Evidence map›Paper›PMID 27353506›Full record

ArticleLupus2017

Can SLE classification rules be effectively applied to diagnose unclear SLE cases?

A Mesa, M Fernandez, W Wu, G Narasimhan, E L Greidinger, D K Mills

Abstract readComparative Study
In one paragraph

Article in Lupus, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Low Expression and Clinical Value of hsa_circ_0049224 and has_circ_0049220 in Systemic Lupus Erythematous Patients.Medical science monitor : international medical journal of experimental and clinical research · 2018
    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

6 authors.

A Mesa1 Department of Surgery, University of Miami Miller School of Medicine, Miami, FL, USA.
M Fernandez2 Bioinformatics Research Group (BioRG), School of Computing and Information Sciences, Florida International University, Miami, FL, USA.
W Wu3 Department of Mathematics and Statistics, Florida International University, Miami, FL, USA.
G Narasimhan2 Bioinformatics Research Group (BioRG), School of Computing and Information Sciences, Florida International University, Miami, FL, USA.
E L Greidinger4 Bruce W Carter Department of Veterans Affairs Medical Center, and University of Miami Miller School of Medicine, Miami, FL, USA.
D K Mills5 Department of Biological Sciences, Florida International University, Miami, FL, USA; International Forensic Research Institute, Florida International University, Miami, FL, USA.

Funding

Immune Response to Small Nuclear Ribonucleoprotein AutoantigensR01AR043308 · NIAMS · UNIVERSITY OF MISSOURI-COLUMBIA · PI GREIDINGER, ERIC L · 1997 to 2011
$3.6M
Innate Immune Response Patterns to Autoantigen-Associated RNAI01BX002047 · VA · MIAMI VA HEALTH CARE SYSTEM · PI GREIDINGER, ERIC L · 2014 to 2017
–
BLRD VA I01 BX002047NIAMS NIH HHS R01 AR043308
6 · The paper itself

Abstract

Objective The objective of this paper is to develop novel classification criteria to distinguish between unclear systemic lupus erythematosus (SLE) and mixed connective tissue disease (MCTD) cases. Methods A total of 205 variables from 111 SLE and 55 MCTD patients were evaluated to uncover unique molecular and clinical markers for each disease. Binomial logistic regressions (BLRs) were performed on currently used SLE and MCTD classification criteria sets to obtain six reduced models with power to discriminate between unclear SLE and MCTD patients that were confirmed by receiving operating characteristic (ROC) curve. Decision trees were employed to delineate novel classification rules to discriminate between unclear SLE and MCTD patients. Results SLE and MCTD patients exhibited contrasting molecular markers and clinical manifestations. Furthermore, reduced models highlighted SLE patients exhibiting prevalence of skin rashes and renal disease while MCTD cases show dominance of myositis and muscle weakness. Additionally decision tree analyses revealed a novel classification rule tailored to differentiate unclear SLE and MCTD patients (Lu-vs-M) with an overall accuracy of 88%. Conclusions Validation of our novel proposed classification rule (Lu-vs-M) includes novel contrasting characteristics (calcinosis, CPK elevated and anti-IgM reactivity for U1-70K, U1A and U1C) between SLE and MCTD patients and showed a 33% improvement in distinguishing these disorders when compared to currently used classification criteria sets. Pending additional validation, our novel classification rule is a promising method to distinguish between patients with unclear SLE and MCTD diagnosis.

Indexed as

Decision Support TechniquesArea Under CurveBiomarkersChi-Square DistributionDecision TreesDiagnosis, DifferentialHumansLogistic ModelsLupus Erythematosus, SystemicMixed Connective Tissue DiseasePhenotypePredictive Value of TestsPrevalenceReproducibility of ResultsROC CurveBiomarkersautoimmune disordersclassification criteriadiagnosisMixed connective tissue disease (MCTD)systemic lupus erythematosus (SLE)

Identifiers

PMID27353506
PMCPMC5192007

What OpenQuestion holds

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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.