Evidence map›Paper›PMID 42584677›Full record

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

Vascular endothelial dysfunction and echocardiographic changes in male and female patients with Fabry disease: a single-center observational study.

Radosław Dziedzic, Piotr Kuszmiersz, Magdalena Szuścik, Anna Drynda, Magdalena Celińska-Löwenhoff, Agnieszka Padjas, Renata Pacholczak-Madej, Lech Zaręba, Jan G Bazan, Stanisława Bazan-Socha and 1 more

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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.

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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

11 authors.

Radosław DziedzicDoctoral School of Medical and Health Sciences, Jagiellonian University Medical College, św. Łazarza 16, Kraków, 31-530, Poland.ORCID http://orcid.org/0000-0003-0321-3557
Piotr KuszmierszClinical Department of Rheumatology, Immunology and Internal Medicine, University Hospital in Kraków, Jakubowskiego 2, Kraków, 30-688, Poland.ORCID http://orcid.org/0000-0002-2031-6657
Magdalena SzuścikStudents' Scientific Group of Immune Diseases and Hypercoagulation, Jagiellonian University Medical College, Jakubowskiego 2, Kraków, 30-688, Poland.ORCID http://orcid.org/0009-0001-8686-8905
Anna DryndaDoctoral School of Medical and Health Sciences, Jagiellonian University Medical College, św. Łazarza 16, Kraków, 31-530, Poland.ORCID http://orcid.org/0009-0009-5556-2637
Magdalena Celińska-LöwenhoffClinical Department of Rheumatology, Immunology and Internal Medicine, University Hospital in Kraków, Jakubowskiego 2, Kraków, 30-688, Poland.ORCID http://orcid.org/0000-0002-4889-2218
Agnieszka PadjasClinical Department of Rheumatology, Immunology and Internal Medicine, University Hospital in Kraków, Jakubowskiego 2, Kraków, 30-688, Poland.ORCID http://orcid.org/0000-0001-6492-6521
Renata Pacholczak-MadejDepartment of Anatomy, Jagiellonian University Medical College, Kopernika 12, Kraków, 31-034, Poland.ORCID http://orcid.org/0000-0002-6535-4841
Lech ZarębaFaculty of Exact and Technical Science, Institute of Computer Science, University of Rzeszów, Pigonia 1, Rzeszów, 35-310, Poland.ORCID http://orcid.org/0000-0002-2221-614X
Jan G BazanFaculty of Exact and Technical Science, Institute of Computer Science, University of Rzeszów, Pigonia 1, Rzeszów, 35-310, Poland.ORCID http://orcid.org/0000-0002-9738-7007
Stanisława Bazan-Socha *Clinical Department of Rheumatology, Immunology and Internal Medicine, University Hospital in Kraków, Jakubowskiego 2, Kraków, 30-688, Poland.ORCID http://orcid.org/0000-0001-9634-0963
Jerzy Dropiński *Clinical Department of Rheumatology, Immunology and Internal Medicine, University Hospital in Kraków, Jakubowskiego 2, Kraków, 30-688, Poland. jerzy.dropinski@uj.edu.pl.ORCID http://orcid.org/0000-0002-0768-5597

Funding

Wydział Lekarski, Uniwersytet Jagielloński Collegium Medicum N41/DBS/000506
6 · The paper itself

Abstract

introductionFabry disease (FD) is a progressive X-linked lysosomal storage disorder characterized by the accumulation of pathological glycosphingolipids in a wide range of cells, leading, among others, to vascular endothelial dysfunction. Advanced atherosclerosis, indicated by increased intima-media thickness (IMT), and endothelial injury, characterized by impaired arterial flow-mediated dilatation (FMD), are associated with a higher cardiovascular risk seen in these patients. Next, echocardiography may provide non-invasive insight into cardiac changes that may also correlate with endothelial dysfunction in FD. However, evidence on that relationship is scarce, especially regarding sex differences. Therefore, we aimed to evaluate endothelial function together with echocardiographic changes in a cohort of Polish FD patients. PATIENTS AND

methodsWe assessed brachial artery FMD, measured common carotid artery IMT, and performed transthoracic echocardiography to evaluate cardiac involvement in 31 FD patients without cardiovascular events in medical history (17 male and 14 female patients) and 31 controls matched by age, sex, and body mass index (BMI).

resultsFD patients exhibited a 54.8% reduction in FMD response and a 25.0% increase in IMT thickness compared to controls (p < 0.001 for both, also after adjustment for sex, age, and BMI). In echocardiography, FD exhibited increased left ventricular wall thickness, a slightly reduced ejection fraction, and a higher pulmonary artery systolic pressure compared to the controls (p < 0.001 for all, also after adjustment for sex, age, and BMI). There were several associations between FMD/IMT and echocardiographic parameters. No differences in FMD or IMT were observed when comparing male and female FD patients.

conclusionsFabry disease is associated with vascular endothelial dysfunction and subclinical arterial wall thickening, as reflected by reduced FMD and increased IMT, respectively. No significant sex-related differences in FMD or IMT were observed in our FD patient group. Overall, these parameters were associated with echocardiographic abnormalities characteristic for FD. Importantly, all of these parameters can be assessed using non-invasive diagnostic methods.

Indexed as

EchocardiographyFabry diseaseFlow-mediated dilatationIntima-media thicknessVascular endothelial dysfunction

Identifiers

PMID42584677

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