Evidence map›Paper›PMID 26613049›Full record

ArticleAutoimmune diseases2015

Pentraxin 3 Plasma Levels and Disease Activity in Systemic Lupus Erythematosus.

Roberto Assandri, Marta Monari, Anna Colombo, Alessandra Dossi, Alessandro Montanelli

Open access · goldAbstract read
In one paragraph

Article in Autoimmune diseases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. The role of pentraxin 3 in pemphigus vulgaris.Postepy dermatologii i alergologii · 2020
    Article
  6. Article
  7. Article
  8. Pentraxin 3 and biopsy status in celiac patients.Gastroenterology and hepatology from bed to bench · 2018
    Article
  9. Article
  10. 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

5 authors at 2 institutions in 1 country.

Roberto AssandriClinical Investigation Laboratory, Humanitas Clinical and Research Center, Rozzano, Milan, Italy.
Marta MonariClinical Investigation Laboratory, Humanitas Clinical and Research Center, Rozzano, Milan, Italy.
Anna ColomboHumanitas Clinical and Research Center, Rozzano, Milan, Italy.
Alessandra DossiClinical Investigation Laboratory, Diagnostics Department, Spedali Civili of Brescia, Brescia, Italy.
Alessandro MontanelliClinical Investigation Laboratory, Diagnostics Department, Spedali Civili of Brescia, Brescia, Italy.
Humanitas University · ITAzienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SLE is an autoimmune disorder that involves polyclonal autoimmunity against multiple autoantigens. PTX3, a marker of the acute-phase inflammatory response, plays an important role in innate immunity and in modulation of the adaptive immune response. Our study tried to resolve some rather controversial aspects of the use of PTX3 as a biomarker of disease activity in SLE patients. We demonstrated that plasma PTX3 concentration of the SLE patients was significantly higher than the healthy control groups and reflected disease activity. ROC curve analysis was used to determine best cut-off point (2.8 ng/mL) with a good sensitivity and specificity. In patients with SLE, PTX3 concentrations were correlated with SLEDAI. Trend to remission (TTR) curve was created by plotting PTX3 levels and SLEDAI and we applied the curve as a model for the analysis of two patients with different follow-up. PTX3 plasma levels declined significantly and this decline occurred parallel to the clinical improvement with a complete remission of disease. In patients who experienced a clinical relapse, an increase in PTX3 levels followed the lupus flare. The proposal of PTX3 cut-off associated with TTR and monitoring of PTX3 plasma levels could be an innovative approach to follow-up of SLE patients.

Identifiers

PMID26613049
PMCPMC4646995
OpenAlexW2183309348

What OpenQuestion holds

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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.