Literature DB >> 26757982

Rare variant associations with waist-to-hip ratio in European-American and African-American women from the NHLBI-Exome Sequencing Project.

Mengyuan Kan1,2, Paul L Auer3, Gao T Wang1, Kristine L Bucasas1, Stanley Hooker1, Alejandra Rodriguez1, Biao Li1, Jaclyn Ellis4, L Adrienne Cupples5,6, Yii-Der Ida Chen7,8,9, Josée Dupuis5,6, Caroline S Fox6, Myron D Gross10, Joshua D Smith11, Nancy Heard-Costa6,12, James B Meigs13, James S Pankow10, Jerome I Rotter7,8, David Siscovick14,15, James G Wilson16, Jay Shendure11, Rebecca Jackson17, Ulrike Peters3, Hua Zhong18, Danyu Lin19, Li Hsu3, Nora Franceschini20, Chris Carlson3, Goncalo Abecasis21, Stacey Gabriel22, Michael J Bamshad11, David Altshuler22, Deborah A Nickerson10, Kari E North20, Leslie A Lange4, Alexander P Reiner3,15, Suzanne M Leal1.   

Abstract

Waist-to-hip ratio (WHR), a relative comparison of waist and hip circumferences, is an easily accessible measurement of body fat distribution, in particular central abdominal fat. A high WHR indicates more intra-abdominal fat deposition and is an established risk factor for cardiovascular disease and type 2 diabetes. Recent genome-wide association studies have identified numerous common genetic loci influencing WHR, but the contributions of rare variants have not been previously reported. We investigated rare variant associations with WHR in 1510 European-American and 1186 African-American women from the National Heart, Lung, and Blood Institute-Exome Sequencing Project. Association analysis was performed on the gene level using several rare variant association methods. The strongest association was observed for rare variants in IKBKB (P=4.0 × 10(-8)) in European-Americans, where rare variants in this gene are predicted to decrease WHRs. The activation of the IKBKB gene is involved in inflammatory processes and insulin resistance, which may affect normal food intake and body weight and shape. Meanwhile, aggregation of rare variants in COBLL1, previously found to harbor common variants associated with WHR and fasting insulin, were nominally associated (P=2.23 × 10(-4)) with higher WHR in European-Americans. However, these significant results are not shared between African-Americans and European-Americans that may be due to differences in the allelic architecture of the two populations and the small sample sizes. Our study indicates that the combined effect of rare variants contribute to the inter-individual variation in fat distribution through the regulation of insulin response.

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Year:  2016        PMID: 26757982      PMCID: PMC4970686          DOI: 10.1038/ejhg.2015.272

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


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