Self-reported sleep and β-amyloid deposition in community-dwelling older adults.

Self-reported sleep and β-amyloid deposition in community-dwelling older adults.
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DOI:
10.1001/jamaneurol.2013.4258
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发表时间:
2013-12
期刊:
影响因子:
29
通讯作者:
Resnick, Susan M.
Resnick, Susan M.
中科院分区:
医学1区
文献类型:
--
作者:
Spira, Adam P.;Gamaldo, Alyssa A.;An, Yang;Wu, Mark N.;Simonsick, Eleanor M.;Bilgel, Murat;Zhou, Yun;Wong, Dean F.;Ferrucci, Luigi;Resnick, Susan M.

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Older adults commonly report disturbed sleep, and recent studies in humans and animals suggest links between sleep and Alzheimer disease biomarkers. Studies are needed that evaluate whether sleep variables are associated with neuroimaging evidence of β-amyloid deposition. To determine the association between self-reported sleep parameters and β-amyloid deposition in community-dwelling older adults. cross-sectional Baltimore Longitudinal Study of Aging, a prospective study of normative aging 70 adults (mean age = 76; range 53 - 91) in the BLSA neuroimaging study β-amyloid burden, measured by [11C] Pittsburgh compound B (PiB) positron emission tomography (PET) distribution volume ratios (DVR) After adjustment for potential confounders, reports of shorter sleep duration were associated with greater β-amyloid burden, measured by mean cortical DVR (cDVR; B = 0.08, 95% confidence interval (CI) 0.03, 0.14, p = 0.005) and precuneus DVR (B = 0.11, 95% CI 0.03, 0.18, p = 0.007). Reports of lower sleep quality were associated with greater β-amyloid burden measured by precuneus DVR (B = 0.08, 95% CI 0.01, 0.15, p = 0.025). Among community-dwelling older adults, reports of shorter sleep duration and lower sleep quality are associated with greater β-amyloid burden. Further studies with objective sleep measures are needed to determine whether sleep disturbance causes or accelerates Alzheimer disease.
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