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The rs1014290 polymorphism of the SLC2A9 gene is associated with type 2 diabetes mellitus in Han Chinese.


ABSTRACT: AIMS: The SLC2A9 gene encodes the glucose transporter 9, with the abilities of transporting both glucose and uric acid and is involved in the pancreatic glucose-stimulated insulin secretion. The single nucleotide polymorphisms (SNPs) of SLC2A9 accounted for 5% variance of serum uric acid (UA). UA was identified as a risk factor for type 2 diabetes mellitus (DM). We investigated whether the SLC2A9 gene variations are associated with type 2 DM in Han Chinese. METHODS: Three common SNPs of the SLC2A9, rs1014290, rs2280205, and rs3733591, were genotyped in 1003 Han Chinese randomly selected from Kaohsiung, Taiwan. RESULTS: The variant SNP rs1014290 is associated with decreased 0.12-fold risk of type 2 DM (P = .002). Per-copy increase in the minor C-allele results in 0.13?mmol/L (P = .037) and 10.03??mol/L (P = .016) decrease in serum glucose and UA, respectively. CONCLUSIONS: The SNP rs1014290 within the SLC2A9 gene is associated with type 2 DM in Han Chinese.

SUBMITTER: Liu WC 

PROVIDER: S-EPMC3092507 | biostudies-literature | 2011

REPOSITORIES: biostudies-literature

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The rs1014290 polymorphism of the SLC2A9 gene is associated with type 2 diabetes mellitus in Han Chinese.

Liu Wan-Chun WC   Hung Chi-Chih CC   Chen Szu-Chia SC   Lin Ming-Yen MY   Chen Ling-I LI   Hwang Daw-Yang DY   Chang Jer-Ming JM   Tsai Jer-Chia JC   Chen Hung-Chun HC   Hwang Shang-Jyh SJ  

Experimental diabetes research 20110414


<h4>Aims</h4>The SLC2A9 gene encodes the glucose transporter 9, with the abilities of transporting both glucose and uric acid and is involved in the pancreatic glucose-stimulated insulin secretion. The single nucleotide polymorphisms (SNPs) of SLC2A9 accounted for 5% variance of serum uric acid (UA). UA was identified as a risk factor for type 2 diabetes mellitus (DM). We investigated whether the SLC2A9 gene variations are associated with type 2 DM in Han Chinese.<h4>Methods</h4>Three common SNP  ...[more]

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