A Pilot Genome-Wide Association Study in Postmenopausal Mexican-Mestizo Women Implicates the RMND1/CCDC170 Locus Is Associated with Bone Mineral Density

Marisela Villalobos‐Comparán, Rogelio F. Jiménez-Ortega, Karol Estrada, Alma Y Parra-Torres, Anahí González‐Mercado, Nelly Patiño, Manuel Castillejos‐López, Manuel Quiterio, Juan Carlos Fernández-López, B Ibarra,

International Journal of Genomics · 2017 · 17 citations · 38 references

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Abstract

To identify genetic variants influencing bone mineral density (BMD) in the Mexican-Mestizo population, we performed a GWAS for femoral neck (FN) and lumbar spine (LS) in Mexican-Mestizo postmenopausal women. In the discovery sample, 300,000 SNPs were genotyped in a cohort of 411 postmenopausal women and seven SNPs were analyzed in the replication cohort (<i>n</i> = 420). The combined results of a meta-analysis from the discovery and replication samples identified two loci, <i>RMND1</i> (rs6904364, <i>P</i> = 2.77 × 10<sup>-4</sup>) and <i>CCDC170</i> (rs17081341, <i>P</i> = 1.62 × 10<sup>-5</sup>), associated with FN BMD. We also compared our results with those of the Genetic Factors for Osteoporosis (GEFOS) Consortium meta-analysis. The comparison revealed two loci previously reported in the GEFOS meta-analysis: <i>SOX6</i> (rs7128738) and <i>PKDCC</i> (rs11887431) associated with FN and LS BMD, respectively, in our study population. Interestingly, rs17081341 rare in Caucasians (minor allele frequency < 0.03) was found in high frequency in our population, which suggests that this association could be specific to non-Caucasian populations. In conclusion, the first pilot Mexican GWA study of BMD confirmed previously identified loci and also demonstrated the importance of studying variability in diverse populations and/or specific populations.

References

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