Evidence map›Paper›PMID 30391651›Full record

ArticleClinical immunology (Orlando, Fla.)2019

A Markov Multi-State model of lupus nephritis urine biomarker panel dynamics in children: Predicting changes in disease activity.

E M D Smith, A Eleuteri, B Goilav, L Lewandowski, A Phuti, T Rubinstein, D Wahezi, C A Jones, S D Marks, R Corkhill and 6 more

Open access · greenAbstract read
In one paragraph

Article in Clinical immunology (Orlando, Fla.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

3 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Arachidonic Acid Metabolism and Kidney Inflammation.International journal of molecular sciences · 2019
    Review
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 6 institutions in 4 countries.

E M D SmithDepartment of Women's & Children's Health, University of Liverpool, Liverpool, UK; Department of Paediatric Rheumatology, Alder Hey Children's NHS Foundation Trust, Liverpool, UK. Electronic address: esmith8@liverpool.ac.uk.
A EleuteriMedical Physics and Clinical Engineering, and Department of Physics, University of Liverpool, Liverpool, UK. Electronic address: antonio.eleuteri@liv.ac.uk.
B GoilavDepartment of Paediatric Nephrology, Albert Einstein College of Medicine, New York, USA. Electronic address: bgoilav@montefiore.org.
L LewandowskiNational Institute of Health, Maryland, USA. Electronic address: laura.lewandowski@nih.gov.
A PhutiPaediatric Rheumatology, University of Cape Town, Cape Town, South Africa. Electronic address: trubinst@montefiore.org.
T RubinsteinDepartment of Paediatric Rheumatology, Albert Einstein College of Medicine, New York, USA. Electronic address: trubinst@montefiore.org.
D WaheziDepartment of Paediatric Rheumatology, Albert Einstein College of Medicine, New York, USA. Electronic address: DWAHEZI@montefiore.org.
C A JonesDepartment of Paediatric Nephrology, Alder Hey Children's NHS Foundation Trust, Liverpool, UK. Electronic address: Caroline.Jones@alderhey.nhs.uk.
S D MarksPaediatric Nephrology, Great Ormond Street Hospital, London, UK. Electronic address: Stephen.Marks@gosh.nhs.uk.
R CorkhillDepartment of Women's & Children's Health, University of Liverpool, Liverpool, UK. Electronic address: rachel.corkhill@liverpool.ac.uk.
C PilkingtonPaediatric Rheumatology, Great Ormond Street Hospital, London, UK. Electronic address: Clarissa.Pilkington@gosh.nhs.uk.
K TullusPaediatric Nephrology, Great Ormond Street Hospital, London, UK. Electronic address: Kjell.Tullus@gosh.nhs.uk.
C PuttermanDepartment of Rheumatology, Albert Einstein College of Medicine, New York, USA. Electronic address: Chaim.Putterman@einstein.yu.edu.
C ScottPaediatric Rheumatology, University of Cape Town, Cape Town, South Africa. Electronic address: chris.scott@uct.ac.za.
A C FisherMedical Physics and Clinical Engineering, and Department of Physics, University of Liverpool, Liverpool, UK. Electronic address: clfs12@liverpool.ac.uk.
M W BeresfordDepartment of Women's & Children's Health, University of Liverpool, Liverpool, UK; Department of Paediatric Rheumatology, Alder Hey Children's NHS Foundation Trust, Liverpool, UK. Electronic address: m.w.beresford@liverpool.ac.uk.
University of Liverpool · GBAlbert Einstein College of Medicine · USGreat Ormond Street Hospital · GBUniversity of Cape Town · ZAAlder Hey Children's NHS Foundation Trust · GBNational Institute of Health · AM

