Cleary Kirsten Lawrence, Roney Kelly, Costantine Maged
Department of Obstetrics and Gynecology, Columbia University Medical Center, 622 W 168th St, 16-66, New York, NY 10032.
Research Triangle Institute International, Research Triangle Park, NC.
Semin Perinatol. 2014 Dec;38(8):523-7. doi: 10.1053/j.semperi.2014.08.019. Epub 2014 Oct 12.
Statins (3-hydroxy-3 methyl-glutaryl coenzyme-A reductase inhibitors) are the most commonly prescribed cholesterol-lowering medications due to their efficacy in reducing cardiovascular mortality and morbidities, tolerability, and safety profiles. Based on pathophysiologic similarities between cardiovascular disease and preeclampsia, a common and dangerous complication of pregnancy, there is an increasing interest in studying this class of medications during pregnancy to prevent and/or treat preeclampsia. Undergoing such a study, which entails the use of a pregnancy class X medication for an off-label indication in pregnancy, requires intensive multidisciplinary involvement of a group of experts in basic and clinical pharmacology, research methods, pregnancy physiology and maternal-fetal medicine, as well as U.S. Food and Drug Administration (FDA) regulatory guidelines and practice. Issues of potential fetal risk, altered maternal-fetal pharmacokinetics and pharmacodynamics, and regulatory challenges are real, and must be carefully considered in the process of research in this arena.
他汀类药物(3-羟基-3-甲基戊二酰辅酶A还原酶抑制剂)是最常用的降胆固醇药物,因为它们在降低心血管疾病死亡率和发病率、耐受性及安全性方面疗效显著。鉴于心血管疾病与子痫前期(一种常见且危险的妊娠并发症)在病理生理上存在相似性,人们对在孕期研究这类药物以预防和/或治疗子痫前期的兴趣日益浓厚。开展此类研究,即使用妊娠X级药物用于孕期的非适应症用药,需要基础和临床药理学、研究方法、妊娠生理学和母胎医学等领域的专家以及美国食品药品监督管理局(FDA)的监管指南和实践进行深入的多学科参与。潜在的胎儿风险、母胎药代动力学和药效学的改变以及监管挑战等问题切实存在,在该领域的研究过程中必须仔细加以考虑。