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中国汉族人群多巴胺D_2受体-141C Ins/Del多态性与海洛因依赖的Meta分析 被引量:1
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作者 胡佩武 李杏莉 +2 位作者 彭莎莎 罗希 刘志胜 《中南大学学报(医学版)》 CAS CSCD 北大核心 2015年第3期233-240,共8页
目的:系统评价多巴胺D2受体基因-141C Ins/Del多态性与中国汉族人群海洛因依赖的相关性。方法:检索中外数据库于建库至2014年3月公开发表的文献,收集有关多巴胺D2受体基因-141C Ins/Del多态性与中国汉族人群海洛因依赖的病例对照研究,使... 目的:系统评价多巴胺D2受体基因-141C Ins/Del多态性与中国汉族人群海洛因依赖的相关性。方法:检索中外数据库于建库至2014年3月公开发表的文献,收集有关多巴胺D2受体基因-141C Ins/Del多态性与中国汉族人群海洛因依赖的病例对照研究,使用Stata12.0软件进行Meta分析。结果:共纳入7项关于多巴胺D2受体基因-141C Ins/Del多态性与海洛因依赖的病例对照研究,其中病例组3 211人,对照组1 979人。Meta分析结果显示各基因型合并后的OR值、OR值95%CI和P值,其中基因型Ins/Ins与基因型Del/Del比较,OR=0.51,95%CI:0.27~0.96,P=0.017;基因型Ins/Ins与基因型Ins/Del+Del/Del比较,OR=0.82,95%CI:0.72~0.94,P=0.448;基因型Ins/Ins+Ins/Del与基因型Del/Del比较,OR=0.53,95%CI:0.28~0.98,P=0.019;基因型Ins/Del与基因型Del/Del比较,OR=0.59,95%CI:0.32~1.07,P=0.045;Ins等位基因与Del等位基因比较,OR=0.79,95%CI:0.71~0.89,P=0.101。结论:多巴胺D2受体基因-141C Ins/Del多态性与中国汉族人群海洛因依赖存在关联,携带有Ins等位基因的个体可能不易对海洛因产生依赖。 展开更多
关键词 多巴胺D2受体 -141C ins/del多态性 海洛因依赖 META分析
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NF-κB1基因启动子-94ins/del ATTG的基因多态性与动脉粥样硬化性脑梗死的关系 被引量:3
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作者 王锐 张俊和 +1 位作者 陈立杰 蒋殿飞 《中国神经免疫学和神经病学杂志》 CAS 北大核心 2012年第3期231-233,237,共4页
目的探讨核因子κB1(NF-κB1)基因启动子-94ins/del ATTG基因多态性与动脉粥样硬化性脑梗死(ACI)的关系。方法采用PCR限制性片段长度多态性分析(PCR-RFLP)法检测191例ACI患者(其中中国东北地区ACI患者101例,湖北省ACI患者90例)和171名... 目的探讨核因子κB1(NF-κB1)基因启动子-94ins/del ATTG基因多态性与动脉粥样硬化性脑梗死(ACI)的关系。方法采用PCR限制性片段长度多态性分析(PCR-RFLP)法检测191例ACI患者(其中中国东北地区ACI患者101例,湖北省ACI患者90例)和171名健康对照(其中东北地区90名,湖北省81名)的NF-κB 1基因启动子-94ins/del ATTG基因型,分析该基因多态性与ACI的关系。结果 ACI组患者的NF-κB1-94ins/del ATTG 2种基因型频率(WW和DD型)和2种等位基因频率(W和D型)与健康对照者间比较有统计学差异(P<0.01);东北地区健康对照组与东北ACI组DD基因型频率和等位基因频率(W和D型)存在统计学差异(P<0.05),湖北地区健康对照组与ACI组WW、DD基因型频率和等位基因频率(W和D型)存在统计学差异(P<0.05),两地区健康对照组之间比较以及ACI组间比较均无统计学差异(P>0.05)。结论 NF-κB1基因启动子-94ins/del ATTG基因多态性与ACI发病有一定相关性,但其相关性不存在地区差异。 展开更多
关键词 NF-κB1基因启动子-94ins/del ATTG 动脉粥样硬化性脑梗死 基因多态性
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Association of NFKB1 gene polymorphism (rs28362491) with levels of inflammatory biomarkers and susceptibility to diabetic nephropathy in Asian Indians 被引量:4
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作者 Amar Gautam Stuti Gupta +5 位作者 Mohit Mehndiratta Mohini Sharma Kalpana Singh Om P Kalra Sunil Agarwal Jasvinder K Gambhir 《World Journal of Diabetes》 SCIE CAS 2017年第2期66-73,共8页
