Abstract
Objective
Low-density lipoprotein cholesterol (LDL-C) lowering constitutes a cornerstone of secondary prevention of atherosclerotic cardiovascular disease (ASCVD), yet a considerable number of patients do not achieve guideline-recommended LDL‑C targets. The 2016 European guidelines recommended titration of LDL‑C lowering medication in a set number of steps, starting with oral medication. We aimed to investigate the effects of this stepwise approach in post-acute coronary syndrome (ACS) patients.
Methods
In a multicentre, prospective, non-randomised trial, we evaluated a three-step strategy aiming to reduce LDL‑C to ≤ 1.8 mmol/l in post-ACS patients with prior ASCVD and/or diabetes mellitus. Steps, undertaken every 4–6 weeks, included: 1) start high-intensity statin (HIST); 2) addition of ezetimibe; 3) addition of proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9i). The primary outcome was the proportion of patients achieving LDL-C ≤ 1.8 mmol/l after Steps 1 and 2 (using oral medications alone). Secondary outcomes examined the prevalence of meeting the target throughout all steps (https://onderzoekmetmensen.nl/nl/trial/21157).
Results
Out of 999 patients, 84% (95% confidence intervals (CI): 81–86) achieved the LDL‑C target using only statin and/or ezetimibe. In an intention-to-treat analysis, the percentages of patients meeting the LDL‑C target after each step were 69% (95% CI: 67–72), 84% (95% CI: 81–86), and 87% (95% CI: 85–89), respectively. There were protocol deviations for 23, 38 and 23 patients at each respective step.
Conclusion
Through stepwise intensification of lipid-lowering therapy, 84% of very high-risk post-ACS patients achieved an LDL‑C target of ≤ 1.8 mmol/l with oral medications alone. Addition of PCSK9i further increased this rate to 87% (95% CI: 85–89).
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National and European guidelines recommend applying a stepwise approach to lower low-density lipoprotein cholesterol (LDL-C) to target, but low success rates have been observed in previous studies.
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Through a stepwise approach to cholesterol lowering, 84% of very high-risk cardiovascular patients reached target LDL‑C using only oral and affordable medication, increasing to 87% with additional use of PCSK9 inhibitors.
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A step-wise approach to LDL-lowering can be easily aligned with local considerations and implemented into clinical practice to improve and accelerate LDL‑C management in very high-risk patients.
Introduction
Patients with atherosclerotic cardiovascular disease (ASCVD) and elevated low-density lipoprotein cholesterol (LDL-C) have a high residual cardiovascular risk [1]. International guidelines recommending strict LDL‑C targets are slowly being adopted in regional guidelines [2,3,4,5,6]. Statins are recommended as the first-choice medication to lower LDL‑C [2]. If LDL‑C targets are not met with high-intensity statin therapy (HIST), the addition of ezetimibe is indicated which may further reduce LDL‑C by up to 15–27% [4, 7]. Proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9i), used on top of statin therapy, reduce LDL‑C levels by an additional ~60% [8, 9]. Therefore, PCSK9i therapy is recommended for very high-risk patients in whom LDL‑C goals are not met despite a combination of maximum tolerated statin therapy and ezetimibe [2, 4,5,6]. While PCSK9i are highly effective in selected patients, they are not considered cost-effective for all ASCVD patients [10].
Despite guideline-based LDL‑C targets, there is a marked disparity with real-world clinical practice. Observational studies such as EUROASPIRE V and the DA VINCI study report that 29 and 54% of ASCVD patients, respectively, achieve LDL-C ≤ 1.8 mmol/l values. This proportion increases to 60% in a meta-analysis of statin trials [11,12,13]. These results underscore the challenges in effectively implementing lipid-lowering treatment, particularly considering the increasingly stringent LDL‑C guidelines in recent years.
