۲۹ فروردین ۱۴۰۴
اميرحسين احمدي

امیرحسین احمدی

مرتبه علمی: استادیار
نشانی: دانشکده علوم و فناوری نانو و زیستی - گروه علوم زیستی
تحصیلات: دکترای تخصصی / ژنتیک مولکولی
تلفن: ۰۷۷۳۳۴۴۱۴۹۷
دانشکده: دانشکده علوم و فناوری نانو و زیستی

مشخصات پژوهش

عنوان Association of IL2RA and multiple sclerosis risk: A case control, systematic review, and meta-analysis study
نوع پژوهش مقالات در نشریات
کلیدواژه‌ها
Multiple sclerosis, IL2RA, rs2104286, Meta-analysis, Iranian population
مجله JOURNAL OF THE NEUROLOGICAL SCIENCES
شناسه DOI https://doi.org/10.1016/j.jns.2025.123461
پژوهشگران فاطمه رنگانی (نفر اول) ، ناهید رخشانی (نفر دوم) ، زهرا کدخدا مزرجی (نفر سوم) ، آسیه علیخواه (نفر چهارم) ، ریحانه دهقان زاد (نفر پنجم) ، بابک عباسی (نفر ششم به بعد) ، امیرحسین احمدی (نفر ششم به بعد) ، عباس نیک روش (نفر ششم به بعد) ، مجید پهلوان کاخکی (نفر ششم به بعد)

چکیده

Abstract The interleukin-2 receptor alpha chain (IL2RA) gene has been implicated in multiple sclerosis (MS) susceptibility, particularly through the rs2104286 and rs12722489 SNPs. However, previous studies have yielded inconsistent results across different populations, likely due to small sample sizes and ethnic variations. This study aimed to investigate the association of IL2RA SNPs with MS risk in eastern Iranian population and through a comprehensive meta-analysis. Our case-control study included 400 Iranian individuals from North Khorasan and Sistan & Baluchistan provinces, comprising 200 MS patients across all subtypes and genders and 200 controls. The meta-analysis incorporated pooled odds ratios (ORs) with 95 % confidence intervals (CIs) to assess the strength of these associations. Our case-control findings demonstrated a significant association between rs2104286 and MS risk, which was further supported by the meta-analysis in Iranian populations. Specifically, the association was observed at both the genotype (P = 0.001) and allelic (P = 0.003) levels in North Khorasan and at the genotype level in Sistan & Baluchistan (P = 0.001). A global meta-analysis of rs2104286, encompassing 24,931 MS patients and 36,036 controls, revealed a significant association between the A allele and all genotype models with increased MS risk (P < 0.05). Similarly, a meta-analysis of rs12722489, including 19,797 MS patients and 32,085 controls, identified the CC + CT genotype as a risk factor for MS (P = 0.04). In conclusion, our findings suggest that the rs2104286 A allele and rs12722489 CC + CT genotype are associated with an increased risk of MS in both Caucasian and Asian populations, including Iranians.