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Sex Differences in Cardiovascular Outcomes and Cholesterol-Lowering Efficacy of PCSK9 Inhibitors: Systematic Review and Meta-Analysis.

Publication ,  Journal Article
Rivera, FB; Cha, SW; Aparece, JP; Rocimo, A; Ong, BA; Golbin, JM; Alfonso, PG; Enkhmaa, B; Khan, SU; Cainzos-Achirica, M; Volgman, AS ...
Published in: JACC Adv
November 2023

BACKGROUND: Guideline-recommended low-density lipoprotein cholesterol (LDL-C) thresholds are often not achieved in women. The proprotein convertase subtilisin/kexin type-9 inhibitor (PCSK9i) monoclonal antibodies can help further reduce LDL-C and major adverse cardiovascular events (MACE) although differences in efficacy by sex and type are less understood. OBJECTIVES: The authors sought to determine if there are differences in the efficacy of LDL-C lowering and reduction in the risk of MACE by sex and type of PCSK9i. METHODS: A comprehensive literature search was done through October 17, 2022, for published trials comparing PCSK9i vs control. Outcomes assessed were LDL-C reduction and incidence of MACE following the use of PCSK9i vs placebo, stratified by sex and type of PCSK9i used. RESULTS: We identified 16 trials with 54,996 adults, and 15,143 (27.5%) of them were female. PCSK9i significantly reduced MACE compared to placebo in both women (HR: 0.86, 95% CI: 0.74-0.97, P < 0.001) and men (HR: 0.85, 95% CI: 0.79-0.91, P < 0.001) with no significant sex difference (MD -0.01, 95% CI: -0.14 to -0.13, P = 0.930). PCSK9i also significantly reduced LDL-C levels in both sexes at 12 weeks (females: MD -62.57, 95% CI: -70.24 to -54.91, P < 0.001; males: MD -66.19, 95% CI: -72.03 to -60.34, P < 0.001) and 24 weeks (females: MD -47.52, 95% CI: -52.94 to -42.09, P < 0.001; males: MD -54.07, 95% CI: -59.46 to -48.68, P < 0.001). Significant sex difference was seen in the LDL reduction of PCSK9i for both 12 weeks (males vs females: MD -4.55, 95% CI: -7.34 to -1.75, P < 0.01) and 24 weeks (males vs females: MD -7.11, 95% CI: -9.99 to -4.23, P < 0.001). CONCLUSIONS: The use of PCSK9i results in significant LDL-C and MACE reduction in both males and females. While there is no significant sex difference in MACE reduction, LDL-C reduction is greater in males than in females. Our data support the equal use of PCSK9i in all eligible patients, regardless of sex.

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Published In

JACC Adv

DOI

EISSN

2772-963X

Publication Date

November 2023

Volume

2

Issue

9

Start / End Page

100669

Location

United States
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Rivera, F. B., Cha, S. W., Aparece, J. P., Rocimo, A., Ong, B. A., Golbin, J. M., … Shah, N. P. (2023). Sex Differences in Cardiovascular Outcomes and Cholesterol-Lowering Efficacy of PCSK9 Inhibitors: Systematic Review and Meta-Analysis. JACC Adv, 2(9), 100669. https://doi.org/10.1016/j.jacadv.2023.100669
Rivera, Frederick Berro, Sung Whoy Cha, John Paul Aparece, Aubrey Rocimo, Bradley Ashley Ong, Jem Marie Golbin, Pia Gabrielle Alfonso, et al. “Sex Differences in Cardiovascular Outcomes and Cholesterol-Lowering Efficacy of PCSK9 Inhibitors: Systematic Review and Meta-Analysis.JACC Adv 2, no. 9 (November 2023): 100669. https://doi.org/10.1016/j.jacadv.2023.100669.
Rivera FB, Cha SW, Aparece JP, Rocimo A, Ong BA, Golbin JM, et al. Sex Differences in Cardiovascular Outcomes and Cholesterol-Lowering Efficacy of PCSK9 Inhibitors: Systematic Review and Meta-Analysis. JACC Adv. 2023 Nov;2(9):100669.
Rivera, Frederick Berro, et al. “Sex Differences in Cardiovascular Outcomes and Cholesterol-Lowering Efficacy of PCSK9 Inhibitors: Systematic Review and Meta-Analysis.JACC Adv, vol. 2, no. 9, Nov. 2023, p. 100669. Pubmed, doi:10.1016/j.jacadv.2023.100669.
Rivera FB, Cha SW, Aparece JP, Rocimo A, Ong BA, Golbin JM, Alfonso PG, Enkhmaa B, Khan SU, Cainzos-Achirica M, Volgman AS, Navar AM, Shah NP. Sex Differences in Cardiovascular Outcomes and Cholesterol-Lowering Efficacy of PCSK9 Inhibitors: Systematic Review and Meta-Analysis. JACC Adv. 2023 Nov;2(9):100669.

Published In

JACC Adv

DOI

EISSN

2772-963X

Publication Date

November 2023

Volume

2

Issue

9

Start / End Page

100669

Location

United States