Physicians' Academy for Cardiovascular Education

Data from clinical care: less LDL-c reduction with PCSK9 antibodies in women than men

Sex differences in efficacy and safety of PCSK9 monoclonal antibodies: A real-world registry

Literature - Galema-Boers AMH, Mulder JWCM, Steward K, et al. - Atherosclerosis. 2023 Mar 30;S0021-9150(23)00115-6 [Online ahead of print]. doi: 10.1016/j.atherosclerosis.2023.03.013

Introduction and methods


Sex-specific analyses of the FOURIER and ODYSSEY clinical trials showed that treatment with PCSK9 monoclonal antibodies results in slightly less LDL-c reduction in women than men [1-3]. However, real-world studies have reported conflicting results, with some confirming the trial findings [4-8], while others presented no sex differences [9,10]. These real-world studies did have limitations such as a small population size, a short follow-up duration, and an unbalanced sex distribution.

Aim of the study

The study aim was to assess sex differences in the effectiveness and safety of PCSK9 monoclonal antibodies in a clinical real-world setting using a large registry.


Data were extracted from a prospective open-cohort registry that included consecutive adult patients who started subcutaneous treatment with evolocumab (140 mg per 2 weeks) or alirocumab (75 or 150 mg per 2 weeks), as part of clinical care, at the outpatient lipid clinic of the Erasmus Medical Center in Rotterdam, the Netherlands. According to Dutch reimbursement criteria, patients qualify for reimbursement of PCSK9 inhibitor therapy if they do not meet the LDL-c target level despite maximum-tolerated lipid-lowering therapy and are at very high CVD risk.

For the current study, patients who had homozygous familial hypercholesterolemia, received treatment with inclisiran), or had participated in a previous PCSK9 inhibitor trial were excluded, leaving 436 patients (of whom 209 women (48%)) to be included in the analysis.


Main outcomes were percentage LDL-c change compared with baseline and reported side effects at 6 months. Secondary outcomes were absolute and percentage changes in LDL-c reduction over time, specific side effects, and treatment discontinuation.

Main results




In this Dutch, single-center, real-world study of patients at very high CVD risk who received maximum-tolerated lipid-lowering therapy, PCSK9 monoclonal antibody therapy resulted in less relative LDL-c reduction at 6 months in women compared with men. Although the mean absolute LDL-c reduction was similar in both sexes, women had a higher mean baseline LDL-c level. During the remainder of follow-up (up to 24 months), mean LDL-c levels remained stable in both women and men. In addition, women were less likely to reach LDL-c targets than men. No sex differences in reported side effects or treatment discontinuation were observed.

Although further research is needed, the authors point out that “[a]n explanation for the unequal relative LDL-c reduction between sexes could be the sex difference in circulating levels of PCSK9.” Based on their results, they also offer some recommendations for clinical practice, for example, to start with a full dose of the PCSK9 monoclonal antibody and uptitrate statins in all patients in whom this therapy is initiated, especially women.


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