Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci

Niha Zubair(Fred Hutch Cancer Center), Mariaelisa Graff, José Luis Ambite(University of Southern California), William S. Bush(Case Western Reserve University), Gleb Kichaev(University of California, Los Angeles), Yingchang Lu(Icahn School of Medicine at Mount Sinai), Ani Manichaikul(University of Virginia), Wayne Huey‐Herng Sheu(Taichung Veterans General Hospital), Devin Absher(HudsonAlpha Institute for Biotechnology), Themistocles L. Assimes(Stanford University), Suzette J. Bielinski(Mayo Clinic), Erwin P. Böttinger(Icahn School of Medicine at Mount Sinai), Petra Bůžková(University of Washington), Lee‐Ming Chuang(National Taiwan University), Ren‐Hua Chung(National Health Research Institutes), Barbara Cochran, Logan Dumitrescu(Vanderbilt University), Omri Gottesman(Icahn School of Medicine at Mount Sinai), Jeffrey Haessler(Fred Hutch Cancer Center), Christopher A. Haiman(University of Southern California), Gerardo Heiss, Chao A. Hsiung(National Health Research Institutes), Yi‐Jen Hung(Tri-Service General Hospital), Chii‐Min Hwu(National Yang Ming Chiao Tung University), Jyh‐Ming Jimmy Juang(National Taiwan University Hospital), Loı̈c Le Marchand(University of Hawaiʻi at Mānoa), I‐Te Lee(Taichung Veterans General Hospital), Wen‐Jane Lee(Taichung Veterans General Hospital), Li‐An Lin(The University of Texas Health Science Center at Houston), D. Y. Lin(University of North Carolina at Chapel Hill), Shih-Yi Lin(Taichung Veterans General Hospital), Rachel H. Mackey(University of Pittsburgh), Lisa W. Martin(George Washington University), Bogdan Paşaniuc(University of California, Los Angeles), Ulrike Peters(Fred Hutch Cancer Center), Irene M. Predazzi(Oregon Health & Science University), Thomas Quertermous(Stanford University), Alex P. Reiner(Fred Hutch Cancer Center), Jennifer G. Robinson(University of Iowa), Jerome I. Rotter(The Lundquist Institute), Kelli K. Ryckman(University of Iowa), Pamela J. Schreiner(University of Minnesota), Eli A. Stahl(Icahn School of Medicine at Mount Sinai), Ran Tao(University of North Carolina at Chapel Hill), Michael Y. Tsai(University of Minnesota), Lindsay L. Waite(HudsonAlpha Institute for Biotechnology), Tzung‐Dau Wang(National Taiwan University Hospital), Steven Buyske(Rutgers, The State University of New Jersey), Yii‐Der Ida Chen(The Lundquist Institute), Iona Cheng(Cancer Prevention Institute of California), Dana C. Crawford(Case Western Reserve University), Ruth J. F. Loos(Icahn School of Medicine at Mount Sinai), Stephen S. Rich(University of Virginia), Myriam Fornage(The University of Texas Health Science Center at Houston), Kari E. North, Charles Kooperberg(Fred Hutch Cancer Center), Cara L. Carty(Children's National)
Human Molecular Genetics
October 26, 2016
Cited by 27Open Access
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Abstract

Genome-wide association studies have identified over 150 loci associated with lipid traits, however, no large-scale studies exist for Hispanics and other minority populations. Additionally, the genetic architecture of lipid-influencing loci remains largely unknown. We performed one of the most racially/ethnically diverse fine-mapping genetic studies of HDL-C, LDL-C, and triglycerides to-date using SNPs on the MetaboChip array on 54,119 individuals: 21,304 African Americans, 19,829 Hispanic Americans, 12,456 Asians, and 530 American Indians. The majority of signals found in these groups generalize to European Americans. While we uncovered signals unique to racial/ethnic populations, we also observed systematically consistent lipid associations across these groups. In African Americans, we identified three novel signals associated with HDL-C (LPL, APOA5, LCAT) and two associated with LDL-C (ABCG8, DHODH). In addition, using this population, we refined the location for 16 out of the 58 known MetaboChip lipid loci. These results can guide tailored screening efforts, reveal population-specific responses to lipid-lowering medications, and aid in the development of new targeted drug therapies.


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