Saint Luke's Mid America Heart Institute and the University of Kanas City-Missouri, Kansas City, MO.
Saint Luke's Mid America Heart Institute and the University of Kanas City-Missouri, Kansas City, MO.
J Card Fail. 2021 Jul;27(7):812-815. doi: 10.1016/j.cardfail.2021.02.018. Epub 2021 Mar 20.
Statins are recommended in heart transplant patients, but are sometimes poorly tolerated. Alternative agents are often considered including proprotein convertase subtilisin/kexin type-9 inhibitors (PCSK9i). We sought to investigate the use of PCSK9i after heart transplantation.
We identified patients who received a heart transplant from 1999 to 2019 and were started on PCSK9i at our institution. Clinical, laboratory, and coronary angiography with intravascular ultrasound results were compared. Among 65 patients initiated on PCSK9i (48 for statin intolerance and 17 for refractory hyperlipidemia), the median time from transplant was 5.5 years (interquartile range [IQR], 2.8-9.9 years) with a median PCSK9 treatment duration of 1.6 years (IQR, 0.8-3.2 years) and 80% still on treatment. Evolocumab was used in 73.8%, alirocumab in 12.3%, and both in 13.8% owing to insurance coverage. All patients required prior authorization; initial denial occurred in 18.5% and 32.3% had denials in subsequent years. The median low-density lipoprotein cholesterol decreased from 130 mg/dL (IQR, 102-148 mg/dL) to 55 mg/dL (IQR, 35-74 mg/dL) after starting PCSK9i (P < .001), with 72% of patients achieving a low-density lipoprotein cholesterol of <70 mg/dL after treatment. There were also significant reductions of total cholesterol, non-high-density lipoprotein cholesterol, total/high-density lipoprotein cholesterol ratio, and triglycerides, with a modest increase in high-density lipoprotein cholesterol. These changes were durable at latest follow-up. In 33 patients with serial coronary angiography and intravascular ultrasound, PCSK9i were associated with stable coronary plaque thickness and lumen area.
Among heart transplant recipients, PCSK9i are effective in lowering cholesterol levels and stabilizing coronary intimal hyperplasia with minimal side effects. Despite favorable effects, access and affordability remain a challenge.
他汀类药物被推荐用于心脏移植患者,但有时耐受性较差。通常会考虑使用其他药物,包括前蛋白转化酶枯草溶菌素/糜蛋白酶 9 抑制剂(PCSK9i)。我们旨在研究心脏移植后 PCSK9i 的使用情况。
我们确定了 1999 年至 2019 年在我院接受心脏移植并开始使用 PCSK9i 的患者。比较了临床、实验室和冠状动脉造影及血管内超声结果。在开始使用 PCSK9i 的 65 名患者中(48 名因他汀类药物不耐受,17 名因难治性高脂血症),移植后中位时间为 5.5 年(四分位距 [IQR],2.8-9.9 年),中位 PCSK9 治疗时间为 1.6 年(IQR,0.8-3.2 年),80%仍在接受治疗。依洛尤单抗的使用率为 73.8%,阿利鲁单抗为 12.3%,由于保险覆盖,两种药物的使用率均为 13.8%。所有患者均需要事先授权;初始拒绝率为 18.5%,随后几年的拒绝率为 32.3%。开始使用 PCSK9i 后,低密度脂蛋白胆固醇中位数从 130mg/dL(IQR,102-148mg/dL)降至 55mg/dL(IQR,35-74mg/dL)(P<0.001),治疗后 72%的患者达到低密度脂蛋白胆固醇<70mg/dL。总胆固醇、非高密度脂蛋白胆固醇、总/高密度脂蛋白胆固醇比值和甘油三酯也显著降低,高密度脂蛋白胆固醇略有增加。在最新随访时,这些变化仍然持久。在 33 名接受连续冠状动脉造影和血管内超声检查的患者中,PCSK9i 与稳定的冠状动脉斑块厚度和管腔面积有关。
在心脏移植受者中,PCSK9i 可有效降低胆固醇水平并稳定冠状动脉内膜增生,副作用极小。尽管效果良好,但获取途径和可负担性仍是一个挑战。