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Admixture mapping and fine-mapping of birth weight loci in the Black Women's Health Study.
Ochs-Balcom, Heather M; Shaw, Holly; Preus, Leah; Palmer, Julie R; Haddad, Stephen A; Rosenberg, Lynn; Ruiz-Narváez, Edward A.
Affiliation
  • Ochs-Balcom HM; Department of Epidemiology and Environmental Health, School of Public Health and Health Professions, University at Buffalo, Buffalo, NY, USA.
  • Shaw H; Department of Epidemiology and Environmental Health, School of Public Health and Health Professions, University at Buffalo, Buffalo, NY, USA.
  • Preus L; Department of Epidemiology and Environmental Health, School of Public Health and Health Professions, University at Buffalo, Buffalo, NY, USA.
  • Palmer JR; Slone Epidemiology Center, Boston University, Boston, MA, USA.
  • Haddad SA; Slone Epidemiology Center, Boston University, Boston, MA, USA.
  • Rosenberg L; Slone Epidemiology Center, Boston University, Boston, MA, USA.
  • Ruiz-Narváez EA; Department of Nutritional Sciences, University of Michigan School of Public Health, 1860 SPH I, 1415 Washington Heights, Ann Arbor, MI, USA. eruiznar@umich.edu.
Hum Genet ; 137(6-7): 535-542, 2018 Jul.
Article in En | MEDLINE | ID: mdl-30006737
ABSTRACT
Several genome-wide association studies (GWAS) have identified genetic variants associated with birth weight. To date, however, most GWAS of birth weight have focused primarily on European ancestry samples even though prevalence of low birth weight is higher among African-Americans. We conducted admixture mapping using 2918 ancestral informative markers in 2596 participants of the Black Women's Health Study, with the goal of identifying novel genomic regions where local African ancestry is associated with birth weight. In addition, we performed a replication analysis of 11 previously identified index single nucleotide polymorphisms (SNPs), and fine-mapped those genetic loci to identify better or new genetic variants associated with birth weight in African-Americans. We found that high African ancestry at 12q14 was associated with low birth weight, and we identified multiple independent birth weight-lowering variants in this genomic region. We replicated the association of a previous GWAS SNP in ADRB1 and our fine-mapping efforts suggested the presence of new birth weight-associated variants in ADRB1, HMGA2, and SLC2A4. Further studies are needed to determine whether birth weight-associated loci can in part explain race-associated birth weight disparities.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Birth Weight / Black or African American / Polymorphism, Single Nucleotide / Genetic Loci Type of study: Clinical_trials / Risk_factors_studies Limits: Adult / Female / Humans / Middle aged Language: En Journal: Hum Genet Year: 2018 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Birth Weight / Black or African American / Polymorphism, Single Nucleotide / Genetic Loci Type of study: Clinical_trials / Risk_factors_studies Limits: Adult / Female / Humans / Middle aged Language: En Journal: Hum Genet Year: 2018 Type: Article Affiliation country: United States