The KCNJ11 E23K and ABCC8 exon 31 variants contribute to susceptibility to type 2 diabetes, glucose intolerance and altered insulin secretion in a Russian population

被引:4
|
作者
Chistiakov, Dimitry A. [1 ]
Potapov, Viktor A. [1 ]
Khodirev, Dimitry S. [1 ]
Shamkhalova, Minara S. [2 ]
Shestakova, Marina V. [2 ]
Nosikov, Valery V. [1 ]
机构
[1] Natl Res Ctr GosNIIgenetika, Bldg 1,1st Dorozhny Proezd, Moscow 113545, Russia
[2] Endocrinol Res Ctr, Moscow, Russia
关键词
Glucose tolerance; Insulin secretion; ABCC8; KCNJ11; Russian population; Susceptibility; Type; 2; diabetes;
D O I
10.1016/j.dsx.2008.04.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: The KCNJ11 and ABCC8 genes encode components of the ATP-sensitive potassium (KATP) channel, which regulates insulin secretion by beta-cells. Alterations in the activity of pancreatic KATP could be involved in the pathogenesis of type 2 diabetes (T2D). We studied the KCNJ11 E23K and ABCC8 exon 31 variants for association with T2D, glucose intolerance and altered insulin secretion in a Russian population. Methods: Using a polymerase chain reaction (PCR) with the following digestion of a PCR product with a corresponding restriction enzyme, genomic DNA from Russian T2D patients (N = 127) and controls (N = 117) were genotyped. Fasting and 2 h glucose and insulin were measured in blood of all subjects studied. Biochemical parameters in diabetic and control individuals were compared by the unpaired Student's t-test. chi(2)-test was used to compare allele and genotype frequencies of the polymorphisms studied. Results: The KCNJ11 E23 variant and the ABCC8 exon 31 allele A were associated with higher risk of T2D (Odds Ratio (OR) of 1.53 (p = 0.023) and 2.41 (p = 1.95 x 10(-5)), respectively. T2D patients with the EE variant of KCNJ11 have elevated 2 h serum insulin (EE (87.3 +/- 34.9 mU/l) vs. KK + EK (82.1 +/- 31.1 mU/l), p = 0.038). Diabetic carriers of the ABCC8 G/G variant had reduced 2 h glucose compared to A/A + A/G (p = 0.031). The G/G genotype of ABCC8 was also significantly associated with increased both fasting and 2 h serum insulin in diabetic and non-diabetic patients. A HOMA-beta value characterizing the beta-cell homeostasis was higher in the non-diabetic carriers homozygous for G/G (98.0 +/- 46.9) than for other genotypes (HOMA-beta = 85.6 +/- 45.5 for A/A + A/G, p = 0.0015). Conclusions: The KCNJ11 E23K and ABCC8 exon31 variants contribute to susceptibility to T2D diabetes, glucose intolerance and altered insulin secretion in a Russian population. (C) 2008 Diabetes India. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:185 / 191
页数:7
相关论文
共 37 条
  • [21] Association of common KCNJ11 polymorphism E23K with type 2 diabetes and markers of glycaemic control, inflammation and obesity
    Bego, T.
    Causevic, A.
    Dujic, T.
    Malenica, M.
    Velija-Asimi, Z.
    Prnjavorac, B.
    Bego, Z.
    Nekvindova, J.
    Palicka, V.
    Semiz, S.
