Evidence map›Paper›PMID 36005422›Full record

ReviewJournal of cardiovascular development and disease2022

Recent Update on PCSK9 and Platelet Activation Experimental Research Methods: In Vitro and In Vivo Studies.

Meidi Utami Puteri, Nuriza Ulul Azmi, Salbiah Ridwan, Muhammad Iqbal, Tresni Fatimah, Tri Diana Puspita Rini, Mitsuyasu Kato, Fadlina Chany Saputri

Open access · goldAbstract readReview
In one paragraph

Review in Journal of cardiovascular development and disease, 2022. 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
1.1field-weighted citation impact, top 23% of its field
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, 6 citations in OpenAlex.

  1. Platelet subpopulations and contribution to hemostasis.Blood science (Baltimore, Md.) · 2026
    Review
  2. Review
  3. Article
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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 at 2 institutions in 2 countries.

Meidi Utami PuteriDepartment of Pharmacology-Toxicology, Faculty of Pharmacy, Universitas Indonesia, Depok 16424, Indonesia.ORCID 0000-0003-1550-8627
Nuriza Ulul AzmiDepartment of Pharmacology-Toxicology, Faculty of Pharmacy, Universitas Indonesia, Depok 16424, Indonesia.
Salbiah RidwanMagister Program, Faculty of Pharmacy, Universitas Indonesia, Depok 16424, Indonesia.
Muhammad IqbalMagister Program, Faculty of Pharmacy, Universitas Indonesia, Depok 16424, Indonesia.
Tresni FatimahMagister Program, Faculty of Pharmacy, Universitas Indonesia, Depok 16424, Indonesia.
Tri Diana Puspita RiniMagister Program, Faculty of Pharmacy, Universitas Indonesia, Depok 16424, Indonesia.
Mitsuyasu KatoDepartment of Experimental Pathology, Faculty of Medicine, University of Tsukuba, Tsukuba 305-8575, Japan.ORCID 0000-0001-9905-2473
Fadlina Chany SaputriDepartment of Pharmacology-Toxicology, Faculty of Pharmacy, Universitas Indonesia, Depok 16424, Indonesia.ORCID 0000-0002-6668-8915
University of Indonesia · IDUniversity of Tsukuba · JP

Funding

Universitas Indonesia Hibah PUTI RA 2022
6 · The paper itself

Abstract

Proprotein convertase subtilisin/kexin type 9 (PCSK9) is a crucial factor in the development and progression of cardiovascular diseases. PCSK9 has been demonstrated to modify LDL plasma levels and increase platelet activation, which promotes atherosclerosis, a defining feature of nearly all cardiovascular diseases. Platelet activation has been shown to promote and maintain the response to atherosclerosis development, from beginning to progression and exacerbation, which can lead to advanced cardiovascular events including myocardial infarction (MI) or death. Research on PCSK9 and platelet activation is currently underway with the main goal of reducing the risk of advanced cardiovascular events by preventing or slowing down atherosclerosis progression. Both in vitro and in vivo studies have been used to explore PCSK9 functions to develop new drugs targeting PCSK9. Finding the most suitable study models that represent the pathological and physiological systems found in humans is very important to achieving the goal. This review aimed to present a current and comprehensive overview of the experimental models that have been used to investigate the role of PCSK9 in platelet activation-induced atherosclerotic cardiovascular diseases.

Indexed as

animal modelsatherosclerosiscardiovascular diseaseexperimental methodsmyocardial infarctionplatelet activationproprotein convertase subtilisin/kexin type 9

Identifiers

PMID36005422
PMCPMC9409389
OpenAlexW4291002226

What OpenQuestion 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 OpenQuestion graph.