Evidence map›Paper›PMID 17384211›Full record

ArticleThe Journal of molecular diagnostics : JMD2007

Identification of molecular biomarkers for multiple sclerosis.

Sallyanne C Fossey, Cindy L Vnencak-Jones, Nancy J Olsen, Subramaniam Sriram, Gladys Garrison, Xenquing Deng, Philip S Crooke, Thomas M Aune

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of molecular diagnostics : JMD, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

  1. A Perspective on Artificial Intelligence for Molecular Pathologists.The Journal of molecular diagnostics : JMD · 2025
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Serum DNA motifs predict disease and clinical status in multiple sclerosis.The Journal of molecular diagnostics : JMD · 2010
    Article
  11. Article
  12. Article
  13. Review
  14. Definition of non-responders: biological markers.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2008
    Review
  15. 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

8 authors at 2 institutions in 4 countries.

Sallyanne C FosseyDepartment of Pathology, Vanderbilt University School of Medicine, Nashvill, Tennessee, USA.
Cindy L Vnencak-Jones
Nancy J Olsen
Subramaniam Sriram
Gladys Garrison
Xenquing Deng
Philip S Crooke
Thomas M Aune
Vanderbilt University · USThe University of Texas Southwestern Medical Center · US

Funding

Gene Expression and Diagnosis of Autoimmune DiseaseR42AI053984 · NIAID · ARTHROCHIP, LLC · PI AUNE, THOMAS M. · 2004 to 2010
$3.4M
Gene Expression and Diagnosis of Autoimmune DiseaseR41AI053984 · NIAID · ARTHROCHIP, LLC · PI AUNE, THOMAS M. · 2003 to 2003
$134k
NIAID NIH HHS AI053984NIAID NIH HHS R41 AI053984NIAID NIH HHS R42 AI053984
6 · The paper itself

Abstract

Multiple sclerosis is a demyelinating disease of the central nervous system with a presumed autoimmune etiology. Previous microarray analyses identified conserved gene expression signatures in peripheral blood mononuclear cells of patients with autoimmune diseases. We used quantitative real-time polymerase chain reaction analysis to identify a minimum number of genes of which transcript levels discriminated multiple sclerosis patients from patients with other chronic diseases and from controls. We used a computer program to search quantitative transcript levels to identify optimum ratios that distinguished among the different categories. A combination of a 4-ratio equation using expression levels of five genes segregated the multiple sclerosis cohort (n=55) from the control cohort (n=49) with a sensitivity of 91% and specificity of 98%. When autoimmune and other chronic disease groups were included (n=78), this discriminator still performed with a sensitivity of 79% and a specificity of 87%. This approach may have diagnostic utility not only for multiple sclerosis but also for other clinically complex autoimmune diseases.

Indexed as

AdultAgedBiomarkersDiscriminant AnalysisFemaleGenetic TestingHumansMaleMiddle AgedMultiple SclerosisRNA, MessengerROC CurveSensitivity and SpecificitySoftwareTranscription, GeneticBiomarkersRNA, Messenger

Identifiers

PMID17384211
PMCPMC1867435
OpenAlexW2046728308

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.