Genetic variation of Neurogenin 3 is slightly associated with hyperproinsulinaemia and progression toward type 2 diabetes

被引:8
作者
Li, J. [1 ]
Bergmann, A.
Reimann, M. [1 ]
Schulze, J. [1 ]
Bornstein, S. R. [1 ]
Schwarz, P. E. H. [1 ]
机构
[1] Tech Univ Dresden, Med Fac Carl Gustav Carus, Med Clin 3, Dept Endocrinopathies & Metab Dis, D-01309 Dresden, Germany
关键词
Neurogenin; 3; proinsulin; progression of type 2; diabetes;
D O I
10.1055/s-2007-992156
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Transcription factor Neurogenin 3 (NGN3) is considered as a candidate gene for the development of type 2 diabetes. The aim of the current study was to investigate the relevance of NGN3 variants for the clinical spectrum of diabetes development and disease progressions. Research Design and Methods: A total of 552 subjects with increased risk of type 2 diabetes were investigated. They underwent a 75g OGTT with measurements of plasma glucose, insulin and proinsulin at fasting and at 30, 60,90 and 120 minutes after the glucose challenge, repeated after 3 years. The NGN3 SNPs, Gly167Arg and Ser199Phe were genotyped. Result: Patients with type 2 diabetes carrying the variant genotype at SNP199 presented with significantly higher proinsulin levels. Proinsulin level was also associated with progression of diabetes mellitus. There was a discrete association of the Ser199Phe variant with evolution of the disease status. Conclusion: A genetic variation in NGN3 gene may be among the genetic determinants involved in the pathogenesis of diabetes.
引用
收藏
页码:178 / 183
页数:6
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