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过氧化物酶体增殖物激活受体 γ 多态性与日本孕妇牙周炎的关系。

Peroxisome proliferator-activated receptor gamma polymorphism and periodontitis in pregnant Japanese women.

机构信息

Division of Periodontology, Department of Oral Biological Science, Graduate School of Medical and Dental Sciences, Niigata University, Niigata 951-8514, Japan.

出版信息

J Periodontol. 2010 Jun;81(6):897-906. doi: 10.1902/jop.2010.090669.

Abstract

BACKGROUND

Recent studies suggest an association between maternal periodontitis and preterm birth, although the association remains controversial. It was suggested that mechanisms such as a genetic predisposition for a hyperinflammatory response cause periodontitis and preterm births. Peroxisome proliferator-activated receptor gamma (PPARgamma) is a nuclear hormone receptor and ligand-dependent transcription factor. PPARgamma inhibits the transcriptional activity of the genes that produce proinflammatory mediators and repress periodontitis. Recently, a common polymorphism, proline(PRO)-to-alanine(ALA) mutation at codon12 in exonB (Pro12Ala: rs 1801282) PPARgamma, was reported to reduce the ability to transactivate responsive promoters. In this study, we tested whether the PPARgammaPro12Ala polymorphism was associated with maternal periodontitis and/or preterm birth.

METHODS

Genomic DNA was isolated from the venous blood of pregnant Japanese women (term birth: n = 72; preterm birth: n = 58). The PPARgammaPro12Ala genotype was determined by polymerase chain reaction (PCR)-restriction fragment length polymorphism. Within 5 days after labor, clinical periodontal parameters were evaluated, and periodontopathic bacteria from the subgingival plaque were detected by species-specific PCR.

RESULTS

The mean clinical attachment level (P = 0.012), mean probing depth (P = 0.031), mean gingival index (P = 0.037), and percentages of sites with bleeding on probing (P = 0.041) in women with the PPARgammaPro12Ala genotype were significantly higher than in women with the PPARgammaPro12Pro genotype. However, there was no association between preterm birth and periodontitis.

CONCLUSION

We suggest that the PPARgammaPro12Ala polymorphism may represent a genetic susceptibility factor for the clinical measurements of periodontitis in a limited number of pregnant Japanese women, but it probably cannot influence the relationship between periodontitis and preterm birth.

摘要

背景

最近的研究表明,母体牙周炎与早产之间存在关联,尽管这种关联仍存在争议。有人认为,导致牙周炎和早产的机制是遗传易感性导致的过度炎症反应。过氧化物酶体增殖物激活受体 γ(PPARγ)是一种核激素受体和配体依赖性转录因子。PPARγ 抑制产生促炎介质的基因的转录活性并抑制牙周炎。最近,报道了一种常见的多态性,即在exonB 中的密码子 12 处脯氨酸(PRO)到丙氨酸(ALA)突变(Pro12Ala:rs1801282)PPARγ,该突变降低了转录激活反应启动子的能力。在这项研究中,我们测试了 PPARγPro12Ala 多态性是否与母体牙周炎和/或早产有关。

方法

从日本孕妇的静脉血中分离基因组 DNA(足月分娩:n=72;早产:n=58)。通过聚合酶链反应(PCR)-限制性片段长度多态性确定 PPARγPro12Ala 基因型。分娩后 5 天内,评估临床牙周参数,并通过物种特异性 PCR 检测龈下菌斑中的牙周病细菌。

结果

PPARγPro12Ala 基因型女性的平均临床附着水平(P=0.012)、平均探诊深度(P=0.031)、平均牙龈指数(P=0.037)和探诊出血位点百分比(P=0.041)显著高于 PPARγPro12Pro 基因型女性。然而,早产与牙周炎之间没有关联。

结论

我们认为,PPARγPro12Ala 多态性可能代表了有限数量的日本孕妇牙周炎临床测量的遗传易感性因素,但它可能不能影响牙周炎与早产之间的关系。

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