Abstract
Substantial progress has been made in identification of type 2 diabetes (T2D) risk loci in the past few years, but our understanding of the genetic basis of T2D in ethnically diverse populations remains limited. We performed a genome-wide association study and a replication study in Chinese Hans comprising 8,569 T2D case subjects and 8,923 control subjects in total, from which 10 single nucleotide polymorphisms were selected for further follow-up in a de novo replication sample of 3,410 T2D case and 3,412 control subjects and an in silico replication sample of 6,952 T2D case and 11,865 control subjects. Besides confirming seven established T2D loci (
CDKAL1
,
CDKN2A/B
,
KCNQ1
,
CDC123
,
GLIS3
,
HNF1B
, and
DUSP9
) at genome-wide significance, we identified two novel T2D loci, including G-protein–coupled receptor kinase 5 (
GRK5
) (rs10886471:
P
= 7.1 × 10
−9
) and
RASGRP1
(rs7403531:
P
= 3.9 × 10
−9
), of which the association signal at
GRK5
seems to be specific to East Asians. In nondiabetic individuals, the T2D risk-increasing allele of
RASGRP1
-rs7403531 was also associated with higher HbA
1c
and lower homeostasis model assessment of β-cell function (
P
= 0.03 and 0.0209, respectively), whereas the T2D risk-increasing allele of
GRK5
-rs10886471 was also associated with higher fasting insulin (
P
= 0.0169) but not with fasting glucose. Our findings not only provide new insights into the pathophysiology of T2D, but may also shed light on the ethnic differences in T2D susceptibility.