TY - JOUR
T1 - Effects of proprotein convertase subtilisin/kexin type 9 antibodies in adults with hypercholesterolemia
T2 - A systematic review and meta-analysis
AU - Navarese, Eliano Pio
AU - Kołodziejczak, Michalina
AU - Schulze, Volker
AU - Gurbel, Paul A.
AU - Tantry, Udaya
AU - Lin, Yingfeng
AU - Brockmeyer, Maximilian
AU - Kandzari, David E.
AU - Kubica, Julia M.
AU - D'Agostino, Ralph B.
AU - Kubica, Jacek
AU - Volpe, Massimo
AU - Agewall, Stefan
AU - Kereiakes, Dean J.
AU - Kelm, Malte
N1 - Publisher Copyright:
© 2015 American College of Physicians.
Copyright:
Copyright 2015 Elsevier B.V., All rights reserved.
PY - 2015/7/7
Y1 - 2015/7/7
N2 - Background: Guidelines recommend statins as first-line therapy for dyslipidemia. Monoclonal antibodies targeting proprotein convertase subtilisin/kexin type 9 (PCSK9) is a new lipid-lowering approach. Purpose: To assess the efficacy and safety of PCSK9 antibodies in adults with hypercholesterolemia. Data Sources: MEDLINE, PubMed Central, and Google Scholar; conference proceedings; and the ClinicalTrials.gov registry through 4 April 2015. Study Selection: Phase 2 or 3 randomized, controlled trials (RCTs) comparing treatment using PCSK9 antibodies with no anti-PCSK9 therapy in adults with hypercholesterolemia. Data Extraction: Two investigators independently extracted data on study characteristics and lipid and clinical outcomes, and rated risk of bias of trials. Prespecified primary end points were all-cause and cardiovascular mortality. Data Synthesis: Twenty-four RCTs comprising 10 159 patients were included. Compared with no antibody, treatment with PCSK9 antibodies led to marked reductions in low-density lipoprotein cholesterol levels (mean difference,-47.49% [95% CI,-69.64% to-25.35%]; P < 0.001] and other atherogenic lipid fractions, and it reduced all-cause mortality (odds ratio [OR], 0.45 [CI, 0.23 to 0.86]; P = 0.015; heterogeneity P = 0.63; I2 = 0%) and cardiovascular mortality (OR, 0.50 [CI, 0.23 to 1.10]; P = 0.084; heterogeneity P = 0.78; I2 = 0%). The rate of myocardial infarction was significantly reduced with use of PCSK9 antibodies (OR, 0.49 [CI, 0.26 to 0.93]; P = 0.030; heterogeneity P = 0.45; I2 = 0%), and increases in the serum creatine kinase level were reduced (OR, 0.72 [CI, 0.54 to 0.96]; P = 0.026; heterogeneity P = 0.65; I2 = 0%). Serious adverse events did not increase with administration of PCSK9 antibodies. Limitation: Results were derived from study-level data rather than patient-level data, and clinical outcome data are rare. Conclusion: PCSK9 antibodies seem to be safe and effective for adults with dyslipidemia.
AB - Background: Guidelines recommend statins as first-line therapy for dyslipidemia. Monoclonal antibodies targeting proprotein convertase subtilisin/kexin type 9 (PCSK9) is a new lipid-lowering approach. Purpose: To assess the efficacy and safety of PCSK9 antibodies in adults with hypercholesterolemia. Data Sources: MEDLINE, PubMed Central, and Google Scholar; conference proceedings; and the ClinicalTrials.gov registry through 4 April 2015. Study Selection: Phase 2 or 3 randomized, controlled trials (RCTs) comparing treatment using PCSK9 antibodies with no anti-PCSK9 therapy in adults with hypercholesterolemia. Data Extraction: Two investigators independently extracted data on study characteristics and lipid and clinical outcomes, and rated risk of bias of trials. Prespecified primary end points were all-cause and cardiovascular mortality. Data Synthesis: Twenty-four RCTs comprising 10 159 patients were included. Compared with no antibody, treatment with PCSK9 antibodies led to marked reductions in low-density lipoprotein cholesterol levels (mean difference,-47.49% [95% CI,-69.64% to-25.35%]; P < 0.001] and other atherogenic lipid fractions, and it reduced all-cause mortality (odds ratio [OR], 0.45 [CI, 0.23 to 0.86]; P = 0.015; heterogeneity P = 0.63; I2 = 0%) and cardiovascular mortality (OR, 0.50 [CI, 0.23 to 1.10]; P = 0.084; heterogeneity P = 0.78; I2 = 0%). The rate of myocardial infarction was significantly reduced with use of PCSK9 antibodies (OR, 0.49 [CI, 0.26 to 0.93]; P = 0.030; heterogeneity P = 0.45; I2 = 0%), and increases in the serum creatine kinase level were reduced (OR, 0.72 [CI, 0.54 to 0.96]; P = 0.026; heterogeneity P = 0.65; I2 = 0%). Serious adverse events did not increase with administration of PCSK9 antibodies. Limitation: Results were derived from study-level data rather than patient-level data, and clinical outcome data are rare. Conclusion: PCSK9 antibodies seem to be safe and effective for adults with dyslipidemia.
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U2 - 10.7326/M14-2957
DO - 10.7326/M14-2957
M3 - Review article
C2 - 25915661
AN - SCOPUS:84931849550
SN - 0003-4819
VL - 163
SP - 40
EP - 51
JO - Annals of internal medicine
JF - Annals of internal medicine
IS - 1
ER -