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Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.

Authors :
Ganesh SK
Zakai NA
van Rooij FJ
Soranzo N
Smith AV
Nalls MA
Chen MH
Kottgen A
Glazer NL
Dehghan A
Kuhnel B
Aspelund T
Yang Q
Tanaka T
Jaffe A
Bis JC
Verwoert GC
Teumer A
Fox CS
Guralnik JM
Ehret GB
Rice K
Felix JF
Rendon A
Eiriksdottir G
Levy D
Patel KV
Boerwinkle E
Rotter JI
Hofman A
Sambrook JG
Hernandez DG
Zheng G
Bandinelli S
Singleton AB
Coresh J
Lumley T
Uitterlinden AG
Vangils JM
Launer LJ
Cupples LA
Oostra BA
Zwaginga JJ
Ouwehand WH
Thein SL
Meisinger C
Deloukas P
Nauck M
Spector TD
Gieger C
Gudnason V
van Duijn CM
Psaty BM
Ferrucci L
Chakravarti A
Greinacher A
O'Donnell CJ
Witteman JC
Furth S
Cushman M
Harris TB
Lin JP
Source :
Nature genetics [Nat Genet] 2009 Nov; Vol. 41 (11), pp. 1191-8. Date of Electronic Publication: 2009 Oct 11.
Publication Year :
2009

Abstract

Measurements of erythrocytes within the blood are important clinical traits and can indicate various hematological disorders. We report here genome-wide association studies (GWAS) for six erythrocyte traits, including hemoglobin concentration (Hb), hematocrit (Hct), mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), mean corpuscular hemoglobin concentration (MCHC) and red blood cell count (RBC). We performed an initial GWAS in cohorts of the CHARGE Consortium totaling 24,167 individuals of European ancestry and replication in additional independent cohorts of the HaemGen Consortium totaling 9,456 individuals. We identified 23 loci significantly associated with these traits in a meta-analysis of the discovery and replication cohorts (combined P values ranging from 5 x 10(-8) to 7 x 10(-86)). Our findings include loci previously associated with these traits (HBS1L-MYB, HFE, TMPRSS6, TFR2, SPTA1) as well as new associations (EPO, TFRC, SH2B3 and 15 other loci). This study has identified new determinants of erythrocyte traits, offering insight into common variants underlying variation in erythrocyte measures.

Details

Language :
English
ISSN :
1546-1718
Volume :
41
Issue :
11
Database :
MEDLINE
Journal :
Nature genetics
Publication Type :
Academic Journal
Accession number :
19862010
Full Text :
https://doi.org/10.1038/ng.466