Joint effect of mid- and late-life blood pressure on the brain: the AGES-Reykjavik study
- PMID: 24898928
- PMCID: PMC4113458
- DOI: 10.1212/WNL.0000000000000517
Joint effect of mid- and late-life blood pressure on the brain: the AGES-Reykjavik study
Abstract
Objective: We hypothesized that in participants with a history of hypertension, lower late-life blood pressure (BP) will be associated with more brain pathology.
Methods: Participants are 4,057 older men and women without dementia with midlife (mean age 50 ± 6 years) and late-life (mean age 76 ± 5 years) vascular screening, cognitive function, and brain structures on MRI ascertained as part of the Age, Gene/Environment Susceptibility (AGES)-Reykjavik Study.
Results: The association of late-life BP to brain measures depended on midlife hypertension history. Higher late-life systolic and diastolic BP (DBP) was associated with an increased risk of white matter lesions and cerebral microbleeds, and this was most pronounced in participants without a history of midlife hypertension. In contrast, in participants with a history of midlife hypertension, lower late-life DBP was associated with smaller total brain and gray matter volumes. This finding was reflected back in cognitive performance; in participants with midlife hypertension, lower DBP was associated with lower memory scores.
Conclusion: In this large population-based cohort, late-life BP differentially affects brain pathology and cognitive performance, depending on the history of midlife hypertension. Our study suggests history of hypertension is critical to understand how late-life BP affects brain structure and function.
© 2014 American Academy of Neurology.
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Comment in
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Joint effect of mid- and late-life blood pressure on the brain: the AGES-Reykjavik Study.Neurology. 2015 Jan 20;84(3):329. doi: 10.1212/01.wnl.0000460552.36620.a9. Neurology. 2015. PMID: 25601884 No abstract available.
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Joint effect of mid- and late-life blood pressure on the brain: the AGES-Reykjavik Study. Author response.Neurology. 2015 Jan 20;84(3):329-30. Neurology. 2015. PMID: 25759868 No abstract available.
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