Evidence map›Paper›PMID 39463005›Full record

ReviewDevelopment, growth & differentiation2024

Transition from fetal to postnatal state in the heart: Crosstalk between metabolism and regeneration.

Tai Sada, Wataru Kimura

Abstract readReview
In one paragraph

Review in Development, growth & differentiation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. 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

2 authors.

Tai SadaLaboratory for Heart Regeneration, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan.ORCID https://orcid.org/0009-0000-3087-4890
Wataru KimuraLaboratory for Heart Regeneration, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan.ORCID https://orcid.org/0000-0001-6548-6353

Funding

Bristol-Myers SquibbHoansha FoundationJapan Agency for Medical Research and Development, PRIMEJapanese Circulation SocietyJapan Society for the Promotion of Science 17H05083Japan Society for the Promotion of Science 19K22629Japan Society for the Promotion of Science 20H03680Japan Society for the Promotion of Science 21K18273JST FOREST JPMJFR210OJST SPRING JPMJSP2138Mitsubishi FoundationMochida Memorial Foundation for Medical and Pharmaceutical ResearchNaito FoundationPrincess Takamatsu Cancer Research FundSenri Life Science FoundationTakeda Science FoundationToray Science FoundationUehara Memorial Foundation
6 · The paper itself

Abstract

Cardiovascular disease is the leading cause of mortality worldwide. Myocardial injury resulting from ischemia can be fatal because of the limited regenerative capacity of adult myocardium. Mammalian cardiomyocytes rapidly lose their proliferative capacities, with only a small fraction of adult myocardium remaining proliferative, which is insufficient to support post-injury recovery. Recent investigations have revealed that this decline in myocardial proliferative capacity is closely linked to perinatal metabolic shifts. Predominantly glycolytic fetal myocardial metabolism transitions towards mitochondrial fatty acid oxidation postnatally, which not only enables efficient production of ATP but also causes a dramatic reduction in cardiomyocyte proliferative capacity. Extensive research has elucidated the mechanisms behind this metabolic shift, as well as methods to modulate these metabolic pathways. Some of these methods have been successfully applied to enhance metabolic reprogramming and myocardial regeneration. This review discusses recently acquired insights into the interplay between metabolism and myocardial proliferation, emphasizing postnatal metabolic transitions.

Indexed as

HeartMyocardiumRegenerationAnimalsCell ProliferationHumansMyocytes, Cardiacamino acidsBCAAcardiac metabolismenvironment shiftfatty acid oxidationglycolysisheart regenerationketone bodymitochondriamTOR

Identifiers

PMID39463005
PMCPMC11659109

What OpenQuestion holds

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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.