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Safety and efficacy of PCSK9 inhibitors and effect on coronary plaque phenotype in statin-treated patients following acute coronary syndrome: a systematic review and meta-analysis
被引:2
作者:
Hakim, Dennis Ievan
[1
]
Qhabibi, Faqrizal Ria
[1
,2
]
Yusuf, Muhammad
[1
]
Amar, Nasim
[1
]
Prasetya, Indra
[3
]
Ambari, Ade Meidian
[4
]
机构:
[1] Brawijaya Univ, Fac Med, Med Sch Dept, Jl Vet,Lowokwaru, Malang 65145, Indonesia
[2] Natl Cardiovasc Ctr Harapan Kita, Dept Cardiovasc Prevent & Rehabil, West Jakarta, Jakarta, Indonesia
[3] Brawijaya Univ, Dr Saiful Anwar Hosp, Fac Med, Dept Cardiol & Vasc Med, Malang, Indonesia
[4] Univ Indonesia, Fac Med, Natl Cardiovasc Ctr Harapan Kita, Dept Cardiol & Vasc Med, Jakarta, Indonesia
关键词:
Acute coronary syndrome;
Atherosclerosis;
LDL-C;
Proprotein convertase subtilisin/kexin type 9;
Statin;
ARTERY-DISEASE;
EVOLOCUMAB;
RISK;
MANAGEMENT;
AGE;
D O I:
10.1186/s43044-024-00567-2
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
BackgroundAcute coronary syndrome continues to be a significant cardiovascular issue. Statins are commonly acknowledged as medications that reduce LDL-C levels and stabilize plaques. Nevertheless, their efficacy is limited. Presently, PCSK9 inhibitors are suggested to be advantageous in patients who are already receiving statin treatment. The study seeks to assess the safety and effectiveness of PCSK9 inhibitors in individuals who have been treated with statins after experiencing acute coronary syndrome (ACS), as well as investigate the impact on the characteristics of coronary plaque. MethodsArticles were identified from PubMed, Cochrane Central Register of Controlled Trials, and ProQuest. Our analysis comprised trials and observational studies that compared the plaque phenotype, lipid profile, and safety outcomes between PCSK9 inhibitors and a control group in patients with acute coronary syndrome who were already being treated with statins. The random-effect model was used to measure the pooled effect, which was presented in terms of mean difference, standardized mean difference, and risk ratio. ResultsAcquired 12 studies that fulfilled our criteria. The addition of PCSK9 inhibitors ameliorates the plaque phenotype significantly in terms of percent atheroma volume (P = 0.02), total atheroma volume (P < 0.010), fibrous cap thickness (P < 0.00001), lipid arc (P < 0.00001), quantitative flow ratio (P = 0.003), and diameter of stenosis (P = 0.0003) but not in lipid/lesion length (P = 0.17). The administration of PCSK9 inhibitors led to a considerable improvement in all lipid profiles (P < 0.00001). Regarding safety analysis, there is no substantial disparity in the likelihood of non-serious side events (RR 1.21; P = 0.2), however, a significant reduction in the risk of serious adverse effects (RR 0.77; P = 0.04) in the PCSK9 inhibitor group. ConclusionsThe addition of PCSK9 inhibitors compared to statin-only treatment led to a majority of patients experiencing significant benefits in terms of safety and efficacy following ACS.
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