Luizon Marcelo R, Palei Ana Ct, Cavalli Ricardo C, Sandrim Valeria C
Department of Pharmacology, Institute of Biosciences of Botucatu, Universidade Estadual Paulista (UNESP), Botucatu, Sao Paulo 18680-000, Brazil.
Department of General Biology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais 31270-901, Brazil.
Pharmacogenomics. 2017 Apr;18(6):571-583. doi: 10.2217/pgs-2016-0198. Epub 2017 Mar 30.
Pre-eclampsia (PE) is defined as pregnancy-induced hypertension and proteinuria, and is a major cause of maternal and perinatal morbidity and mortality. A large subgroup of pregnant women with PE is nonresponsive to antihypertensive drugs, including methyldopa, nifedipine and hydralazine. Pharmacogenomics may help to guide the individualized therapy for this nonresponsive subgroup. However, just a few pharmacogenetic studies examined the effects of genetic polymorphisms on response to antihypertensive drugs in PE, and the criteria of responsiveness used to define responsive or nonresponsive subgroups to antihypertensive therapy should be replicated by others. We review these gene-drugs interactions, novel approaches to pharmacogenomics research and potential novel drugs for PE therapy. Finally, we discuss the challenges and perspectives of pharmacogenetics in the treatment of PE.
子痫前期(PE)被定义为妊娠诱发的高血压和蛋白尿,是孕产妇和围产期发病及死亡的主要原因。很大一部分患子痫前期的孕妇对包括甲基多巴、硝苯地平和肼屈嗪在内的抗高血压药物无反应。药物基因组学可能有助于指导对这一无反应亚组的个体化治疗。然而,仅有少数药物遗传学研究考察了基因多态性对子痫前期患者抗高血压药物反应的影响,用于定义抗高血压治疗反应性或无反应性亚组的反应标准应得到其他人的重复验证。我们综述了这些基因 - 药物相互作用、药物基因组学研究的新方法以及子痫前期治疗的潜在新药。最后,我们讨论了药物遗传学在子痫前期治疗中的挑战和前景。