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牙周疾病中内皮型一氧化氮合酶Glu298Asp基因多态性

Endothelial nitric oxide synthase Glu298Asp gene polymorphism in periodontal diseases.

作者信息

Berdeli Afig, Gürkan Ali, Emingil Gülnur, Atilla Gül, Köse Timur

机构信息

Molecular Medicine Laboratory, Department of Pediatrics, School of Medicine, Ege University, Izmir, Turkey.

出版信息

J Periodontol. 2006 Aug;77(8):1348-54. doi: 10.1902/jop.2006.050320.

Abstract

BACKGROUND

Endothelial nitric oxide synthase (eNOS) is involved in key steps of immune response. The aim of the present study was to evaluate genotype distribution and genotype-phenotype association in periodontal disease regarding Glu298Asp polymorphism of the eNOS gene.

METHODS

A total of 272 subjects were included into the study. Genomic DNA was obtained from the peripheral blood of 51 chronic periodontitis (CP) patients, 48 generalized aggressive periodontitis (GAgP), and 173 reference controls. Polymerase chain reaction (PCR) amplification and subsequent BanII restriction fragment length polymorphism (RFLP) analysis were used to detect eNOS Glu298Asp polymorphism. Probing depth, clinical attachment loss, plaque accumulation, and bleeding on probing (BOP) were recorded. The data were analyzed by the chi2 test, logistic regression, and Mann-Whitney U test.

RESULTS

The distributions of eNOS Glu298Asp genotypes and alleles were similar among study groups. Subjects with the Asp allele (Asp+) were statistically higher in the CP group compared to the control group (odds ratio [OR] = 1.957; 95% confidence interval [95% CI] = 1.038 to 3.689). In the GAgP group, BOP (%) was significantly higher in patients with the 298Asp allele (Asp+) compared to patients without the Asp allele (Asp-) (P = 0.015).

CONCLUSIONS

The present study showed that eNOS Glu298Asp polymorphism is associated with BOP in GAgP patients. Moreover, the 298Asp allele of the eNOS gene might be related to CP in the Turkish population.

摘要

背景

内皮型一氧化氮合酶(eNOS)参与免疫反应的关键步骤。本研究的目的是评估牙周病中eNOS基因Glu298Asp多态性的基因型分布及基因型与表型的关联。

方法

共纳入272名受试者。从51例慢性牙周炎(CP)患者、48例广泛侵袭性牙周炎(GAgP)患者和173例对照者的外周血中获取基因组DNA。采用聚合酶链反应(PCR)扩增及随后的BanII限制性片段长度多态性(RFLP)分析来检测eNOS Glu298Asp多态性。记录探诊深度、临床附着丧失、菌斑积聚和探诊出血(BOP)情况。数据采用卡方检验、逻辑回归和Mann-Whitney U检验进行分析。

结果

研究组间eNOS Glu298Asp基因型和等位基因的分布相似。与对照组相比,CP组中携带Asp等位基因(Asp+)的受试者在统计学上更高(优势比[OR]=1.957;95%置信区间[95%CI]=1.038至3.689)。在GAgP组中,携带298Asp等位基因(Asp+)的患者的BOP(%)显著高于不携带Asp等位基因(Asp-)的患者(P=0.015)。

结论

本研究表明,eNOS Glu298Asp多态性与GAgP患者的BOP相关。此外,在土耳其人群中,eNOS基因的298Asp等位基因可能与CP有关。

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