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学科主题: 临床医学
题名:
Association between vascular endothelial growth factor gene promoter polymorphisms and sporadic amyotrophic lateral sclerosis in a Han Chinese population Case-control study
作者: Sui, Wei1; Liu, Na1; Zhang, Nan1; Zhang, Jun1; Wang, Liping1; Zhang, Xiaoyan2; Zhang, Huagang1; Li, Lingsong2; Chen, Dafang3; Fan, Dongsheng1
关键词: amyotrophic lateral sclerosis ; genetic polymorphisms ; vascular endothelial growth factor
刊名: NEURAL REGENERATION RESEARCH
发表日期: 2009-12-01
DOI: 10.3969/j.issn.1673-5374.2009.12.025
卷: 4, 期:12, 页:1110-1115
收录类别: SCI
文章类型: Article
WOS标题词: Science & Technology
类目[WOS]: Cell Biology ; Neurosciences
研究领域[WOS]: Cell Biology ; Neurosciences & Neurology
关键词[WOS]: MOTOR-NEURON DEGENERATION ; FACTOR VEGF GENE ; PROLONGS SURVIVAL ; IN-VITRO ; ALS ; HYPOXIA ; MECHANISMS ; EXPRESSION ; DELETION ; MODEL
英文摘要:

BACKGROUND: Studies have shown that vascular endothelial growth factor (VEGF) gene polymorphisms highly correlate with sporadic amyotrophic lateral sclerosis (ALS), although this remains controversial. To date, the relationship between VEGF gene polymorphism and sporadic ALS in a Han Chinese population remains unclear.

OBJECTIVE: To explore the relationship between sporadic ALS and VEGF gene promoter 7 locus polymorphisms in a Han Chinese population, and to investigate whether this relationship exhibits gender differences.

DESIGN, TIME AND SETTING: A case-control study regarding genetic association was performed at the Central Laboratory of Peking University Third Hospital from 2002 to 2006.

PARTICIPANTS: A total of 93 patients, who were diagnosed with definite or probable ALS according to El Escorial-revised diagnostic criteria, were selected from the Outpatient Department of Neurology, Peking University Third Hospital from 2002 to 2006. All patients were from Han populations, with no family history of ALS. In addition, 103 gender- and age-matched healthy volunteers were selected as controls.

METHODS: Peripheral venous blood was collected, and whole blood genomic DNA was extracted. VEGF gene promoter 7 locus polymorphisms were analyzed by PCR using the fluorescent Taqman system. The relationship between VEGF gene promoter single nucleotide polymorphisms and ALS was analyzed using Logistic regression model analysis and was stratified according to gender.

MAIN OUTCOME MEASURES: 7 VEGF gene promoter polymorphisms genotype distribution and allele frequencies.

RESULTS: There were no significant differences in VEGF gene promoter 7 locus genotype distribution and allele frequency between case and control groups (P > 0.05). Stratified analysis based on gender demonstrated that female Han subjects carrying the VEGF genotype -1154AA, -2549TT, -634CC genotype were more susceptible to ALS than those carrying -1154GG, -2549CC, -634GG (VEGF-1154AA: OR = 8.9,95%CI = 1.0-77.3, P = 0.047; VEGF-2549TT: OR = 3.1, 95% CI = 1.0-9.6, P = 0.049, VEGF-634CC: OR = 0.2, 95%CI = 0.1-0.7, P = 0.012). Moreover, in female Han populations, people carrying allele -1154A, -2549T, -634C exhibited an increased risk of ALS (VEGF -1154A: OR = 2.3,95%CI = 1.2-4.5, P = 0.018; VEGF-2549T: OR = 3.1, 95%CI = 1.4-6.9, P = 0.005; VEGF-634C: OR = 0.5, 95%CI = 0.3-0.9, P = 0.015).

CONCLUSION: Results showed that VEGF 7 gene promoter polymorphisms were associated with ALS in Han Chinese women. The VEGF gene -1154A, -2549T, -634C allele and -1154AA, -2549TT, -634CC genotype could function as susceptibility genes for ALS in Han Chinese women.

语种: 英语
WOS记录号: WOS:000273468500025
Citation statistics:
内容类型: 期刊论文
URI标识: http://ir.bjmu.edu.cn/handle/400002259/50156
Appears in Collections:北京大学第三临床医学院_神经内科_期刊论文

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作者单位: 1.Peking Univ, Hosp 3, Dept Neurol, Beijing 100191, Peoples R China
2.Peking Univ, Stem Cell Res Ctr, Beijing 100191, Peoples R China
3.Peking Univ, Dept Epidemiol & Stat, Sch Publ Hlth, Beijing 100191, Peoples R China

Recommended Citation:
Sui, Wei,Liu, Na,Zhang, Nan,et al. Association between vascular endothelial growth factor gene promoter polymorphisms and sporadic amyotrophic lateral sclerosis in a Han Chinese population Case-control study[J]. NEURAL REGENERATION RESEARCH,2009,4(12):1110-1115.
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