Insomnia symptom severity and cognitive performance: Moderating role of APOE genotype. Issue 3 (26th July 2021)

• Record Type: Journal Article
• Authors: Baril, Andrée‐Ann; Beiser, Alexa S.; Sanchez, Erlan; Mysliwiec, Vincent; Redline, Susan; Gottlieb, Daniel J.; O'Connor, George T.; Gonzales, Mitzi M.; Himali, Dibya; Seshadri, Sudha; Himali, Jayandra J.; Pase, Matthew P.
• Is Part Of: Alzheimer's & dementia. Volume 18:Issue 3(2022)
• Page Start: 408
• Page End: 421
• Publication Date: 2021-07-26
• Subjects: aging -- Alzheimer's disease -- apolipoprotein E ε4 -- cognition -- cognitive aging -- C‐reactive protein -- dementia -- inflammation -- insomnia -- memory -- neuropsychology -- sleep; Alzheimer's disease -- Periodicals; Alzheimer Disease -- Periodicals; Dementia -- Periodicals; Démence; Maladie d'Alzheimer; Périodique électronique (Descripteur de forme); Ressource Internet (Descripteur de forme); 616.83
• DOI: 10.1002/alz.12405
• Languages: English
• ISSNs: 1552-5260

Abstract

Abstract: Introduction: We evaluated whether insomnia symptom severity was associated with cognitive function, and whether this relationship was modified by biomarkers associated with Alzheimer's disease risk. Methods: We examined insomnia symptoms and neuropsychological performance 3.4 years later in 511 dementia‐free Framingham Heart Study participants (62.65 ± 8.7 years, 50.9% male). Additionally, we explored insomnia symptoms combined with self‐reported short habitual sleep duration and effect modification by apolipoprotein E ( APOE ) ε4 allele status. Results: More severe insomnia symptoms were associated with lower performance on global cognition, and immediate and delayed Logical Memory recall, especially when insomnia symptoms were combined with short sleep duration. The association between insomnia symptoms and poorer memory recall was more pronounced in APOE ε4 allele carriers. Discussion: Insomnia symptom severity was associated with worse subsequent global cognitive and memory performance, which was especially apparent in APOE ε4 allele carriers, suggesting that poor sleep might be particularly detrimental when the brain is already vulnerable to neurodegeneration.