Evidence map›Paper›PMID 42189384›Full record

ReviewCurrent cardiology reports2026

Updates on Pathophysiology of Pericarditis to Guide Development of Therapeutics.

Aldo Bonaventura, Alessandra Vecchié, Adolfo Gabriele Mauro, Marco Giuseppe Del Buono, Brittany N Weber, Stefano Toldo, Antonio Abbate

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current cardiology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Aldo BonaventuraMedical Center, Ospedale Di Circolo and Fondazione Macchi, Department of Internal Medicine, S.C. Medicina Generale 1, ASST Sette Laghi, Varese, Italy. aldo.bonaventura@asst-settelaghi.it.
Alessandra VecchiéMedical Center, Ospedale Di Circolo and Fondazione Macchi, Department of Internal Medicine, S.C. Medicina Generale 1, ASST Sette Laghi, Varese, Italy.
Adolfo Gabriele MauroDivision of Pediatric Cardiology, Department of Pediatrics, Children's Hospital of Richmond at Virginia Commonwealth University Hospital System, Richmond, VA, USA.
Marco Giuseppe Del BuonoDepartment of Cardiovascular Sciences, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Brittany N WeberDivision of Cardiology, Department of Internal Medicine and Dermatology, Cardio-Rheumatology Program, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Stefano ToldoDivision of Cardiovascular Medicine, School of Medicine, Robert M. Berne Cardiovascular Research Center, University of Virginia, Charlottesville, VA, USA.
Antonio AbbateDivision of Cardiovascular Medicine, School of Medicine, Robert M. Berne Cardiovascular Research Center, University of Virginia, Charlottesville, VA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of the reviewPericarditis - the inflammation of the pericardial sac - has a generally benign course, although recurrences may occur in 15-30% of patients within 18 months, even after an initial uncomplicated course. For a long time, the scarcity of animal models has limited a deeper understanding of the pathophysiology of pericarditis. RECENT

findingsA number of stimuli, such as talc and bacterial products containing aluminum, were used in animal models to trigger the inflammation of the pericardial sac. Today, we know that such irritants represent canonical stimuli for the activation of the NACHT, leucine-rich repeat, and pyrin domain-containing protein 3 (NLRP3) inflammasome, an intracellular macromolecular complex responsible for the production and secretion of active interleukin-1 β (IL-1β), a pro-inflammatory cytokine that promotes pericardial inflammation. This evidence supports the central role of the NLRP3 inflammasome/IL-1β axis in driving acute inflammation of the pericardium and subsequent flares, as indirectly highlighted in seminal clinical trials of anakinra (AIRTRIP trial), rilonacept (RHAPSODY trial), and goflikicept. More recently, cannabidiol (CBD, derived from Cannabis sativa) has been found to block the NLRP3 inflammasome activation in vitro and in vivo. Preliminary positive findings have been reported in patients with ongoing recurrent pericarditis in the MAvERIC-Pilot study, while the phase III MAVERIC-2 trial is exploring the impact of CBD among patients with a history of recurrent pericarditis in stable control scheduled to discontinue an IL-1 blocker. The activation of the NLRP3 inflammasome/IL-1β axis supports auto-inflammation as a central event driving recurrences, and its targeted therapeutic inhibition results as a game changer to reduce the risk of recurrences and improve patients' quality of life. Accordingly, a shift moving from the prescription of glucocorticoids as second-line therapy in favor of IL-1 blockers, particularly in those patients presenting with an auto-inflammatory phenotype, is ongoing. To this end, an imaging-guided approach may help choosing the best treatment and monitoring its effects across time, thus allowing a personalized approach to patients with recurrent pericarditis.

Indexed as

PericarditisAnimalsHumansInflammasomesInterleukin-1betaInterleukin 1 Receptor Antagonist ProteinNLR Family, Pyrin Domain-Containing 3 ProteinRecombinant Fusion ProteinsInflammasomesInterleukin-1betaInterleukin 1 Receptor Antagonist ProteinNLR Family, Pyrin Domain-Containing 3 ProteinRecombinant Fusion ProteinsrilonaceptAnakinraCannabidiolGoflikiceptIL-1βNLRP3 inflammasomeRecurrent pericarditisRilonacept

Identifiers

What OpenQuestion holds

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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.