Evidence map›Paper›PMID 42519385›Full record

ReviewFrontiers in cardiovascular medicine2026

Spontaneous coronary artery dissection as a threshold disorder of coronary wall integrity.

Zhongwei Liu, Jun Wang

Abstract readReview
In one paragraph

Review in Frontiers in cardiovascular medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Zhongwei LiuDepartment of Cardiology, Shaanxi Provincial People's Hospital, Xi'an, China.
Jun WangDepartment of Anesthesiology, Shaanxi Provincial Cancer Hospital, Xi'an, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spontaneous coronary artery dissection (SCAD) is an increasingly recognized cause of non-atherosclerotic acute myocardial infarction, predominantly affecting young and middle-aged women and patients during pregnancy or the postpartum period. Although major progress has been made in clinical recognition, angiographic diagnosis, conservative management, and extracoronary vascular screening, the molecular basis of SCAD remains incompletely understood. Here, we develop a provisional, evidence-integrating framework that conceptualizes SCAD as a threshold disorder of coronary wall integrity rather than as a variant of plaque rupture or a purely intimal tear-driven event. The available evidence indicates that the final common pathological event is intramural hematoma formation and true-lumen compression, whereas the threshold for this event is shaped by inherited susceptibility, extracellular matrix architecture, vascular smooth muscle cell and fibroblast regulation, vascular tone, local hemostatic containment, systemic arteriopathy, and reproductive or stress-related hemodynamic load. We critically evaluate inside-out and outside-in models of SCAD initiation, common and rare genetic architecture, the ambiguous role of fibromuscular dysplasia, pregnancy-associated SCAD, antithrombotic controversies, and emerging strategies for mechanism-informed risk stratification. We also define what is established, what remains controversial, and what should not yet be translated into routine practice. Finally, we propose a research roadmap centered on multiomic prospective cohorts, coronary wall models, high-resolution imaging phenotypes, reproductive vascular biology, and pragmatic clinical trials. The resulting taxonomy is intended to organize current evidence, identify priorities for mechanistic validation, and potentially support precision diagnosis, individualized antithrombotic decisions, reproductive counseling, genetic testing, and prevention of recurrence.

Indexed as

coronary wall integrityextracellular matrixfibromuscular dysplasiaintramural hematomaprecision cardiovascular medicinepregnancy-associated myocardial infarctionspontaneous coronary artery dissectionvascular smooth muscle cell

Identifiers

PMID42519385
PMCPMC13381620

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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.