We examined the impact of a protocolled three-step approach (1st HIST, 2nd HIST + ezetimibe, 3rd HIST + ezetimibe + PCSK9i) on achieving LDL‑C guideline-recommended targets in post-ACS patients, who are categorised as very high risk. While the 2019 and 2021 ESC Prevention and Dyslipidaemia guidelines advocate for a step-wise method to reach LDL targets, the practical implementation of such a strategy has not been explored in clinical practice [5, 6].
Methods
Design
The PENELOPE study was an investigator-initiated, multicentre, prospective, non-randomised trial, led and sponsored by the Workgroup Cardiology Centres Netherlands (WCN). The trial was conducted within 23 centres across the Netherlands. Financial support for the trial was provided by Sanofi. Per terms of the contractual agreement, Sanofi had no involvement in the design, execution, planning or publication of the trial.
Study population
We enrolled patients > 18 years who were admitted for a type I ST-elevation myocardial infarction (STEMI) or non-ST-elevation myocardial infarction (NSTEMI), with a history of ASCVD and/or type 2 diabetes mellitus (T2DM). The inclusion criteria were designed to meet the definition of very high-risk ASCVD patients according to the 2016 ESC Guidelines and to fulfil the Dutch reimbursement criteria for PCSK9i (Tab. S1 of the Electronic Supplementary Material; [2, 14]). We excluded patients > 70 years with a Clinical Frailty Score > 3 or with a life expectancy < 1 year as preventive goals in these patients may differ, and patients not eligible for all steps in the protocol (pregnant or lactating women, known intolerance for alirocumab, already using PCSK9i) (Tab. 1) [15, 16].
Intervention and outcomes
Patients underwent a structured, stepwise intensification process, comprising three consecutive steps: Step 1 adding/titrating to HIST, Step 2 adding ezetimibe and Step 3 adding PCSK9i (Fig. 1). After each step, every 4–6 weeks, lipid levels were measured and the next step would be initiated until the LDL‑C target (≤ 1.8 mmol/l) was reached. Therapy of patients on target, either at baseline or after any step, was not modified. Our primary outcome was the prevalence of patients reaching the LDL‑C target using oral medication only. Secondary outcomes included the prevalence of patients reaching target LDL‑C after each of the three steps.
Step 1: Starting or up-titrating HIST
Patients with an LDL‑C level > 1.8 mmol/l at baseline received HIST, atorvastatin (≥ 40 mg) or rosuvastatin (≥ 20 mg), or the highest tolerated statin dosage. A reduced dose or lower-intensity statin was prescribed when necessary due to factors such as low body weight or potential drug interactions. For patients with statin-related muscle symptoms, treatment adhered to the therapeutic guidelines set by the European Atherosclerosis Society Consensus Panel for managing statin-associated muscle symptoms [17].
Step 2: Adding ezetimibe
When LDL‑C persisted above 1.8 mmol/l despite HIST, ezetimibe 10 mg was introduced. Ezetimibe monotherapy was used for those intolerant to at least three distinct statins.
Step 3: Adding PCSK9i
If LDL‑C remained > 1.8 mmol/l after Steps 1 and 2, alirocumab could be added. The alirocumab dosing was left to the clinicians’ discretion which was based on age and LDL‑C level criteria (Electronic Supplementary Material, Box S1) including no alirocumab, or 75 mg or 150 mg every two weeks. This dosing strategy provided flexibility in treatment choices, particularly for lower LDL‑C, while ensuring effective therapy for higher LDL‑C levels. Lipid levels were assessed two weeks after the second alirocumab dose to determine secondary outcomes.
