Brain Volume as an Integrated Marker for the Risk of Death in a Community-Based Sample: Age Gene/Environment Susceptibility--Reykjavik Study.

To access publisher's full text version of this article click on the hyperlink at the bottom of the page Total brain volume is an integrated measure of health and may be an independent indicator of mortality risk independent of any one clinical or subclinical disease state. We investigate the a...

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Published in:The Journals of Gerontology Series A: Biological Sciences and Medical Sciences
Main Authors: Van Elderen, Saskia S G C, Zhang, Qian, Sigurdsson, Sigudur, Haight, Thaddeus J, Lopez, Oscar, Eiriksdottir, Gudny, Jonsson, Palmi, de Jong, Laura, Harris, Tamara B, Garcia, Melissa, Gudnason, Vilmundar, van Buchem, Mark A, Launer, Lenore J
Other Authors: 1 Leiden Univ, Med Ctr, Dept Radiol, NL-2300 RA Leiden, Netherlands 2 NIA, Lab Epidemiol & Populat Sci, Intramural Res Program, NIH, Bethesda, MD 20892 USA 3 Icelandic Heart Assoc, Kopavogur, Iceland 4 Univ Pittsburgh, Dept Neurol, Pittsburgh, PA 15260 USA 5 Landspitali Hosp, Reykjavik, Iceland Organization-Enhanced Name(s) Landspitali National University Hospital
Format: Article in Journal/Newspaper
Language:English
Published: Oxford Univ Press 2016
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Online Access:http://hdl.handle.net/2336/605764
https://doi.org/10.1093/gerona/glu192
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Summary:To access publisher's full text version of this article click on the hyperlink at the bottom of the page Total brain volume is an integrated measure of health and may be an independent indicator of mortality risk independent of any one clinical or subclinical disease state. We investigate the association of brain volume to total and cause-specific mortality in a large nondemented stroke-free community-based cohort. The analysis includes 3,543 men and women (born 1907-1935) participating in the Age, Gene, Environment Susceptibility-Reykjavik Study. Participants with a known brain-related high risk for mortality (cognitive impairment or stroke) were excluded from these analyses. Quantitative estimates of total brain volume, white matter, white matter lesions, total gray matter (GM; cortical GM and subcortical GM separately), and focal cerebral vascular disease were generated from brain magnetic resonance imaging. Brain atrophy was expressed as brain tissue volume divided by total intracranial volume, yielding a percentage. Mean follow-up duration was 7.2 (0-10) years, with 647 deaths. Cox regression was used to analyze the association of mortality to brain atrophy, adjusting for demographics, cardiovascular risk factors, and cerebral vascular disease. Reduced risk of mortality was significantly associated with higher total brain volume (hazard ratio, 95% confidence interval = 0.71, 0.65-0.78), white matter (0.85, 0.78-0.93), total GM (0.74, 0.68-0.81), and cortical GM (0.78, 0.70-0.87). Overall, the associations were similar for cardiovascular and noncardiovascular-related deaths. Independent of multiple risk factors and cerebral vascular damage, global brain volume predicts mortality in a large nondemented stroke-free community-dwelling older cohort. Total brain volume may be an integrated measure reflecting a range of health and with further investigation could be a useful clinical tool when assessing risk for mortality. NIH N01-AG-12100 NIH/NIA Intramural Research Program Hjartavernd (Icelandic Heart ...