A SNP in G6PC2 predicts insulin secretion in type 1 diabetes

被引:0
|
作者
Srinath Sanda
Shan Wei
Tessa Rue
Heather Shilling
Carla Greenbaum
机构
[1] Benaroya Research Institute,
[2] Institute of Translational Health Sciences,undefined
来源
Acta Diabetologica | 2013年 / 50卷
关键词
Translational research; Genetics; Longitudinal studies;
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学科分类号
摘要
We investigated whether single nucleotide polymorphisms in genes related to glucose metabolism correlate with insulin secretion in type 1 diabetes patients. A cohort of 49 type 1 diabetes patients underwent serial mixed meal tolerance tests to assess insulin secretion. Patients were genotyped for SNPs related to glucose metabolism: CDKAL1 rs7754840, G6PC2 rs560887, HHEX rs1111875, KCNJ11 rs5215. Recently diagnosed patients (<100 days) homozygous for the G allele of G6PC2 had higher area under the curve C-peptide on mixed meal tolerance tests compared to non-homozygous patients (344.8 ± 203.2 vs. 167.9 ± 131.5, p = 0.04). Other SNPs did not correlate with insulin secretion in the new onset period. In a longitudinal survival analysis, homozygosity for the minor allele (A) in G6PC2 predicted more rapid loss of insulin secretion over time. A SNP in the beta cell gene G6PC2 may correlate with preserved insulin secretion in type 1 diabetes.
引用
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页码:459 / 462
页数:3
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