Statistical methods
Baseline characteristics are presented using means with standard deviations (SD), medians with interquartile ranges (IQR), or percentages for categorical variables. Anticipating an 80% prevalence of LDL-C ≤ 1.8 mmol/l based on the IMPROVE-IT trial, a sample size of 1000 patients was calculated to achieve a 95% confidence interval (CI) with a 5% width for our primary objective (details in the Electronic Supplementary Material, Box S2; [7]). For each step, the percentage of patients attaining the LDL‑C target and the 5% CI are provided for both the entire cohort (intention-to-treat analysis) and those who rigorously followed the protocol (per-protocol analysis). Target achievement includes patients meeting the goal at the current step or in previous steps, including baseline. When the LDL‑C level was missing, non-high-density lipoprotein (non-HDL) < 2.6 mmol/l was used to determine target achievement. Patients missing both LDL‑C and non-HDL‑C levels were considered off-target in the intention-to-treat group and excluded from the per-protocol group. A post-hoc analysis evaluated patients achieving LDL-C ≤ 1.4 mmol/l, aligning with updated, stricter European guidelines despite not being the original study goal [6]. All analyses were performed in Python (version 3.10).
Results
Baseline characteristics
Between January 2019 and August 2020, 1000 patients were included, one of whom withdrew consent: 707 (70.7%) with NSTEMI and 292 (29.2%) with STEMI. Mean (SD) age was 67 (± 10) years, 23% were women, 74% had a history of ASCVD and 45% of T2DM. At baseline, 380 patients (38%) had LDL-C ≤ 1.8 mmol/l. Medication use at baseline is shown in Tab. 2. Among patients with established ASCVD, 85% were using any lipid-lowering treatment at baseline, and 43% were on target for LDL‑C. In patients with T2DM only, 50% were using any lipid-lowering treatment and 23% had LDL-C ≤ 1.8 mmol/l.
The stepwise lipid-lowering treatment protocol was correctly applied in 915 (92%) patients (per-protocol) (See Box S3 and Fig. S1 in the Electronic Supplementary Material for detailed results per step).
Primary outcome
The primary outcome was reached in 89% (CI: 87–91) of the patients in the per-protocol group, and 84% (CI: 81–86) in the intention-to-treat group. At baseline, 38% (CI: 35–41) of patients were on target. As a cumulative result of treatment with HIST (Step 1), HIST plus ezetimibe (Step 2) and HIST plus ezetimibe plus PCSK9i (Step 3), target LDL‑C was met in 71% (CI: 68–74), 89% (CI: 87–91) and 95% (CI: 94–96) in the per-protocol group (denominator at successive steps: n = 976, n = 938 and n = 915) and 69% (CI: 67–72), 84% (CI: 81–86) and 87% (CI: 85–89) in the intention-to-treat group (n = 999), respectively. The results (Tab. 3) are visualised in Fig. 2.
Step 1: Starting or up-titrating HIST
Of the 618 patients with baseline LDL-C > 1.8 mmol/l, HIST was initiated or statin was titrated to a higher dose in 553 (89%). As a result of Step 1 an additional 314 patients reached target LDL‑C after a median (IQR) of 35 (29–45) days. A total of 694 patients had reached target LDL‑C after Step 1, corresponding with 71% (CI: 68–74) of the per-protocol group and 69% (CI: 67–72) of the intention-to-treat group (Tab. 3). Tab. S2 of the Electronic Supplementary Material shows the prescribed type and dosage of statins.
Step 2: Adding ezetimibe
After ezetimibe was added in 234 of 282 (83%) patients who had not reached target LDL‑C after Step 1, an additional 142 patients achieved target LDL‑C after a median (IQR) of 35 (29–46) days. Cumulatively, corresponding to the primary outcome, after Steps 1 + 2, 836 (84%, CI: 81–86) patients reached target LDL‑C (Tab. 3).
