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Genetic analysis of tumor necrosis factor-alpha (TNF-alpha) G-308A and Saitohin Q7R polymorphisms with Alzheimer's disease

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单位: [1]National Research Institute for Family Planning, Beijing, 100081 China [2]Laboratory for Medical Genetics, Institute of Geriatrics, Beijing hospital, Ministry of Health, Beijing 100730, China [3]Department of Neurology, Beijing Friendship Hospital, Affiliate of Capital University of Medical Sciences, Beijing 100050, China [4]Peking Union Medical College, Beijing, China [5]World Health Organization Collaborating Centre for Research in Human Reproduction, Beijing, China [6]Jiangbin Hospital, Nanning, Guangxi, 530021, China
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关键词: Late-onset Alzheimer's disease APOE ε4 TNF-α STH Case-control study Chinese

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Neuroinflammation and abnormal phosphorylation of TAU proteins have been implicated in the etiology of Alzheimer's disease (AD). Several studies have suggested the G-308A promoter polymorphism in one of the proinflammatory cytokine genes tumor necrosis factor-alpha (TNF-alpha) encoding TNF-alpha may be associated with AD pathogenesis. Association between the Q7R polymorphism in saitohin (STH), a gene nested within the intron of the Tau gene, has also been reported. To determine whether these two polymorphisms contribute to the risk for late-onset AD (LOAD) in Chinese, we have investigated 207 sporadic LOAD patients and 222 healthy controls. The associations of the AA genotype and A-allele with LOAD (chi(2) = 8.74, df = 1, P = 0.0031, and chi(2) = 4.47, df = 1, P = 0.035) were found. After stratifying by apolipoprotein E allele 4 (APOE epsilon4) status, increased LOAD risks associated with the AA genotype and A-allele only in the APOE epsilon4 non-carriers (chi(2) = 9.21, df = 1, P = 0.002; chi(2) = 10.02, df = 1, P = 0.0015) were seen. These results suggested that the TNF-alpha gene G-308A polymorphism might be a risk factor for LOAD and dependent on APOE epsilon4 status in Chinese. Homozygous Q/Q of STH Q7R polymorphism was the only one genotype found in either LOAD group or controls. No R allele was detected in LOAD and control groups. The extremely rare frequency of the ancestral R allele differs sharply from that observed in studies in the Caucasian population, suggesting obvious ethnic differences.

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出版当年[2007]版:
大类 | 3 区 医学
最新[2025]版:
大类 | 3 区 医学
小类 | 3 区 临床神经病学 3 区 神经科学
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出版当年[2006]版:
Q2 CLINICAL NEUROLOGY Q3 NEUROSCIENCES
最新[2023]版:
Q1 CLINICAL NEUROLOGY Q2 NEUROSCIENCES

影响因子: 最新[2023版] 最新五年平均[2021-2025] 出版当年[2006版] 出版当年五年平均[2002-2006] 出版前一年[2005版] 出版后一年[2007版]

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第一作者单位: [1]National Research Institute for Family Planning, Beijing, 100081 China [4]Peking Union Medical College, Beijing, China
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通讯机构: [1]National Research Institute for Family Planning, Beijing, 100081 China [2]Laboratory for Medical Genetics, Institute of Geriatrics, Beijing hospital, Ministry of Health, Beijing 100730, China [4]Peking Union Medical College, Beijing, China [5]World Health Organization Collaborating Centre for Research in Human Reproduction, Beijing, China [*1]Center for Genetics, National Research Institute for Family Planning, 12, Dahuisi Road, Haidian, Beijing, 100081 China.
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