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Interleukin-6 and C-reactive protein as predictors of cognitive decline in late midlife

OBJECTIVE: Peripheral inflammatory markers are elevated in patients with dementia. In order to assess their etiologic role, we examined whether interleukin-6 (IL-6) and C-reactive protein (CRP) measured in midlife predict concurrently assessed cognition and subsequent cognitive decline. METHODS: Mea...

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Autores principales: Singh-Manoux, Archana, Dugravot, Aline, Brunner, Eric, Kumari, Meena, Shipley, Martin, Elbaz, Alexis, Kivimaki, Mika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141998/
https://www.ncbi.nlm.nih.gov/pubmed/24991031
http://dx.doi.org/10.1212/WNL.0000000000000665
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author Singh-Manoux, Archana
Dugravot, Aline
Brunner, Eric
Kumari, Meena
Shipley, Martin
Elbaz, Alexis
Kivimaki, Mika
author_facet Singh-Manoux, Archana
Dugravot, Aline
Brunner, Eric
Kumari, Meena
Shipley, Martin
Elbaz, Alexis
Kivimaki, Mika
author_sort Singh-Manoux, Archana
collection PubMed
description OBJECTIVE: Peripheral inflammatory markers are elevated in patients with dementia. In order to assess their etiologic role, we examined whether interleukin-6 (IL-6) and C-reactive protein (CRP) measured in midlife predict concurrently assessed cognition and subsequent cognitive decline. METHODS: Mean value of IL-6 and CRP, assessed on 5,217 persons (27.9% women) in 1991–1993 and 1997–1999 in the Whitehall II longitudinal cohort study, were categorized into tertiles to examine 10-year decline (assessments in 1997–1999, 2002–2004, and 2007–2009) in standardized scores (mean = 0, SD = 1) of memory, reasoning, and verbal fluency using mixed models. Mini-Mental State Examination (MMSE) was administered in 2002–2004 and 2007–2009; decline ≥3 points was modeled with logistic regression. Analyses were adjusted for baseline age, sex, education, and ethnicity; further analyses were also adjusted for smoking, obesity, Framingham cardiovascular risk score, and chronic diseases (cancer, coronary heart disease, stroke, diabetes, and depression). RESULTS: In cross-sectional analysis, reasoning was 0.08 SD (95% confidence interval [CI] −0.14, −0.03) lower in participants with high compared to low IL-6. In longitudinal analysis, 10-year decline in reasoning was greater (ptrend = 0.01) among participants with high IL-6 (−0.35; 95% CI −0.37, −0.33) than those with low IL-6 (−0.29; 95% CI −0.31, −0.27). In addition, participants with high IL-6 had 1.81 times greater odds ratio of decline in MMSE (95% CI 1.20, 2.71). CRP was not associated with decline in any test. CONCLUSIONS: Elevated IL-6 but not CRP in midlife predicts cognitive decline; the combined cross-sectional and longitudinal effects over the 10-year observation period corresponded to an age effect of 3.9 years.
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spelling pubmed-41419982014-09-10 Interleukin-6 and C-reactive protein as predictors of cognitive decline in late midlife Singh-Manoux, Archana Dugravot, Aline Brunner, Eric Kumari, Meena Shipley, Martin Elbaz, Alexis Kivimaki, Mika Neurology Article OBJECTIVE: Peripheral inflammatory markers are elevated in patients with dementia. In order to assess their etiologic role, we examined whether interleukin-6 (IL-6) and C-reactive protein (CRP) measured in midlife predict concurrently assessed cognition and subsequent cognitive decline. METHODS: Mean value of IL-6 and CRP, assessed on 5,217 persons (27.9% women) in 1991–1993 and 1997–1999 in the Whitehall II longitudinal cohort study, were categorized into tertiles to examine 10-year decline (assessments in 1997–1999, 2002–2004, and 2007–2009) in standardized scores (mean = 0, SD = 1) of memory, reasoning, and verbal fluency using mixed models. Mini-Mental State Examination (MMSE) was administered in 2002–2004 and 2007–2009; decline ≥3 points was modeled with logistic regression. Analyses were adjusted for baseline age, sex, education, and ethnicity; further analyses were also adjusted for smoking, obesity, Framingham cardiovascular risk score, and chronic diseases (cancer, coronary heart disease, stroke, diabetes, and depression). RESULTS: In cross-sectional analysis, reasoning was 0.08 SD (95% confidence interval [CI] −0.14, −0.03) lower in participants with high compared to low IL-6. In longitudinal analysis, 10-year decline in reasoning was greater (ptrend = 0.01) among participants with high IL-6 (−0.35; 95% CI −0.37, −0.33) than those with low IL-6 (−0.29; 95% CI −0.31, −0.27). In addition, participants with high IL-6 had 1.81 times greater odds ratio of decline in MMSE (95% CI 1.20, 2.71). CRP was not associated with decline in any test. CONCLUSIONS: Elevated IL-6 but not CRP in midlife predicts cognitive decline; the combined cross-sectional and longitudinal effects over the 10-year observation period corresponded to an age effect of 3.9 years. Lippincott Williams & Wilkins 2014-08-05 /pmc/articles/PMC4141998/ /pubmed/24991031 http://dx.doi.org/10.1212/WNL.0000000000000665 Text en © 2014 American Academy of Neurology This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Singh-Manoux, Archana
Dugravot, Aline
Brunner, Eric
Kumari, Meena
Shipley, Martin
Elbaz, Alexis
Kivimaki, Mika
Interleukin-6 and C-reactive protein as predictors of cognitive decline in late midlife
title Interleukin-6 and C-reactive protein as predictors of cognitive decline in late midlife
title_full Interleukin-6 and C-reactive protein as predictors of cognitive decline in late midlife
title_fullStr Interleukin-6 and C-reactive protein as predictors of cognitive decline in late midlife
title_full_unstemmed Interleukin-6 and C-reactive protein as predictors of cognitive decline in late midlife
title_short Interleukin-6 and C-reactive protein as predictors of cognitive decline in late midlife
title_sort interleukin-6 and c-reactive protein as predictors of cognitive decline in late midlife
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141998/
https://www.ncbi.nlm.nih.gov/pubmed/24991031
http://dx.doi.org/10.1212/WNL.0000000000000665
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