MEFV Common mutations detection in Iranian Azeri Turk patients with Ulcerative colitis: a case –control study.
MEFV Common mutations detection in Iranian Azeri Turk patients with Ulcerative colitis: a case –control study.
نویسندگان: محمد حسین صومی , مرتضی جبارپور بنیادی , سید کاظم میری نژاد , مسعود فقیه دینوری , مریم سلیمان پور
کلمات کلیدی: Ulcerative colitis, MEFV gene, Iranian Azeri Turkish patients, mutations
نشریه: 22960 , 4 , 10 , 2013
| نویسنده ثبت کننده مقاله |
سید کاظم میری نژاد |
| مرحله جاری مقاله |
تایید نهایی |
| دانشکده/مرکز مربوطه |
بیماری های گوارش و کبد |
| کد مقاله |
72189 |
| عنوان فارسی مقاله |
MEFV Common mutations detection in Iranian Azeri Turk patients with Ulcerative colitis: a case –control study. |
| عنوان لاتین مقاله |
MEFV Common mutations detection in Iranian Azeri Turk patients with Ulcerative colitis: a case –control study. |
| ناشر |
5 |
| آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ |
خیر |
| عنوان نشریه (خارج از لیست فوق) |
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| نوع مقاله |
Original Article |
| نحوه ایندکس شدن مقاله |
ایندکس شده سطح چهار – Index Copernicus |
| آدرس لینک مقاله/ همایش در شبکه اینترنت |
|
| Background Ulcerative colitis and Crohn’s disease constitute the two major forms of chronic
inflammatory bowel diseases with unknown etiology. It is suggested that genetic background and environmental
factors are important factors in the diseases susceptibility and patient's response to therapy. Familial Mediterranean
fever is an auto-inflammatory disease mainly inherited as an autosomal recessive condition. Since there are
similarities between FMF and IBD, the responsible gene for FMF (MEFV) has been introduced as a modifier gene
for IBD. Study: This case –control study was conducted in a setting of 139 unrelated patients referred with UC
compatible symptoms and 200 matched controls without any positive familial history of Behcet syndrome, FMF or
IBD in Azerbaijan during 2008-2010.They were screened for the five most common MEFV mutations (E148Q,
V726A, M680I, M694I, and M694V) applying PCR-RFLP and ARMS-PCR techniques. All cases, being of Azeri
Turk origin were matched in terms of age, sex and race. Results Thirty one (22.3%) patients and 52 (26%) control
individuals carried one of the studied mutations. All studied types of MEFV mutations except for M694I and V726A
could be detected in the patients. However, E148Q and V726A mutations were only observed in the control group.
E148Q was the most frequent mutation observed in this cohort. There was a significant difference between the two
groups regarding M694V mutation (p=0.002). Conclusion Although the correlation between M694V mutation and
UC seems to be significant among the Iranian Azeri Turk patients, studies on a large number of UC and control
series and also on further MEFV mutations are required to determine the role of MEFV mutations in UC. |
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تاریخ درج فایل |
اندازه فایل |
دانلود |
| MEFV Common mutations detection in Iranian Azeri.pdf | 1399/02/21 | 122667 | دانلود |