Transethnic Evaluation Identifies Low-Frequency Loci Associated With 25-Hydroxyvitamin D Concentrations.

Published

Journal Article

Context: Vitamin D inadequacy is common in the adult population of the United States. Although the genetic determinants underlying vitamin D inadequacy have been studied in people of European ancestry, less is known about populations with Hispanic or African ancestry. Objective: The Trans-Ethnic Evaluation of Vitamin D (TRANSCEN-D) genomewide association study (GWAS) consortium was assembled to replicate genetic associations with 25-hydroxyvitamin D [25(OH)D] concentrations from the Study of Underlying Genetic Determinants of Vitamin D and Highly Related Traits (SUNLIGHT) meta-analyses of European ancestry and to identify genetic variants related to vitamin D concentrations in African and Hispanic ancestries. Design: Ancestry-specific (Hispanic and African) and transethnic (Hispanic, African, and European) meta-analyses were performed with Meta-Analysis Helper software (METAL). Patients or Other Participants: In total, 8541 African American and 3485 Hispanic American (from North America) participants from 12 cohorts and 16,124 European participants from SUNLIGHT were included in the study. Main Outcome Measures: Blood concentrations of 25(OH)D were measured for all participants. Results: Ancestry-specific analyses in African and Hispanic Americans replicated single nucleotide polymorphisms (SNPs) in GC (2 and 4 SNPs, respectively). An SNP (rs79666294) near the KIF4B gene was identified in the African American cohort. Transethnic evaluation replicated GC and DHCR7 region SNPs. Additionally, the transethnic analyses revealed SNPs rs719700 and rs1410656 near the ANO6/ARID2 and HTR2A genes, respectively. Conclusions: Ancestry-specific and transethnic GWASs of 25(OH)D confirmed findings in GC and DHCR7 for African and Hispanic American samples and revealed findings near KIF4B, ANO6/ARID2, and HTR2A. The biological mechanisms that link these regions with 25(OH)D metabolism warrant further investigation.

Full Text

Duke Authors

Cited Authors

  • Hong, J; Hatchell, KE; Bradfield, JP; Bjonnes, A; Chesi, A; Lai, C-Q; Langefeld, CD; Lu, L; Lu, Y; Lutsey, PL; Musani, SK; Nalls, MA; Robinson-Cohen, C; Roizen, JD; Saxena, R; Tucker, KL; Ziegler, JT; Arking, DE; Bis, JC; Boerwinkle, E; Bottinger, EP; Bowden, DW; Gilsanz, V; Houston, DK; Kalkwarf, HJ; Kelly, A; Lappe, JM; Liu, Y; Michos, ED; Oberfield, SE; Palmer, ND; Rotter, JI; Sapkota, B; Shepherd, JA; Wilson, JG; Basu, S; de Boer, IH; Divers, J; Freedman, BI; Grant, SFA; Hakanarson, H; Harris, TB; Kestenbaum, BR; Kritchevsky, SB; Loos, RJF; Norris, JM; Norwood, AF; Ordovas, JM; Pankow, JS; Psaty, BM; Sanghera, DK; Wagenknecht, LE; Zemel, BS; Meigs, J; Dupuis, J; Florez, JC; Wang, T; Liu, C-T; Engelman, CD; Billings, LK

Published Date

  • April 1, 2018

Published In

Volume / Issue

  • 103 / 4

Start / End Page

  • 1380 - 1392

PubMed ID

  • 29325163

Pubmed Central ID

  • 29325163

Electronic International Standard Serial Number (EISSN)

  • 1945-7197

Digital Object Identifier (DOI)

  • 10.1210/jc.2017-01802

Language

  • eng

Conference Location

  • United States