Association study between ACE gene polymorphisms and migraine
سال انتشار: 1396
نوع سند: مقاله کنفرانسی
زبان: انگلیسی
مشاهده: 510
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شناسه ملی سند علمی:
NGCMED10_083
تاریخ نمایه سازی: 16 تیر 1397
چکیده مقاله:
Introduction: In the present study, we investigated the association between the ACE gene I/D and rs4343polymorphisms and susceptibility to migraine. As a possible underlying mechanism, the pain may be caused bythe high vascular tension and blood pressure. The serum level of the angiotensin I-converting enzyme (ACE)influences the blood pressure and is reported to be higher in the migraine patients. In this regard, it ishypothesized that polymorphisms located in the ACE gene may be associated with migraine through theirpossible effects on the gene expression level.Methods: Genotyping of the ACE I/D and rs4343 polymorphisms were performed in 148 unrelated migraineurs(105 were diagnosed with migraine without aura [MO] and 43 with aura [MA]) and 149 matched healthycontrols using conventional PCR and TP-ARMS-PCR, respectively.Results: The association was found between rs4343 A/G polymorphism and migraine (P= 0.019; OR = 0.48;95% CI, 0.28-0.89). No significant differences in genotype or allele frequencies were found for I/Dpolymorphism and migraine between migraineurs and controls.Conclusions: In the present study, for the first time, we found evidence for association between rs4343 andmigraine. By considering the role of the rs4343 on the ACE serum level, this polymorphism may be consideredin the future pharmacogenetics studies for treatment of migraine. However, in order to confirm the presentresults, further studies are required to validate the significance of the studied genetic variation in diverse ethnicpopulations.
کلیدواژه ها:
نویسندگان
Atieh abedin do
Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Sara Pouriamanesh
Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Zeeba Kamaliyan
Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Reza Mirfakhraie
Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran