Elevated lipoprotein(a) and adverse pregnancy outcomes.

IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL
Annals of Medicine and Surgery Pub Date : 2026-09-10 eCollection Date: 2026-10-01 DOI:10.1097/MS9.0000000000005411
Ugochukwu Ebubechukwu, Toluwalase Awoyemi, Onyinye Ugoala, Ike Kendra Bolakale-Rufai, Valentine C Nriagu, Chukwuemelie Okeke, Chukwuebuka Stanley Asogwa, Queen Ugochinyere Alu, Oluwaremilekun Tolu-Akinnawo, Emmanuel Daniel, Christabel Uche-Orji, Oluwaseun Adeleke, Anandita Agarwala, Lynn M Yee
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Abstract

Lipoprotein(a) [Lp(a)] is gaining attention as a potential marker for adverse pregnancy outcomes, in addition to its well-established role in cardiovascular disease. This review explores the evolving understanding of Lp(a) in pregnancy, focusing on its links to hypertensive disorders of pregnancy, gestational diabetes mellitus, fetal growth restriction, and preterm birth, while also addressing diagnostic and management challenges. During pregnancy, Lp(a) levels rise substantially, nearly doubling between weeks 10 and 35. Although this increase is universal, its clinical implications are unclear. Lp(a) exerts pro-inflammatory, pro-thrombotic, and pro-atherogenic effects, the mechanisms of which are discussed in detail in the body of this review. However, research into Lp(a)'s specific role in increasing the risk of adverse pregnancy outcomes, such as hypertensive disorders of pregnancy, has produced mixed results, highlighting the need for further investigation. Routine screening for Lp(a) during pregnancy is not standard practice, though some experts suggest that it could be beneficial, particularly for high-risk pregnant people. Similar to managing other cardiovascular disease risk factors, managing elevated Lp(a) during pregnancy requires a comprehensive approach, from preconception counseling to lifestyle adjustments such as improving diet, increasing physical activity, and quitting smoking. Pharmacological options like statins and proprotein convertase subtilisin/kexin type 9 inhibitors have shown promise in non-pregnant populations, but their safety during pregnancy remains a concern, limiting their use. Further research is needed to clarify Lp(a)'s role in adverse pregnancy outcomes and to identify safe, effective treatments for managing elevated Lp(a) levels before and during pregnancy.

脂蛋白升高(a)和不良妊娠结局。
脂蛋白(a) [Lp(a)]作为不良妊娠结局的潜在标记物越来越受到关注,除了在心血管疾病中具有公认的作用。这篇综述探讨了对妊娠期Lp(a)的不断发展的认识,重点关注其与妊娠期高血压疾病、妊娠期糖尿病、胎儿生长受限和早产的联系,同时也解决了诊断和管理方面的挑战。在怀孕期间,Lp(a)水平大幅上升,在第10周至35周之间几乎翻了一番。虽然这种增加是普遍的,但其临床意义尚不清楚。Lp(a)具有促炎症、促血栓形成和促动脉粥样硬化作用,其机制将在本文正文中详细讨论。然而,对Lp(a)在增加妊娠不良结局(如妊娠高血压疾病)风险中的具体作用的研究产生了不同的结果,强调了进一步研究的必要性。妊娠期常规筛查Lp(a)不是标准做法,尽管一些专家认为这可能是有益的,特别是对高危孕妇。与控制其他心血管疾病风险因素类似,控制妊娠期Lp(a)升高需要综合方法,从孕前咨询到生活方式调整,如改善饮食、增加体育活动和戒烟。他汀类药物和蛋白转化酶枯草杆菌素/kexin 9型抑制剂等药物选择在非怀孕人群中显示出希望,但它们在怀孕期间的安全性仍然是一个问题,限制了它们的使用。需要进一步的研究来阐明Lp(a)在不良妊娠结局中的作用,并确定安全、有效的治疗方法来控制妊娠前和妊娠期间Lp(a)水平升高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Annals of Medicine and Surgery
Annals of Medicine and Surgery MEDICINE, GENERAL & INTERNAL-
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5.90%
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1665
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