ReviewEJIFCC2026
Endothelial-to-Mesenchymal Transition in Post-Myocardial Infarction Fibrosis: A Maladaptive but Targetable Pathway.
Review in EJIFCC, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Myocardial infarction (MI) initiates a healing response in which fibroblasts and other cells deposit extracellular matrix to form a stabilizing scar. This scarring is essential for preventing ventricular rupture, yet when excessive or diffuse, it becomes maladaptive: fibrosis stiffens the ventricle, impairs filling, and drives progression to heart failure. Traditional antifibrotic approaches, such as broad TGF-β blockade or collagen cross-linking inhibition, have largely failed because fibroblast activity is required for early scar integrity, while established fibrosis is difficult to reverse. This review highlights endothelial-to-mesenchymal transition (EndMT) as a distinct and underappreciated contributor to post-MI fibrosis. Experimental studies indicate that EndMT supplies 10-30% of fibroblast-like cells, and evidence of EndMT is present in human ischemic cardiomyopathy. Unlike fibroblast-driven repair, EndMT is maladaptive in the adult heart: it promotes fibrosis without enhancing scar strength and reduces endothelial cell numbers, leading to microvascular rarefaction and impaired perfusion. EndMT is regulated by discrete, targetable pathways-including TGF-β/Smad, Notch, Wnt/β-catenin, HIF-1α, and microRNA networks (e.g., miR-21, miR-29)-and exhibits partial reversibility. This opens opportunities for time-limited, pathway-specific interventions during the proliferative phase of healing. Emerging diagnostic tools, such as extracellular volume mapping, fibroblast activation protein PET, collagen peptide assays, and circulating fibrosis-related microRNAs, provide clinical means to detect EndMT activity. By integrating mechanistic insights with advances in molecular imaging and biomarker profiling, this review proposes EndMT-directed, biomarker-guided therapies as a precision strategy to limit maladaptive fibrosis, preserve vascular networks, and improve outcomes after MI.
Indexed as
Identifiers
41659298PMC12882090What OpenQuestion holds
Registered trials
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.