Arj-Ong Sakda, Thakkinstian Ammarin, McEvoy Mark, Attia John
Section for Clinical Epidemiology and Biostatistics, Ramathibodi Hospital, Bangkok, Thailand.
Pediatr Int. 2010 Aug;52(4):527-32. doi: 10.1111/j.1442-200X.2010.03105.x.
There have been genetic studies assessing the association between tumor necrosis factor (TNF)-α-308 and Kawasaki disease (KD) but the results have been conflicting due to lack of power. Therefore, a systematic review and meta-analysis was conducted to increase the power for identifying the association between the TNF-α-308 polymorphism and KD.
Studies were identified from MEDLINE and EMBASE databases and were included if the subjects were children and the frequencies between TNF-α-308 and KD were reported. Data were pooled using a random effect model if heterogeneity between studies was present.
Thirteen studies were identified however only six studies were included. The pooled prevalence of minor A allele was 5.2% (95% confidence interval [CI]: 0.1%-9.5%). Gene effect was assessed using per-allele and per-genotype approaches. The pooled odds ratio of G versus A with the random effect model was 1.13 (95%CI: 0.34-3.27). The genotype effects for GG versus GA+AA was estimated and the pooled odds ratio was 1.08 (95%CI: 0.42-2.92).
This review suggests a trend of association between the TNF-α-308 G-allele and KD. However, the gene effects are heterogeneous and assessing sources of heterogeneity are limited. An updated meta-analysis is needed if more studies are published.
已有基因研究评估肿瘤坏死因子(TNF)-α -308与川崎病(KD)之间的关联,但由于样本量不足,结果存在冲突。因此,进行了一项系统评价和荟萃分析,以增强识别TNF-α -308多态性与KD之间关联的效能。
从MEDLINE和EMBASE数据库中检索研究,如果研究对象为儿童且报告了TNF-α -308与KD之间的频率,则纳入研究。如果研究之间存在异质性,则使用随机效应模型合并数据。
共识别出13项研究,但仅纳入了6项研究。次要A等位基因的合并患病率为5.2%(95%置信区间[CI]:0.1%-9.5%)。使用每等位基因和每基因型方法评估基因效应。随机效应模型下G与A的合并比值比为1.13(95%CI:0.34-3.27)。估计了GG与GA+AA的基因型效应,合并比值比为1.08(95%CI:0.42-2.92)。
本综述提示TNF-α -308 G等位基因与KD之间存在关联趋势。然而,基因效应存在异质性,且评估异质性来源的研究有限。如果有更多研究发表,需要进行更新的荟萃分析。