Aleksova Natasha, Umar Fraz, Bernick Jordan, Mielniczuk Lisa M, Ross Heather J, Chih Sharon
Peter Munk Cardiac Centre, Toronto General Hospital, Toronto, Ontario, Canada.
Heart Failure and Transplantation, Division of Cardiology, University of Ottawa Heart Institute, Ottawa, Ontario, Canada.
CJC Open. 2021 Jul 16;3(12):1453-1462. doi: 10.1016/j.cjco.2021.07.011. eCollection 2021 Dec.
Unlike the relationship with atherosclerotic coronary artery disease, that between low-density lipoprotein cholesterol (LDL-C) and cardiac allograft vasculopathy (CAV) is unclear. Our objectives were to characterize lipid profiles early after heart transplantation (HT) and evaluate the relationship between early LDL-C and the development of CAV.
We retrospectively reviewed consecutive adults who underwent HT at 2 centres during the time period 2010-2018. The primary outcome was the incidence of angiographic CAV. The relationship between LDL-C and CAV was assessed using Cox proportional hazards and logistic regression models adjusted a priori for clinically important covariates, including recipient and donor age, recipient sex, ischemic time, and pre-HT diabetes.
A total of 386 patients followed for a median (range) of 4.4 (2.8-6.8) years were included. LDL-C at baseline (2.11 ± 0.86 mmol/L) and 1 year after HT (2.20 ± 0.88 mmol/L) was similar ( = 0.21), but it was lower at the end of follow-up (1.89 ± 0.74 mmol/L, < 0.01). Of 309 patients who underwent angiography, 54% had CAV. The risk of CAV did not vary according to baseline, 1-year, or change from baseline to 1-year LDL-C. The odds of CAV at 1 year were equally likely across LDL-C values (adjusted odds ratio 1.00, 95% confidence interval: 0.61-1.63 for baseline, and adjusted odds ratio 1.25, 95% confidence interval: 0.74-2.10 for 1-year LDL-C).
No association was identified between early LDL-C and the development of CAV. Our findings do not support targeting a specific LDL-C for patients who do not otherwise meet criteria for guideline-recommended LDL-C target levels. Randomized studies are warranted to determine if lipid-lowering to a specific LDL-C target level modifies the risk of CAV.
与动脉粥样硬化性冠状动脉疾病的关系不同,低密度脂蛋白胆固醇(LDL-C)与心脏移植血管病变(CAV)之间的关系尚不清楚。我们的目标是描述心脏移植(HT)后早期的血脂谱,并评估早期LDL-C与CAV发生之间的关系。
我们回顾性分析了2010年至2018年期间在2个中心接受HT的连续成年患者。主要结局是血管造影CAV的发生率。使用Cox比例风险模型和逻辑回归模型评估LDL-C与CAV之间的关系,这些模型事先针对临床重要协变量进行了调整,包括受者和供者年龄、受者性别、缺血时间和HT前糖尿病。
共纳入386例患者,中位(范围)随访时间为4.4(2.8 - 6.8)年。基线时(2.11±0.86 mmol/L)和HT后1年时(2.20±0.88 mmol/L)的LDL-C相似(P = 0.21),但随访结束时较低(1.89±0.74 mmol/L,P < 0.01)。在309例行血管造影的患者中,54%有CAV。CAV的风险并不因基线、1年时或从基线到1年时LDL-C的变化而不同。LDL-C各值在1年时发生CAV的几率相同(基线时调整后的优势比为1.00,95%置信区间:0.61 - 1.63;1年时LDL-C调整后的优势比为1.25,95%置信区间:0.74 - 2.10)。
未发现早期LDL-C与CAV发生之间存在关联。我们的研究结果不支持对未达到指南推荐LDL-C目标水平标准的患者设定特定的LDL-C目标值。有必要进行随机研究以确定将LDL-C降至特定目标水平是否会改变CAV的风险。