Peyter Anne-Christine, Baud David, Tolsa Jean-François
Neonatal Research Laboratory, Department Woman-Mother-Child, Lausanne University Hospital and University of Lausanne, 1011 Lausanne, Switzerland.
Obstetric Service, Department Woman-Mother-Child, Lausanne University Hospital and University of Lausanne, 1011 Lausanne, Switzerland.
Biomedicines. 2024 Oct 14;12(10):2329. doi: 10.3390/biomedicines12102329.
Fetal growth restriction (FGR) is a common complication of pregnancy, associated with major perinatal mortality and morbidity, and with an increased risk to develop cardiometabolic diseases later in life. There is currently no effective approach to prevent or treat FGR, despite numerous animal and human studies assessing substances likely to improve fetal growth. Phosphodiesterase (PDE) inhibitors appeared as promising drugs to improve FGR management. However, to date, studies have led to somewhat disappointing or controversial results. In this Opinion article, we would like to draw attention to the need to consider the biological sex and the relative reactivity of human umbilical vein and arteries when developing therapeutic interventions to improve human umbilical circulation using PDE inhibitors. Indeed, we suspect that fetal sex, vessel type and the presence of FGR may influence subcellular compartmentation, which could jeopardize beneficial effects of PDE inhibitors.
胎儿生长受限(FGR)是一种常见的妊娠并发症,与围产期主要死亡率和发病率相关,并且会增加日后患心脏代谢疾病的风险。尽管有大量动物和人体研究评估了可能改善胎儿生长的物质,但目前尚无预防或治疗FGR的有效方法。磷酸二酯酶(PDE)抑制剂似乎是改善FGR管理的有前景的药物。然而,迄今为止,研究结果有些令人失望或存在争议。在这篇观点文章中,我们想提请注意,在开发使用PDE抑制剂改善人脐循环的治疗干预措施时,需要考虑生物性别以及人脐静脉和动脉的相对反应性。事实上,我们怀疑胎儿性别、血管类型和FGR的存在可能会影响亚细胞区室化,这可能会危及PDE抑制剂的有益效果。