Evidence map›Paper›PMID 26555452›Full record

ReviewCurrent opinion in rheumatology2016

Molecular stratification and precision medicine in systemic sclerosis from genomic and proteomic data.

Viktor Martyanov, Michael L Whitfield

Abstract readReview
In one paragraph

Review in Current opinion in rheumatology, 2016. 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
–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

15 citing papers in PubMed.

  1. Article
  2. Insights Into Systemic Sclerosis from Gene Expression Profiling.Current treatment options in rheumatology · 2021
    Article
  3. Article
  4. Molecular "omic" signatures in systemic sclerosis.European journal of rheumatology · 2020
    Review
  5. Emerging Roles of Matricellular Proteins in Systemic Sclerosis.International journal of molecular sciences · 2020
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Shared and distinct mechanisms of fibrosis.Nature reviews. Rheumatology · 2019
    Review
  11. Biomarkers in systemic sclerosis.Current opinion in rheumatology · 2019
    Review
  12. Article
  13. Evolving insights into the cellular and molecular pathogenesis of fibrosis in systemic sclerosis.Translational research : the journal of laboratory and clinical medicine · 2019
    Review
  14. Article
  15. 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

2 authors.

Viktor MartyanovDepartment of Genetics, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA.
Michael L Whitfield

Funding

Translational studies for identifying and targeting novel pathways in systemic sclerosis pathogenesisP50AR060780 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DOMSIC, ROBYN THERESE · 2011 to 2021
$14.9M
Rheumatic Diseases Research Core CentersP30AR061271 · NIAMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI WHITFIELD, MICHAEL L · 2011 to 2015
$3.1M
Gene Expression Signatures to Predict Treatment Response in Systemic SclerosisR44AR061920 · NIAMS · CELDARA MEDICAL, LLC · PI FANGER, MICHAEL W · 2014 to 2015
$1.5M
Molecular Biomarkers of Improvement for Patients with Systemic Sclerosis in an Open Label Trial of Mycophenolate MofetilR21AR068035 · NIAMS · DARTMOUTH COLLEGE · PI HINCHCLIFF, MONIQUE EVANGELINE, WHITFIELD, MICHAEL L · 2015 to 2016
$400k
NIAMS NIH HHS P30 AR061271NIAMS NIH HHS P30AR061271NIAMS NIH HHS P50 AR060780NIAMS NIH HHS P50AR060780NIAMS NIH HHS R21 AR068035NIAMS NIH HHS R21AR068035NIAMS NIH HHS R44 AR061920NIAMS NIH HHS R44AR061920
6 · The paper itself

Abstract

purpose of reviewThe goal of this review is to summarize recent advances into the pathogenesis and treatment of systemic sclerosis (SSc) from genomic and proteomic studies. RECENT

findingsIntrinsic gene expression-driven molecular subtypes of SSc are reproducible across three independent datasets. These subsets are a consistent feature of SSc and are found in multiple end-target tissues, such as skin and esophagus. Intrinsic subsets as well as baseline levels of molecular target pathways are potentially predictive of clinical response to specific therapeutics, based on three recent clinical trials. A gene expression-based biomarker of modified Rodnan skin score, a measure of SSc skin severity, can be used as a surrogate outcome metric and has been validated in a recent trial. Proteome analyses have identified novel biomarkers of SSc that correlate with SSc clinical phenotypes. SUMMARY: Integrating intrinsic gene expression subset data, baseline molecular pathway information, and serum biomarkers along with surrogate measures of modified Rodnan skin score provides molecular context in SSc clinical trials. With validation, these approaches could be used to match patients with the therapies from which they are most likely to benefit and thus increase the likelihood of clinical improvement.

Indexed as

Gene ExpressionGenomicsHumansPrecision MedicineProteomicsScleroderma, SystemicTranscriptome

Identifiers

PMID26555452
PMCPMC4722537

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.