Large socioeconomic gap in period life expectancy and life years spent with complications of diabetes in the Scottish population with type 1 diabetes, 2013-2018.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2022
Historique:
received: 22 06 2021
accepted: 23 06 2022
entrez: 11 8 2022
pubmed: 12 8 2022
medline: 16 8 2022
Statut: epublish

Résumé

We report the first study to estimate the socioeconomic gap in period life expectancy (LE) and life years spent with and without complications in a national cohort of individuals with type 1 diabetes. This retrospective cohort study used linked healthcare records from SCI-Diabetes, the population-based diabetes register of Scotland. We studied all individuals aged 50 and older with a diagnosis of type 1 diabetes who were alive and residing in Scotland on 1 January 2013 (N = 8591). We used the Scottish Index of Multiple Deprivation (SIMD) 2016 as an area-based measure of socioeconomic deprivation. For each individual, we constructed a history of transitions by capturing whether individuals developed retinopathy/maculopathy, cardiovascular disease, chronic kidney disease, and diabetic foot, or died throughout the study period, which lasted until 31 December 2018. Using parametric multistate survival models, we estimated total and state-specific LE at an attained age of 50. At age 50, remaining LE was 22.2 years (95% confidence interval (95% CI): 21.6 - 22.8) for males and 25.1 years (95% CI: 24.4 - 25.9) for females. Remaining LE at age 50 was around 8 years lower among the most deprived SIMD quintile when compared with the least deprived SIMD quintile: 18.7 years (95% CI: 17.5 - 19.9) vs. 26.3 years (95% CI: 24.5 - 28.1) among males, and 21.2 years (95% CI: 19.7 - 22.7) vs. 29.3 years (95% CI: 27.5 - 31.1) among females. The gap in life years spent without complications was around 5 years between the most and the least deprived SIMD quintile: 4.9 years (95% CI: 3.6 - 6.1) vs. 9.3 years (95% CI: 7.5 - 11.1) among males, and 5.3 years (95% CI: 3.7 - 6.9) vs. 10.3 years (95% CI: 8.3 - 12.3) among females. SIMD differences in transition rates decreased marginally when controlling for time-updated information on risk factors such as HbA1c, blood pressure, BMI, or smoking. In addition to societal interventions, tailored support to reduce the impact of diabetes is needed for individuals from low socioeconomic backgrounds, including access to innovations in management of diabetes and the prevention of complications.

Sections du résumé

BACKGROUND
We report the first study to estimate the socioeconomic gap in period life expectancy (LE) and life years spent with and without complications in a national cohort of individuals with type 1 diabetes.
METHODS
This retrospective cohort study used linked healthcare records from SCI-Diabetes, the population-based diabetes register of Scotland. We studied all individuals aged 50 and older with a diagnosis of type 1 diabetes who were alive and residing in Scotland on 1 January 2013 (N = 8591). We used the Scottish Index of Multiple Deprivation (SIMD) 2016 as an area-based measure of socioeconomic deprivation. For each individual, we constructed a history of transitions by capturing whether individuals developed retinopathy/maculopathy, cardiovascular disease, chronic kidney disease, and diabetic foot, or died throughout the study period, which lasted until 31 December 2018. Using parametric multistate survival models, we estimated total and state-specific LE at an attained age of 50.
RESULTS
At age 50, remaining LE was 22.2 years (95% confidence interval (95% CI): 21.6 - 22.8) for males and 25.1 years (95% CI: 24.4 - 25.9) for females. Remaining LE at age 50 was around 8 years lower among the most deprived SIMD quintile when compared with the least deprived SIMD quintile: 18.7 years (95% CI: 17.5 - 19.9) vs. 26.3 years (95% CI: 24.5 - 28.1) among males, and 21.2 years (95% CI: 19.7 - 22.7) vs. 29.3 years (95% CI: 27.5 - 31.1) among females. The gap in life years spent without complications was around 5 years between the most and the least deprived SIMD quintile: 4.9 years (95% CI: 3.6 - 6.1) vs. 9.3 years (95% CI: 7.5 - 11.1) among males, and 5.3 years (95% CI: 3.7 - 6.9) vs. 10.3 years (95% CI: 8.3 - 12.3) among females. SIMD differences in transition rates decreased marginally when controlling for time-updated information on risk factors such as HbA1c, blood pressure, BMI, or smoking.
CONCLUSIONS
In addition to societal interventions, tailored support to reduce the impact of diabetes is needed for individuals from low socioeconomic backgrounds, including access to innovations in management of diabetes and the prevention of complications.

