Genome-wide association study of a lipedema phenotype among women in the UK Biobank identifies multiple genetic risk factors

Lipedema is a common disorder characterized by excessive deposition of subcutaneous adipose tissue (SAT) in the legs, hips, and buttocks, mainly occurring in adult women. Although it appears to be heritable, no specific genes have yet been identified. To identify potential genetic risk factors for l...

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Veröffentlicht in:European journal of human genetics : EJHG 2023-03, Vol.31 (3), p.338-344
Hauptverfasser: Klimentidis, Yann C, Chen, Zhao, Gonzalez-Garay, Manuel L, Grigoriadis, Dionysios, Sackey, Ege, Pittman, Alan, Ostergaard, Pia, Herbst, Karen L
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Sprache:eng
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Zusammenfassung:Lipedema is a common disorder characterized by excessive deposition of subcutaneous adipose tissue (SAT) in the legs, hips, and buttocks, mainly occurring in adult women. Although it appears to be heritable, no specific genes have yet been identified. To identify potential genetic risk factors for lipedema, we used bioelectrical impedance analysis and anthropometric data from the UK Biobank to identify women with and without a lipedema phenotype. Specifically, we identified women with both a high percentage of fat in the lower limbs and a relatively small waist, adjusting for hip circumference. We performed a genome-wide association study (GWAS) for this phenotype, and performed multiple sensitivity GWAS. In an independent case/control study of lipedema based on strict clinical criteria, we attempted to replicate our top hits. We identified 18 significant loci (p 
ISSN:1018-4813
1476-5438
DOI:10.1038/s41431-022-01231-6