PCR技术鉴定牙周患者牙菌斑周围病原菌及其与白细胞介素-1复合基因型的关系

Prilozi Pub Date : 2019-10-01 DOI:10.2478/prilozi-2019-0019
A. Stojanovska, Saska Todoroska, M. Popovska, Ilijana Muratovska, Linda Zendeli Bedzeti
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引用次数: 2

摘要

摘要:本研究旨在利用PCR技术评估参与慢性牙周炎病原发生的主要微生物类型的存在,并确定复合IL-1基因型的存在及其与所发现细菌的关系。材料与方法:试验组为诊断为慢性牙周炎的20例和未患牙周炎的健康对照20例。测定牙龈指数(GI)、菌斑指数(PI)、探诊出血(BOP)、牙周袋深度(PPD)、临床附着丧失(CAL)等临床参数。龈下牙菌斑用消毒纸尖收集。结果:龈下牙菌斑中检出最多的菌种是密螺旋体(Treponema denticola)和牙龈卟罗单胞菌(Porfiromonas gingivalis), 65%的被检患者检出。在患者中存在阳性基因型方面,试验组与对照组比较p> 0.05 (p = 1.00),差异无统计学意义。χ2=8,17 (p=0,06, p= 0.05 (p= 1.00), p> 0.05 (p= 0.16), p> 0.05 (p= 0.20), p> 0.05 (p= 0.64)均无相关性。结论。这项调查证实了这五种被检查的周围病原体与牙周炎的密切联系。
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Identification of Periopathogenes from Dental Plaque in Periodontal Patients with PCR Technique and Their Association with Composite Interleukin-1 Genotype
Abstract Introduction: The present study aimed to assess the presence of main types of microorganisms involved in the aetiopathogenesis of chronic periodontitis with PCR technique and determinates the presence of composite IL-1 genotype and their associations with founded bacteria. Material and method: The examined group was consisted from 20 subjects with diagnosed chronic periodontitis and 20 healthy control without periodontitis. Clinical parameters like gingival index (GI), plaque index (PI), bleeding on probing (BOP), periodontal pocket depth (PPD) and clinical attachment lost (CAL) were determinates. Subgingival dental plaque was collected using a sterilized paper point. We used Parodontose Plus test, reverse hybridization kit, for the detection of periodontal marker bacteria, as well as for the detection of composite Interleukin -1 Genotype Results: The most present bacterial species detected from subgingival dental plaque was Treponema denticola and Porfiromonas gingivalis which was present in 65% of examined patients. In relation to the presence of positive genotype in patients, there was no significant difference between the test and control group for p> 0.05 (p = 1.00). For χ2=8,17 (p=0,06, p<0,05) there is an association between Prevotella intermedia, and composite genotype. Between positive genotype and analyzed bacterial species A. actinomycetem comitans for p> 0.05 (p = 1.00), P. gingivalis for p> 0.05 (p = 0.16), T. Forsythia for p> 0.05 (p = 0.20), T. Denticola for p> 0.05 (p = 0.64) no association was found. Conclusion. This investigations confirmed the strong association of these five examined periopathogenes with periodontitis.
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