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血清、脑脊液肿瘤坏死因子-α水平及其-308G/A基因多态性与多发性硬化的相关性
引用本文:董亚贤,许志荣,林佩玉.血清、脑脊液肿瘤坏死因子-α水平及其-308G/A基因多态性与多发性硬化的相关性[J].中华医学遗传学杂志,2006,23(6):677-679.
作者姓名:董亚贤  许志荣  林佩玉
作者单位:1. 510120,广州医学院第一附属医院神经内科
2. 广东省交通医院内科
摘    要:目的研究中国广东汉族人群中血清、脑脊液(cerebrospinalfluid,CSF)肿瘤坏死因子-α(tumornecrosisfactor-α,TNF-α)水平及其-308G/A基因多态性与多发性硬化之间的相关性。方法采用双抗体夹心ABC-ELISA法测定68例无亲缘关系的急性发作期多发性硬化(multiplesclerosis,MS)患者和55例非免疫系统疾病患者的血清、CSF的TNF-α水平,同时应用聚合酶链反应-限制性片段长度多态性技术检测上述68例MS患者和106名无血缘关系的广东籍健康汉族人的TNF-α-308G/A基因型。结果发作期MS患者血清中TNF-α水平与非免疫系统疾病患者组间差异有统计学意义(P<0·05),分别是(276±71)pg/mL和(234±76)pg/mL;发作期MS患者CSF中TNF-α水平与非免疫系统疾病患者组差异无统计学意义(P>0·05),分别是(265±78)pg/mL和(245±83)pg/mL;TNF-α-308G/A各等位基因型频率在MS组和正常人组比较差异无统计学意义(P>0·05),MS组TNF-α基因AA基因型和A等位基因频率分别为4.4%和14·0%,正常人对照组分别为0和8.5%。结论(1)发作期MS与血清中TNF-α水平相关,与CSF中TNF-α水平不相关。(2)从目前调查的例数中,中国广东汉族人群TNF-α基因-308G/A多态性与广东人群中MS不相关。

关 键 词:多发性硬化  肿瘤坏死因子-α  遗传多态性
收稿时间:2006-04-05
修稿时间:2006年4月5日

Association among serous and cerebrospinal fluid TNF-α level, gene polymorphisms of TNF-α and multiple sclerosis in Han nationality of southern China
DONG Ya-xian,XU Zhi-rong,LIN Pei-yu.Association among serous and cerebrospinal fluid TNF-α level, gene polymorphisms of TNF-α and multiple sclerosis in Han nationality of southern China[J].Chinese Journal of Medical Genetics,2006,23(6):677-679.
Authors:DONG Ya-xian  XU Zhi-rong  LIN Pei-yu
Institution:Department of Neurology, First Affiliated Hospital, Guangzhou Medical College, Guangzhou, Guangdong, 510120, P. R. China. yaxiandong@yahoo.com.cn
Abstract:OBJECTIVE: To investigate the association among serous and cerebrospinal fluid (CSF) TNF-alpha level, gene polymorphisms of TNF-alpha and multiple sclerosis (MS) in Han nationality of southern China. METHODS: MS diagnosis was base on Poser (1983) criteria. Fifty-five patients with nonimmulogical diseases and 68 patients with MS from southern China were enrolled in the study, and their TNF-alpha level of serum and CSF were measured by double antibody sandwich ABC-ELISA. TNF-alpha -308G/A in 106 normal healthy subjects and 68 MS patients was genotyped with polymerase chain reaction-restriction fragment length polymorphism. RESULTS: There was significant difference in the serous TNF-alpha level between nonimmune patients and active MS patients (234+/- 76 pg/mL vs 276+/- 71 pg/mL, P< 0.05), but not in the CSF (245+/- 83 pg/mL vs 265+/- 78 pg/mL, P> 0.05). The gene frequency distribution of TNF-alpha -308G/A was corresponding with Hardy-Weinberg equilibrium. The positive rate of genotype AA and the gene frequency of allele A of TNF-alpha were 4.4% and 14.0% in MS group, and 0 and 8.50% in healthy subjects, there was no statistical significance (P> 0.05). CONCLUSION: The TNF-alpha level in serum is associated with active MS, but not in the CSF. The gene polymorphisms of TNF-alpha -308G/A is not associated with MS in Han nationality of southern China.
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