Evidence map›Paper›PMID 41504912›Full record

ArticleClinical research in cardiology : official journal of the German Cardiac Society2026

Microvascular dysfunction and heart failure with preserved ejection fraction.

Ornela Velollari, Antonio Biancofiore, Maximilian Olschewski, Helen Ullrich-Daub, Thomas Münzel, Karl-Philipp Rommel, Philipp Lurz, Tommaso Gori, Karl-Patrik Kresoja

Abstract read
In one paragraph

Article in Clinical research in cardiology : official journal of the German Cardiac Society, 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
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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

9 authors.

Ornela VelollariDepartment of Cardiology, Cardiology I, University Medical Center Mainz, Mainz, Germany.ORCID http://orcid.org/0009-0009-8458-478X
Antonio BiancofioreDepartment of Interventional Cardiology, Misericordia Hospital, Azienda USL (Unità Sanitaria Locale) Toscana Sud Est, Grosseto, Italy.
Maximilian OlschewskiDepartment of Cardiology, Cardiology I, University Medical Center Mainz, Mainz, Germany.
Helen Ullrich-DaubDepartment of Cardiology, Cardiology I, University Medical Center Mainz, Mainz, Germany.
Thomas MünzelDepartment of Cardiology, Cardiology I, University Medical Center Mainz, Mainz, Germany.
Karl-Philipp RommelDepartment of Cardiology, Cardiology I, University Medical Center Mainz, Mainz, Germany.
Philipp LurzDepartment of Cardiology, Cardiology I, University Medical Center Mainz, Mainz, Germany.
Tommaso GoriDepartment of Cardiology, Cardiology I, University Medical Center Mainz, Mainz, Germany.
Karl-Patrik KresojaDepartment of Cardiology, Cardiology I, University Medical Center Mainz, Mainz, Germany. kresojak@uni-mainz.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimThe impact of coronary microvascular dysfunction (CMD) on parameters of systolic and diastolic function, particularly in patients with heart failure and preserved ejection fraction (HFpEF), is poorly understood. Although these conditions often overlap, their combined impact on parameters of systolic and diastolic function remains unexplored.

methodsConsecutive patients undergoing invasive CMD assessment were enrolled. Systolic function was assessed by global longitudinal strain (GLS), diastolic function by E/E', left atrial reservoir strain (LARS), and non-invasive single-beat pressure-volume relationship stiffness constant (β) estimation.

resultsOf 145 patients, 72 (49.7%) had CMD, 35 (24%) HFpEF, and 23 (16%) both conditions. HFpEF was twice as prevalent in CMD patients as compared to patients without CMD (32% vs. 16%, p = 0.034). Both CMD was associated with parameters of both diastolic (E/E' β = 0.29, p < 0.001, LV stiffness constant β = 0.23; p = 0.006, and LARS β = -0.21, p = 0.02) and systolic function (GLS β = 0.31, p < 0.001). The presence of CMD was associated with an impairment in LV stiffness both in patients with and without HFpEF (p for interaction = 0.044).

conclusionHFpEF is highly prevalent in patients with CMD, and CMD is associated with both systolic and diastolic dysfunction. In patients with HFpEF, an additional worsening of diastolic function is observed.

Indexed as

Coronary CirculationHeart FailureMicrocirculationStroke VolumeVentricular Function, LeftAgedDiastoleFemaleGlobal Longitudinal StrainHumansMaleMiddle AgedSystoleCoronary microvascular dysfunctionDiastolic dysfunctionHeart failure with preserved ejection fraction

Identifiers

PMID41504912
PMCPMC13457450

What Socratic holds

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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 Socratic graph.