Association Between Slow-Wave Sleep Loss and Incident Dementia

Author:

Himali Jayandra J.12345,Baril Andree-Ann167,Cavuoto Marina G.8,Yiallourou Stephanie8,Wiedner Crystal D.2,Himali Dibya15,DeCarli Charles9,Redline Susan1011,Beiser Alexa S.145,Seshadri Sudha12,Pase Matthew P.1812

Affiliation:

1. Framingham Heart Study, Framingham, Massachusetts

2. Glenn Biggs Institute for Alzheimer’s & Neurodegenerative Diseases, UT Health San Antonio, San Antonio, Texas

3. Department of Population Health Sciences, University of Texas Health Science Center, San Antonio

4. Department of Biostatistics, Boston University School of Public Health, Boston, Massachusetts

5. Boston University School of Medicine, Boston, Massachusetts

6. Douglas Mental Health University Institute, Verdun, Quebec, Canada

7. Department of Psychiatry, McGill University, Montreal, Quebec, Canada

8. Turner Institute for Brain and Mental Health, School of Psychological Sciences, Monash University, Clayton, Victoria, Australia

9. Department of Neurology, University of California, Davis

10. Division of Sleep and Circadian Disorders, Brigham and Women’s Hospital, Boston, Massachusetts

11. Department of Medicine, Harvard Medical School, Boston, Massachusetts

12. Harvard T.H. Chan School of Public Health, Harvard University, Boston, Massachusetts

Abstract

ImportanceSlow-wave sleep (SWS) supports the aging brain in many ways, including facilitating the glymphatic clearance of proteins that aggregate in Alzheimer disease. However, the role of SWS in the development of dementia remains equivocal.ObjectiveTo determine whether SWS loss with aging is associated with the risk of incident dementia and examine whether Alzheimer disease genetic risk or hippocampal volumes suggestive of early neurodegeneration were associated with SWS loss.Design, Setting, and ParticipantsThis prospective cohort study included participants in the Framingham Heart Study who completed 2 overnight polysomnography (PSG) studies in the time periods 1995 to 1998 and 2001 to 2003. Additional criteria for individuals in this study sample were an age of 60 years or older and no dementia at the time of the second overnight PSG. Data analysis was performed from January 2020 to August 2023.ExposureChanges in SWS percentage measured across repeated overnight sleep studies over a mean of 5.2 years apart (range, 4.8-7.1 years).Main OutcomeRisk of incident all-cause dementia adjudicated over 17 years of follow-up from the second PSG.ResultsFrom the 868 Framingham Heart Study participants who returned for a second PSG, this cohort included 346 participants with a mean age of 69 years (range, 60-87 years); 179 (52%) were female. Aging was associated with SWS loss across repeated overnight sleep studies (mean [SD] change, −0.6 [1.5%] per year; P < .001). Over the next 17 years of follow-up, there were 52 cases of incident dementia. In Cox regression models adjusted for age, sex, cohort, positivity for at least 1 APOE ε4 allele, smoking status, sleeping medication use, antidepressant use, and anxiolytic use, each percentage decrease in SWS per year was associated with a 27% increase in the risk of dementia (hazard ratio, 1.27; 95% CI, 1.06-1.54; P = .01). SWS loss with aging was accelerated in the presence of Alzheimer disease genetic risk (ie, APOE ε4 allele) but not hippocampal volumes measured proximal to the first PSG.Conclusions and RelevanceThis cohort study found that slow-wave sleep percentage declined with aging and Alzheimer disease genetic risk, with greater reductions associated with the risk of incident dementia. These findings suggest that SWS loss may be a modifiable dementia risk factor.

Publisher

American Medical Association (AMA)

Subject

Neurology (clinical)

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