白细胞介素-1基因型在叙利亚人群冠心病和牙周炎相关性中的作用

ISRN dentistry Pub Date : 2013-04-14 Print Date: 2013-01-01 DOI:10.1155/2013/195678
Lina Bashour, Razan Khattab, Elham Harfoush
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引用次数: 7

摘要

目标。目的:确定叙利亚人群牙周炎患者与非冠心病患者IL-1等位基因IL-1α+4845、IL-1β+3954、IL-1β-511和IL-1RN VNTR位点的分布是否存在差异。背景。白细胞介素-1基因在牙周炎和冠心病之间的作用已在先前的研究中得到证实。没有对叙利亚人口进行研究以评估这种作用。方法:200例叙利亚阿拉伯牙周炎患者(男性184例,女性16例;平均年龄52.61岁)分为两组:病例组冠心病患者100例,其中男性92例,女性8例;平均年龄52.06);对照组100例无冠心病,其中男性92例,女性8例;平均年龄53.16岁)。对患者进行探探深度(PD)、临床附着损失(CAL)和牙槽骨损失(ABL)检测。采集血样,采用PCR- rflp技术对IL-1α+4845、IL-1β+3954和IL-1β-511进行基因分型分析,采用正常PCR对IL-1RN VNTR进行基因分型分析。结果。校正其他混杂因素后发现(CAL和ABL)与冠心病之间存在关联(OR: 7.659, P = 0.001;OR: 3.645, P = 0.006)。IL-1α+4845、IL-1β+3954和IL-1β-511等位基因2与ABL存在相关性。IL-1α+4845和IL-1β-511等位基因2与冠心病患者ABL相关。但在校正其他混杂因素后,只有IL-11α+4845等位基因2与冠心病和严重ABL之间存在关联(OR: 0.189, P < 0.001)。结论。IL-11α+4845等位基因2可能被认为是调查的叙利亚人群中患有冠心病和严重ABL的危险指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Role of Interleukin-1 Genotype in the Association between Coronary Heart Disease and Periodontitis in a Syrian Population.

Objective. To determine whether differences exist between periodontitis subjects with and without Coronary Heart Disease (CHD) in a Syrian population in the distribution of IL-1 alleles at positions IL-1α+4845, IL-1β+3954, IL-1β-511, and IL-1RN VNTR. Background. The role of Interleukin-1 genes in the association between periodontitis and CHD has been demonstrated in previous studies. No study has been carried out on the Syrian population to asses for such a role. Methods. 200 Syrian Arab periodontitis patients (184 males, 16 females; mean age 52.61) were divided into two groups: cases group 100 subjects with CHD (92 males, 8 females; mean age 52.06); controls group 100 subjects without CHD (92 males, 8 females; mean age 53.16). Probing depth (PD), clinical attachment loss (CAL), and alveolar bone loss (ABL) were performed for patients. Blood samples were collected for genotyping analysis of IL-1α+4845, IL-1β+3954, and IL-1β-511 using PCR-RFLP technique and IL-1RN VNTR using normal PCR. Results. An association between both (CAL and ABL) and CHD was shown after adjustment for other confounders (OR: 7.659, P = 0.001; OR: 3.645, P = 0.006, resp.). Also, an association between allele 2 of IL-1α+4845, IL-1β+3954, and IL-1β-511 and ABL was shown. Allele 2 of IL-1α+4845 and IL-1β-511 was associated with ABL among individuals with and without CHD. But after adjustment for other confounders, the association remained only between allele 2 of IL-11α+4845 and both CHD and severe ABL (OR: 0.189, P < 0.001). Conclusion. Allele 2 of IL-11α+4845 may be considered a risk indicator for having both CHD and severe ABL in the investigated Syrian population.

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