Evidence map›Paper›PMID 42897551›Full record

ArticleBMC medical imaging2026

Early detection of myocardial fibrosis in patients with coronary microvascular dysfunction in the absence of late enhancement: role of T1 mapping and extracellular volume analysis.

Runze Wen, Qiang Xie, Bo Pan, Xingxing Zhu, Dan Li, Xuemei Wang

Abstract read
In one paragraph

Article in BMC medical imaging, 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

6 authors.

Runze WenDepartment of Nuclear Medicine, Division of Life Sciences and Medicine, First Affiliated Hospital of USTC, University of Science and Technology of China, 17 Lujiang Road, Hefei, Anhui, 230001, China.
Qiang XieDepartment of Nuclear Medicine, Division of Life Sciences and Medicine, First Affiliated Hospital of USTC, University of Science and Technology of China, 17 Lujiang Road, Hefei, Anhui, 230001, China.
Bo PanDepartment of Nuclear Medicine, Division of Life Sciences and Medicine, First Affiliated Hospital of USTC, University of Science and Technology of China, 17 Lujiang Road, Hefei, Anhui, 230001, China.
Xingxing ZhuDepartment of Nuclear Medicine, Division of Life Sciences and Medicine, First Affiliated Hospital of USTC, University of Science and Technology of China, 17 Lujiang Road, Hefei, Anhui, 230001, China.
Dan LiDepartment of Cardiovascular Medicine, Division of Life Sciences and Medicine, First Affiliated Hospital of USTC, University of Science and Technology of China, 17 Lujiang Road, Hefei, Anhui, 230001, China. li-dan@ustc.edu.cn.
Xuemei WangDepartment of Nuclear Medicine, Division of Life Sciences and Medicine, First Affiliated Hospital of USTC, University of Science and Technology of China, 17 Lujiang Road, Hefei, Anhui, 230001, China. wangxuemei201010@163.com.

Funding

USTC Research Funds of the Double First-Class Initiative YD9110002055
6 · The paper itself

Abstract

backgroundCoronary microvascular dysfunction (CMD) can exacerbate myocardial fibrosis, which may further impair microvascular function. However, the relationship between CMD and the extracellular volume fraction (ECV) in patients with ischemia with no obstructive coronary artery disease (INOCA) who are late gadolinium enhancement (LGE)-negative remains undetermined. We used T1 mapping and ECV to assess diffuse myocardial tissue abnormalities and extracellular compartment expansion in LGE-negative patients with CMD. We then investigated how these markers correlate with global myocardial flow reserve (MFR).

methodsBetween August 2024 and May 2026, we prospectively enrolled 86 LGE-negative patients with INOCA from a single center who underwent a positron emission tomography-magnetic resonance imaging (PET-MRI) protocol. Patients with significant epicardial stenosis (stenosis on coronary angiogram or computed tomography ≥ 50%), prior history of revascularization, known myocardial infarction, or heart failure were excluded. MFR and ECV were derived from PET perfusion imaging and pre- and post-T1 mapping, respectively. CMD was defined as PET-derived MFR of < 2.0 in at least one major coronary artery territory.

resultsAmong the 86 patients included, 39 (45.3%) were diagnosed with CMD. ECV was substantially higher in the CMD group (31.22 [29.93, 33.25]% vs. 26.66 [25.85, 27.55]%, P < 0.001), with a more modest but statistically significant elevation in native T1 (1225 ± 25 ms vs. 1212 ± 21 ms, P = 0.012). Multivariable linear regression revealed that only global MFR (β [95% confidence interval] = - 1.905 [- 2.489, - 1.321], P < 0.001) was an independent predictor of ECV in LGE-negative CMD patients. In the overall cohort, resting myocardial blood flow (MBF) (r = 0.539, P < 0.001) and global MFR (r = - 0.741, P < 0.001) were positively and negatively correlated with ECV, respectively. When participants were stratified into ECV tertiles, global MFR showed a progressive decrease (2.92 vs. 2.48 vs. 1.78; P < 0.001 for trend) with increasing ECV values.

conclusionsIn patients with INOCA with CMD, prolonged native T1 and elevated ECV indicate diffuse interstitial expansion, consistent with early tissue remodeling, even when LGE is absent on CMR. These findings suggest that native T1 and ECV may hold promise as adjunctive tissue markers to support risk stratification, though their role in clinical management requires further validation in larger cohorts.

Indexed as

Coronary Artery DiseaseCoronary VesselsMagnetic Resonance ImagingMyocardiumAgedContrast MediaCoronary CirculationEarly DiagnosisFemaleFibrosisHumansMaleMiddle AgedPerfusion Magnetic Resonance ImagingPositron-Emission TomographyProspective StudiesContrast MediaCardiac magnetic resonanceCoronary microvascular dysfunctionExtracellular volume fractionLate gadolinium enhancementMyocardial flow reserve

Identifiers

PMID42897551
PMCPMC13681898

What OpenQuestion holds

Textmetadata
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.