Suppr超能文献

洛美他派在纯合子家族性高胆固醇血症中的疗效和安全性:泛欧回顾性观察研究。

Efficacy and safety of lomitapide in homozygous familial hypercholesterolaemia: the pan-European retrospective observational study.

机构信息

Department of Translational and Precision Medicine, Sapienza University of Rome, Viale dell'Università 35, 00161, Rome, Italy.

Department of Internal Medicine, Erasmus MC, University Medical Centre Rotterdam, Doctor Molewaterplein 40, 3015 GD Rotterdam, the Netherlands.

出版信息

Eur J Prev Cardiol. 2022 May 5;29(5):832-841. doi: 10.1093/eurjpc/zwab229.

Abstract

AIMS

Lomitapide is a lipid-lowering agent indicated as an adjunct therapy for adult homozygous familial hypercholesterolaemia (HoFH). This study evaluated the medium-term effectiveness and safety of lomitapide in a large cohort of HoFH patients in Europe.

METHODS AND RESULTS

In a multicentre retrospective, observational study including 75 HoFH patients treated with lomitapide in a real-world clinical setting from 9 European countries, low-density lipoprotein cholesterol (LDL-C) changes, adverse events (AEs), and major adverse cardiovascular events (MACE) were assessed. After a median 19 months (interquartile range 11-41 months) of treatment with a mean dosage of 20 mg of lomitapide. Low-density lipoprotein cholesterol decreased by 60%, from baseline 280.5 mg/dL (191.8-405.0 mg/dL) to 121.6 mg/dL (61.0-190.5 mg/dL). At the last visit, 32.0% of patients achieved LDL-C <100 mg/dL and 18.7% <70 mg/dL. At baseline, 38 HoFH patients were receiving LDL apheresis (LA), but after initiation of lomitapide 36.8% of patients discontinued LA. During follow-up, lomitapide was permanently interrupted in 13% of patients. Gastrointestinal AEs occurred in 40% and liver transaminases increased (3-5 × upper limits of normal) in 13% of patients. Among patients with liver ultrasound evaluation (n = 45), a modest increase in hepatic steatosis was noted during treatment; however, liver stiffness measured by elastography in 30 of them remained within the normal range. Among HoFH patients exposed to lomitapide for at least 2 years, MACE incident rate was 7.4 per 1000 person-years in the 2 years after as compared to 21.2 per 1000 person-years before treatment with lomitapide.

CONCLUSION

In this medium-term real-world experience, lomitapide proved to be very effective in reducing LDL-C in HoFH. Gastrointestinal AEs were common, but liver safety was reassuring with no sign of increased risk of liver fibrosis. A signal of cardiovascular protection was also observed.

摘要

目的

洛美他派是一种降脂药物,适用于成人纯合子家族性高胆固醇血症(HoFH)的辅助治疗。本研究评估了洛美他派在欧洲大型 HoFH 患者队列中的中期疗效和安全性。

方法和结果

在一项多中心回顾性观察性研究中,纳入了 9 个欧洲国家的 75 名在真实临床环境中接受洛美他派治疗的 HoFH 患者,评估了低密度脂蛋白胆固醇(LDL-C)变化、不良事件(AE)和主要不良心血管事件(MACE)。在中位 19 个月(11-41 个月)的治疗后,平均使用 20mg 洛美他派,LDL-C 降低了 60%,从基线的 280.5mg/dL(191.8-405.0mg/dL)降至 121.6mg/dL(61.0-190.5mg/dL)。在最后一次就诊时,32.0%的患者 LDL-C<100mg/dL,18.7%的患者 LDL-C<70mg/dL。基线时有 38 名 HoFH 患者正在接受 LDL 吸附(LA)治疗,但在开始使用洛美他派后,36.8%的患者停止了 LA。在随访期间,13%的患者永久中断了洛美他派治疗。40%的患者出现胃肠道 AE,13%的患者肝转氨酶升高(3-5×正常值上限)。在接受肝脏超声评估的 45 名患者中,治疗期间注意到肝脂肪变性略有增加;然而,在其中 30 名患者中,通过弹性成像测量的肝硬度仍在正常范围内。在至少接受 2 年洛美他派治疗的 HoFH 患者中,治疗后 2 年内的 MACE 发生率为每 1000 人年 7.4 例,而治疗前为每 1000 人年 21.2 例。

结论

在这项中期真实世界研究中,洛美他派在降低 HoFH 患者的 LDL-C 方面非常有效。胃肠道 AE 常见,但肝脏安全性令人放心,没有肝纤维化风险增加的迹象。也观察到了心血管保护的信号。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验