Identifiants

pubmed: 35951518
doi: 10.1371/journal.pone.0271110
pii: PONE-D-21-20453
pmc: PMC9371295
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0271110

Déclaration de conflit d'intérêts

All authors have completed and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. TMC reports grants from Diabetes UK Grant: 18/0005786, during the conduct of the study. SHW reports meeting attendance supported by Novo Nordisk, outside the submitted work. RJM reports personal fees from Sanofi, personal fees from NovoNordisk, outside the submitted work. NS reports personal fees from Amgen, personal fees from AstraZeneca, grants and personal fees from Boehringer Ingelheim, personal fees from Eli Lilly, personal fees from Novo Nordisk, personal fees from Pfizer, personal fees from Sanofi, outside the submitted work; HMC reports grants, personal fees and other from Eli Lilly and Company, during the conduct of the study; grants from AstraZeneca LP, other from Novartis Pharmaceuticals, grants from Regeneron, grants from Pfizer Inc, other from Roche Pharmaceuticals, other from Sanofi Aventis, grants and personal fees from Novo Nordisk, outside the submitted work. This does not alter our adherence to PLOS ONE policies on sharing data and materials. No other disclosures were reported.

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Auteurs

Andreas Höhn (A)

School of Geography and Sustainable Development, The University of St. Andrews, St. Andrews, United Kingdom.
Institute of Genetics and Cancer, The University of Edinburgh, Edinburgh, United Kingdom.

Stuart J McGurnaghan (SJ)

Institute of Genetics and Cancer, The University of Edinburgh, Edinburgh, United Kingdom.

Thomas M Caparrotta (TM)

Institute of Genetics and Cancer, The University of Edinburgh, Edinburgh, United Kingdom.

Anita Jeyam (A)

Institute of Genetics and Cancer, The University of Edinburgh, Edinburgh, United Kingdom.

Joseph E O'Reilly (JE)

Institute of Genetics and Cancer, The University of Edinburgh, Edinburgh, United Kingdom.

Luke A K Blackbourn (LAK)

Institute of Genetics and Cancer, The University of Edinburgh, Edinburgh, United Kingdom.

Sara Hatam (S)

Institute of Genetics and Cancer, The University of Edinburgh, Edinburgh, United Kingdom.

Christian Dudel (C)

Max Planck Institute for Demographic Research, Laboratory of Population Health, Rostock, GER.

Rosie J Seaman (RJ)

MRC/CSO Social and Public Health Sciences Unit, University of Glasgow, Glasgow, United Kingdom.

Joseph Mellor (J)

Usher Institute of Population Health Sciences and Informatics, The University of Edinburgh, Edinburgh, United Kingdom.

Naveed Sattar (N)

Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, United Kingdom.

Rory J McCrimmon (RJ)

School of Medicine, University of Dundee, Dundee, United Kingdom.

Brian Kennon (B)

Queen Elizabeth University Hospital, University Glasgow, Glasgow, United Kingdom.

John R Petrie (JR)

Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, United Kingdom.

Sarah Wild (S)

Usher Institute of Population Health Sciences and Informatics, The University of Edinburgh, Edinburgh, United Kingdom.

Paul M McKeigue (PM)

Usher Institute of Population Health Sciences and Informatics, The University of Edinburgh, Edinburgh, United Kingdom.

Helen M Colhoun (HM)

Institute of Genetics and Cancer, The University of Edinburgh, Edinburgh, United Kingdom.
Public Health, NHS Fife, Kirkcaldy, United Kingdom.

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