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首页> 外文期刊>International Journal of Biosciences >Implication of insertion/deletion polymorphism of angiotensin converting enzyme gene in the occurrence of type 2 diabetes in the Gabonese Population
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Implication of insertion/deletion polymorphism of angiotensin converting enzyme gene in the occurrence of type 2 diabetes in the Gabonese Population

机译:血管紧张素转换酶基因的插入/缺失多态性在加蓬人群中2型糖尿病的发生中的意义

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Diabetes is a metabolic disease most often associated with complications when the biological parameters are uncontrolled, so management of diabetes remains a challenge in Africa. The aim of this study was to find a relationship between the I/D polymorphism of the gene encoding for angiotensin converting enzyme (ACE) and type 2 diabetes in Gabonese subjects. This study was carried out in the laboratory of the Research Unit of the University of Health Sciences. The study population consisted of 225 subjects. This panel was composed of 88 controls (normoglycemic and non-hypertensive and not having a family history of diabetes) and 137 type 2 diabetic individuals. The genotypic analysis of the ACE gene of the different subjects was carried out by the technique of Polymerase Chain Reaction (PCR). Categorical and continuous variables were compared between diabetic patients and controls using the Chi-square test (χ2) for categorical and the ANOVA test for continuous. The distribution of DD, ID, and II genotypes in controls and diabetics was 63.6%, 33%; 3.4% respectively and 65.7%; 31.4%; 2.9%. In addition, the allelic distribution showed that the alleles I and D in the controls and the diabetic subjects had proportions of 19.9%; 80.1% vs. 18.6%; 81.4% respectively. The genotypic and allelic differences between the two groups were not significant (p ≥ 0.05). Therefore the allele D would not be the factor involving the I/D polymorphism in the occurrence of type 2 diabetes in the Gabonese population.
机译:当生物学参数不受控制时,糖尿病是一种最常与并发症相关的代谢疾病,因此在非洲,糖尿病的管理仍然是一个挑战。这项研究的目的是发现加蓬人中血管紧张素转化酶(ACE)编码基因的I / D多态性与2型糖尿病之间的关系。这项研究是在健康科学大学研究室的实验室中进行的。研究人群包括225名受试者。该小组由88位对照组(血糖正常和非高血压且没有糖尿病家族史的患者)和137位2型糖尿病患者组成。通过聚合酶链反应(PCR)技术对不同受试者的ACE基因进行基因型分析。使用卡方检验(χ2)进行分类,使用ANOVA检验进行连续性分析,比较糖尿病患者和对照组的分类变量和连续变量。 DD,ID和II基因型在对照组和糖尿病患者中的分布分别为63.6%,33%;分别为3.4%和65.7%; 31.4%; 2.9%。另外,等位基因分布表明,对照组和糖尿病患者中等位基因I和D的比例为19.9%; 80.1%和18.6%;分别为81.4%。两组之间的基因型和等位基因差异不显着(p≥0.05)。因此,等位基因D不会成为加蓬人口中2型糖尿病发生中涉及I / D多态性的因素。

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