Evidence map›Paper›PMID 33131208›Full record

ArticleArthritis & rheumatology (Hoboken, N.J.)2021

Large-Scale Characterization of Systemic Sclerosis Serum Protein Profile: Comparison to Peripheral Blood Cell Transcriptome and Correlations With Skin/Lung Fibrosis.

Chiara Bellocchi, Jun Ying, Ellen A Goldmuntz, Lynette Keyes-Elstein, John Varga, Monique E Hinchcliff, Marka A Lyons, Peter McSweeney, Daniel E Furst, Richard Nash and 7 more

Registry-linked trialOpen access · greenAbstract readComparative Study
In one paragraph

Article in Arthritis & rheumatology (Hoboken, N.J.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00114530 (A Randomized, Open-Label, Phase II Multicenter Study of High-Dose Immunosuppressive Therapy Using Total Body Irradiation, Cyclophosphamide, ATGAM, and Autologous Transplantation With Auto-CD34+HPC Versus Intravenous Pulse Cyclophosphamide for the Treatment of Severe Systemic Sclerosis), which is not on this map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 18% 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.

NCT00114530 phase2 / phase3completednot on this map

A Randomized, Open-Label, