Literature DB >> 20164292

Genome-wide association study of bone mineral density in premenopausal European-American women and replication in African-American women.

Daniel L Koller1, Shoji Ichikawa, Dongbing Lai, Leah R Padgett, Kimberly F Doheny, Elizabeth Pugh, Justin Paschall, Siu L Hui, Howard J Edenberg, Xiaoling Xuei, Munro Peacock, Michael J Econs, Tatiana Foroud.   

Abstract

CONTEXT: Several genome-wide association studies (GWAS) have been performed to identify genes contributing to bone mineral density (BMD), typically in samples of elderly women and men.
OBJECTIVE: The objective of the study was to identify genes contributing to BMD in premenopausal women.
DESIGN: GWAS using the Illumina 610Quad array in premenopausal European-American (EA) women and replication of the top 50 single-nucleotide polymorphisms (SNPs) for two BMD measures in African-American (AA) women.
SUBJECTS: Subjects included 1524 premenopausal EA women aged 20-45 yr from 762 sibships and 669 AA premenopausal women aged 20-44 yr from 383 sibships.
INTERVENTIONS: There were no interventions. MAIN OUTCOME MEASURES: BMD was measured at the lumbar spine and femoral neck by dual-energy x-ray absorptiometry. Age- and weight-adjusted BMD values were tested for association with each SNP, with P values determined by permutation.
RESULTS: SNPs in CATSPERB on chromosome 14 provided evidence of association with femoral neck BMD (rs1298989, P = 2.7 x 10(-5); rs1285635, P = 3.0 x 10(-5)) in the EA women, and some supporting evidence was also observed with these SNPs in the AA women (rs1285635, P = 0.003). Genes identified in other BMD GWAS studies, including IBSP and ADAMTS18, were also among the most significant findings in our GWAS.
CONCLUSIONS: Evidence of association to several novel loci was detected in a GWAS of premenopausal EA women, and SNPs in one of these loci also provided supporting evidence in a sample of AA women.

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Year:  2010        PMID: 20164292      PMCID: PMC2853986          DOI: 10.1210/jc.2009-1903

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


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