کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6282606 | 1615142 | 2013 | 5 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
GAB2 polymorphism rs2373115 confers susceptibility to sporadic Alzheimer's disease
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کلمات کلیدی
APPNINCDS-ADRDAGab2CNKIORGHRMAHWEDSMpresenilin 1 - Presenilin 1Apoe - آپوapolipoprotein E - آپولیپوپروتئین EFAD - بدAlzheimer's disease - بیماری آلزایمرfamilial Alzheimer's disease - بیماری آلزایمر خانوادگیHigh resolution melting analysis - تجزیه و تحلیل ذوب با وضوح بالاHardy–Weinberg equilibrium - تعادل هاردی-وینبرگDiagnostic and Statistical Manual of Mental Disorders - راهنمای تشخیصی و آماری اختلالهای روانیChina National Knowledge Infrastructure - زیرساخت دانش دانش ملی چینconfidence interval - فاصله اطمینانodds ratio - نسبت شانس هاpolymerase chain reaction - واکنش زنجیره ای پلیمرازPCR - واکنش زنجیرهٔ پلیمرازamyloid precursor protein - پروتئین پیش ماده آمیلوئی
موضوعات مرتبط
علوم زیستی و بیوفناوری
علم عصب شناسی
علوم اعصاب (عمومی)
پیش نمایش صفحه اول مقاله
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چکیده انگلیسی
It has been reported that a single nucleotide polymorphism (SNP), rs2373115, in the GRB-associated binding protein 2 (GAB2) gene was associated with late-onset AD in Caucasians. Subsequently, other researchers have attempted to validate this finding in different ethnic populations. However, these findings have produced both negative and positive results. To derive a more precise estimation for whether GAB2 polymorphism rs2373115 is associated with sporadic Alzheimer's disease (SAD), we performed the present meta-analysis. Databases including PubMed, AlzGene, China National Knowledge Infrastructure (CNKI) and Wan Fang were searched to find relevant studies. Odds ratios (ORs) with 95% confidence intervals (CIs) were used to assess the strength of association. All analyses were calculated using STATA Version 11.0 and RevMan (v.5.1) software. Ten total case-control studies were included. The statistical results showed that GAB2 SNP rs2373115 is significantly associated with an increased risk for SAD, and the subgroup analysis showed that SNP rs2373115 may only be associated with an increased risk for SAD risk in Caucasians but not in Asians. Furthermore, in APOE É4 carriers or noncarriers, those with rs2373115 genotype GG did not have a significantly higher risk for SAD compared with those with genotype GT and TT (APOE É4 carriers: ORÂ =Â 1.20, 95% CIÂ =Â 0.92-1.56, PÂ =Â 0.178; APOE É4 noncarriers: ORÂ =Â 1.08, 95% CIÂ =Â 0.97-1.20, PÂ =Â 0.157) in the present study. The current meta-analysis further supports previous findings that the GAB2 gene may be associated with SAD risk.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neuroscience Letters - Volume 556, 27 November 2013, Pages 216-220
Journal: Neuroscience Letters - Volume 556, 27 November 2013, Pages 216-220
نویسندگان
Chunhui Jin, Cheng-Zhu Wu, Xiaowei Liu, Fuquan Zhang, Lin Tian, Jianmin Yuan, Guoqiang Wang, Zaohuo Cheng,