Genome-wide association analysis of red blood cell traits in African Americans: The cogent network

Zhao Chen, Hua Tang, Rehan Qayyum, Ursula M. Schick, Michael A. Nalls, Rober Handsaker, Jin Li, Yingchang Lu, Lisa R. Yanek, Brendan Keating, Yan Meng, Frank J.A. Van Rooij, Yukinori Okada, Michiaki Kubo, Laura Rasmussen-Torvik, Margaux F. Keller, Leslie Lange, Michele Evans, Erwin P. Bottinger, Michael D. LindermanDouglas M. Ruderfer, Hakon Hakonarson, George Papanicolaou, Alan B. Zonderman, Omri Gottesman, Cynthia Thomson, Elad Ziv, Andrew B. Singleton, Ruth J.F. Loos, Patrick M.A. Sleiman, Santhi Ganesh, Steven McCarroll, Diane M. Becker, James G. Wilson, Guillaume Lettre, Alexander P. Reiner

研究成果: Article査読

40 被引用数 (Scopus)

抄録

Laboratory red blood cell (RBC) measurements are clinically important, heritable and differ among ethnic groups. To identify genetic variants that contribute to RBC phenotypes in African Americans (AAs), we conducted a genome-wide association study in up to ~16 500 AAs. The alpha-globin locus on chromosome 16pter [lead SNP rs13335629 in ITFG3 gene; P < 1E-13 for hemoglobin (Hgb), RBC count, mean corpuscular volume (MCV), MCH and MCHC] and the G6PD locus on Xq28 [lead SNP rs1050828; P < 1E - 13 for Hgb, hematocrit (Hct), MCV, RBC count and red cell distribution width (RDW)] were each associated with multiple RBC traits. At the alpha-globin region, both the common African 3.7 kb deletion and common single nucleotide polymorphisms (SNPs) appear to contribute independently to RBC phenotypes among AAs. In the 2p21 region, we identified a novel variant of PRKCE distinctly associated with Hct in AAs. In a genome-wide admixture mapping scan, local European ancestry at the 6p22 region containing HFE and LRRC16A was associated with higher Hgb. LRRC16A has been previously associated with the platelet count and mean platelet volume in AAs, but not with Hgb. Finally, we extended to AAs the findings of association of erythrocyte traits with several loci previously reported in Europeans and/or Asians, including CD164 and HBS1L-MYB. In summary, this large-scale genome-wide analysis in AAs has extended the importance of several RBC-associated genetic loci to AAs and identified allelic heterogeneity and pleiotropy at several previously known genetic loci associated with blood cell traits in AAs.

本文言語English
ページ(範囲)2529-2538
ページ数10
ジャーナルHuman molecular genetics
22
12
DOI
出版ステータスPublished - 06-2013
外部発表はい

All Science Journal Classification (ASJC) codes

  • 分子生物学
  • 遺伝学
  • 遺伝学(臨床)

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