A Genome-Wide Association Study Uncovers a Genetic Locus Associated with Thoracic-to-Hip Ratio in Koreans

• Published in: PloS one 2015-12, Vol.10 (12), p.e0145220-e0145220
• Main Authors: Cha, Seongwon, Park, Ah Yeon, Kang, Changsoo
• Format: Article
• Language: English
• Subjects: Age factors; Aged; Alleles; Analysis; Anthropometry; Asian people; Asians; Bioinformatics; Biomedical materials; Body mass index; Body measurements; Cardiovascular disease; Care and treatment; Chromosomes; Diabetes; Diabetes mellitus; Diabetes Mellitus, Type 2 - epidemiology; Diagnosis; Dosage and administration; Drugs; Epidemiology; Family medical history; Fasting; Female; Genetic diversity; Genetic markers; Genome-wide association studies; Genome-Wide Association Study; Genomes; Genotyping; Health aspects; Health risks; Hip; Hip - anatomy & histology; Hip - growth & development; Human performance; Humans; Hypertension; Hypoglycemic agents; Koreans; Male; Markers; Medicine; Metabolic syndrome; Middle Aged; Obesity; Polymorphism; Polymorphism, Single Nucleotide; Population; Regression analysis; Republic of Korea; Risk factors; Sex Factors; Single nucleotide polymorphisms; Single-nucleotide polymorphism; Studies; Surgical implants; Thorax; Thorax - anatomy & histology; Thorax - growth & development; Type 2 diabetes; Ubiquitin-Protein Ligases - genetics
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0145220

The thoracic-to-hip circumference ratio (THR) is an anthropometric marker recently described as a predictor of type 2 diabetes. In this study, we performed a genome-wide association study (GWAS) followed by confirmatory analyses to identify genetic markers associated with THR. A total of 7,240 Korean subjects (4,988 for the discovery stage and 2,252 for the confirmatory analyses) were recruited for this study, and genome-wide single nucleotide polymorphism (SNP) genotyping of the initial 4,988 individuals was performed using Affymetrix Human SNP array 5.0. Linear regression analysis was then performed to adjust for the effects of age, sex, and current diabetes medication status on the THR of the study subjects. In the initial discovery stage, there was a statistically nominal association between minor alleles of SNP markers on chromosomes 4, 8, 10, and 12, and THR changes (p < 5.0 × 10-6). The subsequent confirmatory analyses of these markers, however, only detected a significant association between two SNPs in the HECTD4 gene and decreased THRs. Notably, this association was detected in male (rs11066280: p = 1.14 × 10-2; rs2074356: p = 1.10 × 10-2), but not in female subjects. Meanwhile, the combined results from the two analyses (initial and confirmatory) indicated that minor alleles of these two intronic variants exhibited a significant genome-wide association with decreased THR in the male subjects (n = 3,155; rs11066280: effect size = -0.008624, p = 6.19 × 10-9; rs2074356: effect size = -0.008762, p = 1.89 × 10-8). Furthermore, minor alleles of these two SNPs exhibited protective effects on patients' risks for developing type 2 diabetes. In conclusion, we have identified two genetic variations in HECTD4 that are associated with THR, particularly in men.