Evidence map›Paper›PMID 38202225›Full record

ArticleJournal of clinical medicine2023

Increased Soluble Interleukin 6 Receptors in Fabry Disease.

Livia Lenzini, Elisabetta Iori, Monica Vettore, Giorgia Gugelmo, Claudia Radu, Andrea Padoan, Gianni Carraro, Paolo Simioni, Lorenzo Calò, Angelo Avogaro and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 43% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

12 authors at 1 institution in 1 country.

Livia LenziniInternal & Emergency Medicine Unit, Department of Medicine, Padova University Hospital, 35128 Padova, Italy.ORCID 0000-0001-6146-3015
Elisabetta IoriDivision of Metabolic Diseases, Department of Medicine, Padova University Hospital, 35128 Padova, Italy.
Monica VettoreDivision of Metabolic Diseases, Department of Medicine, Padova University Hospital, 35128 Padova, Italy.
Giorgia GugelmoDivision of Clinical Nutrition, Department of Medicine, Padova University Hospital, 35128 Padova, Italy.
Claudia RaduGeneral Medicine and Thrombotic and Hemorrhagic Diseases Unit, Department of Medicine, Padova University Hospital, 35128 Padova, Italy.ORCID 0000-0002-5548-9785
Andrea PadoanLaboratory Medicine Unit, Department of Medicine, Padova University Hospital, 35128 Padova, Italy.
Gianni CarraroNephrology, Dialysis and Transplant Unit, Department of Medicine, Padova University Hospital, 35128 Padova, Italy.
Paolo SimioniGeneral Medicine and Thrombotic and Hemorrhagic Diseases Unit, Department of Medicine, Padova University Hospital, 35128 Padova, Italy.ORCID 0000-0002-6744-383X
Lorenzo CalòNephrology, Dialysis and Transplant Unit, Department of Medicine, Padova University Hospital, 35128 Padova, Italy.ORCID 0000-0002-7534-0128
Angelo AvogaroDivision of Metabolic Diseases, Department of Medicine, Padova University Hospital, 35128 Padova, Italy.
Gian Paolo RossiInternal & Emergency Medicine Unit, Department of Medicine, Padova University Hospital, 35128 Padova, Italy.ORCID 0000-0002-7963-0931
Nicola VitturiDivision of Metabolic Diseases, Department of Medicine, Padova University Hospital, 35128 Padova, Italy.ORCID 0000-0002-5147-4367
University of Padua · IT

Funding

University of Padova NA
6 · The paper itself

Abstract

Fabry disease (FD) is an X-linked lysosome storage disease that results in the accumulation of globotriaosylceramide (Gb3) throughout the body leading to irreversible target organ damage. As the role of secondary mediators (inflammatory molecules) and their mechanisms has not been fully elucidated, we focused on the interleukin (IL)-6 system in adult FD patients and in matched healthy subjects. To obtain insights into the complex regulation of IL-6 actions, we used a novel approach that integrates information from plasma and exosomes of FD patients (n = 20) and of healthy controls (n = 15). Soluble IL-6 receptor (sIL-6R) levels were measured in plasma with the ELISA method, and membrane-bound IL-6R was quantified in plasma and urinary exosomes using flow cytometry. In FD patients, the levels of soluble IL-6R in plasma were higher than in control subjects (28.0 ± 5.4 ng/mL vs. 18.9 ± 5.4 ng/mL,

Indexed as

exosomesFabry diseaseinflammationinterleukin 6 receptor

Identifiers

PMID38202225
PMCPMC10780051
OpenAlexW4390403500

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.