{"title":"在接受三联降脂治疗的急性冠状动脉综合征患者中,脂蛋白(a)水平升高减缓了LDL-C的降低","authors":"Jaibharat Sharma MD, Surender Himral MD, Roshan Thakur MD, Raman Puri MD, Pankaj Chandel, Komal Mohite, Aziz Khan MD, Rajeev Agarwala MD, Vinod Vijan MD, Kunal Mahajan MD","doi":"10.1016/j.jacl.2025.04.018","DOIUrl":null,"url":null,"abstract":"<div><h3>Background/Synopsis</h3><div>Elevated lipoprotein(a) [Lp(a)] is recognized as an independent risk factor for adverse outcomes in coronary artery disease patients. Research on Lp(a) reduction in acute coronary syndrome (ACS) is ongoing. The standard of care for ACS includes high-intensity statins (HIS), which can paradoxically increase Lp(a) levels. While ezetimibe and PCSK9 inhibitors reduce Lp(a), bempedoic acid (BA) shows minimal effect. Limited data exist regarding the impact of elevated Lp(a) (50 mg/dL or higher) on LDL-C lowering in ACS patients undergoing aggressive lipid-lowering therapy (LLT).</div></div><div><h3>Objective/Purpose</h3><div>To evaluate changes in Lp(a) levels and their association with LDL-C lowering response in ACS patients treated with a triple combination of 40 mg rosuvastatin, ezetimibe, and BA (REB regimen).</div></div><div><h3>Methods</h3><div>We retrospectively analyzed data from statin-naive ACS patients at our center who received the REB regimen between March 2023 and December 2024. Only patients with consistent LLT for one month and available Lp(a) and LDL-C levels at index ACS admission and one-month post-ACS were included. We assessed the impact of changes in Lp(a) levels, particularly those exceeding 50 mg/dL, on mean LDL-C reduction and the percentage of patients achieving the LDL-C target of < 50 mg/dL.</div></div><div><h3>Results</h3><div>Data from 303 patients were analyzed. Mean LDL-C at admission was 111.8 ± 34.6 mg/dL, decreasing to 44.7 ± 15.9 mg/dL at one month(60% reduction). 70.3% (213/303) of patients achieved LDL-C < 50 mg/dL at one month. Median Lp(a) increased from 28.1 mg/dL at admission to 64.6 mg/dL at one month. The prevalence of Lp(a) 50 mg/dL or higher was 28.7% at admission and 60.4% at one month. Logistic regression analysis indicated that an increase in Lp(a) was associated with a decreased probability of achieving LDL-C < 50 mg/dL at one month [Odds ratio=0.98(0.97-0.99), p<0.01]. The mean LDL-C achieved at one month was significantly higher in patients with elevated Lp(a) 50 mg/dL or higher, both at admission (54.3 ± 16.7 vs 40.9 ± 13.8, p < 0.001) and at one month (48.7 ± 16.1 vs 38.5 ± 13.3, p < 0.001).</div></div><div><h3>Conclusions</h3><div>In ACS patients treated with aggressive LDL-C lowering therapy, elevated Lp(a) levels are associated with a blunted LDL-C response. The increase in Lp(a) during aggressive LDL-C lowering may hinder optimal LDL-C targets. These findings highlight the need for Lp(a) monitoring in ACS patients and suggest that Lp(a)-lowering therapies may optimize cardiovascular risk reduction. Further research is needed to evaluate the clinical impact of Lp(a)-lowering strategies in patients undergoing aggressive LDL-C management post-ACS.</div></div>","PeriodicalId":15392,"journal":{"name":"Journal of clinical lipidology","volume":"19 3","pages":"Page e13"},"PeriodicalIF":3.6000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Elevated lipoprotein(a) levels attenuate LDL-C lowering in acute coronary syndrome patients treated with triple combination lipid-lowering therapy\",\"authors\":\"Jaibharat Sharma MD, Surender Himral MD, Roshan Thakur MD, Raman Puri MD, Pankaj Chandel, Komal Mohite, Aziz Khan MD, Rajeev Agarwala MD, Vinod Vijan MD, Kunal Mahajan MD\",\"doi\":\"10.1016/j.jacl.2025.04.018\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background/Synopsis</h3><div>Elevated lipoprotein(a) [Lp(a)] is recognized as an independent risk factor for adverse outcomes in coronary artery disease patients. Research on Lp(a) reduction in acute coronary syndrome (ACS) is ongoing. The standard of care for ACS includes high-intensity statins (HIS), which can paradoxically increase Lp(a) levels. While ezetimibe and PCSK9 inhibitors reduce Lp(a), bempedoic acid (BA) shows minimal effect. Limited data exist regarding the impact of elevated Lp(a) (50 mg/dL or higher) on LDL-C lowering in ACS patients undergoing aggressive lipid-lowering therapy (LLT).</div></div><div><h3>Objective/Purpose</h3><div>To evaluate changes in Lp(a) levels and their association with LDL-C lowering response in ACS patients treated with a triple combination of 40 mg rosuvastatin, ezetimibe, and BA (REB regimen).</div></div><div><h3>Methods</h3><div>We retrospectively analyzed data from statin-naive ACS patients at our center who received the REB regimen between March 2023 and December 2024. Only patients with consistent LLT for one month and available Lp(a) and LDL-C levels at index ACS admission and one-month post-ACS were included. We assessed the impact of changes in Lp(a) levels, particularly those exceeding 50 mg/dL, on mean LDL-C reduction and the percentage of patients achieving the LDL-C target of < 50 mg/dL.</div></div><div><h3>Results</h3><div>Data from 303 patients were analyzed. Mean LDL-C at admission was 111.8 ± 34.6 mg/dL, decreasing to 44.7 ± 15.9 mg/dL at one month(60% reduction). 