Evidence map›Paper›PMID 40627153›Full record

Observational studyRheumatology international2025

Endothelial function and vascular events in patients with limited cutaneous systemic sclerosis (EFVELSS): a prospective observational study.

Philipp Jud, Philipp Douschan, Teresa Sassmann, Günther Silbernagel, Katharina Gütl, Reinhard B Raggam, Peter Rief, Leyla Schweiger, Nikolaus John, Gerald Seinost and 10 more

Abstract readObservational Study
In one paragraph

Observational study in Rheumatology international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

20 authors.

Philipp JudDivision of Angiology, Department of Internal Medicine, Medical University of Graz, Auenbruggerplatz 15, Graz, 8036, Austria. philipp.jud@medunigraz.at.ORCID 0000-0002-0832-1322
Philipp DouschanDivision of Pulmonology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.ORCID 0000-0003-2505-7831
Teresa SassmannDivision of Pulmonology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Günther SilbernagelDivision of Angiology, Department of Internal Medicine, Medical University of Graz, Auenbruggerplatz 15, Graz, 8036, Austria.ORCID 0000-0001-9323-329X
Katharina GütlDivision of Angiology, Department of Internal Medicine, Medical University of Graz, Auenbruggerplatz 15, Graz, 8036, Austria.ORCID 0000-0002-1659-7185
Reinhard B RaggamDivision of Angiology, Department of Internal Medicine, Medical University of Graz, Auenbruggerplatz 15, Graz, 8036, Austria.
Peter RiefDivision of Angiology, Department of Internal Medicine, Medical University of Graz, Auenbruggerplatz 15, Graz, 8036, Austria.ORCID 0000-0002-7378-2846
Leyla SchweigerDivision of Angiology, Department of Internal Medicine, Medical University of Graz, Auenbruggerplatz 15, Graz, 8036, Austria.ORCID 0009-0006-5680-8115
Nikolaus JohnDivision of Pulmonology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.ORCID 0009-0003-0663-7627
Gerald SeinostDivision of Angiology, Department of Internal Medicine, Medical University of Graz, Auenbruggerplatz 15, Graz, 8036, Austria.ORCID 0000-0002-2577-9984
Vasile ForisDivision of Pulmonology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.ORCID 0000-0002-8863-0298
Gabor KovacsDivision of Pulmonology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.ORCID 0000-0003-3709-2183
Thomas GaryDivision of Angiology, Department of Internal Medicine, Medical University of Graz, Auenbruggerplatz 15, Graz, 8036, Austria.
Viktoria NemeczDivision of Angiology, Department of Internal Medicine, Medical University of Graz, Auenbruggerplatz 15, Graz, 8036, Austria.
Andreas MeinitzerClinical Institute of Medical and Chemical Laboratory Diagnostics, Medical University of Graz, Graz, Austria.ORCID 0000-0002-7883-7973
Heimo StrohmaierCenter of Medical Research (ZMF), Medical University of Graz, Graz, Austria.ORCID 0000-0002-4037-3608
Balazs OdlerDivision of Nephrology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.ORCID 0000-0002-8176-5202
Florentine Moazedi-FürstDivision of Rheumatology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.ORCID 0000-0002-2720-8261
Marianne BrodmannDivision of Angiology, Department of Internal Medicine, Medical University of Graz, Auenbruggerplatz 15, Graz, 8036, Austria.ORCID 0000-0001-6493-3799
Franz HafnerDivision of Angiology, Department of Internal Medicine, Medical University of Graz, Auenbruggerplatz 15, Graz, 8036, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Evaluating the predictive role of endothelial dysfunction in the development of vasculopathy-mediated complications in patients with limited cutaneous systemic sclerosis (lcSSc). 38 patients with lcSSc who were naïve for vasculopathy-mediated complications, defined as absent pre-existing digital ulcers (DU), pulmonary hypertension (PH) and symptomatic atherosclerotic cardiovascular diseases, were prospectively observed during a 3-years follow-up period. At study enrolment, functional and laboratory parameters of endothelial dysfunction were assessed. Microvascular events, defined as the development of DU and PH, macrovascular events, defined as newly symptomatic atherosclerotic cardiovascular diseases, and clinical events, defined as additional interstitial lung disease (ILD), renal crisis and esophageal dysfunction, were recorded annually. 33 patients (86.8%) completed all follow-up study visits. During the follow-up period, DU, PH, carotid and vertebral artery disease and ILD occurred in eight (24.2%), one (3.0%), one (3.0%) and two patients (6.1%), respectively, without recorded renal crisis and esophageal dysfunction. Number of pathologic FMD, NMD and/or PWV values was significantly associated with the development of clinical events (p = 0.035), but was not a significant predictor for microvascular events. Number of pathologic FMD, NMD and/or PWV values was a significant predictor for disease activity assessed by EUSTAR index ≥ 2.5 at last study visit (OR 5.47 [95% CI 1.01-29.03], p = 0.049). Distinct endothelial dysfunction may promote the development of disease complications and disease activity in patients with lcSSc.

Indexed as

Endothelium, VascularScleroderma, LimitedAdultAgedFemaleHumansHypertension, PulmonaryLung Diseases, InterstitialMaleMiddle AgedProspective StudiesRisk FactorsSkin UlcerEndotheliumInterstitial lung diseaseMicrocirculationPulmonary hypertensionSystemic sclerosis

Identifiers

PMID40627153
PMCPMC12238130

What OpenQuestion 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 OpenQuestion graph.