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地中海热(MEFV)基因突变频率在风湿性心脏病成人中并未增加。

Mediterranean fever (MEFV) gene mutation frequency is not increased in adults with rheumatic heart disease.

机构信息

Division of Rheumatology, Gulhane School of Medicine, Ankara, Turkey.

出版信息

Clin Rheumatol. 2011 Apr;30(4):491-5. doi: 10.1007/s10067-010-1537-9. Epub 2010 Jul 20.

Abstract

It is well established that there are people with higher risk of developing acute rheumatic fever (ARF) and rheumatic heart disease (RHD). Mediterranean fever (MEFV) gene mutations might be one of the genetic predisposition factors in the development of ARF/RHD since defect in familial Mediterranean fever (FMF) patients is proposed to be heightened inflammatory response to certain stimuli. Previous clinical observations suggested a relationship between FMF and ARF/RHD. The aim of this study was to investigate the role of the MEFV gene mutations in the susceptibility to RHD in Turkish patients. A total of 100 patients with RHD and 100 healthy controls were included in the study. Diagnosis of RHD was based on echocardiographic findings in which a predominant mitral stenosis was used as an inclusion criterion. Genetic analysis was carried out by sequence analysis investigating two hot spots (exons 2 and 10) for MEFV mutations. Mutation analysis showed that 22 RHD patients (22%) and 24 healthy controls (24%) carried at least one mutated allele. MEFV mutations were identified in 22 of 200 (11%) chromosomes in RHD patients while 26 of the 200 (13%) chromosomes of healthy controls were found to carry a mutated allele. No difference was found in allele frequencies and their distribution between the patients and healthy controls (p = 0.54). MEFV mutations are not associated with a predisposition to develop RHD in adult Turkish patients.

摘要

已知有些人患急性风湿热(ARF)和风湿性心脏病(RHD)的风险较高。MEFV 基因突变可能是 ARF/RHD 发展的遗传易感性因素之一,因为家族性地中海热(FMF)患者的缺陷被认为是对某些刺激产生增强的炎症反应。先前的临床观察表明 FMF 与 ARF/RHD 之间存在关系。本研究旨在探讨 MEFV 基因突变在土耳其患者 RHD 易感性中的作用。共有 100 例 RHD 患者和 100 名健康对照者纳入研究。RHD 的诊断基于超声心动图发现,其中主要二尖瓣狭窄被用作纳入标准。通过序列分析对 MEFV 突变的两个热点(外显子 2 和 10)进行遗传分析。突变分析显示,22 例 RHD 患者(22%)和 24 名健康对照者(24%)携带至少一个突变等位基因。在 RHD 患者的 200 个(11%)染色体中发现了 22 个 MEFV 突变,而在健康对照者的 200 个(13%)染色体中发现了 26 个携带突变等位基因。患者和健康对照者之间等位基因频率及其分布无差异(p=0.54)。MEFV 突变与土耳其成年患者发生 RHD 的易感性无关。

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