dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorUniversidade Federal de Minas Gerais (UFMG)
dc.contributorUniversity of Mississippi Medical Center
dc.contributorUniversidade de São Paulo (USP)
dc.date.accessioned2018-12-11T17:11:12Z
dc.date.available2018-12-11T17:11:12Z
dc.date.created2018-12-11T17:11:12Z
dc.date.issued2017-04-01
dc.identifierPharmacogenomics, v. 18, n. 6, p. 571-583, 2017.
dc.identifier1744-8042
dc.identifier1462-2416
dc.identifierhttp://hdl.handle.net/11449/174457
dc.identifier10.2217/pgs-2016-0198
dc.identifier2-s2.0-85017404286
dc.description.abstractPre-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.
dc.languageeng
dc.relationPharmacogenomics
dc.relation0,845
dc.rightsAcesso restrito
dc.sourceScopus
dc.subjectantihypertensive therapy
dc.subjectgenotypes
dc.subjectgestational hypertension
dc.subjecthaplotypes
dc.subjectpharmacogenetics
dc.subjectpharmacogenomics
dc.subjectpolymorphisms
dc.subjectpre-eclampsia
dc.titlePharmacogenetics in the treatment of pre-eclampsia: Current findings, challenges and perspectives
dc.typeOtros


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