Evidence map›Paper›PMID 41008604›Full record

ArticleBiomolecules2025

Assessment of Cardiorenal Involvement in Systemic Sclerosis Patients.

Chiara Pellicano, Giancarlo D'Ippolito, Annalisa Villa, Ottavio Martellucci, Umberto Basile, Valeria Carnazzo, Valerio Basile, Edoardo Rosato, Mariapaola Marino, Antonietta Gigante

Abstract read
In one paragraph

Article in Biomolecules, 2025. 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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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

10 authors.

Chiara PellicanoDepartment of Translational and Precision Medicine, La Sapienza University of Rome, Piazzale Aldo Moro 5, 00185 Rome, Italy.ORCID 0000-0003-1077-4846
Giancarlo D'IppolitoDepartment of Translational and Precision Medicine, La Sapienza University of Rome, Piazzale Aldo Moro 5, 00185 Rome, Italy.
Annalisa VillaDepartment of Translational and Precision Medicine, La Sapienza University of Rome, Piazzale Aldo Moro 5, 00185 Rome, Italy.
Ottavio MartellucciDepartment of Translational and Precision Medicine, La Sapienza University of Rome, Piazzale Aldo Moro 5, 00185 Rome, Italy.
Umberto BasileDipartimento di Patologia Clinica, Ospedale Santa Maria Goretti, A.U.S.L. Latina, 04100 Latina, Italy.ORCID 0000-0002-8328-2570
Valeria CarnazzoDipartimento di Patologia Clinica, Ospedale Santa Maria Goretti, A.U.S.L. Latina, 04100 Latina, Italy.
Valerio BasileClinical Pathology Unit and Cancer Biobank, Department of Research and Advanced Technologies, I.R.C.C.S. Regina Elena National Cancer Institute, 00144 Rome, Italy.ORCID 0000-0002-9716-070X
Edoardo RosatoDepartment of Translational and Precision Medicine, La Sapienza University of Rome, Piazzale Aldo Moro 5, 00185 Rome, Italy.ORCID 0000-0002-7417-8093
Mariapaola MarinoSezione di Patologia Generale, Dipartimento di Medicina e Chirurgia Traslazionale, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.ORCID 0000-0001-9155-6378
Antonietta GiganteDepartment of Translational and Precision Medicine, La Sapienza University of Rome, Piazzale Aldo Moro 5, 00185 Rome, Italy.ORCID 0000-0002-2015-765X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic sclerosis (SSc) is an autoimmune disease associated with a high burden of morbidity and mortality due to organ complications. Pulmonary arterial hypertension (PAH) and cardiac involvement, characterized by chronic right ventricular (RV) pressure overload with consequent RV dysfunction and ultimately right heart failure (HF), are among these. A common comorbidity in SSc is chronic kidney disease (CKD). CKD is often present at the time of PAH diagnosis or a decline in renal function may occur during the course of the disease. CKD is strongly and independently associated with mortality in patients with PAH and HF. The cardiovascular and renal systems are closely interconnected, and disruption of this balance may result in cardiorenal syndrome (CRS). Type 2 CRS refers to CKD as a consequence of chronic HF. In clinical practice, non-specific markers such as troponin, B-type natriuretic peptide (BNP), N-terminal pro-BNP (NT-proBNP), and serum creatinine aid in CRS diagnosis. More specific biomarkers, including cystatin C (CysC), neutrophil gelatinase-associated lipocalin (NGAL), galectin-3, and soluble urokinase plasminogen activator receptor (suPAR), have shown value for diagnosis and prognosis in CRS. This study aimed to evaluate comprehensively heart/kidney damage markers related to CRS in SSc patients compared with healthy controls (HC) and to examine their association with renal and cardiac ultrasound parameters. SSc patients showed significantly higher CRS markers than HC (

Indexed as

Cardio-Renal SyndromeRenal Insufficiency, ChronicScleroderma, SystemicAdultAgedBiomarkersCystatin CFemaleGalectin 3HumansLipocalin-2MaleMiddle AgedNatriuretic Peptide, BrainPeptide FragmentsBiomarkersCystatin CGalectin 3LCN2 protein, humanLipocalin-2Natriuretic Peptide, BrainPeptide Fragmentspro-brain natriuretic peptide (1-76)cardiorenal syndromechronic kidney diseasepulmonary arterial hypertensionsystemic sclerosis

Identifiers

PMID41008604
PMCPMC12467943

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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.