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Multi-ancestry genome-wide gene–sleep interactions identify novel loci for blood pressure

Abstract:
Long and short sleep duration are associated with elevated blood pressure (BP), possibly through effects on molecular pathways that influence neuroendocrine and vascular systems. To gain new insights into the genetic basis of sleep-related BP variation, we performed genome-wide gene by short or long sleep duration interaction analyses on four BP traits (systolic BP, diastolic BP, mean arterial pressure, and pulse pressure) across five ancestry groups in two stages using 2 degree of freedom (df) joint test followed by 1df test of interaction effects. Primary multi-ancestry analysis in 62,969 individuals in stage 1 identified three novel gene by sleep interactions that were replicated in an additional 59,296 individuals in stage 2 (stage 1 + 2 Pjoint < 5 × 10−8), including rs7955964 (FIGNL2/ANKRD33) that increases BP among long sleepers, and rs73493041 (SNORA26/C9orf170) and rs10406644 (KCTD15/LSM14A) that increase BP among short sleepers (Pint < 5 × 10−8). Secondary ancestry-specific analysis identified another novel gene by long sleep interaction at rs111887471 (TRPC3/KIAA1109) in individuals of African ancestry (Pint = 2 × 10−6). Combined stage 1 and 2 analyses additionally identified significant gene by long sleep interactions at 10 loci including MKLN1 and RGL3/ELAVL3 previously associated with BP, and significant gene by short sleep interactions at 10 loci including C2orf43 previously associated with BP (Pint < 10−3). 2df test also identified novel loci for BP after modeling sleep that has known functions in sleep–wake regulation, nervous and cardiometabolic systems. This study indicates that sleep and primary mechanisms regulating BP may interact to elevate BP level, suggesting novel insights into sleep-related BP regulation.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/s41380-021-01087-0

Authors


More by this author
Role:
Author
ORCID:
0000-0002-1486-7495
More by this author
Role:
Author
ORCID:
0000-0003-1424-0673
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Nuffield Department of Population Health
Sub department:
Clinical Trial Service Unit
Role:
Author
ORCID:
0000-0002-8944-1771
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Nuffield Department of Population Health
Oxford college:
St Cross College
Role:
Author
ORCID:
0000-0002-2374-9204
et al.


Publisher:
Springer Nature
Journal:
Molecular Psychiatry More from this journal
Volume:
26
Issue:
11
Pages:
6293–6304
Publication date:
2021-04-15
Acceptance date:
2021-03-29
DOI:
EISSN:
1476-5578
ISSN:
1359-4184
Pmid:
33859359


Language:
English
Keywords:
Pubs id:
1172746
Local pid:
pubs:1172746
Deposit date:
2021-06-25

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