Journal Article

Common variants at the GCK, GCKR, G6PC2-ABCB11 and MTNR1B loci are associated with fasting glucose in two Asian populations

Yamori, Y, Ikegami, H, Wickremasinghe, R, Nakashima, E, Kono, S, Kobayashi, S, Kato, N, Chakrewarthy, S, Ogihara, T, Ohnaka, K, Yamamoto, K, Yamaguchi, S, Takayanagi, R, Fujisawa, T, Kasturiratne, A, de Silva, A, Serizawa, M, Fujioka, A, Nabika, T, Katsuya, T, Takeuchi, F, Sugiyama, T

2010

Overview

Aims/hypothesis To test fasting glucose association at four loci recently identified or verified by genome-wide association (GWA) studies of European populations, we performed a replication study in two Asian populations. Methods We genotyped five common variants previously reported in Europeans: rs1799884 (GCK), rs780094 (GCKR), rs560887 (G6PC2-ABCB11) and both rs1387153 and rs10830963 (MTNR1B) in the general Japanese (n = 4,813) and Sri Lankan (n = 2,319) populations. To identify novel variants, we further examined genetic associations near each locus by using GWA scan data on 776 non-diabetic Japanese samples. Results Fasting glucose association was replicated for the five single nucleotide polymorphisms (SNPs) at p < 0.05 (one-tailed test) in South Asians (Sri Lankan) as well as in East Asians (Japanese). In fine-mapping by GWA scan data, we identified in the G6PC2-ABCB11 region a novel SNP, rs3755157, with significant association in Japanese (p = 2.6 × 10⁻⁸) and Sri Lankan (p = 0.001) populations. The strength of association was more prominent at rs3755157 than that of the original SNP rs560887, with allelic heterogeneity detected between the SNPs. On analysing the cumulative effect of associated SNPs, we found the per-allele gradients (β = 0.055 and 0.069 mmol/l in Japanese and Sri Lankans, respectively) to be almost equivalent to those reported in Europeans. Conclusions/interpretation Fasting glucose association at four tested loci was proven to be replicable across ethnic groups. Despite this overall consistency, ethnic diversity in the pattern and strength of linkage disequilibrium certainly exists and can help to appreciably reduce potential causal variants after GWA studies.

• Publisher: Berlin/Heidelberg : Springer-Verlag,Springer-Verlag,Springer,Springer Nature B.V
• Subject: Adaptor Proteins, Signal Transducing - genetics / Alleles / Asian Continental Ancestry Group - genetics / ATP Binding Cassette Subfamily B Member 11 / ATP-Binding Cassette Transporters - genetics / Biological and medical sciences / Blood Glucose - metabolism / Chromosome Mapping - methods / Diabetes. Impaired glucose tolerance / Endocrine pancreas. Apud cells (diseases) / Endocrinopathies / Ethnic Groups - genetics / Etiopathogenesis. Screening. Investigations. Target tissue resistance / Fasting - physiology / Genetic Variation / Glucose-6-Phosphatase - genetics / Haplotypes - genetics / Human Physiology / Humans / Internal Medicine / Japan / Medical sciences / Medicine / Medicine & Public Health / Metabolic Diseases / Polymorphism, Single Nucleotide / Protein-Serine-Threonine Kinases - genetics / Receptor, Melatonin, MT2 - genetics / Regression Analysis / Sri Lanka