Association between C1019T polymorphism of connexin37 and acute myocardial infarction:: a study in patients from Sicily

被引:55
|
作者
Listì, F
Candore, G
Lio, D
Russo, M
Colonna-Romano, G
Caruso, M
Hoffmann, E
Caruso, C
机构
[1] Univ Palermo, Dept Biopatol & Metodol Biomed, Grp Studio Immunosenescenza, I-90134 Palermo, Italy
[2] Univ Palermo, Dipartimento Med Interna Malattie Cardiovasc & Ne, Palermo, Italy
关键词
acute myocardial infarction; atherosclerosis; connexin37; gap junction; SNP;
D O I
10.1016/j.ijcard.2004.05.031
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
During atherogenesis, a critical role is played by intercellular communication via gap junctions, cell membrane channels linking the cytoplasmic compartments of adjacent cells. The component protein subunits of these channels, called connexin (Cx), belong to a multigene family. Cx37 is involved in growth, regeneration after injury and ageing of the endothelial cells, suggesting its role in atherosclerosis. The C1019 single nucleotide polymorphismi (SNP) of Cx37 gene was associated with thickening of the carotid intima in Swedish men and was also associated with coronary artery disease in a Taiwanese population. On the other hand, in two more recent studies performed in male Japanese population, T1019 Cx37 SNP has shown to be a risk factor for acute myocardial infarction (AMI). In the light of these discrepant results, we have studied the frequency of this SNP in a very homogeneous cohort of young male people affected by AML We analysed 97 male Sicilian patients (mean age 40, age range 20-46) and 196 healthy male controls (mean age 39, age range 20-55) for C1019T of the Cx37. The 1019T SNP was significantly increased in the patients compared to the controls (43.8% vs. 34.4%; p=0.03 by chi(2) test with Yates' correction; odds ratio (OR) 1.5, (1.0-2.1) 95% confidence interval (CI). The present case control study performed in a homogeneous Caucasoid population confirms the Japanese results that T SNP of Cx37 gene is involved in AMI phenotype, demonstrating the consistency of the association across past studies and across different populations. The differences between patients and controls are significant but relatively small with an odd ratio risk of 1.5. However, as AMI is a multifactorial disease, any single mutation will only provide a small or modest contribution to risk, also depending on interaction with other genes and/or a particular environment. (c) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:269 / 271
页数:3
相关论文
共 50 条
  • [1] Contribution of Connexin37 Gene Polymorphism (C1019T) in the Incidence of Acute Myocardial Infarction in the Egyptians
    El Tahry, Fadwa
    Hashad, Ingy
    Farouk, Mohamed
    Gad, Mohamed
    PROTEIN SCIENCE, 2015, 24 : 16 - 16
  • [2] Association of Connexin37 C1019T with myocardial infarction and coronary artery disease: a meta-analysis
    Wen, Dan
    Du, Xin
    Nie, Shao-Ping
    Dong, Jian-Zeng
    Ma, Chang-Sheng
    EXPERIMENTAL GERONTOLOGY, 2014, 58 : 203 - 207
  • [3] Association between C1019T polymorphism of the connexin37 gene and coronary heart disease in patients with in-stent restenosis
    Guo, Su-Xia
    Yang, Zhen-Yu
    Wang, Ru-Xing
    Yang, Ying
    Cao, Hua-Ming
    Zhang, Tao
    EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2013, 5 (02) : 539 - 544
  • [4] Connexin37 1019 gene polymorphism in myocardial infarction patients and centenarians
    Listi, Florinda
    Candore, Giuseppina
    Balistreri, Carmela Rita
    Caruso, Marco
    Incalcaterra, Egle
    Hoffmann, Enrico
    Lio, Domenico
    Caruso, Calogero
    ATHEROSCLEROSIS, 2007, 191 (02) : 460 - 461
  • [5] C1019T polymorphism in Connexin37 gene and ischemic cerebrovascular disease in the Japanese population
    Ito, D
    Tanahashi, N
    Murata, M
    Watanabe, K
    Yoshida, T
    Fukuuchi, Y
    STROKE, 2000, 31 (11) : 2861 - 2861
  • [6] Association of C1019T polymorphism in the connexin37 gene and coronary artery disease in the Chinese Han population.
    Xi, S. Y.
    Han, Y. L.
    Zhang, X. L.
    Yan, C. H.
    Kang, J.
    AMERICAN JOURNAL OF CARDIOLOGY, 2007, 99 (08): : 63F - 63F
  • [7] The Connexin37 Gene C1019T Polymorphism and Risk of Coronary Artery Disease: A Meta-analysis
    Wu, Zhijun
    Lou, Yuqing
    Jin, Wei
    Liu, Yan
    Lu, Lin
    Chen, Qiujing
    Zhang, Ruiyan
    ARCHIVES OF MEDICAL RESEARCH, 2014, 45 (01) : 21 - 30
  • [8] Association Between C1019T Polymorphism in the Connexin 37 Gene and Helicobacter Pylori Infection in Patients with Gastric Cancer
    Jing, Yuan-Ming
    Guo, Su-Xia
    Zhang, Xiao-Ping
    Sun, Ai-Jing
    Tao, Feng
    Qian, Hai-Xin
    ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, 2012, 13 (05) : 2363 - 2367
  • [9] Analysis of Connexin37 gene C1019T polymorphism and PCOS susceptibility in South Indian population: case-control study
    Guruvaiah, Praveen
    Govatati, Suresh
    Reddy, Tumu Venkat
    Beeram, Himabindu
    Deenadayal, Mamata
    Shivaji, Sisinthy
    Bhanoori, Manjula
    EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 2016, 196 : 17 - 20
  • [10] The influence of smoking and homocysteine on subclinical atherosclerosis is modified by the connexin37 C1019T polymorphism -: The Cardiovascular Risk in Young Finns Study
    Collings, Auni
    Raitakari, Olli T.
    Juonala, Markus
    Mansikkaniemi, Kristiina
    Kahonen, Mika
    Hutri-Kahonen, Nina
    Marniemi, Jukka
    Viikari, Jorma S. A.
    Lehtimaki, Terho J.
    CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2008, 46 (08) : 1102 - 1108