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用于家族性地中海热分子诊断的聚合酶链反应-限制性片段长度多态性(PCR-RFLP)和反向杂交方法结果的比较。

Comparison of the results of PCR-RFLP and reverse hybridization methods used in molecular diagnosis of FMF.

作者信息

Sahin Feride Iffet, Yilmaz Zerrin, Yurtcu Erkan, Baskin Esra

机构信息

Department of Medical Genetics, Baskent University Faculty of Medicine, Ankara, Turkey.

出版信息

Genet Test. 2008 Mar;12(1):171-4. doi: 10.1089/gte.2007.0085.

Abstract

Familial Mediterranean fever (FMF) is characterized by recurrent fever, serositis, and arthritis. Due to the abundance of mutations and clinical heterogeneity of the disease, different screening methods have been developed. In this study, we aimed to compare our findings of mutations determined by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) with reverse hybridization (RH) methods. In 152 of 263 patients (57.79%) different mutations were determined with RH. Allelic frequencies were E148Q 6.84%, M680I(G/C) 3.61%, M694V 20.91%, V726A 7.03%, P369S 1.33%, F479L 0.19%, M680I(G/A) 0.76%, M694I 0.57%, K695R 0.57%, A744S 0.38%, R731H 0.38%, and del1692 0%. Frequent mutations were also confirmed by PCR-RFLP. There were no conflicting results between the two methods. Four of these genotypes were homozygous for a single mutation, 15 were heterozygous for two mutations, 8 were heterozygous for a single mutation, 1 was heterozygous for three mutations, and 1 was homozygous for one mutation and heterozygous for another mutation. It has been reported that analytical sensitivity of RH is 97%. We did not find a discrepancy between the two methods. In 21 patients, we detected additional mutations with RH. This finding was regarded as an advantage of RH, and we concluded that this assay is a useful method for detection of first stage FMF mutation screening.

摘要

家族性地中海热(FMF)的特征为反复发热、浆膜炎和关节炎。由于该疾病存在大量突变且临床具有异质性,因此已开发出不同的筛查方法。在本研究中,我们旨在比较通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)与反向杂交(RH)方法确定的突变结果。在263例患者中的152例(57.79%)中,通过RH确定了不同的突变。等位基因频率分别为:E148Q 6.84%、M680I(G/C) 3.61%、M694V 20.91%、V726A 7.03%、P369S 1.33%、F479L 0.19%、M680I(G/A) 0.76%、M694I 0.57%、K695R 0.57%、A744S 0.38%、R731H 0.38%,del1692为0%。常见突变也通过PCR-RFLP得到了证实。两种方法之间没有相互矛盾的结果。这些基因型中,4种为单个突变的纯合子,15种为两个突变的杂合子,8种为单个突变的杂合子,1种为三个突变的杂合子,1种为一个突变的纯合子和另一个突变的杂合子。据报道,RH的分析灵敏度为97%。我们未发现两种方法之间存在差异。在21例患者中,我们通过RH检测到了额外的突变。这一发现被视为RH的一个优势,我们得出结论,该检测方法是用于第一阶段FMF突变筛查的一种有用方法。

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