Evidence map›Paper›PMID 41514239›Full record

SynthesisBMC cardiovascular disorders2026

Inclisiran SiRNA therapy for durable LDL-C reduction: a systematic review and meta-analysis highlighting a breakthrough in long-term cardiovascular risk management.

Shakta Mani Satyam, Mohamed El-Tanani, Mohamed Anas Patni, Abdul Rehman, Sara Muhammad Irshad, Reem Raheem, Esha Junais, Ashika Anu John, Rena Yusuf Rassal, Rashmi Kumari and 1 more

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in BMC cardiovascular disorders, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Shakta Mani SatyamDepartment of Pharmacology, Translational Medical Research Centre & Central Animal Research Facility, RAK College of Medical Sciences, RAK Medical and Health Sciences University, Ras Al Khaimah, United Arab Emirates. satyam@rakmhsu.ac.ae.
Mohamed El-TananiRAK College of Pharmacy, Ras Al Khaimah Medical and Health Sciences University, Ras Al Khaimah, 11172, United Arab Emirates. eltanani@rakmhsu.ac.ae.
Mohamed Anas PatniDepartment of Community Medicine, RAK College of Medical Sciences, RAK Medical and Health Sciences University, Ras Al Khaimah, United Arab Emirates.
Abdul RehmanDepartment of Pathological Sciences, College of Medicine, Ajman University, Ajman, United Arab Emirates.
Sara Muhammad IrshadDepartment of Pharmacology, Translational Medical Research Centre & Central Animal Research Facility, RAK College of Medical Sciences, RAK Medical and Health Sciences University, Ras Al Khaimah, United Arab Emirates.
Reem RaheemDepartment of Pharmacology, Translational Medical Research Centre & Central Animal Research Facility, RAK College of Medical Sciences, RAK Medical and Health Sciences University, Ras Al Khaimah, United Arab Emirates.
Esha JunaisDepartment of Pharmacology, Translational Medical Research Centre & Central Animal Research Facility, RAK College of Medical Sciences, RAK Medical and Health Sciences University, Ras Al Khaimah, United Arab Emirates.
Ashika Anu JohnDepartment of Pharmacology, Translational Medical Research Centre & Central Animal Research Facility, RAK College of Medical Sciences, RAK Medical and Health Sciences University, Ras Al Khaimah, United Arab Emirates.
Rena Yusuf RassalDepartment of Pharmacology, Translational Medical Research Centre & Central Animal Research Facility, RAK College of Medical Sciences, RAK Medical and Health Sciences University, Ras Al Khaimah, United Arab Emirates.
Rashmi KumariA. J. Institute of Hospital Management, A. J. Hospital & Research Centre, Mangalore, India. rashmisatyam1203@gmail.com.
Sainath PDepartment of Perfusion Technology, Manipal College of Health Professions, Manipal Academy of Higher Education, Udupi, Manipal, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInclisiran is a novel small interfering RNA therapeutic developed to lower lipid levels by targeting hepatic production of proprotein convertase subtilisin/kexin type 9. Unlike monoclonal antibodies, Inclisiran silences messenger RNA expression, resulting in sustained reductions in low-density lipoprotein cholesterol with infrequent dosing. This study aimed to systematically evaluate the efficacy and clinical applicability of Inclisiran across randomized controlled trials.

methodsA systematic literature search was conducted in PubMed, Scopus, Embase, and Cochrane CENTRAL databases up to December 2024. This meta-analysis updates the global evidence base by incorporating 14 randomized trials (> 13,000 participants) identified through December 2024. Beyond earlier syntheses, it provides pooled analyses of multiple lipid parameters, phenotype-stratified subgroup and sensitivity analyses, and meta-regression for baseline LDL-C and statin use, thereby offering the most comprehensive and clinically differentiated evaluation of inclisiran to date. The primary outcome was the mean change in low-density lipoprotein cholesterol levels in patients treated with Inclisiran compared to placebo. Data was pooled using a random-effects model. Heterogeneity was assessed using the I² statistic, and publication bias was evaluated with funnel plot analysis.

resultsInclisiran treatment resulted in a significant mean reduction of 44.9% in low-density lipoprotein cholesterol levels compared to placebo (95% confidence interval: 39.54% to 50.25%; p < 0.001). While statistical heterogeneity was high (I² = 90.3%), visual assessment of the funnel plot suggested minimal risk of publication bias. Subgroup analyses supported consistent efficacy across patient populations, including those with statin intolerance or poor adherence to conventional therapies.

conclusionsInclisiran provides a durable, twice-yearly injectable option for lipid management, offering substantial reductions in low-density lipoprotein cholesterol. Its unique RNA-based mechanism and long-acting profile make it particularly suitable for patients who struggle with adherence or have limited response to traditional lipid-lowering medications. These findings support Inclisiran’s role as a promising addition to current strategies for cardiovascular risk reduction.

Indexed as

Cardiovascular DiseasesCholesterol, LDLDyslipidemiasRNAi TherapeuticsRNA, Small InterferingAgedBiomarkersFemaleHeart Disease Risk FactorsHumansMaleMiddle AgedPCSK9 InhibitorsProprotein Convertase 9Randomized Controlled Trials as TopicRisk AssessmentALN-PCSBiomarkersCholesterol, LDLPCSK9 InhibitorsPCSK9 protein, humanProprotein Convertase 9RNA, Small InterferingCardiovascular risk managementInclisiranLDL cholesterol reductionLipid-lowering agentsPCSK9 inhibitionSiRNA therapy

Identifiers

PMID41514239
PMCPMC12853707

What OpenQuestion holds

Texttitle and abstract
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.