70.3% (213/303) of patients achieved LDL-C < 50 mg/dL at one month. Median Lp(a) increased from 28.1 mg/dL at admission to 64.6 mg/dL at one month. The prevalence of Lp(a) 50 mg/dL or higher was 28.7% at admission and 60.4% at one month. Logistic regression analysis indicated that an increase in Lp(a) was associated with a decreased probability of achieving LDL-C < 50 mg/dL at one month [Odds ratio=0.98(0.97-0.99), p<0.01]. The mean LDL-C achieved at one month was significantly higher in patients with elevated Lp(a) 50 mg/dL or higher, both at admission (54.3 ± 16.7 vs 40.9 ± 13.8, p < 0.001) and at one month (48.7 ± 16.1 vs 38.5 ± 13.3, p < 0.001).</div></div><div><h3>Conclusions</h3><div>In ACS patients treated with aggressive LDL-C lowering therapy, elevated Lp(a) levels are associated with a blunted LDL-C response. The increase in Lp(a) during aggressive LDL-C lowering may hinder optimal LDL-C targets. These findings highlight the need for Lp(a) monitoring in ACS patients and suggest that Lp(a)-lowering therapies may optimize cardiovascular risk reduction. Further research is needed to evaluate the clinical impact of Lp(a)-lowering strategies in patients undergoing aggressive LDL-C management post-ACS.</div></div>\",\"PeriodicalId\":15392,\"journal\":{\"name\":\"Journal of clinical lipidology\",\"volume\":\"19 3\",\"pages\":\"Page e13\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2025-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of clinical lipidology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1933287425000947\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of clinical lipidology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1933287425000947","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
Elevated lipoprotein(a) levels attenuate LDL-C lowering in acute coronary syndrome patients treated with triple combination lipid-lowering therapy
Background/Synopsis
Elevated lipoprotein(a) [Lp(a)] is recognized as an independent risk factor for adverse outcomes in coronary artery disease patients. Research on Lp(a) reduction in acute coronary syndrome (ACS) is ongoing. The standard of care for ACS includes high-intensity statins (HIS), which can paradoxically increase Lp(a) levels. While ezetimibe and PCSK9 inhibitors reduce Lp(a), bempedoic acid (BA) shows minimal effect. Limited data exist regarding the impact of elevated Lp(a) (50 mg/dL or higher) on LDL-C lowering in ACS patients undergoing aggressive lipid-lowering therapy (LLT).
Objective/Purpose
To evaluate changes in Lp(a) levels and their association with LDL-C lowering response in ACS patients treated with a triple combination of 40 mg rosuvastatin, ezetimibe, and BA (REB regimen).
Methods
We retrospectively analyzed data from statin-naive ACS patients at our center who received the REB regimen between March 2023 and December 2024. Only patients with consistent LLT for one month and available Lp(a) and LDL-C levels at index ACS admission and one-month post-ACS were included. We assessed the impact of changes in Lp(a) levels, particularly those exceeding 50 mg/dL, on mean LDL-C reduction and the percentage of patients achieving the LDL-C target of < 50 mg/dL.
Results
Data from 303 patients were analyzed. Mean LDL-C at admission was 111.8 ± 34.6 mg/dL, decreasing to 44.7 ± 15.9 mg/dL at one month(60% reduction). 70.3% (213/303) of patients achieved LDL-C < 50 mg/dL at one month. Median Lp(a) increased from 28.1 mg/dL at admission to 64.6 mg/dL at one month. The prevalence of Lp(a) 50 mg/dL or higher was 28.7% at admission and 60.4% at one month. Logistic regression analysis indicated that an increase in Lp(a) was associated with a decreased probability of achieving LDL-C < 50 mg/dL at one month [Odds ratio=0.98(0.97-0.99), p<0.01]. The mean LDL-C achieved at one month was significantly higher in patients with elevated Lp(a) 50 mg/dL or higher, both at admission (54.3 ± 16.7 vs 40.9 ± 13.8, p < 0.001) and at one month (48.7 ± 16.1 vs 38.5 ± 13.3, p < 0.001).
Conclusions
In ACS patients treated with aggressive LDL-C lowering therapy, elevated Lp(a) levels are associated with a blunted LDL-C response. The increase in Lp(a) during aggressive LDL-C lowering may hinder optimal LDL-C targets. These findings highlight the need for Lp(a) monitoring in ACS patients and suggest that Lp(a)-lowering therapies may optimize cardiovascular risk reduction. Further research is needed to evaluate the clinical impact of Lp(a)-lowering strategies in patients undergoing aggressive LDL-C management post-ACS.
期刊介绍:
Because the scope of clinical lipidology is broad, the topics addressed by the Journal are equally diverse. Typical articles explore lipidology as it is practiced in the treatment setting, recent developments in pharmacological research, reports of treatment and trials, case studies, the impact of lifestyle modification, and similar academic material of interest to the practitioner.
Sections of Journal of clinical lipidology will address pioneering studies and the clinicians who conduct them, case studies, ethical standards and conduct, professional guidance such as ATP and NCEP, editorial commentary, letters from readers, National Lipid Association (NLA) news and upcoming event information, as well as abstracts from the NLA annual scientific sessions and the scientific forums held by its chapters, when appropriate.