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Replication of genomewide association studies on age at menarche in the Korean population

Authors :
Haesook Min
Younjhin Ahn
Jae Kyung Park
Seon-Joo Park
Cheong-Sik Kim
Yeonjung Kim
Sung Soo Kim
Kyung-Won Hong
Source :
Genes & Genomics. 35:69-75
Publication Year :
2013
Publisher :
Springer Science and Business Media LLC, 2013.

Abstract

Early menarche is associated with adverse health outcomes, including breast cancer, endometrial cancer, obesity, type 2 diabetes, and cardiovascular disease. Recently, a genomewide association study (GWAS) of age at menarche (AAM) in 104,533 individuals of European ancestry was reported by the ReproGen consortium. They identified 42 loci known and novel loci that were linked to age at menarche. Because age at menarche varies between ethnic groups, we decided to investigate if these results would be replicated in the Korean population. To this end, we examined the association of the SNPs reported in the ReproGen GWAS with AAM in 3,194 individuals from the Korean Genome and Epidemiology Study (KoGES) cohort. Genotype data for total 17 SNPs (6 genotyped SNPs and 11 imputed SNPs) were available for the association analysis using linear regression analysis for age at menarche with controlling current age, waist-to-hip ratio, and body mass index as the covariates. We found replication of the ReproGen study in two SNPs; one SNP (rs466639) in the retinoic acid receptor gamma gene (RXRG), showing a significant association with early menarche (beta = −0.224 ± 0.065, p value = 5.2 × 10−4, Bonferroni-corrected p value = 0.009), and the other (rs10899489), in GRB2 (growth factor receptor bound protein 2)-associated binding protein 2 (GAB2), linked to late menarche (beta = 0.140 ± 0.047, p value = 2.8 × 10−3, Bonferroni-corrected p value = 0.049). This result possibly suggests that genetic factors governing AAM in the Korean population would be distinct from those in the Europeans, implying roles of modulating or interacting factors in determining AAM, including environmental factors such as nutritional status.

Details

ISSN :
20929293 and 19769571
Volume :
35
Database :
OpenAIRE
Journal :
Genes & Genomics
Accession number :
edsair.doi...........d03a230c882b4a3437eb855ab4279113
Full Text :
https://doi.org/10.1007/s13258-013-0060-1