Evidence map›Paper›PMID 28013203›Full record

ReviewRheumatology (Oxford, England)2017

Systemic lupus erythematosus biomarkers: the challenging quest.

Cristina Arriens, Jonathan D Wren, Melissa E Munroe, Chandra Mohan

Abstract readReview
In one paragraph

Review in Rheumatology (Oxford, England), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

49 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

4 authors.

Cristina ArriensDepartment of Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation.
Jonathan D WrenDepartment of Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation.
Melissa E MunroeDepartment of Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation.
Chandra MohanDepartment of Biomedical Engineering, University of Houston, Houston, TX, USA.

Funding

Tracking and Evaluation CoreU54GM104938 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI Robert Hal Scofield · 2013 to 2026
$68.2M
Understanding connective tissue development and disease with PDGFR-driven..... P20GM103636 · NIGMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI THOMPSON, LINDA F · 2013 to 2023
$26.9M
UT Southwestern Center for Translational Medicine (UL1/KL2/TL1)UL1TR001105 · NCATS · UT SOUTHWESTERN MEDICAL CENTER · PI TOTO, ROBERT DANIEL · 2013 to 2017
$24.5M
SNP Confirmation and High Throughput Genotyping CoreP30AR053483 · NIAMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI GUTHRIDGE, JOEL MARVIN · 2007 to 2017
$6.7M
Pre-Clinical Studies to Identify SLE Therapeutic TargetsU19AI082714 · NIAID · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI JAMES, JUDITH A · 2009 to 2018
$6.2M
RENAL CONTROL OF BODY COMPOSITION AND BLOOD PRESSURET32DK007257 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI BAUM, MICHEL GERARD, MOE, ORSON W · 1986 to 2021
$5.0M
Understanding early events in lupus autoimmunity to aid preventionU01AI101934 · NIAID · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI JAMES, JUDITH A · 2012 to 2016
$2.3M
NCATS NIH HHS UL1 TR001105NIAID NIH HHS U01 AI101934NIAID NIH HHS U19 AI082714NIAMS NIH HHS P30 AR053483NIDDK NIH HHS T32 DK007257NIGMS NIH HHS P20 GM103636NIGMS NIH HHS U54 GM104938
6 · The paper itself

Abstract

SLE, a multisystem heterogeneous disease, is characterized by production of antibodies to cellular components, with activation of both the innate and the adaptive immune system. Decades of investigation of blood biomarkers has resulted in incremental improvements in the understanding of SLE. Owing to the heterogeneity of immune dysregulation, no single biomarker has emerged as a surrogate for disease activity or prediction of disease. Beyond identification of surrogate biomarkers, a multitude of clinical trials have sought to inhibit elevated SLE biomarkers for therapeutic benefit. Armed with new -omics technologies, the necessary yet daunting quest to identify better surrogate biomarkers and successful therapeutics for SLE continues with tenacity.

Indexed as

AngiostatinsAntibodies, AntinuclearAutoantibodiesBiomarkersChemokine CCL2Complement System ProteinsCytokinesCytokine TWEAKDNAFerritinsHumansInsulin-Like Growth Factor Binding ProteinsLipocalin-2Lupus Erythematosus, SystemicTumor Necrosis FactorsVascular Cell Adhesion Molecule-1AngiostatinsAntibodies, AntinuclearAutoantibodiesBiomarkersCCL2 protein, humanChemokine CCL2Complement System ProteinsCytokinesCytokine TWEAKDNAFerritinsInsulin-Like Growth Factor Binding ProteinsLipocalin-2TNFSF12 protein, humanTumor Necrosis FactorsVascular Cell Adhesion Molecule-1antibody.autoimmunitybiomarkerschemokinecomplementcytokineimmunosuppressantsinterleukinlupus nephritissystemic lupus erythematosus

Identifiers

PMID28013203
PMCPMC5850341

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.