    FEBS OPEN BIO, 2018, 8 : 245 - 245
  • [22] Association of E23k KCNJ11 variant and progression of neuropathy among type 2 diabetes patients in the north area of Iran
    Parvaneh, Keshavarz Kiasaraei
    Malake, Ghasemi
    Razieh, Habibi
    CLINICAL BIOCHEMISTRY, 2011, 44 (13) : S298 - S299
  • [23] Association between KCNJ11 E23K polymorphism and the risk of type 2 diabetes mellitus: A global meta-analysis
    Ren, Yaxuan
    Zhu, Wenfei
    Shi, Jikang
    Shao, Aiyu
    Cheng, Yi
    Liu, Yawen
    JOURNAL OF DIABETES AND ITS COMPLICATIONS, 2022, 36 (05)
  • [24] Evidence for Association of the E23K Variant of KCNJ11 Gene with Type 2 Diabetes in Tunisian Population: Population-Based Study and Meta-Analysis
    Lasram, Khaled
    Ben Halim, Nizar
    Hsouna, Sana
    Kefi, Rym
    Arfa, Imen
    Ghazouani, Welid
    Jamoussi, Henda
    Benrahma, Houda
    Kharrat, Najla
    Rebai, Ahmed
    Ben Ammar, Slim
    Bahri, Sonia
    Barakat, Abdelhamid
    Abid, Abdelmajid
    Abdelhak, Sonia
    BIOMED RESEARCH INTERNATIONAL, 2014, 2014
  • [25] The E23K and A190A variations of the KCNJ11 gene are associated with early-onset type 2 diabetes and blood pressure in the Chinese population
    Langen Zhuang
    Yu Zhao
    Weijing Zhao
    Ming Li
    Ming Yu
    Ming Lu
    Rong Zhang
    Xiaoxu Ge
    Taishan Zheng
    Can Li
    Jun Yin
    Jingyuan Yin
    Yuqian Bao
    Limei Liu
    Weiping Jia
    Yanjun Liu
    Molecular and Cellular Biochemistry, 2015, 404 : 133 - 141
  • [26] The E23K and A190A variations of the KCNJ11 gene are associated with early-onset type 2 diabetes and blood pressure in the Chinese population
    Zhuang, Langen
    Zhao, Yu
    Zhao, Weijing
    Li, Ming
    Yu, Ming
    Lu, Ming
    Zhang, Rong
    Ge, Xiaoxu
    Zheng, Taishan
    Li, Can
    Yin, Jun
    Yin, Jingyuan
    Bao, Yuqian
    Liu, Limei
    Jia, Weiping
    Liu, Yanjun
    MOLECULAR AND CELLULAR BIOCHEMISTRY, 2015, 404 (1-2) : 133 - 141
  • [27] Association of KCNJ11 E23K/rs5219 Gene Polymorphism with Type 2 Diabetes and Diabetes-Related Cardiovascular Disease
    Buraczynska, Monika
    Boczkowska, Sylwia
    Zaluska, Wojciech
    DIABETES METABOLIC SYNDROME AND OBESITY, 2025, 18 : 653 - 661
  • [28] Association of the E23K (rs5219) polymorphism in the potassium channel (KCNJ11) gene with diabetic neuropathy in type 2 diabetes
    Elzehery, Rasha
    Abd El-Hafez, Hala
    Elsehely, Ibrahim
    Barakat, Amira
    Foda, Engy Ahmed Ebrahim
    Hendawy, Shimaa Rabea
    Gameil, Mohammed Ali
    Nada, Hyam Sameh
    EL-Sebaie, Ahmed
    GENE, 2024, 921
  • [29] Relationship between E23K (an established type II diabetes-susceptibility variant within KCNJ11), polycystic ovary syndrome and androgen levels
    Thomas M Barber
    Amanda J Bennett
    Anna L Gloyn
    Christopher J Groves
    Ulla Sovio
    Aimo Ruokonen
    Hannu Martikainen
    Anneli Pouta
    Saara Taponen
    Michael N Weedon
    Anna-Liisa Hartikainen
    John A H Wass
    Marjo-Riitta Järvelin
    Eleftheria Zeggini
    Stephen Franks
    Mark I McCarthy
    European Journal of Human Genetics, 2007, 15 : 679 - 684
  • [30] Relationship between E23K (an established type II diabetes-susceptibility variant within KCNJ11), polycystic ovary syndrome and androgen levels
    Barber, Thomas M.
    Bennett, Amanda J.
    Gloyn, Anna L.
    Groves, Christopher J.
    Sovio, Ulla
    Ruokonen, Aimo
    Martikainen, Hannu
    Pouta, Anneli
    Taponen, Saara
    Weedon, Michael N.
    Hartikainen, Anna-Liisa
    Wass, John A. H.
    Jarvelin, Marjo-Riitta
    Zeggini, Eleftheria
    Franks, Stephen
    McCarthy, Mark I.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2007, 15 (06) : 679 - 684