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:: Volume 19, Issue 1 (spring 2019) ::
J Ardabil Univ Med Sci 2019, 19(1): 110-116 Back to browse issues page
MEFV Gene Variant Alleles in Normal Population of Northwest of Iran, Ardabil Province
Farhad Salehzadeh , Afshan Sharghi , Atena Moteyagheni , Saeid Hosseini asl , Mahsa Mottaghi , Sepehr Sarkhanloo *
Medical Student, School of Medicine, Ardabil University of Medical Sciences, Ardabil, Iran , sepehr.sarkhanloo@gmail.com
Abstract:   (5609 Views)
Background & objectives: MEFV gene has a major role in Familial Mediterranean Fever (FMF) as an auto-inflammatory disorder. FMF is most often seen in the people of the Mediterranean area. Considering the significant role of the MEFV gene in many rheumatologic diseases and even non-rheumatologic disorders, it is necessary to identify different variations of these mutations in the healthy and normal population of this area.
Methods: 224 healthy people entered into this study. The blood samples were screened for the 12 most common MEFV gene variants according to manufacturer’s instructions. (FMF Strip Assay, Vienna lab, Vienna, Austria)
They filled a questionnaire containing the required information. All patients were initially evaluated for the FMF symptoms and signs in themselves and their first-degree relatives based on clinical criteria. Chi-squared test and t-test were employed for statistical analysis using SPSS ver.24.  
Results: Among 224 cases, 113 cases (50.4%) were male, and 111 cases (49.6%) were female. MEFV mutations were detected in 57 patients (25%) of them, 28 cases were male (49.1%) and 29 cases were female (50.9%). The most frequent mutations were E148Q (18.3%, 41cases), followed by P369S (3.1%, 7 cases), V726A (2.2%, 5cases), A744S (1.3%, 3cases), F479L, M694V and R761H (0.8%, each 2 cases), and eventually K695R (0.4%) respectively. Some mutations such as M694I, M680I (G/C), M680I (G/A), I692del were not seen in these samples. There were compound heterozygous mutations of E148Q/P369S, E148Q/V726A, E148Q/P369S, and P369S / F479L in normal population without any findings in favor of FMF.
Conclusion: Twenty-five percent of the normal population of the northwest of Iran carrying a heterozygous variant of the MEFV gene, E148Q (18.3%) as a most common mutation, which can be considered as a normal variant in the healthy population. The presence of M694I, M680I (G/C), M680I (G/A) and I692del mutations in the normal population can be interpreted with cautiously, while particular compound heterozygous mutations can be considered as normal variants.
 
Keywords: MEFV mutations, FMF Gene, Northwest of Iran, Ardabil
Full-Text [PDF 125 kb]   (1437 Downloads)    
Type of Study: article | Subject: ژنتیک و پزشکی مولکولی
Received: 2019/01/26 | Accepted: 2020/06/29 | Published: 2020/06/29
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Salehzadeh F, Sharghi A, Moteyagheni A, Hosseini asl S, Mottaghi M, Sarkhanloo S. MEFV Gene Variant Alleles in Normal Population of Northwest of Iran, Ardabil Province . J Ardabil Univ Med Sci 2019; 19 (1) :110-116
URL: http://jarums.arums.ac.ir/article-1-1664-en.html


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Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Volume 19, Issue 1 (spring 2019) Back to browse issues page
مجله دانشگاه علوم پزشکی اردبیل Journal of Ardabil University of Medical Sciences
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