Combined Use of Statin and PCSK9 Inhibitor in a Pregnant Woman with Possible Familial Hypercholesterolemia and Coronary Artery Stenosis.

IF 2.8 2区 医学 Q2 PERIPHERAL VASCULAR DISEASE
Yusaku Shimizu, Tae Yokouchi-Konishi, Chizuko Aoki-Kamiya, Mai Temukai, Kotaro Hizuka, Masami Sawada, Aiko Kakigano, Naoko Iwanaga, Takeshi Kanagawa, Kota Murai, Hisashi Makino, Jun Yoshimatsu
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Abstract

Although the risk of acute coronary syndrome increases during pregnancy and the postpartum period compared to the non-pregnant state, dyslipidemia-one of the key risk factors for atherosclerotic cardiovascular disease-is often undertreated in this population. Several lipid-lowering medications, including statin, have not been used due to concerns about their impact on the fetus. Herein, we report a pregnant woman with possible familial hypercholesterolemia (FH) and coronary artery stenosis, whose low-density lipoprotein cholesterol (LDL-C) level was managed by a combination of statin and proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor for the secondary prevention of coronary artery disease.A 37-year-old pregnant woman with dyslipidemia was found to have severe coronary artery stenosis. She was suspected of having FH, and her lipid control was initiated with the goal of lowering LDL-C levels to <100 mg/dL. Although ezetimibe and colestimide were administered at 14 weeks, the target LDL-C level was not achieved. Thus, treatment with pravastatin was started at 23 weeks and evolocumab at 32 weeks of gestation. With the combination of pravastatin and evolocumab, her LDL-C levels decreased to 67 mg/dL after 35 weeks of gestation. The patient delivered vaginally at 37 weeks of gestation without any cardiac events, and her baby did not present with any abnormalities. In conclusion, the combined use of statin and PCSK9 inhibitor could effectively manage LDL-C levels, and it might be a safe option during pregnancy. Nevertheless, further research is required to assess the safety and efficacy of this combination therapy during pregnancy.

他汀类药物和PCSK9抑制剂在可能有家族性高胆固醇血症和冠状动脉狭窄的孕妇中的联合应用
尽管与非妊娠期相比,妊娠期和产后急性冠状动脉综合征的风险增加,但血脂异常——动脉粥样硬化性心血管疾病的关键危险因素之一——在这一人群中往往得不到充分治疗。包括他汀类药物在内的几种降脂药物由于担心对胎儿的影响而未被使用。在此,我们报告了一名可能患有家族性高胆固醇血症(FH)和冠状动脉狭窄的孕妇,其低密度脂蛋白胆固醇(LDL-C)水平由他汀类药物和枯草杆菌蛋白转化酶/ keexin 9型(PCSK9)抑制剂联合控制,用于冠状动脉疾病的二级预防。一位37岁患有血脂异常的孕妇被发现有严重的冠状动脉狭窄。她被怀疑患有FH,并开始了脂质控制,目标是将LDL-C水平降低到<100 mg/dL。尽管在14周时给予依折麦比和colestimide,但未达到目标LDL-C水平。因此,普伐他汀治疗在妊娠23周开始,evolocumab治疗在妊娠32周开始。结合普伐他汀和evolocumab,她的LDL-C水平在妊娠35周后降至67 mg/dL。患者于妊娠37周顺产,无任何心脏事件,胎儿无任何异常。综上所述,他汀类药物联合PCSK9抑制剂可有效控制LDL-C水平,可能是妊娠期的安全选择。然而,需要进一步的研究来评估这种联合治疗在妊娠期间的安全性和有效性。
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来源期刊
CiteScore
6.60
自引率
15.90%
发文量
271
审稿时长
1 months
期刊介绍: JAT publishes articles focused on all aspects of research on atherosclerosis, vascular biology, thrombosis, lipid and metabolism.
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