Nastri L, Caruso F
Dipartimento di Discipline Odontostomatologiche, Ortodontiche e Chirurgiche, Facoltà di Medicina e Chirurgia, Seconda Università degli Studi di Napoli, Napoli, Italy.
Minerva Stomatol. 2003 Jun;52(6):253-9.
Interleukin-1 (IL-1) is a bone resorption stimulating cytokine that is implicated in the development of periodondal lesions. Recent studies suggest that the production of this mediator depends for quantity on a specific allelic combination in its genetic cluster. Periodontitis severity was correlated with the extent of the form 2 allele at the position -889 in the gene IL-1A, together with the form 2 allele at the position +3953 of the gene IL-1B. Aim of the study was to evaluate the relationship between the prevalence of the previously mentioned composite genotype and severity of periodontal lesions.
A group of 20 subjects aged more than 35 with clinical and radiographic signs of severe periodontitis (cases) underwent the salivary genetic test to single out the alleles of the genes IL-1A and IL-1B, by the PCR technique. The same test was performed to a group of 10 periodontally healthy people (controls) recruited by the same conditions. Excluding criteria were: smoking (actual or past), systemic diseases, drug absumption.
Only 7/20 patients of the case-group were positive for the composite genotype (Allele 2 of both the genes IL-1A and IL-1B), consisting in the 35% of the group. In the control-group, 4/10 subjects were positive (40%). In the case group it was not possible to underline any difference in clinical signs between positive and negative patients (respectively: Mean Probing Depth 5.05 mm vs 5.27 mm; Full Mouth Bleeding Score 56.43% vs 43.33%; Full Mouth Plaque Score 49.7% vs 41.75%)
The results obtained lead us to consider of little value the meaning of this genetic test. The test did not supply any useful element in discriminating controls from severe periodontal cases; therefore, it is not useful in the formulation of the prognosis.
白细胞介素 -1(IL -1)是一种刺激骨吸收的细胞因子,与牙周病变的发展有关。最近的研究表明,这种介质的产生量取决于其基因簇中的特定等位基因组合。牙周炎的严重程度与IL -1A基因 -889位点的2型等位基因以及IL -1B基因 +3953位点的2型等位基因的存在程度相关。本研究的目的是评估上述复合基因型的患病率与牙周病变严重程度之间的关系。
一组20名年龄超过35岁、有严重牙周炎临床和影像学表现的受试者(病例组)通过聚合酶链反应(PCR)技术进行唾液基因检测,以筛选出IL -1A和IL -1B基因的等位基因。对一组在相同条件下招募的10名牙周健康者(对照组)进行同样的检测。排除标准为:吸烟(现吸或既往吸烟)、全身性疾病、药物滥用。
病例组中只有7/20的患者复合基因型呈阳性(IL -1A和IL -1B基因均为2型等位基因),占该组的35%。对照组中,4/10的受试者呈阳性(40%)。在病例组中,无法明确阳性和阴性患者在临床体征上有任何差异(分别为:平均探诊深度5.05毫米对5.27毫米;全口出血评分56.43%对43.33%;全口菌斑评分49.7%对41.75%)。
所得结果使我们认为该基因检测意义不大。该检测在区分对照组和严重牙周病例方面未提供任何有用信息;因此,它对预后的判断没有帮助。