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Noordam, Raymond;
Bos, Maxime M.;
Wang, Heming;
Winkler, Thomas W.;
Bentley, Amy R.;
Kilpeläinen, Tuomas O.;
de Vries, Paul S.;
Sung, Yun Ju;
Schwander, Karen;
Cade, Brian E.;
Manning, Alisa;
Aschard, Hugues;
Brown, Michael R.;
Chen, Han;
Franceschini, Nora;
Musani, Solomon K.;
Richard, Melissa;
Vojinovic, Dina;
Aslibekyan, Stella;
Bartz, Traci M.;
de las Fuentes, Lisa;
Feitosa, Mary;
Horimoto, Andrea R.;
Ilkov, Marjan;
[...]
Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration
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- Medientyp: E-Artikel
- Titel: Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration
- Beteiligte: Noordam, Raymond; Bos, Maxime M.; Wang, Heming; Winkler, Thomas W.; Bentley, Amy R.; Kilpeläinen, Tuomas O.; de Vries, Paul S.; Sung, Yun Ju; Schwander, Karen; Cade, Brian E.; Manning, Alisa; Aschard, Hugues; Brown, Michael R.; Chen, Han; Franceschini, Nora; Musani, Solomon K.; Richard, Melissa; Vojinovic, Dina; Aslibekyan, Stella; Bartz, Traci M.; de las Fuentes, Lisa; Feitosa, Mary; Horimoto, Andrea R.; Ilkov, Marjan; [...]
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Erschienen:
Springer Science and Business Media LLC, 2019
- Erschienen in: Nature Communications, 10 (2019) 1
- Sprache: Englisch
- DOI: 10.1038/s41467-019-12958-0
- ISSN: 2041-1723
- Entstehung:
- Anmerkungen:
- Beschreibung: AbstractBoth short and long sleep are associated with an adverse lipid profile, likely through different biological pathways. To elucidate the biology of sleep-associated adverse lipid profile, we conduct multi-ancestry genome-wide sleep-SNP interaction analyses on three lipid traits (HDL-c, LDL-c and triglycerides). In the total study sample (discovery + replication) of 126,926 individuals from 5 different ancestry groups, when considering either long or short total sleep time interactions in joint analyses, we identify 49 previously unreported lipid loci, and 10 additional previously unreported lipid loci in a restricted sample of European-ancestry cohorts. In addition, we identify new gene-sleep interactions for known lipid loci such asLPLandPCSK9. The previously unreported lipid loci have a modest explained variance in lipid levels: most notable, gene-short-sleep interactions explain 4.25% of the variance in triglyceride level. Collectively, these findings contribute to our understanding of the biological mechanisms involved in sleep-associated adverse lipid profiles.
- Zugangsstatus: Freier Zugang