Dyslipidaemia management in pregnant patients: a 2024 update

Author:

Lewek Joanna12,Bielecka-Dąbrowa Agata12,Toth Peter P3,Banach Maciej1234ORCID

Affiliation:

1. Department of Preventive Cardiology and Lipidology, Medical University of Lodz (MUL) , Rzgowska 281/289, 93-338 Lodz , Poland

2. Department of Cardiology and Congenital Diseases of Adults, Polish Mother’s Memorial Hospital Research Institute (PMMHRI) , Rzgowska 281/289, 93-338 Lodz , Poland

3. The Ciccarone Center for the Prevention of Cardiovascular Disease, Johns Hopkins University School of Medicine , 600 N. Wolfe St, Carnegie 591, Baltimore, MD 21287 , USA

4. Cardiovascular Research Centre , Zyty 28, 65-417 Zielona Góra , Poland

Abstract

Abstract Over several decades, the approach to treating dyslipidaemias during pregnancy remains essentially unchanged. The lack of advancement in this field is mostly related to the fact that we lack clinical trials of pregnant patients both with available as well as new therapies. While there are numerous novel therapies developed for non-pregnant patients, there are still many limitations in dyslipidaemia treatment during pregnancy. Besides pharmacotherapy and careful clinical assessment, the initiation of behavioural modifications as well as pre-conception management is very important. Among the various lipid-lowering medications, bile acid sequestrants are the only ones officially approved for treating dyslipidaemia in pregnancy. Ezetimibe and fenofibrate can be considered if their benefits outweigh potential risks. Statins are still considered contraindicated, primarily due to animal studies and human case reports. However, recent systematic reviews and meta-analyses as well as data on familial hypercholesterolaemia (FH) in pregnant patients have indicated that their use may not be harmful and could even be beneficial in certain selected cases. This is especially relevant for pregnant patients at very high cardiovascular risk, such as those who have already experienced an acute cardiovascular event or have homozygous or severe forms of heterozygous FH. In these cases, the decision to continue therapy during pregnancy should weigh the potential risks of discontinuation. Bempedoic acid, olezarsen, evinacumab, evolocumab and alirocumab, and inclisiran are options to consider just before and after pregnancy is completed. In conclusion, decisions regarding lipid-lowering therapy for pregnant patients should be personalized. Despite the challenges in designing and conducting studies in pregnant women, there is a strong need to establish the safety and efficacy of dyslipidaemia treatment during pregnancy.

Publisher

Oxford University Press (OUP)

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