Step 3: Adding PCSK9i
Patients remaining off-target after Steps 1 and 2 (n = 102) were eligible to receive PCSK9i. In 40 patients alirocumab was added on top of statin and/or ezetimibe, after which the target LDL‑C was met in an additional 34 patients. Prescribed dosages can be found in Box S1 in the Electronic Supplementary Material. In 39 patients with LDL-C ≤ 2.6 mmol/l PCSK9i therapy was not initiated because of the physician’s or patient’s preference. Overall, after completing Steps 1 + 2 + 3, target LDL‑C was reached in 870 patients, corresponding to 95% (CI: 94–96) of the per-protocol group and 87% (CI: 85–89) of the intention-to-treat group. The median (IQR) time to complete all three steps was 45 (32–77) days. The distribution of LDL‑C at baseline and after the final step is shown in Fig. 3. Even though medication adjustments were aimed at achieving an LDL-C ≤ 1.8 mmol/l, 43% of patients reached an LDL-C ≤ 1.4 mmol/l. The number of patients reaching LDL-C ≤ 1.4 mmol/l after each successive step is shown in Tab. 3.
Protocol deviations
Overall, despite an LDL-C > 1.8 mmol/l, the protocol was not followed in 122 patients (12%): 22 patients were not prescribed HIST (Step 1), 38 patients were not prescribed ezetimibe (Step 2) and 62 patients were not prescribed PCSK9i (Step 3). The reasons for protocol deviation in the first two steps were study burden as perceived by the patient (n = 25), unknown reasons (n = 18), statin-related symptoms (n = 4), physician discretion (n = 4), deceased (n = 4), missing LDL‑C and non-HDL values (n = 1). The reasons for protocol deviation in Step 3 were not fulfilling reimbursement criteria due to ezetimibe intolerance in 7 patients; 16 patients with LDL-C ≥ 2.6 mmol/l did not receive PCSK9i due to patients’ and/or physicians’ choice. A detailed overview is shown in Tab. S3 of the Electronic Supplementary Material.
Treatment intolerance
At baseline, 78 patients (7.8%) reported a history of statin intolerance; 55 of them had tried ≤ 2 statins before inclusion. Among those 55 patients, 51 (93%) tolerated a rechallenge with a third statin during Step 1 (HIST). Twenty-three patients with a documented history of intolerance to ≥ 3 statins were treated with ezetimibe instead of being rechallenged with statins. In the 553 patients without a history of statin intolerance, 46 (8%) patients developed muscle complaints, causing 12 patients (2%) to cease statin therapy. For ezetimibe, 12 (4%) patients reported side effects during the study.
Discussion
This study evaluated a stepwise lipid-lowering strategy to achieve an LDL‑C of ≤ 1.8 mmol/l in post-ACS patients categorised as very high-risk patients. Utilising only statins and/or ezetimibe, 84% of the patients reached the target LDL‑C in two successive steps.
This stepwise approach combining statins, ezetimibe and PCSK9i led to better LDL‑C attainment rates than in most observational studies [11, 12, 18]. In line with the reigning 2016 ESC guideline at the beginning of this study, the LDL‑C target was set at ≤ 1.8 mmol/l. Although this still corresponds with current applicable Dutch cardiovascular guidelines and PCSK9i reimbursement criteria, the 2019 ESC guideline introduced a more stringent target of ≤ 1.4 mmol/l. Although medication adjustments were not aimed at the latter target, an LDL-C ≤ 1.4 mmol/l was achieved in 43% of the patients (Fig. 3 and Tab. 3). This demonstrates that the stepwise approach is adaptable to varied local thresholds and suggests it could be superior to commonly used titration strategies that depend on the healthcare professional’s discretion.
Implementing stepwise lipid-lowering treatment protocols requires a robust infrastructure due to the frequent visits and associated workload (Electronic Supplementary Material, Box S3). Yet, 84% of patients achieved LDL‑C targets exclusively using oral therapeutics, underscoring their affordability. Prioritising appropriate and early prescription of oral lipid-lowering treatment in such protocols may improve the accessibility and affordability of post-ACS care.
In this study, a low incidence of statin- and ezetimibe-related complaints was observed, even among patients with a prior history of statin-related issues. Re-challenging such patients might enhance the likelihood of achieving LDL targets with oral medications. These observations resonate with the findings from both the SAMSON and StatinWISE trials, which reported no significant differences in muscle-related symptoms between the statin and placebo groups [19, 20].
