Nibali L, Donos N, Brett P M, Parkar M, Ellinas T, Llorente M, Griffiths G S
Periodontology Unit, Eastman Dental Institute and Hospital, University College London, London, UK.
J Periodontal Res. 2008 Dec;43(6):627-34. doi: 10.1111/j.1600-0765.2007.01039.x. Epub 2008 Aug 22.
Family history is a primary diagnostic criterion for current classification of aggressive periodontitis (AgP). However, results of previous studies have shed controversy over the degree of familiarity of AgP and its possible inheritance mechanisms. The aims of this study were to estimate the percentage of affected relatives of AgP individuals, to analyse the disease phenotypes in relatives and to explore the distributions of genetic polymorphisms of interleukin-6 (IL-6) in AgP patients and in diseased and healthy relatives.
Patients with AgP were clinically examined and asked to provide relatives for examination. First-degree relatives were clinically and radiographically diagnosed. Blood samples were collected, DNA was extracted and analysis of single nucleotide polymorphisms of IL-6 (at positions -174, -1363 and -1480) by polymerase chain reaction was performed in patients and relatives.
Fifty-five AgP patients provided relatives for examination. A total of 100 first-degree relatives were assessed and 10 of them (10%) were found to have AgP. All relatives diagnosed with AgP had the same disease as the corresponding proband (localized AgP/localized AgP or generalized AgP/generalized AgP). The same IL-6 genotypes (-174 GG, -1480 CC) previously associated with AgP showed a tendency for association with AgP in relatives.
This pilot study confirmed a relatively high risk for relatives of AgP patients to have AgP (10%). Genetic polymorphisms in the IL-6 gene may have an impact in aetiopathogenesis. This study provides a sample size calculation for a novel study design using healthy relatives as control subjects.
家族史是目前侵袭性牙周炎(AgP)分类的主要诊断标准。然而,既往研究结果对AgP的家族聚集程度及其可能的遗传机制存在争议。本研究的目的是评估AgP患者患病亲属的比例,分析亲属中的疾病表型,并探讨AgP患者及其患病和健康亲属中白细胞介素-6(IL-6)基因多态性的分布情况。
对AgP患者进行临床检查,并要求其提供亲属进行检查。对一级亲属进行临床和影像学诊断。采集血样,提取DNA,并对患者及其亲属进行聚合酶链反应检测IL-6(-174、-1363和-1480位点)的单核苷酸多态性。
55例AgP患者提供了亲属进行检查。共评估了100名一级亲属,其中10人(10%)被发现患有AgP。所有被诊断为AgP的亲属与相应先证者患有相同的疾病(局限性AgP/局限性AgP或广泛性AgP/广泛性AgP)。先前与AgP相关的相同IL-6基因型(-174 GG,-1480 CC)在亲属中显示出与AgP相关的趋势。
这项初步研究证实,AgP患者的亲属患AgP的风险相对较高(10%)。IL-6基因的多态性可能对发病机制有影响。本研究为一项以健康亲属作为对照的新研究设计提供了样本量计算方法。