TY - JOUR
T1 - Poor sleep is associated with impaired cognitive function in older women
T2 - The study of osteoporotic fractures
AU - Blackwell, Terri
AU - Yaffe, Kristine
AU - Ancoli-Israel, Sonia
AU - Schneider, Jennifer L.
AU - Cauley, Jane A.
AU - Hillier, Teresa A.
AU - Fink, Howard A.
AU - Stone, Katie L.
N1 - Funding Information:
ACKNOWLEDGMENTS This project is supported by National Institutes of Health grants AG05407, AR35582, AG05394, AR35584, AR35583, and AG08415. Dr. Yaffe is a Beeson Faculty Scholar in Aging and is supported by National Institute on Aging grant R01 AG021918.
PY - 2006/4
Y1 - 2006/4
N2 - Background. The association between objectively measured sleep and cognition among community-dwelling elderly persons remains understudied. This observational, cross-sectional analysis examined this association. Methods. Results are from 2932 women (mean age 83.5 years) in the Study of Osteoporotic Fractures between 2002 and 2004. Cognitive function was measured by Mini-Mental State Examination (MMSE) and Trail Making B Test (Trails B). Cognitive impairment was denned as MMSE < 26 or Trails B > 278 seconds. Sleep parameters measured objectively using actigraphy included total sleep time, sleep efficiency, sleep latency, wake after sleep onset (WASO), and total nap time. Results. There were 305 women (10.6%) with MMSE < 26 and 257 women (9.3%) with Trails B > 278 seconds. Compared with women with sleep efficiency >70%, those with <70% had a higher risk of cognitive impairment (MMSE < 26 multivariate odds ratio [MOR]=1.61; 95% confidence interval [CI], 1.20-2.16; Trails B > 278 MOR=1.96; 95% CI, 1.43-2.67). Higher sleep latency was associated with higher risk of cognitive impairment (per half hour: MMSE < 26 MOR=1.23; 95% CI, 1.13-1.33; Trails B > 278 MOR=1.13; 95% CI, 1.04-1.24), as was higher WASO (per half hour: MMSE < 26 MOR=1.15; 95% CI, 1.06-1.23; Trails B > 278 MOR=1.24; 95% CI, 1.15-1.34). Women who napped >2 hours per day had a higher risk (MMSE < 26 MOR=1.42; 95% CI, 1.05-1.93; Trails B > 278 MOR=1.74; 95% CI, 1.26-2.40). There was no significant relationship for total sleep time. Conclusion. Objectively measured disturbed sleep was consistently related to poorer cognition, whereas total sleep time was not. This finding may suggest that it is disturbance of sleep rather than quantity that affects cognition.
AB - Background. The association between objectively measured sleep and cognition among community-dwelling elderly persons remains understudied. This observational, cross-sectional analysis examined this association. Methods. Results are from 2932 women (mean age 83.5 years) in the Study of Osteoporotic Fractures between 2002 and 2004. Cognitive function was measured by Mini-Mental State Examination (MMSE) and Trail Making B Test (Trails B). Cognitive impairment was denned as MMSE < 26 or Trails B > 278 seconds. Sleep parameters measured objectively using actigraphy included total sleep time, sleep efficiency, sleep latency, wake after sleep onset (WASO), and total nap time. Results. There were 305 women (10.6%) with MMSE < 26 and 257 women (9.3%) with Trails B > 278 seconds. Compared with women with sleep efficiency >70%, those with <70% had a higher risk of cognitive impairment (MMSE < 26 multivariate odds ratio [MOR]=1.61; 95% confidence interval [CI], 1.20-2.16; Trails B > 278 MOR=1.96; 95% CI, 1.43-2.67). Higher sleep latency was associated with higher risk of cognitive impairment (per half hour: MMSE < 26 MOR=1.23; 95% CI, 1.13-1.33; Trails B > 278 MOR=1.13; 95% CI, 1.04-1.24), as was higher WASO (per half hour: MMSE < 26 MOR=1.15; 95% CI, 1.06-1.23; Trails B > 278 MOR=1.24; 95% CI, 1.15-1.34). Women who napped >2 hours per day had a higher risk (MMSE < 26 MOR=1.42; 95% CI, 1.05-1.93; Trails B > 278 MOR=1.74; 95% CI, 1.26-2.40). There was no significant relationship for total sleep time. Conclusion. Objectively measured disturbed sleep was consistently related to poorer cognition, whereas total sleep time was not. This finding may suggest that it is disturbance of sleep rather than quantity that affects cognition.
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U2 - 10.1093/gerona/61.4.405
DO - 10.1093/gerona/61.4.405
M3 - Article
C2 - 16611709
AN - SCOPUS:33645998100
SN - 1079-5006
VL - 61
SP - 405
EP - 410
JO - Journals of Gerontology - Series A Biological Sciences and Medical Sciences
JF - Journals of Gerontology - Series A Biological Sciences and Medical Sciences
IS - 4
ER -