Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels.

Détails

Ressource 1Télécharger: BIB_35AFF34A673F.P001.pdf (851.19 [Ko])
Etat: Public
Version: Final published version
ID Serval
serval:BIB_35AFF34A673F
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels.
Périodique
Nature Communications
Auteur⸱e⸱s
Kilpeläinen T.O., Carli J.F., Skowronski A.A., Sun Q., Kriebel J., Feitosa M.F., Hedman Å.K., Drong A.W., Hayes J.E., Zhao J., Pers T.H., Schick U., Grarup N., Kutalik Z., Trompet S., Mangino M., Kristiansson K., Beekman M., Lyytikäinen L.P., Eriksson J., Henneman P., Lahti J., Tanaka T., Luan J., Del Greco M F., Pasko D., Renström F., Willems S.M., Mahajan A., Rose L.M., Guo X., Liu Y., Kleber M.E., Pérusse L., Gaunt T., Ahluwalia T.S., Ju Sung Y., Ramos Y.F., Amin N., Amuzu A., Barroso I., Bellis C., Blangero J., Buckley B.M., Böhringer S., I Chen Y.D., de Craen A.J., Crosslin D.R., Dale C.E., Dastani Z., Day F.R., Deelen J., Delgado G.E., Demirkan A., Finucane F.M., Ford I., Garcia M.E., Gieger C., Gustafsson S., Hallmans G., Hankinson S.E., Havulinna A.S., Herder C., Hernandez D., Hicks A.A., Hunter D.J., Illig T., Ingelsson E., Ioan-Facsinay A., Jansson J.O., Jenny N.S., Jørgensen M.E., Jørgensen T., Karlsson M., Koenig W., Kraft P., Kwekkeboom J., Laatikainen T., Ladwig K.H., LeDuc C.A., Lowe G., Lu Y., Marques-Vidal P., Meisinger C., Menni C., Morris A.P., Myers R.H., Männistö S., Nalls M.A., Paternoster L., Peters A., Pradhan A.D., Rankinen T., Rasmussen-Torvik L.J., Rathmann W., Rice T.K., Brent Richards J., Ridker P.M., Sattar N., Savage D.B., Söderberg S., Timpson N.J., Vandenput L., van Heemst D., Uh H.W., Vohl M.C., Walker M., Wichmann H.E., Widén E., Wood A.R., Yao J., Zeller T., Zhang Y., Meulenbelt I., Kloppenburg M., Astrup A., Sørensen T.I., Sarzynski M.A., Rao D.C., Jousilahti P., Vartiainen E., Hofman A., Rivadeneira F., Uitterlinden A.G., Kajantie E., Osmond C., Palotie A., Eriksson J.G., Heliövaara M., Knekt P.B., Koskinen S., Jula A., Perola M., Huupponen R.K., Viikari J.S., Kähönen M., Lehtimäki T., Raitakari O.T., Mellström D., Lorentzon M., Casas J.P., Bandinelli S., März W., Isaacs A., van Dijk K.W., van Duijn C.M., Harris T.B., Bouchard C., Allison M.A., Chasman D.I., Ohlsson C., Lind L., Scott R.A., Langenberg C., Wareham N.J., Ferrucci L., Frayling T.M., Pramstaller P.P., Borecki I.B., Waterworth D.M., Bergmann S., Waeber G., Vollenweider P., Vestergaard H., Hansen T., Pedersen O., Hu F.B., Eline Slagboom P., Grallert H., Spector T.D., Jukema J.W., Klein R.J., Schadt E.E., Franks P.W., Lindgren C.M., Leibel R.L., Loos R.J.
ISSN
2041-1723 (Electronic)
ISSN-L
2041-1723
Statut éditorial
Publié
Date de publication
2016
Peer-reviewed
Oui
Volume
7
Pages
10494
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, N.I.H., Extramural ; Research Support, N.I.H., Intramural ; Research Support, Non-U.S. Gov't
Publication Status: epublish
Résumé
Leptin is an adipocyte-secreted hormone, the circulating levels of which correlate closely with overall adiposity. Although rare mutations in the leptin (LEP) gene are well known to cause leptin deficiency and severe obesity, no common loci regulating circulating leptin levels have been uncovered. Therefore, we performed a genome-wide association study (GWAS) of circulating leptin levels from 32,161 individuals and followed up loci reaching P<10(-6) in 19,979 additional individuals. We identify five loci robustly associated (P<5 × 10(-8)) with leptin levels in/near LEP, SLC32A1, GCKR, CCNL1 and FTO. Although the association of the FTO obesity locus with leptin levels is abolished by adjustment for BMI, associations of the four other loci are independent of adiposity. The GCKR locus was found associated with multiple metabolic traits in previous GWAS and the CCNL1 locus with birth weight. Knockdown experiments in mouse adipose tissue explants show convincing evidence for adipogenin, a regulator of adipocyte differentiation, as the novel causal gene in the SLC32A1 locus influencing leptin levels. Our findings provide novel insights into the regulation of leptin production by adipose tissue and open new avenues for examining the influence of variation in leptin levels on adiposity and metabolic health.
Mots-clé
Adipose Tissue/metabolism, Animals, Gene Expression Regulation/physiology, Gene Knockdown Techniques, Genome-Wide Association Study, Leptin/blood, Leptin/genetics, Male, Mice, RNA, Messenger/genetics, RNA, Messenger/metabolism, Tissue Culture Techniques
Pubmed
Web of science
Open Access
Oui
Création de la notice
19/02/2016 16:52
Dernière modification de la notice
20/08/2019 14:23
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