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Association of Matrix Metalloproteinase 9 (MMP-9) Polymorphisms with Asthma Risk: A Meta-Analysis

机译:基质金属蛋白酶9(MMP-9)具有哮喘风险的多态性的关系:META分析

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Published data on the association between MMP-9 polymorphisms (?1562 C??T, rs3918242; Gln279Arg, rs17576 Arg668Gln, rs17577) and asthma susceptibility are inconclusive. To derive a more precise estimation of this association, a meta-analysis was performed. A literature search was conducted in PubMed, Web of Science, EMBASE, Wanfang, and China National Knowledge Infrastructure (CNKI) databases to identify eligible studies. The pooled odds ratios (ORs) and corresponding 95% confidence intervals (CIs) were used to calculate the strength of association. Sensitivity analysis was performed to evaluate the influence of individual studies on the overall effect estimates, and funnel plots and Egger’s test were inspected for indication of publication bias. Seven studies with 1592 asthma patients and 1987 controls were finally identified. Overall, we found no significant association between ?1562 C??T, rs3918242 polymorphism, and asthma susceptibility in any of the genetic model comparisons. After categorizing studies into different subgroups on the basis of ethnicity and age, there is still no significant association. For the Gln279Arg, rs17576 polymorphism, there seems to be a significant association in the allelic genetic model in regard to the P value (OR?=?1.11, 95% CI?=?1.00–1.22, I2?=?0%, PZ=0.044); however, the value of lower 95% CI is 1.0. For the Arg668Gln, rs17577 polymorphism, a high significant association was observed in the dominant model comparison (OR?=?1.65, 95% CI?=?1.28–2.11, I2?=?22.50%, PZ=0), recessive model comparison (OR?=?2.40, 95% CI?=?1.23–4.72, I2?=?0%, PZ=0.011), homozygote genotype comparison (OR?=?2.69, 95% CI?=?1.36–5.33, I2?=?0%, PZ=0.004), and allelic genetic model (OR?=?1.59, 95% CI?=?1.29–1.97, I2?=?36.9%, PZ=0). Sensitivity analysis demonstrated the stability of our results, and publication bias was not evident. The present meta-analysis suggests that MMP-9 Arg668Gln, rs17577 polymorphism may be the risk factor for asthma susceptibility.
机译:发布关于MMP-9多态性之间的关联的数据(?1562 C?>?T,RS3918242; GLN279ARG,RS17576 ARG668GLN,RS17577)和哮喘敏感性是不确定的。为了获得这种关联的更精确估计,进行了META分析。文学搜索是在PubMed,Embase,Wanfang和中国国家知识基础设施(CNKI)数据库中进行的PubMed,Web,以确定合格的研究。汇集的差距(或)和相应的95%置信区间(CIS)用于计算关联的强度。进行敏感性分析以评估个体研究对整体效果估计的影响,检查漏斗图和EGGER测试是否符合出版物偏见。最终确定了七项哮喘患者和1987例对照的研究。总体而言,我们发现在任何遗传模型比较中的任何遗传模型比较中没有显着关联?1562 c?> ?? t,rs3918242多态性和哮喘易感性。在基于种族和年龄的基础上对不同亚组进行分类后,仍然没有重大关联。对于GLN279ARG,RS17576多态性,在P值(或?= 1.11,95%CI?=?1.00-1.22,I2?= 0%,PZ中,似乎在等位基因遗传模型中似乎是一个重要的关联。 = 0.044);但是,低95%CI的值为1.0。对于ARG668GLN,RS17577多态性,在主导模型比较中观察到高显着关联(或?=?1.65,95%CI?=?1.28-2.11,I2?= 22.50%,PZ = 0),隐性模型比较(或?=?2.40,95%ci?=?1.23-4.72,I2?= 0%,pz = 0.011),homozygote基因型比较(或?=Δ2.69,95%ci?=?1.36-5.33,i2 ?= 0%,pz = 0.004)和等位基因遗传模型(或?=?1.59,95%CI?=?1.29-1.97,I2?= 36.9%,PZ = 0)。敏感性分析证明了我们的结果稳定性,出版物偏见并不明显。本元分析表明,MMP-9 Arg668GLN,RS17577多态性可能是哮喘易感性的危险因素。

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