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An Immune Risk Phenotype, Cognitive Impairment, and Survival in Very Late Life: Impact of Allostatic Load in Swedish Octogenarian and Nonagenarian Humans
Abstract
In the previous OCTO longitudinal study, we identified an immune risk phenotype (IRP) of high CD8 and low CD4 numbers and poor proliferative response. We also demonstrated that cognitive impairment constitutes a major predictor of nonsurvival. In the present NONA longitudinal study, we simultaneously examine in a model of allostatic load IRP and compromised cognition in 4-year survival in a population-based sample (n = 138, 86–94 years). Immune system measurements consisted of determinations of T-cell subsets, plasma interleukin 6 and cytomegalovirus and Epstein–Barr virus serology. Interleukin 2 responsiveness to concanavalin A, using data from the previous OCTO (octogenarians) immune study, hereafter OCTO immune, was also examined. Cognitive status was rated using a battery of neuropsychological tests. Logistic regression indicated that the IRP and cognitive impairment together predicted 58% of observed deaths. IRP was associated with late differentiated CD8+CD28−CD27− cells (p <.001), decreased interleukin 2 responsiveness (p <.05) and persistent viral infection (p <.01). Cognitive impairment was associated with increased plasma interleukin 6 (p <.001). IRP individuals with cognitive impairment were all deceased at the follow-up, indicating an allostatic overload.
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Metadata
- Authors
- Wikby, A., Ferguson, F., Forsey, R., Thompson, J., Strindhall, J., Löfgren, S., Nilsson, B.-O., Ernerudh, J., Pawelec, G., & Johansson, B.
- Affiliations
- Jönköping University (SE)
- Corresponding author
- Wikby, Anders
- Venue
- The Journals of Gerontology Series A: Biological Sciences and Medical Sciences
- Publisher
- Oxford University Press (OUP)
- Published
- 2005-05-01
- Volume
- 60
- Issue
- 5
- Pages
- 556-565
- ISSN
- 1079-5006 (ISSN-L)
- 1758-535X
- OpenAlex
- W2153840275
- Cited by
- 407
- References
- 57
- Citations by year
- 2026: 11 · 2025: 8 · 2024: 12 · 2023: 7 · 2022: 14 · 2021: 22 · 2020: 20 · 2019: 30 · 2018: 22 · 2017: 30 · 2016: 29 · 2015: 18 · 2014: 27 · 2013: 18 · 2012: 21
- FWCI
- 23.42
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journals of Gerontology Series A (publishedVersion)
- PubMed (publishedVersion)
- Funders
- European Commission
- Topics
- Social Sciences › Psychology › Developmental and Educational Psychology › Aging and Gerontology Research
- Social Sciences › Health › Health disparities and outcomes
- Health Sciences › Medicine › Geriatrics and Gerontology › Frailty in Older Adults
- Keywords
- allostatic load, cognitive impairment, survival, octogenarians, nonagenarians, interleukin-2 responsiveness, interleukin-6, cytomegalovirus serology, Epstein-Barr virus serology, viral persistence, T cell subsets, mortality prediction, oldest old
- MeSH terms
- Aged, Aged, 80 and over, Aging, Analysis of Variance, Cognition Disorders, Female, Health Status Indicators, Humans, Interleukin-2, Life Expectancy, Longevity, Longitudinal Studies, Male, Phenotype, Probability, Sweden, Cohort Studies, Geriatric Assessment, Antigens, CD, Interleukin-6, Survival Rate, CD4-CD8 Ratio, Immunocompromised Host, Risk Assessment, Statistics, Nonparametric
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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