评价他汀类药物在血液透析患者中的应用:临床和安全性结果的回顾性分析。

IF 4.3 3区 医学 Q2 CHEMISTRY, MEDICINAL
Pharmaceuticals Pub Date : 2025-06-18 DOI:10.3390/ph18060911
Abdulmalik S Alotaibi, Mohamed A Albekery, Ahmed A Alanazi, Ibrahim S Alhomoud, Khalid A Alamer, Mohammad Shawaqfeh, Reem H Alshammari, Fayez Alhejaili, Muthana Al Sahlawi, Ibrahim Aldossary, Hajar Adel Aljuayl, Mohammad Alkathiri, Shmeylan Alharbi, Abdulkareem Albekairy, Abdulmalik Alkatheri
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引用次数: 0

摘要

背景:脂质代谢紊乱在终末期肾病(ESRD)血液透析(HD)患者中很常见,导致血脂异常,其特征是血浆脂质和脂蛋白异常。尽管大型随机对照试验通常没有证明他汀类药物治疗在接受血液透析的患者中具有生存益处,但有限的观察性研究报道了他汀类药物治疗与改善该人群临床结果的潜在关联。方法:本回顾性队列研究调查了2018年1月1日至2019年12月30日两年期间,他汀类药物在患有HD的ESRD患者中使用的临床和安全性结果。主要终点通过评估特定脂质参数的变化来评估他汀类药物的临床结果,包括低密度脂蛋白胆固醇(LDL-C)、甘油三酯(TG)、总胆固醇(TC)和高密度脂蛋白胆固醇(HDL-C)。次要终点通过监测肝酶和肌酸激酶(CK)水平来评估安全性。结果:179名参与者中,糖尿病患者134例(74.9%),高血压患者168例(93.9%)。95例(53.1%)发生心血管事件。146例患者(82.0%)接受了他汀类药物治疗,其中阿托伐他汀是最常用的他汀类药物(69.3%)。瑞舒伐他汀组和阿托伐他汀组LDL-C水平略有下降,而辛伐他汀组和非他汀组LDL-C水平略有上升。这些组内变化均无统计学意义。在阿托伐他汀组,LDL-C从2.058略微下降到2.003 mmol/L。瑞舒伐他汀组LDL-C从2.607降至2.113 mmol/L。相反,辛伐他汀组LDL-C从1.550增加到1.901 mmol/L。非他汀类药物组LDL-C由2.678升高至2.820 mmol/L。肝酶和CK水平略有波动,但仍在正常范围内。结论:本研究评估了他汀类药物治疗血液透析患者的血脂异常。尽管在阿托伐他汀和瑞舒伐他汀组中观察到LDL-C水平的适度降低,但他汀类药物治疗并没有降低伴有血脂异常的血液透析患者动脉粥样硬化事件的发生率。此外,他汀类药物的使用与任何临床或统计学上显著的影响无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Statins Use in Hemodialysis Patients: A Retrospective Analysis of Clinical and Safety Outcomes.

Background: Lipid metabolism disturbances are common in end-stage renal disease (ESRD) patients on hemodialysis (HD), leading to dyslipidemia, which is characterized by abnormal plasma lipids and lipoproteins. Although large randomized controlled trials have generally not demonstrated a survival benefit associated with statin therapy among patients receiving hemodialysis, limited observational studies have reported potential associations with improved clinical outcomes in this population. Methods: This retrospective cohort study investigated the clinical and safety outcomes of statin use in ESRD patients on HD with documented dyslipidemia over a two-year period from 1 January 2018 to 30 December 2019. The primary endpoints evaluated the clinical outcomes of statins by assessing changes in specific lipid parameters, including low-density lipoprotein cholesterol (LDL-C), triglycerides (TG), total cholesterol (TC), and high-density lipoprotein cholesterol (HDL-C). The secondary endpoints assessed safety by monitoring liver enzymes and creatine kinase (CK) levels. Results: Among 179 participants, diabetes mellitus was present in 134 patients (74.9%), while 168 patients (93.9%) had hypertension. Cardiovascular events occurred in 95 patients (53.1%). Statin therapy was administered to 146 patients (82.0%), with atorvastatin being the most frequently prescribed statin (69.3%). Modest reductions in LDL-C levels were observed in the rosuvastatin and atorvastatin groups, whereas slight increases were noted in the simvastatin and non-statin groups. None of these within-group changes were statistically significant. In the atorvastatin group, LDL-C decreased slightly from 2.058 to 2.003 mmol/L. The rosuvastatin group experienced a more pronounced LDL-C reduction from 2.607 to 2.113 mmol/L. Conversely, the simvastatin group showed an LDL-C increase from 1.550 to 1.901 mmol/L. Among the non-statin group, LDL-C increased from 2.678 to 2.820 mmol/L. Liver enzyme and CK levels fluctuated slightly but remained within normal ranges. Conclusions: This study evaluated statin therapy in hemodialysis patients with dyslipidemia. Although modest reductions in LDL-C levels were observed in the atorvastatin and rosuvastatin groups, statin therapy did not reduce the incidence of atherosclerotic events in hemodialysis patients with dyslipidemia. Additionally, statin use was not associated with any clinically or statistically significant effects.

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来源期刊
Pharmaceuticals
Pharmaceuticals Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
6.10
自引率
4.30%
发文量
1332
审稿时长
6 weeks
期刊介绍: Pharmaceuticals (ISSN 1424-8247) is an international scientific journal of medicinal chemistry and related drug sciences.Our aim is to publish updated reviews as well as research articles with comprehensive theoretical and experimental details. Short communications are also accepted; therefore, there is no restriction on the maximum length of the papers.
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