Gürkan Ali, Emingil Gülnur, Saygan Buket Han, Atilla Gül, Köse Timur, Baylas Haluk, Berdeli Afig
Department of Periodontology, School of Dentistry, Ege University, Izmir, Turkey.
J Clin Periodontol. 2009 Mar;36(3):204-11. doi: 10.1111/j.1600-051X.2008.01379.x.
Evidence suggests that the ultimate product of the renin-angiotensin system (RAS), angiotensin II, exerts inflammatory actions. The present study aimed to evaluate the inter-relation between gene polymorphisms of the RAS components; angiotensin converting enzyme (ACE), angiotensinogen (AGT) and angiotensin II type-I receptor (AT1R), and severe chronic periodontitis (CP).
DNA was obtained from peripheral blood of 90 CP patients and 126 periodontally healthy subjects, and the clinical parameters were recorded. ACE I/D, AGT M235T and AT1R A1166C polymorphisms were genotyped by the PCR-RFLP method. Chi-square, anova and logistic regression methods were used in statistical analyses.
The frequency of the ACE D allele was significantly lower in the CP group than the healthy group (p(corr)=0.015). CP subjects exhibited increased C allele carriage and C allele frequency of the AT1R gene (p(corr)=0.03 and p(corr)=0.03, respectively). All clinical parameters of CP patients were found to be similar in variant allele-carrying and non-carrying subjects (p>0.05).
The present findings suggest that ACE I/D and AT1R polymorphisms might be associated with susceptibility to CP but not with disease severity. The D allele of ACE I/D might be associated with decreased, whereas the C variant of AT1R A1166C might be associated with an elevated risk for CP in Turkish population.
有证据表明肾素 - 血管紧张素系统(RAS)的最终产物血管紧张素II具有炎症作用。本研究旨在评估RAS组分;血管紧张素转换酶(ACE)、血管紧张素原(AGT)和血管紧张素II 1型受体(AT1R)的基因多态性与重度慢性牙周炎(CP)之间的相互关系。
从90例CP患者和126例牙周健康受试者的外周血中获取DNA,并记录临床参数。采用聚合酶链反应 - 限制性片段长度多态性(PCR - RFLP)方法对ACE I/D、AGT M235T和AT1R A1166C多态性进行基因分型。统计分析采用卡方检验、方差分析和逻辑回归方法。
CP组中ACE D等位基因的频率显著低于健康组(p(校正)=0.015)。CP受试者中AT1R基因的C等位基因携带率和C等位基因频率增加(分别为p(校正)=0.03和p(校正)=0.03)。在携带和不携带变异等位基因的CP患者中,所有临床参数均相似(p>0.05)。
目前的研究结果表明,ACE I/D和AT1R多态性可能与CP易感性相关,但与疾病严重程度无关。在土耳其人群中,ACE I/D的D等位基因可能与CP风险降低相关,而AT1R A1166C的C变异可能与CP风险升高相关。