevalence and mortality rates.

            The degree of generalisability of patient databases to the general population is important for interpreting database research. This report describes the representativeness of The Health Improvement Network (THIN), a UK primary care database, of the UK population. Demographics, deprivation (Townsend), Quality and Outcomes Framework (QOF) condition prevalence and deaths from THIN were compared with national statistical and QOF 2006/2007 data. Demographics were similar although THIN contained fewer people aged under 25 years. Condition prevalence was comparable, e.g. 3.5% diabetes prevalence in THIN, 3.7% nationally. More THIN patients lived in the most affluent areas (23.5% in THIN, 20% nationally). Between 1990 and 2009, standardised mortality ratio ranged from 0.81 (95% CI: 0.39-1.49; 1990) to 0.93 (95% CI: 0.48-1.64; 1995). Adjusting for demographics/deprivation, the 2006 THIN death rate was 9.08/1000 population close to the national death rate of 9.4/1000 population. THIN is generalisable to the UK for demographics, major condition prevalence and death rates adjusted for demographics and deprivation.
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              Young-onset type 2 diabetes mellitus — implications for morbidity and mortality

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                Author and article information

                Contributors
                sambhupaul@hotmail.com , sanjoy.paul@unimelb.edu.au
                Journal
                Diabetologia
                Diabetologia
                Diabetologia
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0012-186X
                1432-0428
                5 September 2022
                5 September 2022
                2022
                : 65
                : 12
                : 2066-2077
                Affiliations
                [1 ]GRID grid.1008.9, ISNI 0000 0001 2179 088X, Melbourne EpiCentre, Department of Medicine at Royal Melbourne Hospital, , University of Melbourne, ; Melbourne, VIC Australia
                [2 ]GRID grid.266100.3, ISNI 0000 0001 2107 4242, Department of Family and Community Medicine, , University of California, ; San Diego, CA USA
                [3 ]GRID grid.417815.e, ISNI 0000 0004 5929 4381, Present Address: AstraZeneca, ; London, UK
                Article
                5764
                10.1007/s00125-022-05764-9
                9630215
                36059021
                8ef9bbf1-a362-4693-9aa7-a000eb39b056
                © The Author(s) 2022

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 13 December 2021
                : 3 May 2022
                Funding
                Funded by: University of Melbourne
                Categories
                Article
                Custom metadata
                © Springer-Verlag GmbH Germany, part of Springer Nature 2022

                Endocrinology & Diabetes
                antidepressants,depression,diabetes,mental illness,real-world evidence
                Endocrinology & Diabetes
                antidepressants, depression, diabetes, mental illness, real-world evidence

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