Evidence map›Paper›PMID 26331941›Full record

ArticleJournal of clinical laboratory analysis2016

Endocan, Novel Potential Biomarker for Systemic Sclerosis: Results of a Pilot Study.

Paul Bălănescu, Anca Lădaru, Eugenia Bălănescu, Theodor Voiosu, Cristian Băicuş, Gheorghe Andrei Dan

Open access · bronzeAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

11 citing papers in PubMed, 23 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Treatable Traits in Systemic Sclerosis.Clinical reviews in allergy & immunology · 2023
    Review
  5. Article
  6. Article
  7. Article
  8. Article
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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

6 authors at 3 institutions in 1 country.

Paul BălănescuCDPC Clinical Immunology Department, Colentina Clinical Hospital, Bucharest, Romania. plbalanescu@gmail.com.
Anca LădaruPediatrics Department, Institute for Mother and Child Protection "Alfred Rusescu," Bucharest, Romania.
Eugenia BălănescuCDPC Clinical Immunology Department, Colentina Clinical Hospital, Bucharest, Romania.
Theodor VoiosuInternal Medicine Chair, University of Medicine and Pharmacy "Carol Davila", Bucharest, Romania.
Cristian BăicuşInternal Medicine Chair, University of Medicine and Pharmacy "Carol Davila", Bucharest, Romania.
Gheorghe Andrei DanInternal Medicine Chair, University of Medicine and Pharmacy "Carol Davila", Bucharest, Romania.
Spitalul Clinic Colentina · ROCarol Davila University of Medicine and Pharmacy · ROInstitutul National pentru Sanatatea Mamei si Copilului "Alessandrescu-Rusescu" · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSystemic sclerosis (Ssc) is an autoimmune disease characterized by vascular alterations of small arteries and microvessels with subsequent tissue fibrosis. Endocan is expressed by endothelial cells and associated with endothelial dysfunction; therefore it could be a potential biomarker for Ssc patients.

methodsTwenty-one Ssc patients and 20 sex- and age-matched healthy controls were recruited for the study. Serum endocan levels were determined using ELISA method in all patients and controls.

resultsSerum endocan levels were superior in Ssc patients (median 2.53 (1.10-7 ng/ml)) compared with controls (0.79 (0-2 ng/ml), P < 0.05). Higher serum endocan expression was seen in diffuse Ssc subset and associated with the presence of digital ulcers and daily Raynaud's phenomenon (P < 0.05). Higher serum endocan levels were associated with a modified Rodnan skin score >14 and longer disease duration (P < 0.05). Values of areas under the receiver operating curves showed that serum endocan had good discriminative power for Ssc diagnosis, differentiating diffuse from limited subset type and differentiating patients with modified Rodnan skin score above and under 14 (area under curve: 0.94, 0.81, 0.75, respectively).

conclusionThe results of this pilot study suggest endocan as a potential biomarker for microvascular manifestations and complications in Ssc patients. These encouraging results could promote future prospective studies in order to determine the exact role played by endocan as a biomarker for Ssc.

Indexed as

AdultAgedAutoantibodiesBiomarkersCase-Control StudiesEnzyme-Linked Immunosorbent AssayFemaleHumansMaleMiddle AgedNeoplasm ProteinsPilot ProjectsProteoglycansScleroderma, SystemicStatistics, NonparametricAutoantibodiesBiomarkersESM1 protein, humanNeoplasm ProteinsProteoglycansbiomarkerendocanischemic digital ulcerRaynaud's phenomenonskin fibrosissystemic sclerosisvascular alteration

Identifiers

PMID26331941
PMCPMC6807019
OpenAlexW1926185720

What OpenQuestion holds

Textmetadata
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.