VEGF promoter haplotype and amyotrophic lateral sclerosis (ALS)

被引:34
作者
Terry, PD
Kamel, F
Umbach, DM
Lehman, TA
Hu, H
Sandler, DP
Taylor, JA
机构
[1] NIEHS, Epidemiol Branch, NIH, Dept Hlth & Human Serv, Res Triangle Pk, NC 27709 USA
[2] Karolinska Inst, Dept Med Epidemiol & Biostat, Stockholm, Sweden
[3] NIEHS, Biostat Branch, NIH, Dept Hlth & Human Serv, Res Triangle Pk, NC 27709 USA
[4] Harvard Univ, Sch Med, Boston, MA 02115 USA
[5] Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
[6] BioServe Biotechnol Ltd, Laurel, MD 20707 USA
[7] NIEHS, Mol Carcinogenesis Lab, NIH, Dept Hlth & Human Serv, Res Triangle Pk, NC 27709 USA
关键词
vascular endothelial growth factor; amyotrophic lateral sclerosis; epidemiologic studies; haplotypes;
D O I
10.1080/01677060490894450
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Vascular endothelial growth factor (VEGF) is a cytokine essential for angiogenesis. A recent study found that haplotypes, determined by three SNPs (-2,578C/A, -1,154 G/A, and -634G/C) in the VEGF upstream promoter/leader sequence, were associated with risk of amyotrophic lateral sclerosis (ALS). We used samples and data from a case-control study to examine the relation of ALS to VEGF haplotype. Genotypes at each of the three polymorphic sites were determined using allele-specific primer extension reactions followed by MALDI-TOF. We found a 3-fold increased risk among individuals homozygous for the AAG or AGG haplotypes (95% CI=0.7-13.4), consistent with the findings of the previous study. Given the wide confidence interval, our findings should be interpreted cautiously.
引用
收藏
页码:429 / 434
页数:6
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