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

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. T...

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Bibliographische Detailangaben
Hauptverfasser: Kilpeläinen, Tuomas O. (VerfasserIn) , Kleber, Marcus E. (VerfasserIn) , Delgado Gonzales de Kleber, Graciela (VerfasserIn) , März, Winfried (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 1 Feb 2016
In: Nature Communications
Year: 2016, Jahrgang: 7
ISSN:2041-1723
DOI:10.1038/ncomms10494
Online-Zugang:Verlag, Volltext: http://dx.doi.org/10.1038/ncomms10494
Verlag, Volltext: https://www-nature-com.ezproxy.medma.uni-heidelberg.de/articles/ncomms10494
Volltext
Verfasserangaben:Tuomas O. Kilpeläinen et al.
Beschreibung
Zusammenfassung: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.
Beschreibung:Gesehen am 30.01.2019
Beschreibung:Online Resource
ISSN:2041-1723
DOI:10.1038/ncomms10494

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