Common MEFV mutations (M۶۹۴V, V۷۲۶A, M۶۸۰I, M۶۹۴I, and E۱۴۸Q ) in patients with Behcet's disease in Ardabil
- سال انتشار: 1401
- محل انتشار: فصلنامه زیست پزشکی جرجانی، دوره: 10، شماره: 3
- کد COI اختصاصی: JR_JOBJ-10-3_002
- زبان مقاله: انگلیسی
- تعداد مشاهده: 95
نویسندگان
Department of Internal Medicine, School of Medicine, Ardabil University of Medical Science,Ardabil,Iran
Molecular-Genetic Laboratory, Imam Khomeini Hospital, Ardabil University of Medical Sciences, Ardabil, Iran.
Department of Internal Medicine, School of Medicine, Ardabil University of Medical Science,Ardabil,Iran
Department of Pediatrics, School of Medicine, Ardabil University of Medical Science,Ardabil,Iran
School of Medicine, Ardabil University of Medical Science,Ardabil,Iran
چکیده
Background and objectives: Behcet's Disease (BD) is a rare severe recurrent inflammatory disorder affecting several body organs. Since Familial Mediterranean Fever (FMF) and BD affect almost a specific population, both diseases can mimic the other clinically, and these two diseases sometimes occur in the same family and the same patient, also due to the high prevalence of BD in Iran and performing a small number of studies about MEFV gene mutations in patients with BD, this study aimed to determine the frequency of MEFV gene mutations in Ardabil patients with BD. Material and Methods: Fifty patients with BD were diagnosed according to the International Study Group criteria for BD (for oral pests, genital pests, and ocular lesions, ۲ points each, skin symptoms, vascular symptoms, positive pathogenesis test, and neurological symptoms, ۱ point each). A score of ۴ or higher indicated BD. All patients were analyzed for five common MEFV mutations (M۶۹۴V, V۷۲۶A, M۶۸۰I, M۶۹۴I, and E۱۴۸Q) using amplification refractory mutation system and Polymerase Chain Reaction (PCR) restriction-digestion testing methods. A cohort of ۲۲۴ healthy people who had been previously genotyped regarding the five common MEFV mutations served as the control group. Results: The mean age of patients was ۳۸.۶۸±۱۱ years. Most BD patients (۵۶%) and ۵۰.۴% of the control group were women. Of all patients, ۶۶% (۳۳) mentioned that their parents had no family relationship. Among ۵۰ patients with BD, ۱۲ (۲۴%) had mutations in the MEFV gene, of which seven patients (۵۸.۳%) had E۱۴۸Q mutation. Among healthy individuals, ۵۷ patients (۲۵.۴%) had mutations, of which ۳۹ (۶۸.۴%) had E۱۴۸Q mutation. The difference between the two groups was not significant. Conclusion: Results showed that most patients with BD had mutations in the MEFV gene and the most common case was E۱۴۸Q mutation which was similar to the healthy population in terms of BD agent.کلیدواژه ها
Behcet Syndrome, Mutation, Familial Mediterranean Feverاطلاعات بیشتر در مورد COI
COI مخفف عبارت CIVILICA Object Identifier به معنی شناسه سیویلیکا برای اسناد است. COI کدی است که مطابق محل انتشار، به مقالات کنفرانسها و ژورنالهای داخل کشور به هنگام نمایه سازی بر روی پایگاه استنادی سیویلیکا اختصاص می یابد.
کد COI به مفهوم کد ملی اسناد نمایه شده در سیویلیکا است و کدی یکتا و ثابت است و به همین دلیل همواره قابلیت استناد و پیگیری دارد.