José Javier Gómez-Barrado, Paula Gómez-Turégano, María Beltrán Moreno, Ana Isabel Fernández-Chamorro, Benjamín Roque Rodríguez, Zineb Kounka
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The association of Lp(a) >50 mg/dL with achievement of LDL-C targets was assessed by logistic regression analysis.</div></div><div><h3>Results</h3><div>The prevalence of Lp(a) >50 mg/dL was 30.8%. Patients with Lp(a) >50 mg/dL had higher baseline (142.30 ± 47.54 mg/dL vs 130.47 ± 40.75 mg/dL; p = 0.0001) and current (72.91 ± 26.44 mg/dL vs 64.72 ± 25.30 mg/dL; p = 0.0001), despite the fact that they were treated with more high-potency statins (77.2% vs 70.9%; p = 0.058) and more combination lipid-lowering therapy (LLT) (37.7% vs 25.7%; p = 0.001). The proportion of patients achieving target LDL-C was lower in those with Lp(a) >50 mg/dL. Independent predictors of having elevated Lp(a) levels >50 mg/dL were the use of high-potency statins (OR 1.5; 95% CI 1.08−2.14), combination LLT with ezetimibe (OR 2.0; 95% CI 1.45−2.73) and failure to achieve a LDL-C ≤55 mg/dL (OR 2.3; 95% CI 1.63−3.23).</div></div><div><h3>Conclusions</h3><div>Elevated Lp(a) levels influence LDL-C levels and hinder the achievement of targets in patients at very high cardiovascular risk. New drugs that act directly on Lp(a) are needed in these patients.</div></div>","PeriodicalId":100263,"journal":{"name":"Clínica e Investigación en Arteriosclerosis (English Edition)","volume":"36 5","pages":"Pages 278-285"},"PeriodicalIF":0.0000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Lipoprotein (a) is a predictor of non-achievement of LDL-C goals in patients with chronic heart disease\",\"authors\":\"José Javier Gómez-Barrado, Paula Gómez-Turégano, María Beltrán Moreno, Ana Isabel Fernández-Chamorro, Benjamín Roque Rodríguez, Zineb Kounka\",\"doi\":\"10.1016/j.artere.2024.09.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction and objectives</h3><div>Lipoprotein (a) [Lp(a)] concentration influences serum low-density lipoprotein cholesterol (LDL-C) levels. How it influences the achievement of LDL-C targets established in the guidelines is not well studied. Our aim was to know the prevalence of elevated Lp(a) levels in patients with coronary artery disease (CAD), and to assess its influence on the achievement of LDL-C targets.</div></div><div><h3>Method</h3><div>We conducted a cross-sectional study in a Cardiology department in Spain. A total of 870 patients with stable CAD had their lipid profile determined, including Lp(a). Patients were stratified into two groups according to Lp(a) >50 mg/dL and Lp(a) ≤50 mg/dL. The association of Lp(a) >50 mg/dL with achievement of LDL-C targets was assessed by logistic regression analysis.</div></div><div><h3>Results</h3><div>The prevalence of Lp(a) >50 mg/dL was 30.8%. Patients with Lp(a) >50 mg/dL had higher baseline (142.30 ± 47.54 mg/dL vs 130.47 ± 40.75 mg/dL; p = 0.0001) and current (72.91 ± 26.44 mg/dL vs 64.72 ± 25.30 mg/dL; p = 0.0001), despite the fact that they were treated with more high-potency statins (77.2% vs 70.9%; p = 0.058) and more combination lipid-lowering therapy (LLT) (37.7% vs 25.7%; p = 0.001). The proportion of patients achieving target LDL-C was lower in those with Lp(a) >50 mg/dL. Independent predictors of having elevated Lp(a) levels >50 mg/dL were the use of high-potency statins (OR 1.5; 95% CI 1.08−2.14), combination LLT with ezetimibe (OR 2.0; 95% CI 1.45−2.73) and failure to achieve a LDL-C ≤55 mg/dL (OR 2.3; 95% CI 1.63−3.23).