Lipid lowering with inclisiran: a real-world single-centre experience
Open accessAbstract
Objective: The reduction in circulating low-density lipoprotein cholesterol (LDL-c) is the primary aim of lipid-lowering therapies as a method of atherosclerotic cardiovascular disease risk reduction. Inclisiran is a new and potent lipid-lowering drug that is shown to be effective in reducing LDL-c in randomised controlled trials, however, real-world data of its use are not yet known. We sought to analyse the early effects of this drug in a tertiary centre lipid and cardiovascular risk clinic. Methods: We performed a retrospective analysis of the first 80 patients who received a single dose of inclisiran at our lipid clinic between 1 December 2021 and 1 September 2022. Data were collected using electronic healthcare records. Baseline blood tests were taken prior to start of treatment and were repeated at 2 months follow-up. Data on adverse events were also recorded. Results: At 2 months after treatment initiation, mean baseline LDL-c fell from 3.5±1.1 mmol/L by 48.6% to 1.8±1.0 mmol/L and total cholesterol from 5.7±1.3 mmol/L by 33.3% to 3.8±1.1 mmol/L (both p<0.0001). Mean high-density lipoprotein-c rose by 7.7% to 1.4±0.4 mmol/L (p=0.02) and median triglycerides fell by 31.3% to 1.1 mmol/L (IQR 0.9–2) (p=0.001). Adverse events (injection site reaction, fatigue and headache) were recorded in three patients and all had self-resolved by time of follow-up. Conclusion: Inclisiran use in line with National Institute for Health and Care Excellence guidelines led to significant lowering of LDL-c at 2 months, with efficacy similar to that reported in trials with good tolerability.
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Real-world data remain limited and inconclusive regarding whether inclisiran yields better adherence than monoclonal antibodies.
“While inclisiran’s twice-yearly dosing regimen is hypothesized to enhance medication adherence,14 real-world data remain limited and inconclusive regarding whether inclisiran yields better adherence than moAbs.15,16”
From Adherence to PCSK9 Inhibitors in Clinical Practice (2026) · cites this paper as [16]
The Discussion describes this as the first real-world report on inclisiran’s LDL-c reduction, with only two months of follow-up, supporting the point that real-world evidence was limited. It notes that no patient discontinued after the first dose and says this could improve adherence, but it does not compare adherence with monoclonal antibodies or assess whether inclisiran yields better adherence. (LLM, conf=0.84)
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Cites
Two Phase 3 Trials of Inclisiran in Patients with Elevated LDL Cholesterol
Ray, K. K., Wright, R. S., Kallend, D., Koenig, W., Leiter, L. A., Raal, F. J., Bisch, J. A., Richardson, T., Jaros, M., Wijngaard, P. L. J., et al. (2020) · New England Journal of Medicine · doi:10.1056/nejmoa1912387 · Cited by 1,665 · see citing works
Self-citationInclisiran for the Treatment of Heterozygous Familial Hypercholesterolemia
Raal, F. J., Kallend, D., Ray, K. K., Turner, T., Koenig, W., Wright, R. S., Wijngaard, P. L. J., Curcio, D., Jaros, M. J., Leiter, L. A., et al. (2020) · New England Journal of Medicine · doi:10.1056/nejmoa1913805 · Cited by 818 · see citing works
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Harnessing RNA Interference for Cholesterol Lowering: The Bench‐to‐Bedside Story of Inclisiran
Wilkinson, M. J., Bajaj, A., Brousseau, M. E., & Taub, P. R. (2024) · Journal of the American Heart Association · doi:10.1161/jaha.123.032031 · Cited by 37 · see citing works
Adherence to PCSK9 Inhibitors in Clinical Practice
Blais, J. E., Zhong, W., Li, C. Y. V., Kongkaew, C., & Chan, A. H. Y. (2026) · JACC: Advances · doi:10.1016/j.jacadv.2026.102733 · Cited by 7 · see citing works
Efficacy, benefit and safety of inclisiran
López-Miranda, J. (2024) · Clínica e Investigación en Arteriosclerosis (English Edition) · doi:10.1016/j.artere.2025.100730 · Cited by 4 · see citing works
- Authors
- Padam, P., Barton, L., Wilson, S., David, A., Walji, S., de Lorenzo, F., Ray, K. K., Jones, B., & Cegla, J.
- Affiliations
- Imperial College Healthcare NHS Trust (GB)
- Lipids and Cardiovascular Risk Service, Department of Cardiology, Imperial College Healthcare NHS Trust, London, UK
- Corresponding author
- Cegla, Jaimini
- Venue
- Open Heart
- Publisher
- BMJ
- Published
- 2022-12
- Volume
- 9
- Issue
- 2
- Pages
- e002184
- ISSN
- 2053-3624 (ISSN-L)
- PMC
- PMC9748986
- OpenAlex
- W4311309800
- Cited by
- 41
- References
- 2
- Citations by year
- 2026: 6 · 2025: 14 · 2024: 13 · 2023: 8
- FWCI
- 8.36
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Open Heart (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Spiral (Imperial College London) (submittedVersion, other-oa)
- Funders
- National Institute for Health and Care Research (CL-2017-21-002, ACF-2010-21-012)
- Academy of Medical Sciences (SGL019\1078)
- Medical Research Council (MR/K023667/1)
- Topics
- Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipid metabolism and disorders
- Health Sciences › Medicine › Surgery › Cholesterol and Lipid Metabolism
- Keywords
- inclisiran, LDL cholesterol lowering, lipid-lowering therapy, PCSK9 inhibition, real-world effectiveness, atherosclerotic cardiovascular disease, hypercholesterolemia, total cholesterol, HDL cholesterol, triglycerides, adverse events, injection site reactions, NICE guidelines
- MeSH terms
- Hypolipidemic Agents, Cardiovascular Diseases, Humans, Cholesterol, LDL, Retrospective Studies, RNA, Small Interfering
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