Bhatia Harpreet S, Dweck Marc R, Craig Neil, Capoulade Romain, Pibarot Philippe, Trainor Patrick J, Whelton Seamus P, Rikhi Rishi, Lidani Karita C F, Post Wendy S, Tsai Michael Y, Criqui Michael H, Shapiro Michael D, Budoff Matthew J, DeFilippis Andrew P, Thanassoulis George, Tsimikas Sotirios
Division of Cardiology, Department of Medicine, University of California-San Diego, La Jolla, California, USA.
Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, United Kingdom.
J Am Coll Cardiol. 2024 Dec 17;84(25):2430-2441. doi: 10.1016/j.jacc.2024.08.070. Epub 2024 Nov 15.
BACKGROUND: Oxidized phospholipids (OxPLs) are carried by apolipoprotein B-100-containing lipoproteins (OxPL-apoB) including lipoprotein(a) (Lp[a]). Both OxPL-apoB and Lp(a) have been associated with calcific aortic valve disease (CAVD). OBJECTIVES: This study aimed to evaluate the associations between OxPL-apoB, Lp(a) and the prevalence, incidence, and progression of CAVD. METHODS: OxPL-apoB and Lp(a) were evaluated in MESA (Multi-Ethnic Study of Atherosclerosis) and a participant-level meta-analysis of 4 randomized trials of participants with established aortic stenosis (AS). In MESA, the association of OxPL-apoB and Lp(a) with aortic valve calcium (AVC) at baseline and 9.5 years was evaluated using multivariable ordinal regression models. In the meta-analysis, the association between OxPL-apoB and Lp(a) with AS progression (annualized change in peak aortic valve jet velocity) was evaluated using multivariable linear regression models. RESULTS: In MESA, both OxPL-apoB and Lp(a) were associated with prevalent AVC (OR per SD: 1.19 [95% CI: 1.07-1.32] and 1.13 [95% CI: 1.01-1.27], respectively) with a significant interaction between the two (P < 0.01). Both OxPL-apoB and Lp(a) were associated with incident AVC at 9.5 years when evaluated individually (interaction P < 0.01). The OxPL-apoB∗Lp(a) interaction demonstrated higher odds of prevalent and incident AVC for OxPL-apoB with increasing Lp(a) levels. In the meta-analysis, when analyzed separately, both OxPL-apoB and Lp(a) were associated with faster increase in peak aortic valve jet velocity, but when evaluated together, only OxPL-apoB remained significant (ß: 0.07; 95% CI: 0.01-0.12). CONCLUSIONS: OxPL-apoB is a predictor of the presence, incidence, and progression of AVC and established AS, particularly in the setting of elevated Lp(a) levels, and may represent a novel therapeutic target for CAVD.
背景:氧化磷脂(OxPLs)由含载脂蛋白B - 100的脂蛋白(OxPL - apoB)携带,包括脂蛋白(a) [Lp(a)]。OxPL - apoB和Lp(a)均与钙化性主动脉瓣疾病(CAVD)相关。 目的:本研究旨在评估OxPL - apoB、Lp(a)与CAVD的患病率、发病率及病情进展之间的关联。 方法:在动脉粥样硬化多族裔研究(MESA)以及一项针对已确诊主动脉瓣狭窄(AS)参与者的4项随机试验的参与者水平荟萃分析中评估OxPL - apoB和Lp(a)。在MESA中,使用多变量有序回归模型评估基线时及9.5年后OxPL - apoB和Lp(a)与主动脉瓣钙化(AVC)的关联。在荟萃分析中,使用多变量线性回归模型评估OxPL - apoB和Lp(a)与AS进展(主动脉瓣峰值射流速度的年化变化)之间的关联。 结果:在MESA中,OxPL - apoB和Lp(a)均与AVC患病率相关(每标准差的OR:分别为1.19 [95%CI:1.07 - 1.32]和1.13 [95%CI:1.01 - 1.27]),二者之间存在显著交互作用(P < 0.01)。单独评估时,OxPL - apoB和Lp(a)均与9.5年后的AVC发病率相关(交互作用P < 0.01)。OxPL - apoB∗Lp(a)交互作用表明,随着Lp(a)水平升高,OxPL - apoB的AVC患病率和发病率几率更高。在荟萃分析中,单独分析时,OxPL - apoB和Lp(a)均与主动脉瓣峰值射流速度的更快增加相关,但共同评估时,只有OxPL - apoB仍具有显著性(ß:0.07;95%CI:0.01 - 0.12)。 结论:OxPL - apoB是AVC存在、发病及进展以及已确诊AS的预测指标,尤其是在Lp(a)水平升高的情况下,可能代表CAVD的一个新治疗靶点。
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