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他汀类药物联合依折麦布在脯氨酰肽酶枯草溶菌素/前蛋白转化酶 9 抑制剂时代。

Statins plus ezetimibe in the era of proprotein convertase subtilisin/ kexin type 9 inhibitors.

机构信息

Department of Cardiosciences, Division of Cardiology, Azienda Ospedaliera San Camillo­‑Forlanini, Rome, Italy.

Department of Pharmacological and Biomolecular Sciences, University of Milano, Milan, Italy; IRCCS Multimedica, Milan, Italy

出版信息

Kardiol Pol. 2020 Sep 25;78(9):850-860. doi: 10.33963/KP.15529. Epub 2020 Jul 24.

DOI:10.33963/KP.15529
PMID:32716152
Abstract

Statins are first‑line agents used in patients with dyslipidemia, which show established benefits in reducing low‑density lipoprotein cholesterol (LDL‑C) levels and decreasing the rate of cardiovascular events. However, a considerable number of patients on statins do not achieve target LDL‑C levels, even at maximally tolerated statin doses, or are intolerant to intensive statin therapy. These patients can benefit from the addition of a nonstatin lipid‑lowering agent, and recent cholesterol guidelines have put greater focus on combination lipid‑lowering therapy. In patients who cannot achieve target treatment goals with statin therapy alone, the addition of a cholesterol absorption inhibitor, ezetimibe, leads to further LDL‑C reduction with good tolerability and decreases cardiovascular morbidity and mortality. The more recent proprotein convertase subtilisin‑like / kexin type 9 (PCSK‑9) inhibitors can lower LDL‑C by additional 45% to 65% and are also well tolerated. These complementary approaches for LDL‑C lowering in patients treated with statins decrease LDL‑C levels more effectively than statin monotherapy. As no threshold level has been established below which LDL‑C lowering benefits disappear, the early application of a combination treatment strategy may lead to improved cardiovascular outcomes, particularly in high‑risk patients. This review examines the rationale, advantages, and potential barriers to combination lipid‑lowering therapy with reference to the current guideline recommendations.

摘要

他汀类药物是治疗血脂异常患者的一线药物,其降低 LDL-C 水平和减少心血管事件的作用已得到充分证实。然而,相当数量的他汀类药物使用者并未达到 LDL-C 目标水平,即使在最大耐受他汀类药物剂量下,或不耐受强化他汀类药物治疗。这些患者可以从添加非他汀类降脂药物中获益,最近的胆固醇指南更加关注联合降脂治疗。对于单独使用他汀类药物无法达到治疗目标的患者,添加胆固醇吸收抑制剂依折麦布可进一步降低 LDL-C,且耐受性良好,降低心血管发病率和死亡率。最近的前蛋白转化酶枯草溶菌素 9(PCSK9)抑制剂可使 LDL-C 进一步降低 45%至 65%,且耐受性良好。这些方法与他汀类药物联合使用,可更有效地降低 LDL-C 水平,优于单独使用他汀类药物。由于尚未确定 LDL-C 降低获益消失的下限,因此早期应用联合治疗策略可能会改善心血管结局,尤其是高危患者。本综述参考当前指南建议,探讨了联合降脂治疗的原理、优势和潜在障碍。

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