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Mediterranean Fever Gene Mutations and Messenger Ribonucleic Acid Expressions in Pediatric Patients With Familial Mediterranean Fever in the Trakya Region of Turkey

机译:土耳其特拉基亚地区小儿家族性地中海热患者的地中海热基因突变和信使核糖核酸表达

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Objectives: This study aims to investigate the possible relationship between Mediterranean fever (MEFV) gene mutations and messengerribonucleic acid (mRNA) expressions and to identify the link between phenotype and genotype of pediatric patients with Familial Mediterraneanfever (FMF).Patients and methods: Seventy-one pediatric FMF patients who were identified with FMF symptoms and diagnosed with FMF according toTel Hashomer criteria were included at Trakya University, Faculty of Medicine, Department of Paediatric Nephrology. The control group consistedof 73 healthy pediatric participants. Genomic deoxyribonucleic acid was isolated from whole blood samples and the following mutations of MFEVgene were analyzed: E148Q, P369S, H478Y, H479L, S675N, G678E, M680L, M680I (G>A and G>C), T681I, I692del, M694V, M694L, M694I, M695R,M695M, R717S, I720M, V722M, V726A, A744S and R761H. Total RNA isolation from leukocytes was performed and MEFV mRNA expression levelsof the patients were compared by using real-time quantitative polymerase chain reaction method. β2 microglobulin was selected as the controlgene. The comparison of mRNA expression levels among the patients was performed using the ΔCT method.Results: The most common clinical findings were abdominal pain, fever and vomiting. The mutation detection rate in the patient group wasOR=4.1 (95% CI: 1.8-9.0) times higher than that of the control group. The MEFV mRNA expression level of the patients with MEFV gene mutationswas lower compared to the control group, indicating statistical significance.Conclusion: Our study results support the findings of previous studies indicating that the MEFV mRNA expression levels of pediatric FMF patientswith MEFV gene mutation are lower than the MEFV mRNA expression levels of healthy controls.
机译:目的:本研究旨在探讨地中海热(MEFV)基因突变与信使核糖核酸(mRNA)表达之间的可能关系,并确定儿童家族性地中海热(FMF)患者的表型与基因型之间的联系。患者与方法:70特拉基亚大学医学院儿科肾脏病学系收治了1名根据Tel Hashomer标准诊断为FMF症状并诊断为FMF的小儿FMF患者。对照组由73名健康的儿科参与者组成。从全血样本中分离出基因组脱氧核糖核酸并分析了MFEVgene的以下突变:E148Q,P369S,H478Y,H479L,S675N,G678E,M680L,M680I(G> A和G> C),T681I,I692del,M694V,M694L ,M694I,M695R,M695M,R717S,I720M,V722M,V726A,A744S和R761H。采用实时定量聚合酶链反应法从白细胞中分离总RNA,比较患者MEFV mRNA表达水平。选择β2微球蛋白作为对照基因。结果:最常见的临床表现为腹痛,发烧和呕吐。患者组的突变检测率是对照组的OR = 4.1(95%CI:1.8-9.0)倍。结论:我们的研究结果支持以往的研究结果,表明具有MEFV基因突变的小儿FMF患者的MEFV mRNA表达水平较低,因此,具有统计学意义。高于健康对照组的MEFV mRNA表达水平。

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