Cullinan M P, Westerman B, Hamlet S M, Palmer J E, Faddy M J, Lang N P, Seymour G J
The University of Queensland School of Dentistry, Oral Care Research Programme, Brisbane, Australia.
J Clin Periodontol. 2001 Dec;28(12):1137-44. doi: 10.1034/j.1600-051x.2001.281208.x.
Cross-sectional studies have demonstrated that a specific polymorphism (allele 2 of both IL-1A +4845 and IL-1B +3954) in the IL-1 gene cluster has been associated with an increased susceptibility to severe periodontal disease and to an increased bleeding tendency during periodontal maintenance. The aim of the present study was to investigate the relationship between IL-1 genotype and periodontitis in a prospective longitudinal study in an adult population of essentially European heritage.
From an ongoing study of the Oral Care Research Programme of The University of Queensland, 295 subjects consented to genotyping for IL-1 allele 2 polymorphisms. Probing depths and relative attachment levels were recorded at baseline, 6, 12, 24, 36, 48 and 60 months using the Florida probe. Periodontitis progression at a given site was defined as attachment loss > or =2 mm at any observation period during the 5 years of the study and the extent of disease progression determined by the number of sites showing attachment loss. Porphyromonas gingivalis, Actinobacillus actinomycetemcomitans and Prevotella intermedia were detected using ELISA.
38.9% of the subjects were positive for the composite IL-1 genotype. A relationship between the IL-1 positive genotype and increased mean probing pocket depth in non-smokers greater than 50 years of age was found. Further, IL-1 genotype positive smokers and genotype positive subjects with P. gingivalis in their plaque had an increase in the number of probing depths > or =3.5 mm. There was a consistent trend for IL-1 genotype positive subjects to experience attachment loss when compared with IL-1 genotype negative subjects.
The results of this study have shown an interaction of the IL-1 positive genotype with age, smoking and P. gingivalis which suggests that IL-1 genotype is a contributory but non-essential risk factor for periodontal disease progression in this population.
横断面研究表明,白细胞介素-1(IL-1)基因簇中的一种特定多态性(IL-1A +4845和IL-1B +3954的等位基因2)与严重牙周病易感性增加以及牙周维护期间出血倾向增加有关。本研究的目的是在一项针对基本为欧洲血统的成年人群的前瞻性纵向研究中,调查IL-1基因型与牙周炎之间的关系。
从昆士兰大学口腔护理研究项目的一项正在进行的研究中,295名受试者同意对IL-1等位基因2多态性进行基因分型。使用佛罗里达探针在基线、6个月、12个月、24个月、36个月、48个月和60个月时记录探诊深度和相对附着水平。在研究的5年期间的任何观察期,给定部位的牙周炎进展定义为附着丧失≥2 mm,疾病进展程度由显示附着丧失的部位数量确定。使用酶联免疫吸附测定法检测牙龈卟啉单胞菌、伴放线放线杆菌和中间普氏菌。
38.9%的受试者复合IL-1基因型呈阳性。发现IL-1阳性基因型与50岁以上非吸烟者平均探诊袋深度增加之间存在关联。此外,IL-1基因型阳性吸烟者以及菌斑中有牙龈卟啉单胞菌的基因型阳性受试者,探诊深度≥3.5 mm的数量增加。与IL-1基因型阴性受试者相比,IL-1基因型阳性受试者存在附着丧失的趋势一致。
本研究结果表明IL-1阳性基因型与年龄、吸烟和牙龈卟啉单胞菌之间存在相互作用,这表明IL-1基因型是该人群牙周病进展的一个促成但非必要的危险因素。