Evidence map›Paper›PMID 37623365›Full record

ReviewJournal of cardiovascular development and disease2023

Autophagy in Heart Failure: Insights into Mechanisms and Therapeutic Implications.

Magdalena Bielawska, Marta Warszyńska, Monika Stefańska, Przemysław Błyszczuk

Open access · goldAbstract readReview
In one paragraph

Review in Journal of cardiovascular development and disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

20 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Cardioprotective Role of CalhexCell biochemistry and biophysics · 2026
    Review
  3. Review
  4. Review
  5. The pathophysiological role of MiRNAs in heart failure.Frontiers in cardiovascular medicine · 2026
    Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Research progress of autophagy in heart failure.American journal of translational research · 2024
    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

4 authors at 1 institution in 2 countries.

Magdalena BielawskaDepartment of Clinical Immunology, Jagiellonian University Medical College, University Children's Hospital, Wielicka 265, 30-663 Cracow, Poland.
Marta WarszyńskaDepartment of Clinical Immunology, Jagiellonian University Medical College, University Children's Hospital, Wielicka 265, 30-663 Cracow, Poland.
Monika StefańskaDepartment of Clinical Immunology, Jagiellonian University Medical College, University Children's Hospital, Wielicka 265, 30-663 Cracow, Poland.
Przemysław BłyszczukDepartment of Clinical Immunology, Jagiellonian University Medical College, University Children's Hospital, Wielicka 265, 30-663 Cracow, Poland.ORCID 0000-0003-2521-3232
Jagiellonian University · PL

Funding

National Science Center 2019/35/B/NZ5/00551
6 · The paper itself

Abstract

Autophagy, a dynamic and complex process responsible for the clearance of damaged cellular components, plays a crucial role in maintaining myocardial homeostasis. In the context of heart failure, autophagy has been recognized as a response mechanism aimed at counteracting pathogenic processes and promoting cellular health. Its relevance has been underscored not only in various animal models, but also in the human heart. Extensive research efforts have been dedicated to understanding the significance of autophagy and unravelling its complex molecular mechanisms. This review aims to consolidate the current knowledge of the involvement of autophagy during the progression of heart failure. Specifically, we provide a comprehensive overview of published data on the impact of autophagy deregulation achieved by genetic modifications or by pharmacological interventions in ischemic and non-ischemic models of heart failure. Furthermore, we delve into the intricate molecular mechanisms through which autophagy regulates crucial cellular processes within the three predominant cell populations of the heart: cardiomyocytes, cardiac fibroblasts, and endothelial cells. Finally, we emphasize the need for future research to unravel the therapeutic potential associated with targeting autophagy in the management of heart failure.

Indexed as

autophagyheart failuremolecular mechanismspharmacological interventions

Identifiers

PMID37623365
PMCPMC10456056
OpenAlexW4385978230

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.