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. 2022 Sep;10(9):655-667.
doi: 10.1016/S2213-8587(22)00186-3. Epub 2022 Jul 15.

Burden of diabetes and hyperglycaemia in adults in the Americas, 1990-2019: a systematic analysis for the Global Burden of Disease Study 2019

Collaborators

Burden of diabetes and hyperglycaemia in adults in the Americas, 1990-2019: a systematic analysis for the Global Burden of Disease Study 2019

GBD 2019 Diabetes in the Americas Collaborators. Lancet Diabetes Endocrinol. 2022 Sep.

Abstract

Background: High prevalence of diabetes has been reported in the Americas, but no comprehensive analysis of diabetes burden and related factors for the region is available. We aimed to describe the burden of type 1 and type 2 diabetes and that of hyperglycaemia in the Americas from 1990 to 2019.

Methods: We used estimates from GBD 2019 to evaluate the burden of diabetes in adults aged 20 years or older and high fasting plasma glucose in adults aged 25 years or older in the 39 countries and territories of the six regions in the Americas from 1990 to 2019. The main source to estimate the mortality attributable to diabetes and to chronic kidney disease due to diabetes was vital registration. Mortality due to overall diabetes (ie, diabetes and diabetes due to chronic kidney disease) was estimated using the Cause of Death Ensemble model. Years of life lost (YLLs) were calculated as the number of deaths multiplied by standard life expectancy at the age that the death occurred, years lived with disability (YLDs) were estimated based on the prevalence and severity of complications of diabetes. Disability-adjusted life-years (DALYs) were estimated as a sum of YLDs and YLLs. We assessed the association of diabetes burden with the level of development of a country (according to the Socio-demographic Index), health-care access and quality (estimated with the Healthcare Access and Quality Index), and diabetes prevalence. We also calculated the population attributable fraction (PAF) of diabetes burden due to each of its risk factors. We report the 95% uncertainty intervals for all estimates.

Findings: In 2019, an estimated total of 409 000 (95% uncertainty interval 373 000-443 000) adults aged 20 years or older in the Americas died from diabetes, which represented 5·9% of all deaths. Diabetes was responsible for 2266 (1930-2649) crude DALYs per 100 000 adults in the Americas, and high fasting plasma glucose for 4401 DALYs (3685-5265) per 100 000 adults, with large variation across regions. DALYs were mostly due to type 2 diabetes and distribution was heterogeneous, being highest in central Latin America and the Caribbean and lowest in high-income North America and southern Latin America. Between 1990 and 2019, age-standardised DALYs due to type 2 diabetes increased 27·4% (22·0-32·5). This increase was particularly high in Andean Latin America and high-income North America. Burden for both type 1 and type 2 diabetes across countries increased with higher diabetes prevalence and decreased with greater Socio-demographic and Healthcare Access and Quality Indices. Main risk factors for the burden were high BMI, with a PAF of 63·2% and dietary risks, with a PAF of 27·5%. The fraction of burden due to disability has increased since 1990 and now represents nearly half of the overall burden in 2019.

Interpretation: The burden of diabetes in the Americas is large, increasing, heterogeneous, and expanding. To confront the rising burden, population-based interventions aimed to reduce type 2 diabetes risk and strengthening health systems to provide effective and cost-efficient care for those affected are mandatory.

Funding: Bill & Melinda Gates Foundation.

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Conflict of interest statement

Declaration of interests T Bärnighausen reports support for the present manuscript from Alexander von Humboldt Foundation, Wellcome Trust, German Research Foundation, and US National Institutes of Health (National Institute of Allergy and Infectious Diseases, National Institute on Aging, and Fogarty International Center), paid to his institution. I Filip and A Radfar report support from Avicenna Medical and Clinical Research Institute, outside the submitted work. J A Singh reports consulting fees from Crealta/Horizon, Medisys, Fidia, PK Med, Two labs, Adept Field Solutions, Clinical Care Options, Clearview Healthcare Partners, Putnam Associates, Focus Forward, Navigant Consulting, Spherix, MedIQ, Jupiter Life Science, UBM, Trio Health, Medscape, WebMD, and Practice Point Communications, the National Institutes of Health, and the American College of Rheumatology; payment or honoraria for lectures, presentations, speakers' bureaus, manuscript writing or educational events from Simply Speaking; support for attending meetings or travel from the steering committee of OMERACT; participation on a Data Safety Monitoring Board or Advisory Board with the US Food and Drug Administration Arthritis Advisory Committee; leadership or fiduciary role in board, society, committee or advocacy group, paid or unpaid, with OMERACT as a steering committee member, with the Veterans Affairs Rheumatology Field Advisory Committee as Chair (unpaid), and with the UAB Cochrane Musculoskeletal Group Satellite Center on Network Meta-analysis and editor and director (unpaid); stock or stock options in TPT Global Tech, Vaxart Pharmaceuticals, Atyu Biopharma, Adaptimmune Therapeutics, GeoVax Labs, Pieris Pharmaceuticals, Enzolytics, Seres Therapeutics, Tonix Pharmaceuticals and Charlotte's Web Holdings, and previously owned stock options in Amarin, Viking and Moderna Pharmaceuticals; all outside the submitted work.

