The genetic etiology of periodic limb movement in sleep.
Details
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State: Public
Version: Final published version
License: CC BY-ND 4.0
UNIL restricted access
State: Public
Version: Final published version
License: CC BY-ND 4.0
Serval ID
serval:BIB_13D5DB836FAE
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
The genetic etiology of periodic limb movement in sleep.
Journal
Sleep
ISSN
1550-9109 (Electronic)
ISSN-L
0161-8105
Publication state
Published
Issued date
12/04/2023
Peer-reviewed
Oui
Volume
46
Number
4
Pages
zsac121
Language
english
Notes
Publication types: Meta-Analysis ; Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural
Publication Status: ppublish
Publication Status: ppublish
Abstract
Periodic limb movement in sleep is a common sleep phenotype characterized by repetitive leg movements that occur during or before sleep. We conducted a genome-wide association study (GWAS) of periodic limb movements in sleep (PLMS) using a joint analysis (i.e., discovery, replication, and joint meta-analysis) of four cohorts (MrOS, the Wisconsin Sleep Cohort Study, HypnoLaus, and MESA), comprised of 6843 total subjects.
The MrOS study and Wisconsin Sleep Cohort Study (N = 1745 cases) were used for discovery. Replication in the HypnoLaus and MESA cohorts (1002 cases) preceded joint meta-analysis. We also performed LD score regression, estimated heritability, and computed genetic correlations between potentially associated traits such as restless leg syndrome (RLS) and insomnia. The causality and direction of the relationships between PLMS and RLS was evaluated using Mendelian randomization.
We found 2 independent loci were significantly associated with PLMS: rs113851554 (p = 3.51 × 10-12, β = 0.486), an SNP located in a putative regulatory element of intron eight of MEIS1 (2p14); and rs9369062 (p = 3.06 × 10-22, β = 0.2093), a SNP located in the intron region of BTBD9 (6p12); both of which were also lead signals in RLS GWAS. PLMS is genetically correlated with insomnia, risk of stroke, and RLS, but not with iron deficiency. Pleiotropy adjusted Mendelian randomization analysis identified a causal effect of RLS on PLMS.
Because PLMS is more common than RLS, PLMS may have multiple causes and additional studies are needed to further validate these findings.
The MrOS study and Wisconsin Sleep Cohort Study (N = 1745 cases) were used for discovery. Replication in the HypnoLaus and MESA cohorts (1002 cases) preceded joint meta-analysis. We also performed LD score regression, estimated heritability, and computed genetic correlations between potentially associated traits such as restless leg syndrome (RLS) and insomnia. The causality and direction of the relationships between PLMS and RLS was evaluated using Mendelian randomization.
We found 2 independent loci were significantly associated with PLMS: rs113851554 (p = 3.51 × 10-12, β = 0.486), an SNP located in a putative regulatory element of intron eight of MEIS1 (2p14); and rs9369062 (p = 3.06 × 10-22, β = 0.2093), a SNP located in the intron region of BTBD9 (6p12); both of which were also lead signals in RLS GWAS. PLMS is genetically correlated with insomnia, risk of stroke, and RLS, but not with iron deficiency. Pleiotropy adjusted Mendelian randomization analysis identified a causal effect of RLS on PLMS.
Because PLMS is more common than RLS, PLMS may have multiple causes and additional studies are needed to further validate these findings.
Keywords
Humans, Sleep Initiation and Maintenance Disorders, Cohort Studies, Genome-Wide Association Study, Sleep, Movement, Restless Legs Syndrome/genetics, Mendelian randomization, genome-wide association study, periodic limb movements, restless leg syndrome
Pubmed
Web of science
Open Access
Yes
Create date
20/01/2023 17:00
Last modification date
19/07/2023 5:56