Department of Cardiology, First Hospital of Hebei Medical University, Shijiazhuang, China.
Department of Neurosurgery, Emergency General Hospital, Beijing, China.
Adv Ther. 2021 Jun;38(6):3389-3398. doi: 10.1007/s12325-021-01741-7. Epub 2021 May 21.
To investigate the effect of combined lipid-lowering therapy on low-density lipoprotein cholesterol (LDL-C) variability and cardiovascular adverse events in patients with acute coronary syndrome (ACS).
A total of 200 patients with acute coronary syndrome, admitted to the first Hospital of Hebei Medical University from January 2018 to June 2019, were randomly divided into the observation group (100 cases were treated with combined lipid-lowering drugs, including 10 mg/day atorvastatin and 10 mg/day ezetimibe) and the control group (100 cases were given an intensive statin regimen, including 40 mg/day atorvastatin). The levels of blood lipids, creatine kinase (CK), alanine transaminase (ALT), matrix metalloproteinase-9 (MMP-9) and high-sensitivity C-reactive protein (hsCRP) were observed and compared between the two groups. Focus was laid on the concentration of the above-mentioned parameters and follow-up results including the drug safety and incidence of cardiovascular adverse events.
Before treatment, there was no significant difference in total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), CK, ALT, MMP-9, hsCRP and LDL-C between the two groups (P > 0.05). After 6 months, 12 months and 24 months of treatment, TC, HDL-C, CK, ALT, MMP-9, hsCRP and LDL-C were improved in both groups, and TC, HDL-C, CK, ALT, MMP-9, hsCRP and LDL-C in the observation group elicited greater results than those in the control group with significant difference (P < 0.05). In the course of treatment, the drug safety of the two groups was compared (P > 0.05), and the incidence of cardiovascular adverse events in the observation group was significantly lower than that in the control group (6.59% vs. 11.96%) (P < 0.05).
Combination therapy with atorvastatin and ezetimibe potentially provides remarkable effects in terms of treating acute coronary syndrome, controlling the variation of LDL-C, alleviating the inflammatory state and reducing the incidence of cardiovascular adverse events with a safe profile. Combined lipid-lowering drugs are considered valid and alternative approaches for wide clinical practice.
探讨联合降脂治疗对急性冠状动脉综合征(ACS)患者低密度脂蛋白胆固醇(LDL-C)变异性及心血管不良事件的影响。
选取 2018 年 1 月至 2019 年 6 月河北医科大学第一医院收治的急性冠状动脉综合征患者 200 例,随机分为观察组(100 例采用联合降脂药物治疗,阿托伐他汀 10mg/d,依折麦布 10mg/d)和对照组(100 例采用强化他汀方案治疗,阿托伐他汀 40mg/d)。观察两组患者血脂、肌酸激酶(CK)、丙氨酸氨基转移酶(ALT)、基质金属蛋白酶-9(MMP-9)和高敏 C 反应蛋白(hsCRP)水平,并比较两组患者的上述参数浓度及随访结果,包括药物安全性和心血管不良事件发生率。
治疗前,两组患者总胆固醇(TC)、高密度脂蛋白胆固醇(HDL-C)、CK、ALT、MMP-9、hsCRP 及 LDL-C 比较,差异均无统计学意义(P>0.05)。治疗 6、12、24 个月后,两组患者 TC、HDL-C、CK、ALT、MMP-9、hsCRP 及 LDL-C 均较治疗前改善,且观察组 TC、HDL-C、CK、ALT、MMP-9、hsCRP 及 LDL-C 改善程度优于对照组,差异均有统计学意义(P<0.05)。治疗过程中比较两组患者药物安全性(P>0.05),观察组心血管不良事件发生率明显低于对照组(6.59%比 11.96%),差异有统计学意义(P<0.05)。
阿托伐他汀联合依折麦布治疗急性冠状动脉综合征疗效显著,能有效控制 LDL-C 变异性,改善患者炎症状态,降低心血管不良事件发生率,且安全性良好。联合降脂药物是一种有效的、可供选择的治疗方法,值得临床广泛应用。