Figures

Figure 1
Figure 1
Age-standardised DALY rate in 2019 and percentage change in DALY rate from 1990–2019 for type 1 and type 2 diabetes, both sexes (A) Age-standardised type 2 diabetes DALY rate per 100 000 adults aged 20 years or older in 2019. (B) Percentage change in age-standardised type 2 diabetes DALY rate, 1990–2019. (C) Age-standardised type 1 diabetes DALY rate per 100 000 adults aged 20 years or older in 2019. (D) Percentage change in age-standardised type 1 diabetes DALY rate, 1990–2019. DALY=disability-adjusted life-year. *Aged 20 years or older.
Figure 2
Figure 2
Percentage of total all-age diabetes burden expressed as disability (YLDs) and premature mortality (YLLs) among regions of the Americas in 1990 and 2019, both sexes YLDs=years lived with disability. YLLs=years of life lost. *Aged 20 years or older.
Figure 3
Figure 3
All-age DALY rate due to high fasting plasma glucose in adults (older than 25 years) in the Americas by cause in 2019 The burden includes that resulting directly from diabetes (deaths; acute decompensations, microvascular complications including chronic kidney disease, and the burden of living with diabetes) and indirectly from diabetes and lesser degrees of hyperglycaemia via the occurrence of outcomes in other disease groups. DALY=disability-adjusted life-year. *Aged older than 25 years.
Figure 4
Figure 4
Correlation of the SDI (A), the HAQ Index (B), and prevalence of diabetes (C) with the age-standardised DALY rate due to diabetes in the Americas, 2019 DALY=disability-adjusted life-year. HAQ Index=Healthcare Access and Quality Index. SDI=Socio-demographic Index. *Aged 20 years or older.
Figure 5
Figure 5
Crude population attributable fraction of DALYs due to type 2 diabetes for the main risk factors for diabetes identified by GBD 2019, by region Error bars indicate 95% uncertainty intervals. GBD=Global Burden of Diseases, Injuries, and Risk Factors Study.

Comment in

  • The burden of diabetes in the Americas.
    Bernabe-Ortiz A, Carrillo-Larco RM. Bernabe-Ortiz A, et al. Lancet Diabetes Endocrinol. 2022 Sep;10(9):613-614. doi: 10.1016/S2213-8587(22)00196-6. Epub 2022 Jul 15. Lancet Diabetes Endocrinol. 2022. PMID: 35850130 No abstract available.

References

    1. WHO General meeting of the WHO global coordination mechanism on the prevention and control of noncommunicable diseases: meeting report. International Conference Centre, Geneva, Switzerland, 5-6 November 2018. 2019. https://apps.who.int/iris/handle/10665/310961
    1. Vos T, Lim SS, Abbafati C, et al. Global burden of 369 diseases and injuries in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019. Lancet. 2020;396:1204–1222. - PMC - PubMed
    1. Moradi-Lakeh M, El Bcheraoui C, Khalil I, et al. Diabetes mellitus and chronic kidney disease in the Eastern Mediterranean Region: findings from the Global Burden of Disease 2015 study. Int J Public Health. 2018;63(suppl 1):177–186. - PMC - PubMed
    1. Goodall R, Alazawi A, Hughes W, et al. Trends in type 2 diabetes mellitus disease burden in European Union countries between 1990 and 2019. Sci Rep. 2021;11 - PMC - PubMed
    1. International Diabetes Federation IDF Diabetes Atlas, 9th edn. 2019. https://www.diabetesatlas.org/en/

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