Genetic variation associated with circulating monocyte count in the eMERGE Network.

Journal Article (Clinical Trial;Journal Article;Multicenter Study)

With white blood cell count emerging as an important risk factor for chronic inflammatory diseases, genetic associations of differential leukocyte types, specifically monocyte count, are providing novel candidate genes and pathways to further investigate. Circulating monocytes play a critical role in vascular diseases such as in the formation of atherosclerotic plaque. We performed a joint and ancestry-stratified genome-wide association analyses to identify variants specifically associated with monocyte count in 11 014 subjects in the electronic Medical Records and Genomics Network. In the joint and European ancestry samples, we identified novel associations in the chromosome 16 interferon regulatory factor 8 (IRF8) gene (P-value = 2.78×10(-16), β = -0.22). Other monocyte associations include novel missense variants in the chemokine-binding protein 2 (CCBP2) gene (P-value = 1.88×10(-7), β = 0.30) and a region of replication found in ribophorin I (RPN1) (P-value = 2.63×10(-16), β = -0.23) on chromosome 3. The CCBP2 and RPN1 region is located near GATA binding protein2 gene that has been previously shown to be associated with coronary heart disease. On chromosome 9, we found a novel association in the prostaglandin reductase 1 gene (P-value = 2.29×10(-7), β = 0.16), which is downstream from lysophosphatidic acid receptor 1. This region has previously been shown to be associated with monocyte count. We also replicated monocyte associations of genome-wide significance (P-value = 5.68×10(-17), β = -0.23) at the integrin, alpha 4 gene on chromosome 2. The novel IRF8 results and further replications provide supporting evidence of genetic regions associated with monocyte count.

Full Text

Duke Authors

Cited Authors

  • Crosslin, DR; McDavid, A; Weston, N; Zheng, X; Hart, E; de Andrade, M; Kullo, IJ; McCarty, CA; Doheny, KF; Pugh, E; Kho, A; Hayes, MG; Ritchie, MD; Saip, A; Crawford, DC; Crane, PK; Newton, K; Carrell, DS; Gallego, CJ; Nalls, MA; Li, R; Mirel, DB; Crenshaw, A; Couper, DJ; Tanaka, T; van Rooij, FJA; Chen, M-H; Smith, AV; Zakai, NA; Yango, Q; Garcia, M; Liu, Y; Lumley, T; Folsom, AR; Reiner, AP; Felix, JF; Dehghan, A; Wilson, JG; Bis, JC; Fox, CS; Glazer, NL; Cupples, LA; Coresh, J; Eiriksdottir, G; Gudnason, V; Bandinelli, S; Frayling, TM; Chakravarti, A; van Duijn, CM; Melzer, D; Levy, D; Boerwinkle, E; Singleton, AB; Hernandez, DG; Longo, DL; Witteman, JCM; Psaty, BM; Ferrucci, L; Harris, TB; O'Donnell, CJ; Ganesh, SK; CHARGE Hematology Working Group, ; Larson, EB; Carlson, CS; Jarvik, GP; electronic Medical Records and Genomics (eMERGE) Network,

Published Date

  • May 15, 2013

Published In

Volume / Issue

  • 22 / 10

Start / End Page

  • 2119 - 2127

PubMed ID

  • 23314186

Pubmed Central ID

  • PMC3633369

Electronic International Standard Serial Number (EISSN)

  • 1460-2083

Digital Object Identifier (DOI)

  • 10.1093/hmg/ddt010


  • eng

Conference Location

  • England