The contribution of multiple long-term conditions to widening inequalities in disability-free life expectancy over two decades: Longitudinal analysis of two cohorts using the Cognitive Function and Ageing Studies.

Disability Health expectancy Life expectancy Multimorbidity Socioeconomic status

Journal

EClinicalMedicine
ISSN: 2589-5370
Titre abrégé: EClinicalMedicine
Pays: England
ID NLM: 101733727

Informations de publication

Date de publication:
Sep 2021
Historique:
received: 08 06 2021
revised: 07 07 2021
accepted: 08 07 2021
entrez: 13 8 2021
pubmed: 14 8 2021
medline: 14 8 2021
Statut: epublish

Résumé

: Disability-free life expectancy (DFLE) inequalities by socioeconomic deprivation are widening, alongside rising prevalence of multiple long-term conditions (MLTCs). We use longitudinal data to assess whether MLTCs contribute to the widening DFLE inequalities by socioeconomic deprivation. : The Cognitive Function and Ageing Studies (CFAS I and II) are large population-based studies of those ≥65 years, conducted in three areas in England. Baseline occurred in 1991 (CFAS I, : For people with MLTCs, inequalities in DFLE at age 65 between the most and least affluent widened to around 2.5 years (men:2.4 years, 95% confidence interval (95%CI) 0.4-4.4; women:2.6 years, 95%CI 0.7-4.5) by 2011. Incident disability reduced for the most affluent women (Relative Risk Ratio (RRR):0.6, 95%CI 0.4-0.9), and mortality with disability reduced for least affluent men (RRR:0.6, 95%CI 0.5-0.8). MLTCs prevalence increased only for least affluent men (1991: 58.8%, 2011: 66.9%) and women (1991: 60.9%, 2011: 69.1%). However, DFLE inequalities were as large in people without MLTCs (men:2.4 years, 95%CI 0.3-4.5; women:3.1 years, 95% CI 0.8-5.4). : Widening DFLE inequalities were not solely due to MLTCs. Reduced disability incidence with MLTCs is possible but was only achieved in the most affluent.

Sections du résumé

BACKGROUND BACKGROUND
: Disability-free life expectancy (DFLE) inequalities by socioeconomic deprivation are widening, alongside rising prevalence of multiple long-term conditions (MLTCs). We use longitudinal data to assess whether MLTCs contribute to the widening DFLE inequalities by socioeconomic deprivation.
METHODS METHODS
: The Cognitive Function and Ageing Studies (CFAS I and II) are large population-based studies of those ≥65 years, conducted in three areas in England. Baseline occurred in 1991 (CFAS I,
FINDINGS RESULTS
: For people with MLTCs, inequalities in DFLE at age 65 between the most and least affluent widened to around 2.5 years (men:2.4 years, 95% confidence interval (95%CI) 0.4-4.4; women:2.6 years, 95%CI 0.7-4.5) by 2011. Incident disability reduced for the most affluent women (Relative Risk Ratio (RRR):0.6, 95%CI 0.4-0.9), and mortality with disability reduced for least affluent men (RRR:0.6, 95%CI 0.5-0.8). MLTCs prevalence increased only for least affluent men (1991: 58.8%, 2011: 66.9%) and women (1991: 60.9%, 2011: 69.1%). However, DFLE inequalities were as large in people without MLTCs (men:2.4 years, 95%CI 0.3-4.5; women:3.1 years, 95% CI 0.8-5.4).
INTERPRETATION CONCLUSIONS
: Widening DFLE inequalities were not solely due to MLTCs. Reduced disability incidence with MLTCs is possible but was only achieved in the most affluent.

Identifiants

pubmed: 34386756
doi: 10.1016/j.eclinm.2021.101041
pii: S2589-5370(21)00321-7
pmc: PMC8342913
doi:

Types de publication

Journal Article

Langues

eng

Pagination

101041

Subventions

Organisme : Medical Research Council
ID : G0601022
Pays : United Kingdom
Organisme : Medical Research Council
ID : G9901400
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/K02325X/1
Pays : United Kingdom
Organisme : The Dunhill Medical Trust
ID : RPGF1806/44
Pays : United Kingdom

Informations de copyright

© 2021 The Author(s).

Déclaration de conflit d'intérêts

Dr. Bennett reports grants from Dunhill Medical Trust, grants from Medical Research Council, grants from Alzheimer's Society, grants from National Institute of Health Research, during the conduct of the study; Dr. Kingston reports grants from Dunhill Medical Trust, grants from Legal & General, from UKRI Innovate UK, from NIHR School for Primary Care Research, during the conduct of the study; .Dr. Kingston reports grants from Dunhill Medical Trust, grants from Legal & General, grants from UKRI Innovate UK, grants from NIHR School for Primary Care Research, during the conduct of the study;Dr. Lourida reports grants from Dunhill Medical Trust, grants from Medical Research Council, grants from National Institute of Health Research, grants from Alzheimer's Society, during the conduct of the study; Dr. Robinson reports grants from Dunhill Medical Trust, grants from Medical Research Council, grants from Alzheimer's Society, grants from National Institute of Health Research, during the conduct of the study; Dr. Corner reports grants from Dunhill Medical Trust, grants from Medical Research Council, grants from Alzheimer's Society, grants from National Institute of Health Research, during the conduct of the study; Dr. Brayne reports grants from Dunhill Medical Trust, grants from Medical Research Council, grants from Alzheimer's Society, grants from National Institute of Health Research, during the conduct of the study; Dr. Matthews reports grants from Dunhill Trust, NIHR, Medical Research Council, and the Alzheimer's Society UK, during the conduct of the study; Dr. Jagger reports grants from Dunhill Medical Trust, grants from Medical Research Council, grants from Alzheimer's Society, grants from National Institute of Health Research, during the conduct of the study.

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Auteurs

Holly Q Bennett (HQ)

Population Health Sciences Institute, Faculty of Medical Sciences, Biomedical Research Building, Campus for Ageing and Vitality, Newcastle University, Newcastle upon Tyne, NE4 5PL, UK.

Andrew Kingston (A)

Population Health Sciences Institute, Faculty of Medical Sciences, Biomedical Research Building, Campus for Ageing and Vitality, Newcastle University, Newcastle upon Tyne, NE4 5PL, UK.

Ilianna Lourida (I)

Population Health Sciences Institute, Faculty of Medical Sciences, Biomedical Research Building, Campus for Ageing and Vitality, Newcastle University, Newcastle upon Tyne, NE4 5PL, UK.

Louise Robinson (L)

Population Health Sciences Institute, Faculty of Medical Sciences, Biomedical Research Building, Campus for Ageing and Vitality, Newcastle University, Newcastle upon Tyne, NE4 5PL, UK.

Lynne Corner (L)

Population Health Sciences Institute, Faculty of Medical Sciences, Biomedical Research Building, Campus for Ageing and Vitality, Newcastle University, Newcastle upon Tyne, NE4 5PL, UK.

Carol Eg Brayne (CE)

Cambridge Institute of Public Health, Forvie site, University of Cambridge School of Clinical Medicine, Cambridge Biomedical campus, Cambridge CB2 0SR, UK.

Fiona E Matthews (FE)

Population Health Sciences Institute, Faculty of Medical Sciences, Biomedical Research Building, Campus for Ageing and Vitality, Newcastle University, Newcastle upon Tyne, NE4 5PL, UK.

Carol Jagger (C)

Population Health Sciences Institute, Faculty of Medical Sciences, Newcastle University, Edwardson Building, Campus for Ageing and Vitality, Newcastle upon Tyne NE4 5PL, UK.

Classifications MeSH