1 Department of Cosmetic and Plastic Surgery, Xiangya Hospital, Central South University , Changsha, China .
DNA Cell Biol. 2014 Apr;33(4):234-44. doi: 10.1089/dna.2013.2252.
The contribution of genetic polymorphisms in the vascular endothelial growth factor (VEGF) gene to psoriasis risk is a controversial topic. The aim of this meta-analysis was to investigate large-scale evidence to determine the degree to which four common VEGF polymorphisms (+405C>G [dbSNP: rs2010963], -460T>C [dbSNP: rs833061], -2578C>A [dbSNP: rs699947], and -1154G>A [dbSNP: rs1570360]) are associated with susceptibility to psoriasis. A literature search of PubMed, Embase, Web of Science, Chinese National Knowledge Infrastructure, and Chinese Biomedical Literature Database was conducted to identify all eligible studies published before September 15, 2013. The principal outcome measure for evaluating the strength of the association was crude odds ratios (ORs) along with their corresponding 95% confidence intervals (95% CIs). Two thousand five hundred thirty-one patients and 2670 controls from nine case-control studies detailing a possible association between the VEGF genotypes and psoriasis risk were selected. Our meta-analysis provides evidence that two independent alleles +405G and -460C may be a protective factor for psoriasis in Asians, whereas the -1154A allele had a slight but statistically significant preventive effect on the development of psoriasis in Caucasians. The -2578C>A polymorphism, however, did not correlate with any significant difference between patients and healthy controls, even when the groups were stratified by ethnicity. Results from the meta-analysis do support the hypothesis that single-nucleotide polymorphism markers at +405C>G, -460C>T, and -1154G>A of the VEGF gene may serve as biological markers of psoriasis. Future studies should investigate interactions among multiple genotypes and environmental exposures to identify the role of proangiogenic markers in psoriasis and to delineate the underlying mechanisms of psoriasis.
血管内皮生长因子 (VEGF) 基因遗传多态性对银屑病风险的贡献是一个有争议的话题。本荟萃分析的目的是调查大规模证据,以确定四个常见 VEGF 多态性(+405C>G [dbSNP:rs2010963]、-460T>C [dbSNP:rs833061]、-2578C>A [dbSNP:rs699947]和-1154G>A [dbSNP:rs1570360])与银屑病易感性相关的程度。通过检索 PubMed、Embase、Web of Science、中国国家知识基础设施和中国生物医学文献数据库,我们对截至 2013 年 9 月 15 日之前发表的所有合格研究进行了文献搜索。评估关联强度的主要结果测量是粗比值比(ORs)及其相应的 95%置信区间(95%CI)。我们选择了来自九个病例对照研究的 2531 名患者和 2670 名对照者,这些研究详细描述了 VEGF 基因型与银屑病风险之间的可能关联。我们的荟萃分析提供的证据表明,两个独立的等位基因+405G 和-460C 可能是亚洲人银屑病的保护因素,而-1154A 等位基因对高加索人银屑病的发生有轻微但统计学上显著的预防作用。然而,-2578C>A 多态性与患者和健康对照组之间没有任何显著差异相关,即使按种族对组进行分层也是如此。荟萃分析的结果确实支持这样一种假设,即 VEGF 基因的+405C>G、-460C>T 和-1154G>A 单核苷酸多态性标记可能作为银屑病的生物标志物。未来的研究应该研究多个基因型和环境暴露之间的相互作用,以确定促血管生成标记物在银屑病中的作用,并阐明银屑病的潜在机制。