ArticlePloS one2014
The contribution of diseases to the male-female disability-survival paradox in the very old: results from the Newcastle 85+ study.
Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.
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31 citing papers in PubMed, 1 synthesis or guideline pooled it, 57 citations in OpenAlex.
- Low protein intake, physical activity, and physical function in European and North American community-dwelling older adults: a pooled analysis of four longitudinal aging cohorts.The American journal of clinical nutrition · 2021Pooled it
- A multistate model of health transitions in older people: a secondary analysis of ASPREE clinical trial data.The lancet. Healthy longevity · 2022Trial
- Disability trajectories in the last years of life: a Swedish longitudinal multi-cohort study.The journals of gerontology. Series A, Biological sciences and medical sciences · 2026Article
- Prevalence of functional dependence and chronic diseases in the community-dwelling Brazilian older adults: an analysis by dependence severity and multimorbidity pattern.BMC public health · 2024Article
- Differential Roles of Neural Integrity, Physical Activity and Depression in Frailty: Sex-Related Differences.Brain sciences · 2023Article
- Longevity Science and Women's Health and Wellbeing.Journal of population ageing · 2023Article
- The association between multimorbidity and mobility disability-free life expectancy in adults aged 85 years and over: A modelling study in the Newcastle 85+ cohort.PLoS medicine · 2022Article
- Psychosocial aspects and support networks associated with disability in two longevous populations in Brazil: a cross-sectional study.BMC geriatrics · 2022Article
- Health trajectories after age 60: the role of individual behaviors and the social context.Aging · 2021Article
- Trajectories of middle-aged and elderly people's chronic diseases Disability Adjusted Life Years (DALYs): cohort, socio-economic status and gender disparities.International journal for equity in health · 2021Article
- Article
- Clinical Suspicion of COVID-19 in Nursing Home Residents: Symptoms and Mortality Risk Factors.Journal of the American Medical Directors Association · 2020Article
- Transitions between frailty states in the very old: the influence of socioeconomic status and multi-morbidity in the Newcastle 85+ cohort study.Age and ageing · 2020Article
- Plasma proteomic profile of frailty.Aging cell · 2020Article
- Health profiles and socioeconomic characteristics of nonagenarians residing in Mugello, a rural area in Tuscany (Italy).BMC geriatrics · 2020Article
- Protein intake and transitions between frailty states and to death in very old adults: the Newcastle 85+ study.Age and ageing · 2019Article
- Sex Differences in Comorbidity and Frailty in Europe.International journal of public health · 2019Article
- Protein Intake and Disability Trajectories in Very Old Adults: The Newcastle 85+ Study.Journal of the American Geriatrics Society · 2019Article
- Differences between Men and Women in Mortality and the Health Dimensions of the Morbidity Process.Clinical chemistry · 2019Review
- Factors associated with change in self-reported physical activity in the very old: The Newcastle 85+ study.PloS one · 2019Article
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Authors and funding
8 authors at 2 institutions in 1 country.
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Abstract
backgroundExplanations for the male-female disability-survival paradox - that woman live longer than men but with more disability - include sex differences in diseases and their impact on disability and death. Less is known about the paradox in the very old. We examine sex differences in the presence and impact of disabling and fatal diseases accounting for the male-female disability-survival paradox in very late life.
methodsWe use data from the Newcastle 85+ Study, a cohort of people born in 1921 and all recruited at age 85 in 2006. Participants underwent a health assessment (HA) at baseline, 18 months, 36 months, 60 months, and a review of their GP records (GPRR) at baseline and 36 months. We used multi-state modelling to assess the impact of specific diseases on disability and death. Disability (measured via ADLs/IADLs) was categorised as no disability (difficulty with 0 activities), or disabled (difficulty with one or more activities). Diseases were ascertained from review of general practice records and cognitive impairment which was defined as an sMMSE of 21 or less (from health assessment).
resultsIn participants who had complete HA and GPRR, women had more arthritis (RR = 1.2, 95% CI: 1.1-1.3) and hypertension (RR = 1.2, 95%CI 1.0-1.3), more disability, and were more likely disabled at all follow-ups. From multistate models, women with cerebrovascular disease (HR: 2.6, 95% CI: 2.1-3.4) or respiratory disease (HR: 2.0, 95% CI: 1.4-3.0) were more likely to become disabled than those without but this did not hold for men (sex difference p<0.01). Men were more likely to die from respiratory disease (HR: 2.2, 95% CI: 1.8-2.8) but this did not hold for women (p = 0.002).
conclusionThe disability-survival paradox was still evident at age 85 and appears due to sex differences in the types of diseases and their impact on the disability pathway.
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