Intron polymorphism in the KIAA0350 gene is reproducibly associated with susceptibility to type 1 diabetes (T1D) in the Han Chinese population.

Abstract:

OBJECTIVE:Three independent genome-wide association studies in white populations have reported that single nucleotide polymorphisms (SNPs) in the KIAA0350 gene are associated with susceptibility to type 1 diabetes (T1D). The gene product of KIAA0350 is predicted to be a sugar binding C-type lectin. In the present study, we investigated whether SNPs in this gene were associated with T1D in the Han Chinese population. DESIGN AND METHODS:In this case-controlled association study, a total of 205 T1D patients and 422 non-diabetic subjects of the Han Chinese population were enrolled. Two SNPs, namely, rs17802927 and rs725613, in the KIAA0350 gene were genotyped using a polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) protocol. RESULTS:The intron SNP rs725613 was strongly associated with T1D in the Han Chinese population [P = 0.00007, odds ratio (OR) = 0.527, 95% confidence interval (CI) = 0.383-0.726], and the frequencies of its genotypes in the T1D group significantly differed from those in the control group (P = 0.0001). CONCLUSION:The intron polymorphism rs725613 in the KIAA0350 gene is associated with susceptibility to T1D, and this association is not race specific.

journal_name

Clin Endocrinol (Oxf)

journal_title

Clinical endocrinology

authors

Wu X,Zhu X,Wang X,Ma J,Zhu S,Li J,Liu Y

doi

10.1111/j.1365-2265.2008.03437.x

subject

Has Abstract

pub_date

2009-07-01 00:00:00

pages

46-9

issue

1

eissn

0300-0664

issn

1365-2265

pii

CEN3437

journal_volume

71

pub_type

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