Harpe Roxane de La, Rogne Tormod, Nyberg Michael, Cronjé Héléne T, Burgess Stephen, Karhunen Ville, Gill Dipender
Department of Medicine, University Hospital of Lausanne, Lausanne, Vaud, Switzerland.
Department of Community Medicine and Global Health, University of Oslo, Oslo, Norway.
Int J Hypertens. 2025 May 15;2025:9972031. doi: 10.1155/ijhy/9972031. eCollection 2025.
Preeclampsia, a pregnancy complication marked by hypertension after 20 weeks of gestation, arises from placental factors that impair maternal vascular function. C-type natriuretic peptide (CNP), known for its vasodilatory role, may help counter preeclampsia-related vascular dysfunction. This study aimed to explore the effect of CNP on preeclampsia risk using the Mendelian randomization (MR) framework. Genetic instrumental variables that mimic the effects of CNP signaling (through natriuretic peptide receptor 2 [NPR2] activation or reduced NPR3-mediated clearance) were identified in the genes encoding the two receptors. This discovery emerged from a multiancestry genome-wide association study (GWAS) involving over 5 million individuals. Female-specific genetic association estimates were obtained from individual-level data comprising 198,402 female participants in the UK Biobank. Two-sample MR analyses were conducted to investigate the effects of NPR2 activation and NPR3 function on preeclampsia, utilizing the largest publicly available GWAS on preeclampsia, which included 296,824 female participants. Genetically proxied reduced NPR3 function was associated with a lower risk of preeclampsia (odds ratio (OR): 0.46, 95% confidence interval 0.30-0.69). In contrast, genetically proxied increased NPR2 activation lacked significant association, likely due to underpowered genetic instruments. Sensitivity analyses indicated robust findings with minimal pleiotropy, meaning the genetic variants used primarily influenced preeclampsia through the intended biological pathway rather than affecting multiple unrelated traits. This study employed the MR paradigm to provide genetic evidence supporting the protective effects of CNP (through reduced NPR3 function) on the risk of preeclampsia. However, it is important to gather additional evidence from other sources before moving forward with clinical development efforts to explore CNP as a potential treatment for preeclampsia.
子痫前期是一种妊娠并发症,其特征为妊娠20周后出现高血压,由损害母体血管功能的胎盘因素引起。C型利钠肽(CNP)以其血管舒张作用而闻名,可能有助于对抗子痫前期相关的血管功能障碍。本研究旨在使用孟德尔随机化(MR)框架探讨CNP对子痫前期风险的影响。在编码这两种受体的基因中鉴定出了模拟CNP信号传导作用(通过利钠肽受体2 [NPR2]激活或减少NPR3介导的清除)的遗传工具变量。这一发现源自一项涉及超过500万人的多祖先全基因组关联研究(GWAS)。女性特异性遗传关联估计值来自英国生物银行中198,402名女性参与者的个体水平数据。利用关于子痫前期的最大公开可用GWAS(其中包括296,824名女性参与者)进行两样本MR分析,以研究NPR2激活和NPR3功能对子痫前期的影响。遗传代理的NPR3功能降低与子痫前期风险较低相关(优势比(OR):0.46,95%置信区间0.30 - 0.69)。相比之下,遗传代理的NPR2激活增加缺乏显著关联,可能是由于遗传工具的效能不足。敏感性分析表明结果稳健,多效性最小,这意味着所使用的遗传变异主要通过预期的生物学途径影响子痫前期,而非影响多个不相关的性状。本研究采用MR范式提供了遗传证据,支持CNP(通过降低NPR3功能)对子痫前期风险的保护作用。然而,在推进将CNP作为子痫前期潜在治疗方法的临床开发工作之前,从其他来源收集更多证据很重要。