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Prevalence of angiotensin-converting enzyme gene insertion-deletion polymorphism in patients with primary knee osteoarthritis

机译:原发性膝骨性关节炎患者血管紧张素转换酶基因插入缺失多态性的患病率

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OBJECTIVES:Angiotensin converting enzyme (ACE) plays an important role in a number of inflammatory and immune related disorders. This study was undertaken to investigate an association between Angiotensin converting enzyme (ACE) gene insertion- deletion (I/D) polymorphism and primary knee osteoarthritis (OA) in Kuwait and to explore a correlation between clinical subgroups of OA and ACE I/D polymorphism genotypes.PATIENTS AND METHODS:The prevalence of ACE gene I/D polymorphism was determined in 115 patients with primary knee OA and 111 ethnically matched healthy controls by using polymerase chain reaction (PCR) of the genomic DNA. The association of ACE gene I/D polymorphism genotypes was also studied with age of disease onset, function and radiological grading.RESULTS:No significant difference was detected in the frequency of ACE gene I/D polymorphism genotypes and alleles between knee OA patients and the controls. The frequency of ACE gene polymorphism genotypes was also studied in subgroups on the basis of clinical parameters of age of onset of disease, function and radiological grading and no significant difference was detected between subgroups of OA patients and the controls. This is in sharp contrast to a previous report from Korea in which a significant association has been reported between ACE gene polymorphism and knee OA.CONCLUSIONS:This study did not find an association between ACE gene I/D polymorphism genotypes in Kuwaiti patients with primary knee osteoarthritis and the onset or severity of the disease, which is very different from Korean knee OA patients in which an association has been reported.
机译:目的:血管紧张素转换酶(ACE)在许多炎症和免疫相关疾病中起重要作用。这项研究旨在调查科威特的血管紧张素转换酶(ACE)基因插入-缺失(I / D)多态性与原发性膝骨关节炎(OA)之间的关联,并探讨OA临床亚群与ACE I / D多态性之间的相关性患者和方法:通过基因组DNA的聚合酶链反应(PCR)检测115例原发性膝骨关节炎和111例民族匹配的健康对照者的ACE基因I / D多态性。还研究了ACE基因I / D多态性基因型与疾病发病年龄,功能和影像学分级之间的关系。控制。还根据疾病发病年龄,功能和放射学分级的临床参数在亚组中研究了ACE基因多态性基因型的频率,在OA患者亚组和对照组之间未发现显着差异。这与韩国先前的报道形成鲜明对比,该报道曾报道韩国ACE基因多态性与膝骨关节炎之间存在显着相关性。结论:这项研究未发现科威特原发性膝关节患者ACE基因I / D多态性基因型之间存在关联。骨关节炎和疾病的发作或严重程度,与韩国膝OA患者有很大的不同,后者已被报道。

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