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原发性膝关节骨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

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

作者信息

Shehab D K, Al-Jarallah K F, Alawadhi A M, Al-Herz A, Nahar I, Haider M Z

机构信息

Department of Medicine, Faculty of Medicine, Kuwait University, Kuwait.

出版信息

Clin Exp Rheumatol. 2008 Mar-Apr;26(2):305-10.

Abstract

OBJECTIVE

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.

CONCLUSION

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.

摘要

目的

血管紧张素转换酶(ACE)在多种炎症和免疫相关疾病中起重要作用。本研究旨在调查科威特原发性膝骨关节炎(OA)与血管紧张素转换酶(ACE)基因插入/缺失(I/D)多态性之间的关联,并探讨OA临床亚组与ACE I/D多态性基因型之间的相关性。

患者与方法

采用基因组DNA聚合酶链反应(PCR),对115例原发性膝OA患者和111例种族匹配的健康对照者进行ACE基因I/D多态性患病率测定。还研究了ACE基因I/D多态性基因型与疾病发病年龄、功能及放射学分级的相关性。

结果

膝OA患者与对照组之间,ACE基因I/D多态性基因型和等位基因频率未检测到显著差异。根据疾病发病年龄、功能及放射学分级等临床参数,对亚组患者的ACE基因多态性基因型频率进行研究,OA患者亚组与对照组之间未检测到显著差异。这与韩国之前的一份报告形成鲜明对比,在该报告中,ACE基因多态性与膝OA之间存在显著关联。

结论

本研究未发现科威特原发性膝骨关节炎患者的ACE基因I/D多态性基因型与疾病的发病或严重程度之间存在关联,这与韩国膝OA患者的情况不同,在韩国膝OA患者中已报道存在关联。

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