Associations of Genetically Predicted NPR3 and NPR2 Perturbation and Preeclampsia Risk: A Two-Sample Mendelian Randomization Analysis.

IF 1.9 4区 医学 Q3 PERIPHERAL VASCULAR DISEASE
International Journal of Hypertension Pub Date : 2025-05-15 eCollection Date: 2025-01-01 DOI:10.1155/ijhy/9972031
Roxane de La Harpe, Tormod Rogne, Michael Nyberg, Héléne T Cronjé, Stephen Burgess, Ville Karhunen, Dipender Gill
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引用次数: 0

Abstract

Background: 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. Methods: 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. Results: 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. Conclusion: 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.

遗传预测NPR3和NPR2扰动与子痫前期风险的关联:两样本孟德尔随机化分析。
背景:先兆子痫是妊娠20周后以高血压为特征的妊娠并发症,由胎盘因素损害母体血管功能引起。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。本研究旨在利用孟德尔随机化(MR)框架探讨CNP对子痫前期风险的影响。方法:在编码两种受体的基因中鉴定了模拟CNP信号传导作用的遗传工具变量(通过利钠肽受体2 [NPR2]激活或减少npr3介导的清除)。这一发现来自一项涉及500多万人的多祖先全基因组关联研究(GWAS)。从英国生物银行198,402名女性参与者的个人水平数据中获得了女性特异性遗传关联估计。通过两样本MR分析,研究NPR2激活和NPR3功能对子痫前期的影响,利用最大的公开GWAS,其中包括296,824名女性参与者。结果:基因相关的NPR3功能降低与子痫前期风险降低相关(优势比(OR): 0.46, 95%可信区间0.30-0.69)。相比之下,遗传代理增加的NPR2激活缺乏显著关联,可能是由于功率不足的遗传工具。敏感性分析显示具有最小的多效性,这意味着使用的遗传变异主要通过预期的生物学途径影响先兆子痫,而不是影响多个不相关的性状。结论:本研究采用MR模式提供遗传证据,支持CNP(通过降低NPR3功能)对子痫前期风险的保护作用。然而,在进一步开展临床开发工作以探索CNP作为先兆子痫的潜在治疗方法之前,从其他来源收集更多证据是很重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
International Journal of Hypertension
International Journal of Hypertension Medicine-Internal Medicine
CiteScore
4.00
自引率
5.30%
发文量
45
期刊介绍: International Journal of Hypertension is a peer-reviewed, Open Access journal that provides a forum for clinicians and basic scientists interested in blood pressure regulation and pathophysiology, as well as treatment and prevention of hypertension. The journal publishes original research articles, review articles, and clinical studies on the etiology and risk factors of hypertension, with a special focus on vascular biology, epidemiology, pediatric hypertension, and hypertensive nephropathy.
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