Evidence map›Paper›PMID 37093420›Full record

ReviewAdvances in experimental medicine and biology2023

Statins and Hemostasis: Therapeutic Potential Based on Clinical Evidence.

Yolanda Prado, Diego Aravena, Felipe M Llancalahuen, Cristobal Aravena, Felipe Eltit, Cesar Echeverría, Sebastian Gatica, Claudia A Riedel, Felipe Simon

Abstract readReview
PubMed Publisher
In one paragraph

Review in Advances in experimental medicine and biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
27.3field-weighted citation impact, top 1% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Coronary plaque healing: a safety net or a hazard indicator?Journal of thrombosis and thrombolysis · 2026
    Review
  4. 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

9 authors at 4 institutions in 2 countries.

Yolanda PradoFaculty of Life Sciences, Universidad Andres Bello, Santiago, Chile.
Diego AravenaFaculty of Life Sciences, Universidad Andres Bello, Santiago, Chile.
Felipe M LlancalahuenFaculty of Life Sciences, Universidad Andres Bello, Santiago, Chile.
Cristobal AravenaFaculty of Life Sciences, Universidad Andres Bello, Santiago, Chile.
Felipe EltitDepartment of Urologic Sciences, University of British Columbia, Vancouver, Canada.
Cesar EcheverríaLaboratory of Molecular Biology, Nanomedicine and Genomics, Faculty of Medicine, University of Atacama, Copiapo, Chile.
Sebastian GaticaFaculty of Life Sciences, Universidad Andres Bello, Santiago, Chile.
Claudia A RiedelFaculty of Life Sciences, Universidad Andres Bello, Santiago, Chile.
Felipe SimonFaculty of Life Sciences, Universidad Andres Bello, Santiago, Chile. fsimon@unab.cl.
Millennium Institute on Immunology and Immunotherapy · CLUniversidad Andrés Bello · CLUniversity of Atacama · CLUniversity of British Columbia · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hemostasis preserves blood fluidity and prevents its loss after vessel injury. The maintenance of blood fluidity requires a delicate balance between pro-coagulant and fibrinolytic status. Endothelial cells (ECs) in the inner face of blood vessels maintain hemostasis through balancing anti-thrombotic and pro-fibrinolytic activities. Dyslipidemias are linked to hemostatic alterations. Thus, it is necessary a better understanding of the underlying mechanisms linking hemostasis with dyslipidemia. Statins are drugs that decrease cholesterol levels in the blood and are the gold standard for treating hyperlipidemias. Statins can be classified into natural and synthetic molecules, approved for the treatment of hypercholesterolemia. The classical mechanism of action of statins is by competitive inhibition of a key enzyme in the synthesis pathway of cholesterol, the HMG-CoA reductase. Statins are frequently administrated by oral ingestion and its interaction with other drugs and food supplements is associated with altered bioavailability. In this review we deeply discuss the actions of statins beyond the control of dyslipidemias, focusing on the actions in thrombotic modulation, vascular and cardiovascular-related diseases, metabolic diseases including metabolic syndrome, diabetes, hyperlipidemia, and hypertension, and chronic diseases such as cancer, chronic obstructive pulmonary disease, and chronic kidney disease. Furthermore, we were prompted to delved deeper in the molecular mechanisms by means statins regulate coagulation acting on liver, platelets, and endothelium. Clinical evidence show that statins are effective regulators of dyslipidemia with a high impact in hemostasis regulation and its deleterious consequences. However, studies are required to elucidate its underlying molecular mechanism and improving their therapeutical actions.

Indexed as

Cardiovascular DiseasesDyslipidemiasHydroxymethylglutaryl-CoA Reductase InhibitorsHyperlipidemiasThrombosisCholesterolEndothelial CellsHemostasisHumansCholesterolHydroxymethylglutaryl-CoA Reductase InhibitorsFibrinolysisHemostasisLipidsStatinThrombosis

Identifiers

PMID37093420
OpenAlexW4366822127

What OpenQuestion holds

Texttitle and abstract
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.