POLYMORPHISM OF TISSUE INHIBITORS OF METALLOPROTEINASE-2 (G303 → A) GENE IN PATIENTS WITH INTESTINAL ANASTOMOTIC LEAK IN UKRAINIAN POPULATION

Y. Voitiv
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Abstract

Purpose - to analyze the frequency of polymorphic variants of tissue inhibitors ofmetalloproteinase-2 (G303 → A) gene in patients with intestinal anastomotic leak.Material and methods. The object of the study comprises 61 patients with anastomotic leakand connective tissue pathology, who were treated in the department of thoracoabdominalsurgery of Shalimov National Institute of Surgery and Transplantology during 2017-2020. Laboratory, genetic, histological studies and statistical analysis were performed.Results. As a result of genetic and statistical analysis of the tissue inhibitors ofmetalloproteinase-2 (G303 → A) gene polymorphisms, genotype variants have beenidentified that are associated with the risk of anastomotic leak in the hollow digestiveorgans. Significant differences in the distribution of genotypes in the studied groupswere revealed. Analysis of the multiplicative model of inheritance of tissue inhibitors ofmetalloproteinase-2 (G303 → A) gene showed compliance of genotype distribution withHardy-Weinberg's law. All models of inheritance were analyzed and the best model withthe lowest Akaike Information Criterion, which turned out to be a recessive model, hasbeen determined.Conclusions. It is statistically significant that in the group of patients with intestinalanastomotic leak the GG variant of the TIMP-2 gene was detected in 1,6 times moreoften. Carriers of minor homozygotes of AA genotype in the group with suture failurewere not detected, while a similar genotype in the control group was found in 10%(p <0,05).
乌克兰人群肠吻合口瘘患者金属蛋白酶-2 (g303→a)基因组织抑制剂多态性研究
目的:分析肠吻合口瘘患者金属蛋白酶-2组织抑制因子(G303→A)基因多态性变异的频率。材料和方法。本研究对象为2017-2020年在沙里莫夫国立外科与移植研究所胸腹外科治疗的吻合口漏及结缔组织病理患者61例。进行了实验室、遗传、组织学研究和统计分析。通过对金属蛋白酶-2 (G303→a)组织抑制剂基因多态性的遗传和统计分析,发现基因型变异与空心消化器官吻合口漏的风险相关。结果表明,各研究组基因型分布存在显著差异。对金属蛋白酶-2组织抑制剂(G303→A)基因的遗传增殖模型分析表明,基因型分布符合hardy - weinberg定律。对所有遗传模型进行分析,确定了赤池信息准则最低的最佳遗传模型为隐性遗传模型。在肠吻合口漏患者组中,TIMP-2基因GG变异的检出率高出1、6倍,差异有统计学意义。缝合失败组未检出AA基因型的少量纯合子携带者,而对照组中有10%的AA基因型携带者(p < 0.05)。
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