AIM To investigate the association of NFKB1 gene-94 ATTG insertion/deletion(rs28362491) polymorphism with inflammatory markers and risk of diabetic nephropathy in Asian Indians.METHODS A total of 300 subjects were rec... AIM To investigate the association of NFKB1 gene-94 ATTG insertion/deletion(rs28362491) polymorphism with inflammatory markers and risk of diabetic nephropathy in Asian Indians.METHODS A total of 300 subjects were recruited(100 each), normoglycemic,(NG); type 2 diabetes mellitus(T2DM) without any complications(DM) and T2 DM with diabetic nephropathy [DM-chronic renal disease(CRD)]. Analysis was carried out by polymerase chain reaction-restriction fragment length polymorphism and ELISA. Pearson's correlation, analysis of variance and logistic regression wereused for statistical analysis.RESULTS The allelic frequencies of-94 ATTG insertion/deletion were 0.655/0.345(NG), 0.62/0.38(DM) and 0.775/0.225(DM-CRD). The-94 ATTG ins allele was associated with significantly increased levels of urinary monocyte chemoattractant protein-1(u MCP-1); u MCP-1(P = 0.026) and plasma tumor necrosis factor-alpha(TNF-α); TNF-α(P = 0.030) and almost doubled the risk of diabetic nephropathy(OR = 1.91, 95%CI: 1.080-3.386, P = 0.025).CONCLUSION-94 ATTG ins/ins polymorphism might be associated with increased risk of developing nephropathy in Asian Indian subjects with diabetes mellitus. 展开更多
关键词 糖尿病的 nephropathy 发炎 NFKB1 -94 ATTG ins/del 多型性 尿单核白血球 chemoattractant protein-1 肿瘤坏死 factor-alpha
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Association of NFkB1 Gene Polymorphism with Inflammatory Markers in Patients of Type 2 Diabetes Mellitus with or without Renal Involvement in Eastern India
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作者 Sonalika Behera Andrew Abel Lamare +2 位作者 Roma Rattan Bijan Patnaik Sidhartha Das 《Journal of Diabetes Mellitus》 2020年第3期169-181,共13页
<strong>Aims: </strong>To evaluate the association of Nuclear factor kappa B1(NFkB1) gene polymorphism with inflammatory markers Urinary Monocyte Chemoattractant Protein 1 (UMCP1) and Tumor Necrosis Factor... <strong>Aims: </strong>To evaluate the association of Nuclear factor kappa B1(NFkB1) gene polymorphism with inflammatory markers Urinary Monocyte Chemoattractant Protein 1 (UMCP1) and Tumor Necrosis Factor alfa (TNF alfa) in Patients of diabetes mellitus with or without renal involvement in Eastern India. <strong>Material and Methods: </strong>Consecutive Patients of Type 2 Diabetes Mellitus (DM) with or without microalbuminuria attending SCB MEDICAL COLLEGE and HOSPITAL Medical OPDs in between September 2018 to September 2019 were recruited in this study. Patients were subjected to blood and urine investigations. DNA extraction and Restriction fragment Length Polymorphism (RFLP) was done in Department of Biochemistry. Controls