Literature DB >> 19533015

Transcription factor 7-like 2-gene polymorphism is related to fasting C peptide in latent autoimmune diabetes in adults (LADA).

Barbara Szepietowska1, Dariusz Moczulski, Natalia Wawrusiewicz-Kurylonek, Wladyslaw Grzeszczak, Maria Gorska, Malgorzata Szelachowska.   

Abstract

Common polymorphisms in the transcription factor 7-like 2 gene (TCF7L2) have been associated with type 2 diabetes in different populations and recently with LADA, but not with type 1 diabetes. The aim of our study was to investigate association between the rs7903146 polymorphism in the TCF7L2 gene and LADA in Polish patients. Link between the "high risk for type 2 diabetes genotype" with clinical features was analyzed. 68 newly diagnosed patients with LADA and 195 healthy controls were genotyped for the rs7903146 polymorphism in the TCF7L2 gene using the PCR-based RFLP method. Fasting C peptide level was measured by ELISA. We observed increased frequencies of the TT genotype of the rs7903146 polymorphism in the TCF7L2 gene in LADA patients compared to controls (15 vs. 6%, P = 0.03). Fasting C peptide serum concentration was significantly lower in group of patients with LADA carrying the TT genotype (P < 0.01). In conclusion, the data from this study confirmed previous results showing genetic similarities between patients with LADA and type 2 diabetes. Non-autoimmune mechanism may be related to beta cell dysfunction in patients with LADA.

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Year:  2009        PMID: 19533015     DOI: 10.1007/s00592-009-0133-4

Source DB:  PubMed          Journal:  Acta Diabetol        ISSN: 0940-5429            Impact factor:   4.280


  7 in total

1.  The type 2 diabetes-associated variant in TCF7L2 is associated with latent autoimmune diabetes in adult Europeans and the gene effect is modified by obesity: a meta-analysis and an individual study.

Authors:  K Lukacs; N Hosszufalusi; E Dinya; M Bakacs; L Madacsy; P Panczel
Journal:  Diabetologia       Date:  2011-11-23       Impact factor: 10.122

Review 2.  Overlap of genetic susceptibility to type 1 diabetes, type 2 diabetes, and latent autoimmune diabetes in adults.

Authors:  Kevin J Basile; Vanessa C Guy; Stanley Schwartz; Struan F A Grant
Journal:  Curr Diab Rep       Date:  2014       Impact factor: 4.810

3.  Phenotype variability and neonatal diabetes in a large family with heterozygous mutation of the glucokinase gene.

Authors:  Maciej Borowiec; Malgorzata Mysliwiec; Wojciech Fendler; Karolina Antosik; Agnieszka Brandt; Maciej Malecki; Wojciech Mlynarski
Journal:  Acta Diabetol       Date:  2011-03-25       Impact factor: 4.280

Review 4.  The broad pathogenetic role of TCF7L2 in human diseases beyond type 2 diabetes.

Authors:  Laura Del Bosque-Plata; Eduardo Pavel Hernández-Cortés; Claudia Gragnoli
Journal:  J Cell Physiol       Date:  2021-10-06       Impact factor: 6.513

5.  HLA-DR, HLA-DQB1 and PTPN22 gene polymorphism: association with age at onset for autoimmune diabetes.

Authors:  Anna Okruszko; Barbara Szepietowska; Natalia Wawrusiewicz-Kurylonek; Maria Górska; Adam Krętowski; Małgorzata Szelachowska
Journal:  Arch Med Sci       Date:  2012-11-07       Impact factor: 3.318

6.  TCF7L2 Genetic Variants Contribute to Phenotypic Heterogeneity of Type 1 Diabetes.

Authors:  Maria J Redondo; Susan Geyer; Andrea K Steck; Jay Sosenko; Mark Anderson; Peter Antinozzi; Aaron Michels; John Wentworth; Ping Xu; Alberto Pugliese
Journal:  Diabetes Care       Date:  2017-10-12       Impact factor: 19.112

7.  Association of TCF7L2 mutation and atypical diabetes in a Uruguayan population.

Authors:  Carolina Beloso; Jorge Souto; Matias Fabregat; Gerardo Romanelli; Gerardo Javiel; Adriana Mimbacas
Journal:  World J Diabetes       Date:  2018-09-15
  7 in total

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