Epidemiology of High-Risk Sleep Phenotypes in a Diverse Cohort of Older Adults

Abstract Background Insomnia with objective short sleep duration (ISSD) and objective long sleep duration (LS) are high-risk sleep phenotypes that have not been examined in a diverse group of older adults. Methods We studied 1001 adults in the DORMIR study (average age 64.4[8.6] years, 65.7% female; 28.4% Black, 31.6% Hispanic, 40.1% non-Hispanic White). Insomnia was defined as self-reporting any of the following > =3 times/week: trouble getting to sleep within 30min, waking in the middle of the night/early morning or taking sleep medication. Objective overnight sleep duration was assessed by actigraphy (averaged over 5.9[0.9] days). We examined ISSD (insomnia and sleep duration< 6h), LS (sleep duration>8h), and normal sleep (NS; no insomnia and sleep duration=6-8h). Using ANOVA F-tests or chi-square, we assessed phenotype prevalence overall and according to race/ethnicity, and also examined, within each race/ethnicity group, whether comorbidities (e.g., depression, anxiety, dementia status, physical impairment [Short Physical Performance Battery< 10]) differed among phenotypes. Results ISSD prevalence was 8.1% overall and was higher among Blacks (13.4%; p < 0.001). LS prevalence was 22.1% overall and was higher among Whites (27.2%; p < 0.001). Compared to NS, depression was higher in ISSD and LS across all groups. Anxiety was higher in Hispanics and Whites with ISSD and LS compared with NS. Across all groups, physical impairment was significantly higher in LS compared with NS. Dementia status was not different across phenotypes. Conclusion The prevalence of high-risk sleep phenotypes differs across race/ethnicity groups, while comorbidities associated with phenotypes were similar. Future work should examine the association of phenotypes with adverse outcomes.

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Journal
Innovation in Aging
Published
2025-12-01
DOI
https://doi.org/10.1093/geroni/igaf122.1914
Primary Topic
Sleep and related disorders
Type
article
Field-Weighted Citation Impact
0.00
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article

Epidemiology of High-Risk Sleep Phenotypes in a Diverse Cohort of Older Adults

Clémence Cavaillès, Carrie Peltz, Brienne Miner, Jarett Talarczyk et al.
Innovation in Aging
Sleep and related disorders
article

Epidemiology of High-Risk Sleep Phenotypes in a Diverse Cohort of Older Adults

Clémence Cavaillès, Carrie Peltz, Brienne Miner, Jarett Talarczyk, Kristine Yaffe
article en

Abstract

Abstract Background Insomnia with objective short sleep duration (ISSD) and objective long sleep duration (LS) are high-risk sleep phenotypes that have not been examined in a diverse group of older adults. Methods We studied 1001 adults in the DORMIR study (average age 64.4[8.6] years, 65.7% female; 28.4% Black, 31.6% Hispanic, 40.1% non-Hispanic White). Insomnia was defined as self-reporting any of the following > =3 times/week: trouble getting to sleep within 30min, waking in the middle of the night/early morning or taking sleep medication. Objective overnight sleep duration was assessed by actigraphy (averaged over 5.9[0.9] days). We examined ISSD (insomnia and sleep duration< 6h), LS (sleep duration>8h), and normal sleep (NS; no insomnia and sleep duration=6-8h). Using ANOVA F-tests or chi-square, we assessed phenotype prevalence overall and according to race/ethnicity, and also examined, within each race/ethnicity group, whether comorbidities (e.g., depression, anxiety, dementia status, physical impairment [Short Physical Performance Battery< 10]) differed among phenotypes. Results ISSD prevalence was 8.1% overall and was higher among Blacks (13.4%; p < 0.001). LS prevalence was 22.1% overall and was higher among Whites (27.2%; p < 0.001). Compared to NS, depression was higher in ISSD and LS across all groups. Anxiety was higher in Hispanics and Whites with ISSD and LS compared with NS. Across all groups, physical impairment was significantly higher in LS compared with NS. Dementia status was not different across phenotypes. Conclusion The prevalence of high-risk sleep phenotypes differs across race/ethnicity groups, while comorbidities associated with phenotypes were similar. Future work should examine the association of phenotypes with adverse outcomes.

Innovation in AgingVol. 9(Supplement_2)
University of California, San Francisco (US), Yale University (US), Northern California Institute for Research and Education (US), University of San Francisco (US)
Good health and well-being
Openalex Percentile: Top 26%
Sleep and related disorders
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