Evidence map›Paper›PMID 21181207›Full record

ArticlePediatric nephrology (Berlin, Germany)2011

Markers of childhood lupus nephritis indicating disease activity.

Monika Edelbauer, Sudhir Kshirsagar, Magdalena Riedl, Dieter Haffner, Heiko Billing, Burkhard Tönshoff, Sophia Ross, Jörg Dötsch, Oliver Amon, Henry Fehrenbach and 6 more

Open access · bronzeAbstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

14 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
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  7. Article
  8. A single-cell survey of the human glomerulonephritis.Journal of cellular and molecular medicine · 2021
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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

16 authors at 9 institutions in 2 countries.

Monika EdelbauerDepartment of Pediatrics I, Innsbruck Medical University, Anichstr. 35, 6020, Innsbruck, Austria. monika.edelbauer@i-med.ac.at
Sudhir Kshirsagar
Magdalena Riedl
Dieter Haffner
Heiko Billing
Burkhard Tönshoff
Sophia Ross
Jörg Dötsch
Oliver Amon
Henry Fehrenbach
Christian Steuber
Antje Beissert
Josef Hager
Gottfried Wechselberger
Lutz T Weber
Lothar Bernd Zimmerhackl
Innsbruck Medical University · ATKlinik und Poliklinik für Kinder- und Jugendmedizin · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DEHeidelberg University · DEKlinikum Links der Weser · DELMU Klinikum · DEUniversitäts-Kinderklinik Würzburg · DEUniversity Hospital Heidelberg · DEUniversity of Rostock · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current treatment regimens for childhood lupus nephritis (LN) are associated with significant side-effects and toxicity in vulnerable phases of growth and development. The paucity of biomarkers particularly in childhood impedes the appropriate clinical management and the development of new therapeutics. We analyzed markers of immune system (BAFF, RANTES), complement (Bb, C1q, C3d-CIC, C5a) and endothelial cell activation (sVCAM-1) in children with LN (n=22, mean age 14.8±4.7 years), nephrotic syndrome (n=13) and age-matched healthy controls (n=20) to define parameters that correlate with LN activity. Complement fragments of the alternative (Bb, p=0.0004) classical (C3d-CIC, p<0.0001) and common pathway (C5a, p<0.0001) and the levels of BAFF (p<0.0001), RANTES (p=0.0002) and sVCAM-1 (p=0.0004) were significantly higher in active compared to inactive LN. Activation of complement was associated with the occurrence of anti-C1q antibodies and reduced complement C1q. Complement-activation fragments highly correlated with the markers for immune system and endothelial cell activation. The ensemble of these parameters may be of great value in identifying early flares or remissions of childhood LN, and moreover may prove useful in the assessment of new treatments and in determining the optimization of their use.

Indexed as

Complement ActivationAdolescentAustriaB-Cell Activating FactorBiomarkersCase-Control StudiesChemokine CCL5ChildComplement System ProteinsEndothelial CellsFemaleGermanyHumansImmunosuppressive AgentsLinear ModelsLupus NephritisB-Cell Activating FactorBiomarkersCCL5 protein, humanChemokine CCL5Complement System ProteinsImmunosuppressive AgentsTNFSF13B protein, humanVascular Cell Adhesion Molecule-1

Identifiers

PMID21181207
OpenAlexW2092715423

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.