Division of Endocrinology and Metabolism, Li Ka Shing Knowledge Institute of St. Michael's Hospital, University of Toronto, Toronto, Ontario, Canada
Division of Endocrinology and Metabolism, Li Ka Shing Knowledge Institute of St. Michael's Hospital, University of Toronto, Toronto, Ontario, Canada.
Diabetes Care. 2019 Jan;42(1):173-176. doi: 10.2337/dc18-1491. Epub 2018 Nov 28.
To evaluate the efficacy and safety of inclisiran by diabetes status.
ORION-1 (ClinicalTrials.gov, NCT02597127) randomized 501 subjects with atherosclerotic cardiovascular disease (ASCVD) or ASCVD risk equivalents and high LDL cholesterol (LDL-C), despite maximally tolerated LDL-C-lowering therapies, to one or two doses of placebo or inclisiran. Levels of lipids and proprotein convertase subtilisin/kexin type 9 (PCSK9) at baseline and day 180 were compared.
Inclisiran was associated with marked declines in LDL-C (median -28% to -52%, < 0.0001 and -28% to -55%, < 0.005 for all doses in the without- and with-diabetes groups, respectively) and PCSK9. The inclisiran-treated groups also had lower apolipoprotein B, non-HDL cholesterol, and lipoprotein(a) but higher HDL cholesterol. Inclisiran had an adverse profile similar to that of placebo, and adverse events were proportionally balanced in the baseline with- and without-diabetes groups.
PCSK9-targeted siRNA-driven strategies may provide a novel therapeutic option for managing dyslipidemia in the presence and absence of diabetes.
评估依洛尤单抗依糖尿病状态的疗效和安全性。
ORION-1(ClinicalTrials.gov,NCT02597127)将 501 例患有动脉粥样硬化性心血管疾病(ASCVD)或 ASCVD 风险等同物和高 LDL 胆固醇(LDL-C)的患者随机分为一组或两组,分别接受安慰剂或依洛尤单抗治疗。比较基线和 180 天时的血脂和前蛋白转化酶枯草溶菌素/凝血酶 9(PCSK9)水平。
依洛尤单抗可显著降低 LDL-C(无糖尿病和有糖尿病组的所有剂量中位数分别为-28%至-52%,<0.0001 和-28%至-55%,均<0.005)和 PCSK9。依洛尤单抗治疗组的载脂蛋白 B、非 HDL 胆固醇和脂蛋白(a)也较低,但 HDL 胆固醇较高。依洛尤单抗的不良事件谱与安慰剂相似,且基线时伴或不伴糖尿病的两组间不良反应比例平衡。
PCSK9 靶向 siRNA 驱动的策略可能为伴有或不伴有糖尿病的血脂异常管理提供一种新的治疗选择。