School of Public Health, Bengbu Medical University, Bengbu, Anhui, 233030, China.
School of Public Health, Anhui Medical University, Hefei, Anhui, 230030, China.
BMC Cardiovasc Disord. 2024 Nov 15;24(1):647. doi: 10.1186/s12872-024-04310-2.
The NLRP3 inflammasome, a pivotal mechanism regulating inflammatory responses and featuring the pyrin domain containing 3 (NLRP3) within the NOD-like receptor family, is widely recognized as a central pathogenic factor in cardiovascular diseases. The present study endeavors to delve into the correlation and potential interplay between the rs10754558 polymorphism of NLRP3 and the predisposition to hypertension among the Chinese adult population.
All the participants who came from a community in Bengbu, China were investigated by being interviewed with a questionnaire. Overall, 354 paired case-control participants were analyzed. Genomic DNA was extracted from 5ml venous blood using the Tiangen DNA extraction kit. The rs10754558 polymorphism of the NLRP3 gene was genotyped by TaqMan allelic discrimination real-time PCR.The association between the rs10754558 polymorphism and hypertension risk was investigated by a logistic regression analysis. Furthermore, an additive interaction analysis was conducted using related indicators, including the relative excess risk due to interaction (RERI), attributable proportion due to interaction (AP), and synergy index (SI).
Participants carrying the GG genotype were more likely to develop hypertension than participants carrying the CC genotype (adjusted odds ratio [OR]: 2.16, 95% confidence interval [CI]: 1.33-3.52). A significant additive interaction between the NLRP3 polymorphism and obesity status concerning the risk of hypertension was observed, as estimated by all indicators: RERI (1.12, 95% CI: 0.70-1.5), AP (0.34, 95% CI: 0.14-0.53), and SI (1.92, 95% CI: 1.03-3.59). The values of RERI (1.74, 95% CI: 0.37-3.11), AP (0.46, 95% CI: 0.21-0.70), and SI (2.62, 95% CI: 1.18-5.83) showed that a significant interaction between the rs10754558 polymorphism and a family history of hypertension.
Our findings indicate a significant association between the NLRP3 rs10754558 polymorphism and the risk of hypertension in Chinese adults. Moreover, a notable additive interaction emerges between NLRP3 polymorphisms and obesity status, further amplifying the risk of hypertension.
NLRP3 炎性小体是调节炎症反应的关键机制,其特征在于 NOD 样受体家族中的富含 pyrin 结构域蛋白 3(NLRP3),被广泛认为是心血管疾病的中心致病因素。本研究旨在探讨 NLRP3 基因 rs10754558 多态性与中国成年人群高血压易感性之间的相关性和潜在相互作用。
所有参与者均通过问卷调查在中国蚌埠的一个社区进行调查。总共分析了 354 对病例对照参与者。使用 Tiangen DNA 提取试剂盒从 5ml 静脉血中提取基因组 DNA。使用 TaqMan 等位基因鉴别实时 PCR 对 NLRP3 基因的 rs10754558 多态性进行基因分型。通过 logistic 回归分析探讨 rs10754558 多态性与高血压风险之间的关联。此外,使用相关指标(包括交互归因超额风险[RERI]、交互归因比例[AP]和协同指数[SI])进行了附加交互作用分析。
与携带 CC 基因型的参与者相比,携带 GG 基因型的参与者更有可能患上高血压(调整后的优势比[OR]:2.16,95%置信区间[CI]:1.33-3.52)。通过所有指标(RERI(1.12,95%CI:0.70-1.5)、AP(0.34,95%CI:0.14-0.53)和 SI(1.92,95%CI:1.03-3.59))都发现 NLRP3 多态性与肥胖状态之间存在显著的相加交互作用与高血压的风险有关。RERI(1.74,95%CI:0.37-3.11)、AP(0.46,95%CI:0.21-0.70)和 SI(2.62,95%CI:1.18-5.83)的值表明,rs10754558 多态性与高血压家族史之间存在显著的交互作用。
我们的研究结果表明 NLRP3 rs10754558 多态性与中国成年人高血压风险之间存在显著关联。此外,NLRP3 多态性与肥胖状态之间存在显著的相加交互作用,进一步增加了高血压的风险。