Independence of Lipoprotein(a) and Low-Density Lipoprotein Cholesterol-Mediated Cardiovascular Risk: A Participant-Level Meta-Analysis.

IF 5.2 3区 工程技术 Q2 ENERGY & FUELS Energy & Fuels Pub Date : 2024-11-04 DOI:10.1161/CIRCULATIONAHA.124.069556
Harpreet S Bhatia, Simon Wandel, Peter Willeit, Anastasia Lesogor, Keith Bailey, Paul M Ridker, Paul Nestel, John Simes, Andrew Tonkin, Gregory G Schwartz, Helen Colhoun, Christoph Wanner, Sotirios Tsimikas
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Abstract

Background: Low-density lipoprotein cholesterol (LDL-C) and lipoprotein(a) (Lp[a]) levels are independently associated with atherosclerotic cardiovascular disease (ASCVD). However, the relationship between Lp(a) level, LDL-C level, and ASCVD risk at different thresholds is not well defined.

Methods: A participant-level meta-analysis of 27 658 participants enrolled in 6 placebo-controlled statin trials was performed to assess the association of LDL-C and Lp(a) levels with risk of fatal or nonfatal coronary heart disease events, stroke, or any coronary or carotid revascularization (ASCVD). The multivariable-adjusted association between baseline Lp(a) level and ASCVD risk was modeled continuously using generalized additive models, and the association between baseline LDL-C level and ASCVD risk by baseline Lp(a) level by Cox proportional hazards models with random effects. The joint association between Lp(a) level and statin-achieved LDL-C level with ASCVD risk was evaluated using Cox proportional hazards models.

Results: Compared with an Lp(a) level of 5 mg/dL, increasing levels of Lp(a) were log-linearly associated with ASCVD risk in statin- and placebo-treated patients. Among statin-treated individuals, those with Lp(a) level >50 mg/dL (≈125 nmol/L) had increased risk across all quartiles of achieved LDL-C level and absolute change in LDL-C level. Even among those with the lowest quartile of achieved LDL-C level (3.1-77.0 mg/dL), those with Lp(a) level >50 mg/dL had greater ASCVD risk (hazard ratio, 1.38 [95% CI, 1.06-1.79]) than those with Lp(a) level ≤50 mg/dL. The greatest risk was observed with both Lp(a) level >50 mg/dL and LDL-C level in the fourth quartile (hazard ratio, 1.90 [95% CI, 1.46-2.48]).

Conclusions: These findings demonstrate the independent and additive nature of Lp(a) and LDL-C levels for ASCVD risk, and that LDL-C lowering does not fully offset Lp(a)-mediated risk.

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脂蛋白(a)和低密度脂蛋白胆固醇诱发心血管风险的独立性:一项参与者层面的 Meta 分析。
背景:低密度脂蛋白胆固醇(LDL-C)和脂蛋白(a)(Lp[a])水平与动脉粥样硬化性心血管疾病(ASCVD)密切相关。然而,在不同阈值下,脂蛋白(a)水平、低密度脂蛋白胆固醇(LDL-C)水平与 ASCVD 风险之间的关系尚未明确:对参加 6 项安慰剂对照他汀类药物试验的 27 658 名参与者进行了参与者水平的荟萃分析,以评估低密度脂蛋白胆固醇和脂蛋白(a)水平与致命或非致命冠心病事件、中风或任何冠状动脉或颈动脉血运重建(ASCVD)风险之间的关系。基线脂蛋白(a)水平与ASCVD风险之间的多变量调整关系采用广义加法模型进行连续建模,基线LDL-C水平与ASCVD风险之间的关系采用随机效应的Cox比例危险模型进行建模。使用Cox比例危险模型评估了Lp(a)水平和他汀类药物达到的LDL-C水平与ASCVD风险之间的共同关系:结果:与 5 mg/dL 的脂蛋白(a)水平相比,在他汀类药物和安慰剂治疗的患者中,脂蛋白(a)水平的升高与 ASCVD 风险呈对数线性关系。在他汀类药物治疗的患者中,Lp(a)水平>50 mg/dL(≈125 nmol/L)的患者在达到的 LDL-C 水平的所有四分位数和 LDL-C 水平的绝对变化中风险都会增加。即使在低密度脂蛋白胆固醇水平达到最低四分位数(3.1-77.0 mg/dL)的人群中,脂蛋白(a)水平>50 mg/dL的人群比脂蛋白(a)水平≤50 mg/dL的人群具有更大的ASCVD风险(危险比为1.38 [95% CI, 1.06-1.79])。Lp(a)水平>50 mg/dL和LDL-C水平处于第四四分位数的风险最大(危险比为1.90 [95% CI, 1.46-2.48]):这些研究结果表明,脂蛋白(a)和低密度脂蛋白胆固醇(LDL-C)水平对急性心血管疾病风险具有独立和叠加的性质,降低低密度脂蛋白胆固醇并不能完全抵消脂蛋白(a)介导的风险。
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来源期刊
Energy & Fuels
Energy & Fuels 工程技术-工程:化工
CiteScore
9.20
自引率
13.20%
发文量
1101
审稿时长
2.1 months
期刊介绍: Energy & Fuels publishes reports of research in the technical area defined by the intersection of the disciplines of chemistry and chemical engineering and the application domain of non-nuclear energy and fuels. This includes research directed at the formation of, exploration for, and production of fossil fuels and biomass; the properties and structure or molecular composition of both raw fuels and refined products; the chemistry involved in the processing and utilization of fuels; fuel cells and their applications; and the analytical and instrumental techniques used in investigations of the foregoing areas.
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