Brain-derived neurotrophic factor (BDNF) variants and promoter I methylation are associated with prolonged nocturnal awakenings in older adults.


Journal

Journal of sleep research
ISSN: 1365-2869
Titre abrégé: J Sleep Res
Pays: England
ID NLM: 9214441

Informations de publication

Date de publication:
08 2023
Historique:
revised: 12 01 2023
received: 27 07 2022
accepted: 12 01 2023
medline: 17 7 2023
pubmed: 4 2 2023
entrez: 3 2 2023
Statut: ppublish

Résumé

Brain-derived neurotrophic factor (BDNF) is important for sleep physiology. This study investigates whether BDNF variants and promoter I methylation may be implicated in sleep disturbances in older adults. Genotyping was performed for seven BDNF single nucleotide polymorphisms (SNPs) in 355 community-dwelling older adults (aged ≥65 years) and BDNF exon 1 promoter methylation was measured in blood samples at baseline (n = 153). Self-reported daytime sleepiness and insomnia, ambulatory polysomnography measures of sleep continuity and architecture, and psychotropic drug intake were assayed during follow-up. Logistic regression adjusted for age, sex, comorbidities, body mass index, and psychotropic drug intake. Associations were found specifically between wake time after sleep onset (WASO) and four SNPs in the participants not taking psychotropic drugs, whereas in those taking drugs, the associations were either not significant (rs6265 and rs7103411) or in the reverse direction (rs11030101 and rs28722151). Higher BDNF methylation levels were found at most CpG units in those with long WASO and this varied according to psychotropic drug use. The reference group with short WASO not taking drugs showed the lowest methylation levels and the group with long WASO taking treatment, the highest levels. Some SNPs also modified the associations, the participants carrying the low-risk genotype having the lower methylation levels. This genetic and epigenetic study demonstrated blood BDNF promoter methylation to be a potential biomarker of prolonged nocturnal awakenings in older people. Our results suggest the modifying effect of psychotropic drugs and BDNF genetic variants in the associations between methylation and WASO.

Identifiants

pubmed: 36737401
doi: 10.1111/jsr.13838
doi:

Substances chimiques

Brain-Derived Neurotrophic Factor 0
BDNF protein, human 7171WSG8A2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13838

Subventions

Organisme : Medical Research Council
ID : APP1135727
Pays : United Kingdom

Informations de copyright

© 2023 The Authors. Journal of Sleep Research published by John Wiley & Sons Ltd on behalf of European Sleep Research Society.

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Auteurs

Marie-Laure Ancelin (ML)

INM, INSERM, Univ Montpellier, Montpellier, France.

Isabelle Jaussent (I)

INM, INSERM, Univ Montpellier, Montpellier, France.

Karen Ritchie (K)

INM, INSERM, Univ Montpellier, Montpellier, France.
Institut du Cerveau Trocadéro, Paris, France.

Alain Besset (A)

INM, INSERM, Univ Montpellier, Montpellier, France.

Joanne Ryan (J)

Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.

Yves Dauvilliers (Y)

INM, INSERM, Univ Montpellier, Montpellier, France.
Sleep-Wake Disorders Unit, Department of Neurology, Gui-de-Chauliac Hospital, CHU Montpellier, France.

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