Abstract
Background: Familial hypercholesterolemia (FH) is a prevalent and potentially fatal illness that causes a substantial elevation in low-density lipoprotein cholesterol (LDL-C).
Objective: The aim of this study was to investigate the effects of monoclonal antibodies alirocumab and evolocumab on LDL-C and other lipid parameters, as well as their safety in familial hypercholesterolemia patients.
Methods: A comprehensive search was done on PubMed/MEDLINE, EMBASE, Web of Science (WOS/ ISI), Scopus, ClinicalTrials (www.ClinicalTrials.gov), and conferences/ congress research papers. Random effect models were used to calculate mean differences (%) and risk ratios (RRs), and confidence intervals (95%).
Results: Ten studies (n=1489 patients) were included in this study. PCSK9 inhibitors decreased the levels of LDL-C by -49.59% (95%CI -55.5%, -43.67%) as compared to placebo. They also didn’t alter the Treatment-Emergent Adverse Event (TEAE) and neuronal events by RR 0.92 (0.75, 1.13) and 1.31 (0.66, 2.59), respectively. PCSK9 inhibitors were effective and safe in treating patients with FH.
Conclusion: There was high-quality evidence showing that monoclonal antibodies (alirocumab & evolocumab) lower LDL-C (GRADE: high), lipoprotein (a) (GRADE: High), triglycerides (TG) (GRADE: High), total cholesterol (GRADE: High), non-high-density lipoprotein cholesterol (non- HDL-C) (GRADE: Moderate), and apolipoprotein B (GRADE: High), and increase the HDL-C (GRADE: High) as well as apolipoprotein A1 (GRADE: High). Comparing PCSK9 inhibitors against placebo, neither TEAE (GRADE: high) nor neuronal events (GRADE: moderate) were changed.
[http://dx.doi.org/10.1093/aje/kwh236] [PMID: 15321837]
[PMID: 23776352]
[http://dx.doi.org/10.1515/jomb-2016-0019] [PMID: 28670193]
[http://dx.doi.org/10.3389/fphys.2019.00280] [PMID: 30949068]
[http://dx.doi.org/10.3389/fphar.2018.00707] [PMID: 30050433]
[http://dx.doi.org/10.1016/j.jacc.2013.11.002] [PMID: 24239923]
[http://dx.doi.org/10.1016/j.amjcard.2014.05.035] [PMID: 24996554]
[http://dx.doi.org/10.1586/14779072.6.7.955] [PMID: 18666846]
[http://dx.doi.org/10.1016/j.clinthera.2006.01.005] [PMID: 16490577]
[http://dx.doi.org/10.1007/s40256-013-0053-0] [PMID: 24174174]
[http://dx.doi.org/10.1016/j.ahj.2014.05.004] [PMID: 25066560]
[http://dx.doi.org/10.1093/cvr/cvw194] [PMID: 27496869]
[http://dx.doi.org/10.1016/j.bbalip.2017.05.002] [PMID: 28495363]
[http://dx.doi.org/10.5551/jat.RV17012] [PMID: 28804094]
[PMID: 26766888]
[http://dx.doi.org/10.1007/s40262-017-0620-7] [PMID: 29353350]
[http://dx.doi.org/10.1016/S0895-4356(98)00131-0] [PMID: 10086815]
[http://dx.doi.org/10.1186/1471-2288-14-135] [PMID: 25524443]
[http://dx.doi.org/10.4103/2229-3485.100662] [PMID: 23125963]
[http://dx.doi.org/10.1136/bmj.315.7109.629] [PMID: 9310563]
[http://dx.doi.org/10.1002/0470870168.ch8]
[http://dx.doi.org/10.1136/bmj.39490.551019.BE] [PMID: 18456631]
[http://dx.doi.org/10.1016/j.jacc.2020.05.027] [PMID: 32646561]
[http://dx.doi.org/10.1007/s10557-016-6685-y] [PMID: 27618825]
[http://dx.doi.org/10.1093/eurheartj/ehv370] [PMID: 26330422]
[http://dx.doi.org/10.1093/eurheartj/ehw388] [PMID: 27572070]
[http://dx.doi.org/10.1161/CIRCULATIONAHA.112.144055] [PMID: 23129602]
[http://dx.doi.org/10.1016/S0140-6736(14)61374-X] [PMID: 25282520]
[http://dx.doi.org/10.1016/S0140-6736(14)61399-4] [PMID: 25282519]
[http://dx.doi.org/10.1016/S0140-6736(12)60771-5] [PMID: 22633824]
[http://dx.doi.org/10.1093/eurheartj/ehz430] [PMID: 31270529]
[http://dx.doi.org/10.1007/s11883-002-0058-7] [PMID: 11772418]
[http://dx.doi.org/10.1111/bcp.13066] [PMID: 27478094]
[http://dx.doi.org/10.18553/jmcp.2016.22.6.641] [PMID: 27231792]
[http://dx.doi.org/10.18433/J36C8N] [PMID: 28459663]
[http://dx.doi.org/10.1161/JAHA.115.001937] [PMID: 26077586]
[http://dx.doi.org/10.1007/s40256-018-0303-2] [PMID: 30229525]
[http://dx.doi.org/10.1007/s40618-019-01019-4] [PMID: 30762200]
[http://dx.doi.org/10.1161/JAHA.117.006910] [PMID: 29223954]
[http://dx.doi.org/10.1002/14651858.CD011748.pub2]
[http://dx.doi.org/10.1155/2021/8032978]