Multi-ancestry analysis of gene-sleep interactions in 126,926 individuals identifies multiple novel blood lipid loci that contribute to our understanding of sleep-associated adverse blood lipid profile
Noordam R., Bos M., Wang H., Winkler T., Bentley A., Kilpeläinen T., de Vries P., Sung YJ., Schwander K., Cade B., Manning A., Aschard H., Brown M., Chen H., Franceschini N., Musani S., Richard M., Vojinovic D., Aslibekyan S., Bartz T., de las Fuentes L., Feitosa M., Horimoto A., Ilkov M., Kho M., Kraja A., Li C., Lim E., Liu Y., Mook-Kanamori D., Rankinen T., Tajuddin S., van der Spek A., Wang Z., Marten J., Laville V., Alver M., Evangelou E., Graff M., He M., Kühnel B., Lyytikäinen L-P., Marques-Vidal P., Nolte I., Palmer N., Rauramaa R., Shu X-O., Snieder H., Weiss S., Wen W., Yanek L., Adolfo C., Ballantyne C., Bielak L., Biermasz N., Boerwinkle E., Dimou N., Eiriksdottir G., Gao C., Gharib S., Gottlieb D., Haba-Rubio J., Harris T., Heikkinen S., Heinzer R., Hixson J., Homuth G., Ikram A., Komulainen P., Krieger J., Lee J., Liu J., Lohman K., Luik A., Mägi R., Martin L., Meitinger T., Metspalu A., Milaneschi Y., Nalls M., O’Connell J., Peters A., Peyser P., Raitakari O., Reiner A., Rensen PCN., Rice T., Rich S., Roenneberg T., Rotter J., Schreiner P., Shikany J., Sidney S., Sims M., Sitlani C., Sofer T., Strauch K., Swertz M., Taylor K., Uitterlinden A., Duijn CV., Völzke H., Waldenberger M., Wallance R., Dijk KWV., Yu C., Zonderman A., Becker D., Elliott P., Esko T., Gieger C., Grabe H., Lakka T., Lehtimäki T., Study LC., North K., Penninx BWJH., Vollenweider P., Wagenknecht L., Wu T., Xiang Y-B., Zheng W., Arnett D., Bouchard C., Evans M., Gudnason V., Kardia S., Kelly T., Kritchevsky S., Loos RJF., Pereira A., Province M., Psaty B., Rotimi C., Zhu X., Amin N., Cupples A., Fornage M., Fox E., Guo X., Gauderman J., Rice K., Kooperberg C., Munroe P., Liu C-T., Morrison A., Rao D., Heemst DV., Redline S.
Abstract Both short and long sleep are associated with an adverse lipid profile, likely through different biological pathways. To provide new insights in the biology of sleep-associated adverse lipid profile, we conducted 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 identified 49 novel lipid loci, and 10 additional novel lipid loci in a restricted sample of European-ancestry cohorts. In addition, we identified new gene-sleep interactions for known lipid loci such as LPL and PCSK9 . The novel gene-sleep interactions had a modest explained variance in lipid levels: most notable, gene-short-sleep interactions explained 4.25% of the variance in triglyceride concentration. Collectively, these findings contribute to our understanding of the biological mechanisms involved in sleep-associated adverse lipid profiles.