Evidence map›Paper›PMID 39385797›Full record

ReviewTranslational medicine @ UniSa2024

Novel Targets and Strategies Addressing Residual Cardiovascular Risk in Post-acute Coronary Syndromes Patients.

Francesco P Cancro, Michele Bellino, Angelo Silverio, Marco Di Maio, Luca Esposito, Rossana Palumbo, Martina L Manna, Ciro Formisano, Germano Ferruzzi, Carmine Vecchione and 1 more

Abstract readReview
In one paragraph

Review in Translational medicine @ UniSa, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

11 authors.

Francesco P CancroDepartment of Medicine Surgery and Dentistry, University of Salerno, Baronissi, SA, Italy.
Michele BellinoDepartment of Medicine Surgery and Dentistry, University of Salerno, Baronissi, SA, Italy.
Angelo SilverioDepartment of Medicine Surgery and Dentistry, University of Salerno, Baronissi, SA, Italy.
Marco Di MaioDepartment of Medicine Surgery and Dentistry, University of Salerno, Baronissi, SA, Italy.
Luca EspositoDepartment of Medicine Surgery and Dentistry, University of Salerno, Baronissi, SA, Italy.
Rossana PalumboDepartment of Medicine Surgery and Dentistry, University of Salerno, Baronissi, SA, Italy.
Martina L MannaDepartment of Medicine Surgery and Dentistry, University of Salerno, Baronissi, SA, Italy.
Ciro FormisanoDepartment of Medicine Surgery and Dentistry, University of Salerno, Baronissi, SA, Italy.
Germano FerruzziDepartment of Medicine Surgery and Dentistry, University of Salerno, Baronissi, SA, Italy.
Carmine VecchioneDepartment of Medicine Surgery and Dentistry, University of Salerno, Baronissi, SA, Italy.
Gennaro GalassoDepartment of Medicine Surgery and Dentistry, University of Salerno, Baronissi, SA, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the advancement in secondary cardiovascular prevention strategies for post-acute coronary syndrome (ACS) patients, the development of new drugs addressing dyslipidemia and the personalization of dual antiplatelet therapies (DAPT), these patients continue to suffer a significant incidence of recurrent ischemic events. Therefore, novel targets that can be tackled to reduce cardiovascular risk are needed to improve the outcome of this very high-risk population. The role of chronic inflammation and inflammasome in the development and progression of atherosclerosis has been broadly investigated in patients with established coronary artery disease (CAD) and recent randomized trials have highlighted the possibility to manage these targets with specific drugs such as colchicine and monocolonal antibodies with a significant improvement of cardiovascular outcomes in post-ACS patients. Lipoprotein(a) [Lp(a)] is the most promising non-traditional risk factor and has shown to predict worse outcome in post-ACS patients. Lowering Lp(a) through PCSK9 inhibitors and specific targeted therapies has shown positive results in reducing adverse cardiovascular events in patients with established CAD. The effect of microbiome and its alteration in gut dysbiosis seems to actively participate in residual cardiovascular risk of CAD patients; however, the risk-modifying effect of targeted-microbiome therapies hasn't been yet investigated in large population-based studies. Long-term outcome of post-ACS patients is a complex puzzle of multiple factors. In this minireview, we summarize the emerging risk factors that may interplay in the residual risk of post-ACS patients and their possible prognostic and therapeutic implications.

Indexed as

Acute coronary syndromeCoronary artery diseaseEmerging therapiesInflammasomeInflammationLipoprotein(a)MicrobiotaSecondary prevention

Identifiers

PMID39385797
PMCPMC11460530

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Registered trials

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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.