Wu Fangqin, Liu Dongchen, Xia Xin, Yang Xinlei, Huang Suli, Jiang Xinghua
Department of Cardiovascular Medicine, the Second Affiliated Hospital of Nanchang University, 1Minde Road, Nanchang, China.
Department of Cardiovascular Medicine, the Second Affiliated Hospital of Shantou University Medical College, Shantou, China.
BMC Cardiovasc Disord. 2025 Mar 12;25(1):172. doi: 10.1186/s12872-025-04629-4.
The IL-33/ST2 pathway plays a crucial role in the development of essential hypertension (EH). This study aimed to investigate the relationship between EH and genetic variations in this pathway in the Chinese Han population.
A total of 1,151 EH patients and 1,135 healthy controls were included in the study. Sixteen single nucleotide polymorphisms (SNPs) in the interleukin-33 (IL-33) and interleukin-1receptor associated protein (IL-1RAcP) genes were genotyped using the Sequenom MassArray and TaqMan assays. Genotype and allele frequencies were compared between the EH patients and controls using logistic regression analysis.
The rs16865597 SNP in the IL-1RAcP gene was found to be associated with the risk of EH. Specifically, the presence of the C allele of rs16865597 was negatively correlated with EH susceptibility in both the additive model (P = 0.014, OR = 0.75, 95% CI = 0.59-0.94) and the recessive model (P = 0.011, OR = 0.72, 95% CI = 0.56-0.93). Additionally, rs16865597 was linked to a reduced risk of EH in specific subgroups, including males (OR add = 0.73, 95% CI = 0.56-0.94, P = 0.015), nonsmokers (OR add = 0.72, 95% CI = 0.54-0.96, P = 0.023), nondrinkers (OR add = 0.70, 95% CI = 0.53-0.93, P = 0.013), and individuals with low BMI (OR add = 0.69, 95% CI = 0.51-0.92, P = 0.013). Moreover, the C genotype of rs16865597 was strongly associated with higher interleukin-10 levels in vivo.
The rs16865597 SNP is significantly associated with a reduced risk of EH in the Chinese Han population, potentially due to its role in immune regulation.
白细胞介素-33(IL-33)/ST2信号通路在原发性高血压(EH)的发生发展中起关键作用。本研究旨在探讨中国汉族人群中EH与该信号通路基因变异之间的关系。
本研究共纳入1151例EH患者和1135例健康对照。采用Sequenom MassArray和TaqMan检测法对白细胞介素-33(IL-33)基因和白细胞介素-1受体相关蛋白(IL-1RAcP)基因中的16个单核苷酸多态性(SNP)进行基因分型。采用逻辑回归分析比较EH患者和对照组的基因型和等位基因频率。
发现IL-1RAcP基因中的rs16865597 SNP与EH风险相关。具体而言,在加性模型(P = 0.014,OR = 0.75,95%CI = 0.59 - 0.94)和隐性模型(P = 0.011,OR = 0.72,95%CI = 0.56 - 0.93)中,rs16865597的C等位基因与EH易感性呈负相关。此外,rs16865597与特定亚组中EH风险降低相关,包括男性(加性OR = 0.73,95%CI = 0.56 - 0.94,P = 0.015)、非吸烟者(加性OR = 图0.72,95%CI = 0.54 - 0.96,P = 0.023)、不饮酒者(加性OR = 0.70,95%CI = 0.53 - 0.93,P = 0.013)和低体重指数个体(加性OR = 0.69,95%CI = 0.51 - 0.92,P = 0.013)。此外,rs16865597的C基因型与体内较高的白细胞介素-10水平密切相关。
rs16865597 SNP与中国汉族人群中EH风险降低显著相关,这可能与其在免疫调节中的作用有关。