Evidence mapPaperPMID 39484117Full record

ReviewReviews in cardiovascular medicine2024

Rationale for Early Administration of PCSK9 Inhibitors in Acute Coronary Syndrome.

Salvatore Giordano, Jessica Ielapi, Nadia Salerno, Angelica Cersosimo, Alessandro Lucchino, Alessandro Laschera, Giovanni Canino, Assunta Di Costanzo, Salvatore De Rosa, Daniele Torella and 1 more

Abstract readReview
In one paragraph

Review in Reviews in cardiovascular medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
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  7. 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.

Salvatore GiordanoDepartment of Medical and Surgical Sciences, Division of Cardiology, "Magna Graecia" University, 88100 Catanzaro, Italy.
Jessica IelapiDepartment of Experimental and Clinical Medicine, "Magna Graecia" University, 88100 Catanzaro, Italy.
Nadia SalernoDepartment of Experimental and Clinical Medicine, "Magna Graecia" University, 88100 Catanzaro, Italy.
Angelica CersosimoDepartment of Experimental and Clinical Medicine, "Magna Graecia" University, 88100 Catanzaro, Italy.
Alessandro LucchinoDepartment of Medical and Surgical Sciences, Division of Cardiology, "Magna Graecia" University, 88100 Catanzaro, Italy.
Alessandro LascheraDepartment of Medical and Surgical Sciences, Division of Cardiology, "Magna Graecia" University, 88100 Catanzaro, Italy.
Giovanni CaninoDepartment of Medical and Surgical Sciences, Division of Cardiology, "Magna Graecia" University, 88100 Catanzaro, Italy.
Assunta Di CostanzoDepartment of Medical and Surgical Sciences, Division of Cardiology, "Magna Graecia" University, 88100 Catanzaro, Italy.
Salvatore De RosaDepartment of Medical and Surgical Sciences, Division of Cardiology, "Magna Graecia" University, 88100 Catanzaro, Italy.
Daniele TorellaDepartment of Experimental and Clinical Medicine, "Magna Graecia" University, 88100 Catanzaro, Italy.
Sabato SorrentinoDepartment of Medical and Surgical Sciences, Division of Cardiology, "Magna Graecia" University, 88100 Catanzaro, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute coronary syndromes (ACSs) represent a significant global health challenge arising from atherosclerotic cardiovascular disease (ASCVD), with elevated low-density lipoprotein cholesterol (LDL-C) levels being a primary contributor. Despite standard statin therapy, individuals with ACS remain at high risk for recurrent cardiovascular events, particularly in the initial post-ACS period. Monoclonal antibodies targeting proprotein convertase subtilisin/kexin type 9 (PCSK9), such as evolocumab and alirocumab, offer a potential strategy to reduce LDL-C levels further and mitigate this residual risk. This review delves into the molecular mechanisms, effects on cholesterol metabolism, inflammatory modulation, and clinical outcomes associated with early administration of PCSK9 inhibitors following ACS.

Indexed as

acute coronary syndromelow-density lipoprotein cholesterolproprotein convertase subtilisin/kexin type 9

Identifiers

PMID39484117
PMCPMC11522761

What Socratic holds

Textmetadata
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 Socratic graph.