were unrelated healthy attendants with no history of Diabetes Mellitus, HTN, Chronic Kidney Disease (CKD). <strong>Results:</strong> Mean Systolic BP, Fasting Blood Glucose, Post Prandial Blood Glucose, HBA1c, Total Cholesterol were significantly higher in diabetes mellitus and diabetic nephropathy groups than control group. Estimated Glomerular Filtration Rate was significantly lower in diabetic nephropathy (p value < 0.001). UMCP1, Urinary Albumin Creatinine Ratio, TNF alfa were higher in diabetes mellitus and nephropathy with p value (<0.001, 0.006 < 0.001) respectively. In between DM and Diabetic Nephropathy groups nfkb1 gene expression, umcp1 and tnf alfa levels were significantly increased in Diabetic nephropathy with p value 0.019, <0.01, 0.001 respectively. Insertion/insertion NFkB1 gene polymorphisms were more in diabetic nephropathy group and were positively correlated with inflammatory markers UMCP1 (r = 0.517, p < 0.01) and TNF alfa (r = 0.172, p = 0.19). <strong>Conclusion:</strong> insertion/insertion NFkB1 gene polymorphism increases the risk of nephropathy by 2.52 times (OR = 2.52, 95% CI: 0.04 - 0.63, p value = 0.019) in diabetes patients in eastern India. 展开更多
关键词 DN: Diabetic Nephropathy UACR: Urinary Albumin Creatinine Ratio UMCP1: Urinary Monocyte Chemoattractant Protein 1 TNF Alfa: Tumor Necrosis Factor Alfa NFkB1: Nuclear Factor Kappa B ins/ins Polymorphism: insertion/insertion Polymorphism del/del Polymorphism: deletion/deletion Polymorphism ins/del Polymorphism: insertion/deletion Polymorphism
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NF-κB信号转导通路与复发性口腔溃疡的相关性分析 被引量:8
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作者 张敬 令狐瑞琦 +3 位作者 沙晶晶 胡欣培 李丹 李梦源 《上海口腔医学》 CAS CSCD 北大核心 2018年第5期513-517,共5页
目的:研究NF-κB信号转导通路与复发性口腔溃疡(RAU)易感性的相关性。方法:采用ELISA方法检测124例RAU患者和133例健康对照者中NFκBp50、NFκBp65、IκBα、IKK的血清含量,则用限制性片段长度多态性-聚合酶链式反应(RFLP-PCR)进行NFκB... 目的:研究NF-κB信号转导通路与复发性口腔溃疡(RAU)易感性的相关性。方法:采用ELISA方法检测124例RAU患者和133例健康对照者中NFκBp50、NFκBp65、IκBα、IKK的血清含量,则用限制性片段长度多态性-聚合酶链式反应(RFLP-PCR)进行NFκB-94 ins/del ATTG位点的基因多态性分析,用比值比(OR)和95%可信区间(95%CI)估计相对危险度,采用SPSS 20.0软件包对数据进行统计学分析。结果:RAU组患者血清NFκBp50、NFκBp65、IKK水平均显著低于正常对照组(P<0.05),RAU组患者血清IκBα水平均显著高于正常对照组(P<0.05)。NFκB-94ins/del ATTG位点在基因型频率与等位基因频率的分布上,病例组与正常对照组之间均有显著差异(P<0.05)。NFκB-94 ins/del ATTG位点基因型ID(OR=3.073,95%CI=1.557-6.067)与DD(OR=4.851,95%CI=2.264-10.393)为高风险基因型,D等位基因为高风险等位基因(OR=2.079,95%CI=1.462-2.957)。结论:NF-κB信号转导通路与复发性口腔溃疡有一定关系。NFκB-94 ins/del ATTG位点是RAU患者的易感基因位点。NFκB-94 ins/del ATTG位点携带D等位基因,患RAU的风险性是携带I等位基因的2.079倍。 展开更多
关键词 NFκB-94 ins/del ATTG 复发性口腔溃疡 信号转导通路 基因多态性
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