Isaza-Guzmán Diana M, Hernández-Viana Melissa, Bonilla-León Diego M, Hurtado-Cadavid María C, Tobón-Arroyave Sergio I
POPCAD Research Group, Laboratory of Immunodetection and Bioanalysis, Faculty of Dentistry, University of Antioquia. Medellín, Colombia.
POPCAD Research Group, Laboratory of Immunodetection and Bioanalysis, Faculty of Dentistry, University of Antioquia. Medellín, Colombia.
Arch Oral Biol. 2016 May;65:44-51. doi: 10.1016/j.archoralbio.2016.01.013. Epub 2016 Jan 27.
The focus of the current study was to identify if a possible association between NLRP3 (rs4612666) and IL-1B (rs1143634) single-nucleotide polymorphisms (SNPs) may be implicated in the etiopathogenesis of chronic periodontitis (CP) in a Colombian population.
One hundred and twenty-four CP subjects and 81 periodontally healthy controls (HC) were recruited. Periodontal status was assessed by criteria based on probing depth, clinical attachment level, extent, and severity of periodontal breakdown. Human genomic DNA was obtained from saliva samples of the study subjects. The polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method was used to identify the NLRP3 (rs4612666) and IL-1B (rs1143634) SNPs. The association of polymorphisms with CP was assessed individually and adjusted for confounding using a multivariate binary logistic regression model.
Bivariate analysis showed a weak association between CT genotype of NLRP3 (rs4612666) SNP and CP, however after logistic regression analysis, neither NLRP3 (rs4612666) nor IL-1B (rs1143634) polymorphisms were strongly/independently associated with disease status. Even so, an interaction effect was significantly detected not only among CT/CC genotypes of NLRP3 gene regarding to the age stratum ≥ 48 years, but also between CC genotype of the same gene and smoking habit.
Although the present results do not support that IL-1B (rs1143634) SNP could be identified as a risk predictor for CP in the present population, the synergistic interaction of the CT/CC genotypes of NLRP3 (rs4612666) SNP with ageing and/or smoking habit potentially might play a significant role in the pathogenic pathways of periodontal disease.
本研究的重点是确定 NLRP3(rs4612666)和 IL-1B(rs1143634)单核苷酸多态性(SNP)之间的可能关联是否与哥伦比亚人群慢性牙周炎(CP)的发病机制有关。
招募了 124 名 CP 患者和 81 名牙周健康对照者(HC)。根据探诊深度、临床附着水平、牙周破坏的范围和严重程度等标准评估牙周状况。从研究对象的唾液样本中获取人类基因组 DNA。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法鉴定 NLRP3(rs4612666)和 IL-1B(rs1143634)SNP。分别评估多态性与 CP 的关联,并使用多变量二元逻辑回归模型对混杂因素进行校正。
双变量分析显示 NLRP3(rs4612666)SNP 的 CT 基因型与 CP 之间存在弱关联,然而,经过逻辑回归分析,NLRP3(rs4612666)和 IL-1B(rs1143634)多态性均与疾病状态无强关联/独立关联。即便如此,不仅在年龄≥48 岁的人群中,NLRP3 基因的 CT/CC 基因型之间检测到显著的交互作用,而且在该基因的 CC 基因型与吸烟习惯之间也检测到显著的交互作用。
尽管目前的结果不支持 IL-1B(rs