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Published on: November 10, 2017
The cost-effectiveness of intensive low-density lipoprotein cholesterol lowering in people with peripheral artery
Domenico R Nastasi1, Joseph V Moxon2, Richard Norman3
1Queensland Research Centre for Peripheral Vascular Disease, College of Medicine and Dentistry, James Cook University, Townsville, Queensland, Australia.
Insights
Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors significantly reduce major adverse cardiovascular and limb events in peripheral artery disease patients. Treatment is cost-effective, particularly for those with chronic limb-threatening ischemia (CLTI).
Area of Science:
- Cardiovascular Medicine
- Pharmacoeconomics
- Vascular Surgery
Background:
- Peripheral artery disease (PAD) patients face high risks of major adverse cardiovascular events (MACE) and major adverse limb events (MALE).
- Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors effectively lower low-density lipoprotein cholesterol (LDL-C), reducing cardiovascular and limb events.
- This study evaluates the clinical benefit and cost-effectiveness of PCSK9 inhibitors in PAD patients.
Purpose of the Study:
- To estimate the potential reduction in MACE and MALE with PCSK9 inhibitor therapy in PAD patients.
- To assess the cost-effectiveness of using PCSK9 inhibitors for PAD management.
- To compare the benefits and costs in patients with intermittent claudication (IC) versus chronic limb-threatening ischemia (CLTI).
Main Methods:
- 783 Australian PAD patients (582 IC, 201 CLTI) were prospectively enrolled.
- LDL-C levels were measured, and MACE/MALE occurrences were tracked over a median follow-up of 2.2 years.
- Risk reductions, numbers needed to treat (NNT), and incremental cost-effectiveness ratios (ICER) were calculated.
Main Results:
- PCSK9 inhibition estimated to reduce MACE by 6.1% (NNT 16) and MALE by 13.7% (NNT 7) in CLTI patients.
- For IC patients, estimated reductions were 3.2% for MACE (NNT 32) and 5.3% for MALE (NNT 19).
- Estimated 10-year ICERs were $55,270 USD for IC and $32,800 USD for CLTI.
Conclusions:
- PCSK9 inhibitor treatment is projected to be cost-effective for patients with CLTI.
- The findings support the use of PCSK9 inhibitors as a valuable strategy in managing high-risk PAD patients.
- Intensive LDL-C lowering with PCSK9 inhibitors offers significant clinical benefits and favorable economic outcomes in specific PAD populations.
Background:
People with peripheral artery disease are at a high risk of major adverse cardiovascular events (MACE) and major adverse limb events (MALE). Randomized controlled trials suggest that intensive lowering of low-density lipoprotein cholesterol (LDL-C) with proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors is an effective strategy to prevent these events. This study estimated the potential benefit and cost-effectiveness of administrating PCSK9 inhibitors to a cohort of participants with peripheral artery disease.
Methods:
A total of 783 participants with intermittent claudication (IC; n = 582) or chronic limb-threatening ischemia (CLTI; n = 201) were prospectively recruited from three hospitals in Australia. Serum LDL-C was measured at recruitment, and the occurrence of MACE and MALE was recorded over a median (interquartile range) follow-up of 2.2 years (0.3-5.7 years). The potential benefit of administering a PCSK9 inhibitor was estimated by calculating the absolute risk reduction and numbers needed to treat (NNT) based on relative risk reductions reported in published randomized trials. The incremental cost-effectiveness ratio per quality-adjusted life year gained was estimated.
Results:
Intensive LDL-C lowering was estimated to lead to an absolute risk reduction in MACE of 6.1% (95% confidence interval [CI], 2.0-9.3; NNT, 16) and MALE of 13.7% (95% CI, 4.3-21.5; NNT, 7) in people with CLTI compared with 3.2% (95% CI, 1.1-4.8; NNT, 32) and 5.3% (95% CI, 1.7-8.3; NNT, 19) in people with IC. The estimated incremental cost-effectiveness ratios over a 10-year period were $55,270 USD and $32,800 USD for participants with IC and CLTI, respectively.
Conclusions:
This analysis suggests that treatment with a PCSK9 inhibitor is likely to be cost-effective in people with CLTI.
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