Limitations
Some aspects of our study warrant consideration. First, during the course of the study, the 2019 ESC guidelines changed the LDL‑C target for very high-risk ASCVD patients from < 1.8 mmol/l to < 1.4 mmol/l or even ≤ 1.0 mmol/l. This target, however, is not yet adopted by many national societies and multidisciplinary guidelines, such as the Dutch multidisciplinary cardiovascular risk management guidelines [4]. Therefore, our study target of ≤ 1.8 mmol/l remains relevant [2]. Secondly, our study design purposefully permitted clinicians to decide on HIST and alirocumab dosages. While 623 patients (62%) were on HIST at their final visit, a mere 119 (12%) were on the maximum dosage of atorvastatin (80 mg) or rosuvastatin (40 mg) (Electronic Supplementary Material, Tab. S2). Moreover, of the 10% of the patients with an indication for PCSK9i, only 60% were given this treatment (Electronic Supplementary Material, Box S3). Adjusting to the top-end dosage of statins and ensuring complete PCSK9i coverage for all qualified patients might have enabled more patients to reach their LDL‑C goals. Restraint in prescribing this potent, newer class of lipid-lowering treatment emphasises the need for further education on the benefits, costs and potential risks, especially in this highly vulnerable patient subgroup. Finally, this study lacked a (randomly selected) control group, highlighting the need for future studies comparing protocolled, stepwise lipid-lowering treatment to usual care.
Conclusion
A stepwise lipid-lowering strategy utilising only statins and/or ezetimibe resulted in 84% (95% CI: 81–86) of post-ACS patients—classified as very high-risk—achieving an LDL‑C level of ≤ 1.8 mmol/l. This affordable and simple approach has the potential to enable more patients to reach guideline-based lipid targets.
Data availability statement
The data underlying this article will be shared on reasonable request to the corresponding author.
References
Bhatt DL, Eagle KA, Ohman EM, et al. Comparative determinants of 4‑year cardiovascular event rates in stable outpatients at risk of or with atherothrombosis. JAMA. 2010;304:1350–7.
Catapano AL, Graham I, De Backer G, et al. ESC/EAS Guidelines for the Management of Dyslipidaemias. Eur Heart J. 2016;2016:2999–3058.
Penson PE, Pirro M, Banach MLDL‑C. lower is better for longer-even at low risk. BMC Med. 2020;18:320.
Cardiovasculair risicomanagement (CVRM) richtlijnen 2019 [Available from: https://richtlijnendatabase.nl/richtlijn/cardiovasculair_risicomanagement_cvrm/samenvatting_cvrm.html.
Mach F, Baigent C, Catapano AL, et al. ESC/EAS Guidelines for the management of dyslipidaemias: lipid modification to reduce cardiovascular risk: The Task Force for the management of dyslipidaemias of the European Society of Cardiology (ESC) and European Atherosclerosis Society (EAS). Eur Heart J. 2019;2020:111–88.
Visseren FLJ, Mach F, Smulders YM, et al. 2021 ESC Guidelines on cardiovascular disease prevention in clinical practice. Eur Heart J. 2021;42:3227–337.
Cannon CP, Blazing MA, Giugliano RP, et al. Ezetimibe Added to Statin Therapy after Acute Coronary Syndromes. N Engl J Med. 2015;372:2387–97.
Schwartz GG, Steg PG. Szarek et al. Alirocumab and Cardiovascular Outcomes after Acute Coronary Syndrome. N Engl J Med. 2018;379:2097–107.
Sabatine MS, Giugliano RP, Keech AC, et al. Evolocumab and Clinical Outcomes in Patients with Cardiovascular Disease. N Engl J Med. 2017;376:1713–22.
Kazi DS, Penko J, Coxson PG, et al. Updated Cost-effectiveness Analysis of PCSK9 Inhibitors Based on the Results of the FOURIER Trial. JAMA. 2017;318:748–50.
