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在 LDL-C 水平≥190mg/dL 的韩国患者中,他汀类药物用于一级预防的疗效、安全性和临床结局:一项回顾性队列研究。

Efficacy, safety and clinical outcome associated with statin use for primary prevention in Korean patients with low-density lipoprotein cholesterol level ≥ 190 mg/dL: A retrospective cohort study.

机构信息

Division of Cardiology, Department of Internal Medicine, Boramae Medical Center, Seoul National University College of Medicine, Seoul, Korea.

出版信息

PLoS One. 2023 Jun 12;18(6):e0280586. doi: 10.1371/journal.pone.0280586. eCollection 2023.

DOI:10.1371/journal.pone.0280586
PMID:37307267
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10259785/
Abstract

BACKGROUND

Although the current guideline recommends the use of high-intensity statin to reduce the low-density lipoprotein cholesterol (LDL-C) level by 50% in patients with baseline value of ≥ 190 mg/dL, direct application of this recommendation to Asian populations is still questionable. This study was performed to investigate the statin response of LDL-C in Korean patients with LDL-C ≥ 190 mg/dL.

METHODS

A total of 1,075 Korean patients (age 60.7 ± 12.2 years, women 68%) with baseline LDL-C ≥ 190 mg/dL without cardiovascular disease was retrospectively reviewed. Lipid profiles at 6 months, side effects and clinical outcomes during the follow-up period after statin treatment were assessed according to statin intensity.

RESULTS

Most of the patients (76.3%) were treated with moderate-intensity statins, 11.4% with high-intensity statins, and 12.3% with a statin + ezetimibe. The reductions in LDL-C percentage at 6 months were 48.0%, 56.0% and 53.3% in patients treated with moderate-intensity statins, high-intensity statins and statin + ezetimibe, respectively (P < 0.001). Side effects requiring dose reduction, medication switch or drug interruption were observed in 1.3%, 4.9% and 2.3% of patients treated with moderate-intensity statin, high-intensity statin and statin + ezetimibe, respectively (P = 0.024). During the median follow-duration of 815 days (interquartile range, 408-1,361 days), the incidences of cardiovascular events were not different among the 3 groups (log-rank P = 0.823).

CONCLUSIONS

Compared to high-intensity statin, moderate-intensity statin was effective enough in reaching target goal of LDL-C without increase in cardiovascular risk and with fewer side effects in Korean patients with LDL-C ≥ 190 mg/dL.

摘要

背景

尽管目前的指南建议在基线值≥190mg/dL的患者中使用高强度他汀类药物将低密度脂蛋白胆固醇(LDL-C)水平降低 50%,但直接将这一建议应用于亚洲人群仍存在疑问。本研究旨在探讨韩国 LDL-C≥190mg/dL 患者的 LDL-C 对他汀类药物的反应。

方法

回顾性分析了 1075 例 LDL-C≥190mg/dL 且无心血管疾病的韩国患者(年龄 60.7±12.2 岁,女性占 68%)的基线资料。根据他汀类药物强度评估他汀类药物治疗后 6 个月的血脂谱、副作用和随访期间的临床结局。

结果

大多数患者(76.3%)接受中等强度他汀类药物治疗,11.4%接受高强度他汀类药物治疗,12.3%接受他汀类药物+依折麦布治疗。接受中等强度他汀类药物、高强度他汀类药物和他汀类药物+依折麦布治疗的患者,6 个月时 LDL-C 百分比分别降低 48.0%、56.0%和 53.3%(P<0.001)。因副作用需要减少剂量、更换药物或中断药物治疗的患者分别占接受中等强度他汀类药物、高强度他汀类药物和他汀类药物+依折麦布治疗患者的 1.3%、4.9%和 2.3%(P=0.024)。在中位随访时间 815 天(四分位距,408-1361 天)期间,3 组患者的心血管事件发生率无差异(对数秩检验 P=0.823)。

结论

与高强度他汀类药物相比,中等强度他汀类药物在韩国 LDL-C≥190mg/dL 患者中同样有效,可达到 LDL-C 目标值,且心血管风险无增加,副作用更少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0630/10259785/64a41722fe35/pone.0280586.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0630/10259785/d0ee67ed8611/pone.0280586.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0630/10259785/32f6c3d3f4f4/pone.0280586.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0630/10259785/dceb4a0d4fc3/pone.0280586.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0630/10259785/64a41722fe35/pone.0280586.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0630/10259785/d0ee67ed8611/pone.0280586.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0630/10259785/32f6c3d3f4f4/pone.0280586.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0630/10259785/dceb4a0d4fc3/pone.0280586.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0630/10259785/64a41722fe35/pone.0280586.g004.jpg

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