Funding

ExRNA composition in SLE patients and factors influencing exRNP abundance and thU19CA179564 · NCI · ROCKEFELLER UNIVERSITY · PI TUSCHL, THOMAS · 2013 to 2017
$7.1M
CARRA: Accelerating Toward an Evidence Based Culture in Pediatric RheumatologyRC2AR058934 · NIAMS · DUKE UNIVERSITY · PI ILOWITE, NORMAN T, SANDBORG, CHRISTY IRENE · 2009 to 2010
$6.8M
Multi-Ethnic Translational Research Optimization (METRO) Lupus ConsortiumUH2AR067689 · NIAMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BUYON, JILL P, PUTTERMAN, CHAIM · 2014 to 2020
$6.3M
Vanderbilt-Emory-Cornell-Duke Consortium for Global Health Fellows (VECDor)R25TW009337 · FIC · VANDERBILT UNIVERSITY MEDICAL CENTER · PI HEIMBURGER, DOUGLAS CORBETT, VERMUND, STEN H. · 2012 to 2016
$6.3M
Genetics and pathophysiology of systemic lupus erythematosus in global populationsZIAAR041214 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI LEWANDOWSKI, LAURA · 2021 to 2025
$4.5M
TRAINING PROGRAM IN INFLAMMATORY AND IMMUNOLOGICALT32AI007217 · NIAID · DUKE UNIVERSITY · PI PISETSKY, DAVID STEPHEN · 1985 to 2015
$3.3M
Clinical utility of extracellular RNA as marker of kidney disease progressionUH3TR000933 · NCATS · ROCKEFELLER UNIVERSITY · PI SUTHANTHIRAN, MANIKKAM, TUSCHL, THOMAS · 2015 to 2017
$2.5M
Clinical utility of extracellular RNA as marker of kidney disease progressionUH2TR000933 · NCATS · ROCKEFELLER UNIVERSITY · PI SUTHANTHIRAN, MANIKKAM, TUSCHL, THOMAS · 2013 to 2014
$988k
Arthritis Research UKDepartment of HealthFIC NIH HHS R25 TW009337Intramural NIH HHS Z99 AR999999Intramural NIH HHS ZIA AR041214Medical Research Council JXR11948NCATS NIH HHS UH2 TR000933NCATS NIH HHS UH3 TR000933NCI NIH HHS U19 CA179564NIAID NIH HHS T32 AI007217NIAMS NIH HHS RC2 AR058934NIAMS NIH HHS UH2 AR067689
6 · The paper itself

Abstract

backgroundA urine 'biomarker panel' comprising alpha-1-acid-glycoprotein, ceruloplasmin, transferrin and lipocalin-like-prostaglandin-D synthase performs to an 'excellent' level for lupus nephritis identification in children cross-sectionally. The aim of this study was to assess if this biomarker panel predicts lupus nephritis flare/remission longitudinally.

methodsThe novel urinary biomarker panel was quantified by enzyme linked immunoabsorbant assay in participants of the United Kingdom Juvenile Systemic Lupus Erythematosus (UK JSLE) Cohort Study, the Einstein Lupus Cohort, and the South African Paediatric Lupus Cohort. Monocyte chemoattractant protein-1 and vascular cell adhesion molecule-1 were also quantified in view of evidence from other longitudinal studies. Serial urine samples were collected during routine care with detailed clinical and demographic data. A Markov Multi-State model of state transitions was fitted, with predictive clinical/biomarker factors assessed by a corrected Akaike Information Criterion (AICc) score (the better the model, the lower the AICc score).

resultsThe study included 184 longitudinal observations from 80 patients. The homogeneous multi-state Markov model of lupus nephritis activity AICc score was 147.85. Alpha-1-acid-glycoprotein and ceruloplasmin were identified to be the best predictive factors, reducing the AICc score to 139.81 and 141.40 respectively. Ceruloplasmin was associated with the active-to-inactive transition (hazard ratio 0.60 (95% confidence interval [0.39, 0.93])), and alpha-1-acid-glycoprotein with the inactive-to-active transition (hazard ratio 1.49 (95% confidence interval [1.10, 2.02])). Inputting individual alpha-1-acid-glycoprotein/ceruloplasmin values provides 3, 6 and 12 months probabilities of state transition.

conclusionsAlpha-1-acid-glycoprotein was predictive of active lupus nephritis flare, whereas ceruloplasmin was predictive of remission. The Markov state-space model warrants testing in a prospective clinical trial of lupus nephritis biomarker led monitoring.

Indexed as

Markov ChainsAdolescentBiomarkersCeruloplasminChildFemaleHumansLupus NephritisMaleOrosomucoidBiomarkersCeruloplasminOrosomucoidJuvenile systemic lupus erythematosusLupus NephritisMarkov Multi-State modelUrine biomarker panel

Identifiers

PMID30391651
PMCPMC12448077
OpenAlexW2899453383

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