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血管内皮生长因子基因多态性与肌萎缩侧索硬化症发病年龄的关联。

Association of polymorphisms in vascular endothelial growth factor gene with the age of onset of amyotrophic lateral sclerosis.

作者信息

Chen Dafang, Shen Li, Wang Liping, Lu Aili, Zhang Huagang, Zhang Xiaoyan, Zhang Yingshuang, Shui Wei, Li Linsong, Fan Dongsheng, Zhang Jun

机构信息

Department of Epidemiology and Statistics, School of Public Health, Peking University, Beijing, China.

出版信息

Amyotroph Lateral Scler. 2007 Jun;8(3):144-9. doi: 10.1080/17482960601179373.

Abstract

This study investigated the association between polymorphisms in vascular endothelial growth factor (VEGF) gene (-1558C-T, -1190A-G and -1154A-G) and age at onset of amyotrophic lateral sclerosis (ALS). Between July 2000 and June 2004 we conducted a clinical genetic study at Peking University Third Hospital, China. The analyses included a total of 93 ALS patients. Genotyping was performed by using the 5'-nuclease assay technology (Applied Biosystems) with TaqMan allele-specific fluorogenic oligonucleotide probes. We used multivariate linear regression modelling and haplotype-based association test to analyse the association of VEGF gene polymorphisms with the age of onset, adjusting for initial symptoms and sex. The results indicated that patients with the -1190A/G and -1190G/G genotypes exhibited about a 4.1- and 9.4-years earlier onset of ALS than the patients with the -1190A/A genotype. A similar pattern emerged when the VEGF -1154A-G gene was considered: the beta was -7.9(p<0.001) years and -11.7(p<0.001) years for -1154A/G and -1154G/G genotypes, respectively. The VEGF -1558C-T had a positive effect in the -1558C/T group (p = 0.007, beta = 7.0) and -1558T/T (p<0.001, beta = 9.6) compared to the -1558C/C group. We neither observed an interaction nor haplotype association with age onset among -1558C-T, -1190A-G and -1154A-G. In conclusion, our results indicate, for the first time, that there was an important association between the polymorphism of the VEGF gene and age of ALS onset. This suggests a possible role for VEGF variability in the aetiology of individual differences in ALS onset.

摘要

本研究调查了血管内皮生长因子(VEGF)基因多态性(-1558C-T、-1190A-G和-1154A-G)与肌萎缩侧索硬化症(ALS)发病年龄之间的关联。2000年7月至2004年6月,我们在中国北京大学第三医院开展了一项临床遗传学研究。分析共纳入93例ALS患者。采用应用生物系统公司的5'-核酸酶检测技术及TaqMan等位基因特异性荧光寡核苷酸探针进行基因分型。我们使用多变量线性回归模型和基于单倍型的关联检验来分析VEGF基因多态性与发病年龄的关联,并对初始症状和性别进行了校正。结果表明,-1190A/G和-1190G/G基因型的患者与-1190A/A基因型的患者相比,ALS发病时间分别提前约4.1年和9.4年。考虑VEGF -1154A-G基因时出现了类似模式:-1154A/G和-1154G/G基因型的β值分别为-7.9(p<0.001)年和-11.7(p<0.001)年。与-1558C/C组相比,VEGF -1558C-T在-1558C/T组(p = 0.007,β = 7.0)和-1558T/T组(p<0.001,β = 9.6)中具有正向作用。我们在-1558C-T、-1190A-G和-1154A-G之间未观察到与发病年龄的相互作用或单倍型关联。总之,我们的结果首次表明,VEGF基因多态性与ALS发病年龄之间存在重要关联。这表明VEGF变异性在ALS发病个体差异的病因学中可能发挥作用。

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