Evidence map›Paper›PMID 39699771›Full record

ReviewCurrent atherosclerosis reports2024

"Anti-inflammatory Therapies in Atherosclerosis - Where are we going?"

Natdanai Punnanithinont, Soumya Kambalapalli, Beshoy Iskander, Keishi Ichikawa, Srikanth Krishnan, Suvasini Lakshmanan, Sion K Roy, Matthew Budoff

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current atherosclerosis reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Gut microbiota-mediated cardiovascular effects ofFrontiers in microbiology · 2026
    Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
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

8 authors.

Natdanai PunnanithinontThe Lundquist Institute, UCLA Medical Center Harbor, 1124 W Carson St, CA 90502, Torrance, US. n.punnanithinont@lundquist.org.
Soumya KambalapalliThe Lundquist Institute, UCLA Medical Center Harbor, 1124 W Carson St, CA 90502, Torrance, US.
Beshoy IskanderThe Lundquist Institute, UCLA Medical Center Harbor, 1124 W Carson St, CA 90502, Torrance, US.
Keishi IchikawaThe Lundquist Institute, UCLA Medical Center Harbor, 1124 W Carson St, CA 90502, Torrance, US.
Srikanth KrishnanThe Lundquist Institute, UCLA Medical Center Harbor, 1124 W Carson St, CA 90502, Torrance, US.
Suvasini LakshmananThe Lundquist Institute, UCLA Medical Center Harbor, 1124 W Carson St, CA 90502, Torrance, US.
Sion K RoyThe Lundquist Institute, UCLA Medical Center Harbor, 1124 W Carson St, CA 90502, Torrance, US.
Matthew BudoffThe Lundquist Institute, UCLA Medical Center Harbor, 1124 W Carson St, CA 90502, Torrance, US.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewInflammation has been commonly known for the past decade as a part of the pathophysiology of atherosclerosis, along with lipid accumulation. However, some patients with optimized lipid-lowering therapy still have elevated inflammatory biomarkers. Anti-inflammation therapies were developed to eradicate this residual risk. We summarized the primary inflammatory pathway and recent clinical trials in anti-inflammation therapies. RECENT

findingsColchicine Cardiovascular Outcomes Trial (COLCOT) and LoDoCo2 (Colchicine Reduces Risk of Major Cardiovascular Events in Chronic Coronary Disease) found that low-dose colchicine significantly reduced cardiovascular death, myocardial infarction (MI), ischemic stroke and coronary revascularization in patients with recent MI within 30 days and chronic coronary disease respectively. The US Food and Drug Administration approved low-dose colchicine in 2023 for patients with established atherosclerotic cardiovascular disease (ASCVD). However, its use was limited for chronic kidney disease (CKD) patients. Reduction in Inflammation in Patients with Advanced Chronic Renal Disease Utilizing Antibody Mediated Interleukin-6 Inhibition (RESCUE) was conducted using Ziltivekimab, an IL-6 ligand monoclonal antibody and found that it significantly reduced high-sensitivity C-reactive protein, an inflammatory surrogate marker. There is an ongoing phase-3 clinical trial, Ziltivekimab Versus Placebo Cardiovascular Outcomes in Participants with Atherosclerotic Cardiovascular Disease, Chronic Kidney Disease, and Systemic Inflammation trial (ZEUS), which will be essential for further anti-inflammation therapy for patients with CKD. Numerous clinical trials have investigated anti-inflammation therapies. Colchicine is by far the only one that has the potential to be widely used due to its cost-effectiveness. Further research is needed on other novel anti-inflammation therapies and their real-world implementation.

Indexed as

Anti-Inflammatory AgentsAtherosclerosisInflammationColchicineHumansAnti-Inflammatory AgentsColchicineAnti-inflammationAtherosclerosisColchicineInflammation

Identifiers

PMID39699771

What OpenQuestion holds

Textmetadata
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.