Evidence map›Paper›PMID 37658913›Full record

ArticleClinical research in cardiology : official journal of the German Cardiac Society2024

Coronary microvascular dysfunction is a hallmark of all subtypes of MINOCA.

Andrea Milzi, Rosalia Dettori, Richard Karl Lubberich, Sebastian Reith, Michael Frick, Kathrin Burgmaier, Nikolaus Marx, Mathias Burgmaier

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In one paragraph

Article in Clinical research in cardiology : official journal of the German Cardiac Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 9 citations in OpenAlex.

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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

8 authors at 3 institutions in 1 country.

Andrea MilziDepartment of Internal Medicine I, University Hospital of the RWTH, Aachen, Germany. amilzi@ukaachen.de.ORCID http://orcid.org/0000-0001-7580-8029
Rosalia DettoriDepartment of Internal Medicine I, University Hospital of the RWTH, Aachen, Germany.
Richard Karl LubberichDepartment of Internal Medicine I, University Hospital of the RWTH, Aachen, Germany.
Sebastian ReithDepartment of Cardiology, Angiology and Electrophysiology, St. Franziskus Hospital, Münster, Germany.
Michael FrickDepartment of Internal Medicine I, University Hospital of the RWTH, Aachen, Germany.
Kathrin BurgmaierFaculty of Applied Healthcare Science, Deggendorf Institute of Technology, Deggendorf, Germany.
Nikolaus MarxDepartment of Internal Medicine I, University Hospital of the RWTH, Aachen, Germany.
Mathias BurgmaierDepartment of Internal Medicine I, University Hospital of the RWTH, Aachen, Germany.
RWTH Aachen University · DEDeggendorf Institute of Technology · DESt. Franziskus Hospital · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMyocardial infarction without obstructive coronary artery disease (MINOCA) is a heterogeneous clinical condition presenting with myocardial necrosis not due to an obstruction of a major coronary artery. Recently, a relevant role of coronary microvascular dysfunction (CMD) in the pathogenesis of MINOCA has been suggested; however, data on this are scarce. Particularly, it is unclear if CMD is equally present in all subtypes of MINOCA or differentially identifies one or more of these conditions. Therefore, the aim of this study was to assess CMD in all three coronary vessels of MINOCA patients, relating it with the clinical subtype.

methodsWe retrospectively assessed coronary microvascular function in all three coronary territories by means of angiography-based index of microvascular resistance (aIMR) in 92 patients (64 with working diagnosis of MINOCA, 28 control patients). To further assess the association of CMD with MINOCA subtypes, MINOCA patients were subdivided according to clinical data in coronary cause (n = 13), takotsubo (n = 13), infiltrative or inflammatory cardiomyopathy (n = 9) or unclear (n = 29).

resultsPatients with working diagnosis of MINOCA showed a significantly elevated average aIMR compared to control patients (30.5 ± 7.6 vs. 22.1 ± 5.9, p < 0.001) as a marker of a relevant CMD; these data were consistent in all vessels. Among MINOCA subtypes, no significant difference in average aIMR could be detected between patients with coronary cause (33.2 ± 6.6), takotsubo cardiomyopathy (29.2 ± 6.9), infiltrative or inflammatory cardiomyopathy (28.1 ± 6.8) or unclear cause (30.6 ± 8.5; p = 0.412). Interestingly, aIMR was significantly elevated in the coronary vessel supplying the diseased myocardium compared with other vessels (31.9 ± 11.4 vs. 27.8 ± 8.2, p = 0.049).

conclusionCoronary microvascular dysfunction is a hallmark of all MINOCA subtypes. This study adds to the pathophysiological understanding of MINOCA and sheds light into the role of CMD in MINOCA.

Indexed as

Coronary AngiographyCoronary CirculationCoronary VesselsMicrocirculationAgedCoronary Artery DiseaseFemaleHumansMaleMiddle AgedMyocardial InfarctionRetrospective StudiesVascular ResistanceCoronary arteryCoronary microvascular dysfunctionCoronary physiologyDiseaseMINOCA

Identifiers

PMID37658913
PMCPMC11579118
OpenAlexW4386390953

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Registered trials

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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.