Kotseva K, Wood D, De Bacquer D, et al. EUROASPIRE IV: A European Society of Cardiology survey on the lifestyle, risk factor and therapeutic management of coronary patients from 24 European countries. Eur J Prev Cardiol. 2016;23:636–48.
Ray KK, Molemans B, Schoonen WM, et al. EU-Wide Cross-Sectional Observational Study of Lipid-Modifying Therapy Use in Secondary and Primary Care: the DA VINCI study. Eur J Prev Cardiol. 2021;28:1279–89.
Boekholdt SM, Hovingh GK, Mora S, et al. Very low levels of atherogenic lipoproteins and the risk for cardiovascular events: a meta-analysis of statin trials. J Am Coll Cardiol. 2014;64:485–94.
Overheid N. Bijlage 2 Regeling zorgverzekering 2019 [04-12-2019:[Available from: https://wetten.overheid.nl/jci1.3:c:BWBR0018715&bijlage=2&z=2019-12-04&g=2019-12-04.
Rockwood K, Song X, MacKnight C, et al. A global clinical measure of fitness and frailty in elderly people. Cmaj. 2005;173:489–95.
Franchi C, Lancellotti G, Bertolotti M, et al. Use of Lipid-Lowering Drugs and Associated Outcomes According to Health State Profiles in Hospitalized Older Patients. Clin Interv Aging. 2021;16:1251–64.
Stroes ES, Thompson PD, Corsini A, et al. Statin-associated muscle symptoms: impact on statin therapy-European Atherosclerosis Society Consensus Panel Statement on Assessment, Aetiology and Management. Eur Heart J. 2015;36:1012–22.
Ray KK, Haq I, Bilitou A, et al. Treatment gaps in the implementation of LDL cholesterol control among high- and very high-risk patients in Europe between 2020 and 2021: the multinational observational SANTORINI study. Lancet Reg Health Eur. 2023;29:100624.
Howard JP, Wood FA, Finegold JA, et al. Side Effect Patterns in a Crossover Trial of Statin, Placebo, and No Treatment. J Am Coll Cardiol. 2021;78:1210–22.
Herrett E, Williamson E, Brack K, et al. Statin treatment and muscle symptoms: series of randomised, placebo-controlled n‑of-1 trials. BMJ. 2021;372:n135.
Acknowledgements
Dr Peter Dunselman was the spiritual father and key initiator of this study. After his premature passing, the current authors further developed his idea and designed the PENELOPE study as a posthumous recognition of his work.
Funding
This work was supported by an unrestricted grant by Sanofi-Aventis Netherlands BV. The Workgroup Cardiology Centres Netherlands (WCN) was the sponsor and responsible for operational leadership. WCN also composed the Steering Committee, responsible for scientific leadership such as trial design and analysis. Sanofi funded the trial but had no role in trial execution, content and planning of the trial. This is defined in the contract between the sponsor (WCN) and the funder (Sanofi).
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Conflict of interest
A.-h. Liem: co-author of the Dutch cardiovascular risk management guidelines (CVRM). H.T. Jorstad: Editor for NEHJ. F.M.A.C. Martens: co-author of the Dutch cardiovascular risk management guidelines (CVRM). A.M.W. Alings: consulting fees from Sanofi. A. Omar Khader, T. van Trier, S. van der Brug, B.E. Groenemeijer and A. Schut declare that they have no competing interests.
Ethical standards
The trial was reviewed and approved by the Institutional Review Board, i.e. the ethics committee (Medical Research Ethics Committees United (MEC-U)—66879.100.18_R18.063). All patients signed written informed consent at inclusion.
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Registration: Netherlands Trial Register NL7556
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Omar Khader, A., van Trier, T., van der Brug, S. et al. Effects of a stepwise, structured LDL-C lowering strategy in patients post-acute coronary syndrome. Neth Heart J 32, 206–212 (2024). https://doi.org/10.1007/s12471-023-01851-7
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DOI: https://doi.org/10.1007/s12471-023-01851-7