</div></div><div><h3>Conclusions</h3><div>Elevated Lp(a) levels influence LDL-C levels and hinder the achievement of targets in patients at very high cardiovascular risk. 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引用次数: 0
摘要
导言和目的脂蛋白(a)[Lp(a)]浓度影响血清低密度脂蛋白胆固醇(LDL-C)水平。它如何影响实现指南中规定的低密度脂蛋白胆固醇目标尚未得到充分研究。我们的目的是了解冠状动脉疾病(CAD)患者 Lp(a)水平升高的发生率,并评估其对实现低密度脂蛋白胆固醇目标的影响。共有 870 名稳定型冠状动脉疾病患者接受了包括脂蛋白(a)在内的血脂测定。根据脂蛋白(a)>50 毫克/分升和脂蛋白(a)≤50 毫克/分升将患者分为两组。结果 Lp(a) >50 mg/dL 的患病率为 30.8%。Lp(a) >50 mg/dL 患者的基线(142.30 ± 47.54 mg/dL vs 130.47 ± 40.75 mg/dL;p = 0.0001)和当前(72.91 ± 26.44 mg/dL vs 64.72 ± 25.30 mg/dL; p = 0.0001),尽管他们接受了更多的高效他汀类药物治疗(77.2% vs 70.9%; p = 0.058)和更多的联合降脂治疗(LLT)(37.7% vs 25.7%; p = 0.001)。Lp(a)为 50 mg/dL 的患者达到目标 LDL-C 的比例较低。Lp(a)水平升高>50 mg/dL的独立预测因素是使用高效他汀类药物(OR 1.5;95% CI 1.08-2.14)、与依折麦布联合LLT(OR 2.0;95% CI 1.45-2.73)以及未能达到低密度脂蛋白胆固醇目标值。结论Lp(a)水平升高会影响低密度脂蛋白胆固醇(LDL-C)水平,并阻碍心血管风险极高的患者达到目标。这些患者需要能直接作用于脂蛋白(a)的新药。
Lipoprotein (a) is a predictor of non-achievement of LDL-C goals in patients with chronic heart disease
Introduction and objectives
Lipoprotein (a) [Lp(a)] concentration influences serum low-density lipoprotein cholesterol (LDL-C) levels. How it influences the achievement of LDL-C targets established in the guidelines is not well studied. Our aim was to know the prevalence of elevated Lp(a) levels in patients with coronary artery disease (CAD), and to assess its influence on the achievement of LDL-C targets.
Method
We conducted a cross-sectional study in a Cardiology department in Spain. A total of 870 patients with stable CAD had their lipid profile determined, including Lp(a). Patients were stratified into two groups according to Lp(a) >50 mg/dL and Lp(a) ≤50 mg/dL. The association of Lp(a) >50 mg/dL with achievement of LDL-C targets was assessed by logistic regression analysis.
Results
The prevalence of Lp(a) >50 mg/dL was 30.8%. Patients with Lp(a) >50 mg/dL had higher baseline (142.30 ± 47.54 mg/dL vs 130.47 ± 40.75 mg/dL; p = 0.0001) and current (72.91 ± 26.44 mg/dL vs 64.72 ± 25.30 mg/dL; p = 0.0001), despite the fact that they were treated with more high-potency statins (77.2% vs 70.9%; p = 0.058) and more combination lipid-lowering therapy (LLT) (37.7% vs 25.7%; p = 0.001). The proportion of patients achieving target LDL-C was lower in those with Lp(a) >50 mg/dL. Independent predictors of having elevated Lp(a) levels >50 mg/dL were the use of high-potency statins (OR 1.5; 95% CI 1.08−2.14), combination LLT with ezetimibe (OR 2.0; 95% CI 1.45−2.73) and failure to achieve a LDL-C ≤55 mg/dL (OR 2.3; 95% CI 1.63−3.23).
Conclusions
Elevated Lp(a) levels influence LDL-C levels and hinder the achievement of targets in patients at very high cardiovascular risk. New drugs that act directly on Lp(a) are needed in these patients.