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首页> 外文期刊>Journal of Periodontology >Interleukin-1 gene polymorphisms and chronic periodontitis in adult whites: A systematic review and meta-analysis
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Interleukin-1 gene polymorphisms and chronic periodontitis in adult whites: A systematic review and meta-analysis

机译:白细胞介素1基因多态性与慢性牙周炎:系统评价和荟萃分析

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摘要

Background: Interleukin-1 (IL-1) gene polymorphisms have been associated with increased levels of inflammatory mediators and several inflammatory diseases. Periodontitis is a bacterially induced chronic inflammatory disease that destroys the connective tissues and bone that support the teeth, affects substantial numbers of adults, and has been implicated as a contributing factor in systemic diseases. IL-1 gene polymorphisms, most prominently IL1A (-889), IL1A (+4,845), and IL1B (+3,954), have been associated with chronic periodontitis (CP) in whites. Since the first report, ≥125 studies have examined IL-1 gene variation in relation to periodontal disease. These studies have produced mixed findings in diverse periodontal phenotypes and in different ethnic groups. One previous meta-analysis has been published on this topic and supported an association between IL-1 genes and periodontitis, but considerable doubt remains about the patient populations in which the association may be of clinical relevance. Methods: A systematic review and meta-analysis was conducted in an attempt to clarify whether IL-1 gene variants were associated with welldefined clinical phenotypes of CP in white patients. Study inclusion criteria focused on the analytic framework originally proposed for the IL-1 genetic effect in which overexpression of inflammatory mediators is hypothesized to result in more severe periodontitis in response to a bacterial challenge. Results: Twenty-seven studies were included in the qualitative analysis. Nineteen studies yielded significant associations between carriage of the minor IL-1 alleles and periodontitis. The meta-analysis, based on 13 qualifying studies, found significant effects for the two individual gene variations (IL1A odds ratio [OR] = 1.48; IL1B OR = 1.54) and for a composite genotype that combines minor alleles at each locus (OR = 1.51). Statistically significant heterogeneity was found that could not be explained, but there was no indication of publication bias. Conclusion: This review and meta-analysis show that IL1A and IL1B genetic variations are significant contributors to CP in whites. J Periodontol 2012;83:1407-1419.
机译:背景:白介素-1(IL-1)基因多态性与炎症介质水平升高和几种炎症性疾病有关。牙周炎是一种细菌性引起的慢性炎症性疾病,它破坏了支撑牙齿的结缔组织和骨骼,影响了许多成年人,并被认为是全身性疾病的一个致病因素。 IL-1基因多态性,最突出的是IL1A(-889),IL1A(+4,845)和IL1B(+3,954),与白人的慢性牙周炎(CP)相关。自首次报告以来,≥125项研究检查了与牙周疾病相关的IL-1基因变异。这些研究在不同的牙周表型和不同种族中产生了不同的发现。关于该主题的一项先前的荟萃分析已经发表,并支持IL-1基因与牙周炎之间的关联,但是对于这种关联可能与临床相关的患者人群仍存在相当大的疑问。方法:进行系统的审查和荟萃分析,以试图弄清IL-1基因变异是否与白人患者CP的明确临床表型有关。研究纳入标准侧重于最初提出的针对IL-1遗传效应的分析框架,在该框架中,假设炎症介质的过度表达会导致对细菌攻击的更严重的牙周炎。结果:27项研究被纳入定性分析。十九项研究得出了较小的IL-1等位基因携带与牙周炎之间的显着关联。这项荟萃分析基于13项合格研究,发现对两个单独的基因变异(IL1A优势比[OR] = 1.48; IL1B OR = 1.54)以及在每个基因座处合并了次要等位基因的复合基因型(OR = 1.51)。发现统计学上的显着异质性无法解释,但没有迹象表明存在出版偏倚。结论:这项审查和荟萃分析表明,IL1A和IL1B的遗传变异是白人CP的重要因素。 J牙周病2012; 83:1407-1419。

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