Evidence map›Paper›PMID 26367225›Full record

Trial reportBone marrow transplantation2015

Identification and validation of biomarkers associated with acute and chronic graft versus host disease.

S S Ahmed, X N Wang, J Norden, K Pearce, E El-Gezawy, S Atarod, I Hromadnikova, M Collin, E Holler, A M Dickinson

Erratum issuedAbstract readClinical TrialMulticenter Study
PubMed Publisher
In one paragraph

Trial report in Bone marrow transplantation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
6.1field-weighted citation impact, top 3% 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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 69 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 3 countries.

S S AhmedHaematological Sciences, Institute of Cellular Medicine, Newcastle University, Newcastle-upon-Tyne, UK.
X N WangHaematological Sciences, Institute of Cellular Medicine, Newcastle University, Newcastle-upon-Tyne, UK.
J NordenHaematological Sciences, Institute of Cellular Medicine, Newcastle University, Newcastle-upon-Tyne, UK.
K PearceHaematological Sciences, Institute of Cellular Medicine, Newcastle University, Newcastle-upon-Tyne, UK.
E El-GezawyHaematological Sciences, Institute of Cellular Medicine, Newcastle University, Newcastle-upon-Tyne, UK.
S AtarodHaematological Sciences, Institute of Cellular Medicine, Newcastle University, Newcastle-upon-Tyne, UK.
I HromadnikovaThird Faculty of Medicine, Charles University, Prague, Czech Republic.
M CollinHaematological Sciences, Institute of Cellular Medicine, Newcastle University, Newcastle-upon-Tyne, UK.
E HollerRegensburg University Hospital, Department of Hematology and Oncology, Regensburg, Germany.
A M DickinsonHaematological Sciences, Institute of Cellular Medicine, Newcastle University, Newcastle-upon-Tyne, UK.
Newcastle University · GBAlcyomics (United Kingdom) · GBCharles University · CZUniversity Hospital Regensburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Graft versus host disease (GVHD) is a major complication of haematopoietic SCT (HSCT). A number of inflammatory cytokines/chemokines are implicated in GVHD and have been identified in numerous single centre studies as potential biomarkers for acute and/or chronic GVHD. In this study, we analysed candidate inflammatory biomarkers (B-cell activating factor (BAFF), interleukin 33 (IL-33), CXCL10 and CXCL11) in a two-centre study. Biomarkers were evaluated pre-transplant and at serial time points post transplant in acute and chronic GVHD patient sera with time-matched control samples from patients without GVHD. Further validation was performed using the human skin explant assay, clinical GVHD biopsies and mRNA expression analysis. BAFF was significantly increased pre-transplant. BAFF, IL-33, CXCL10 and CXCL11 showed increased levels in acute GVHD patient sera and high protein expression in grades II-III of the in vitro skin explant graft versus host reaction (GVHR) group. BAFF, CXCL10 and CXCL11 also showed increased mRNA expression levels in clinical biopsies compared with the no/low-grade GVHD group. BAFF, CXCL10 and CXCL11 levels were increased in chronic GVHD patient sera. The results identify BAFF and CXCL10 as predictive biomarkers for acute GVHD and BAFF, CXCL10 and CXCL11 as useful diagnostic biomarkers for acute GVHD and chronic GVHD.

Indexed as

Hematopoietic Stem Cell TransplantationAcute DiseaseAllograftsBiomarkersChronic DiseaseCytokinesFemaleGraft vs Host DiseaseHematologic NeoplasmsHumansMaleBiomarkersCytokines

Identifiers

PMID26367225
OpenAlexW1932854607

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.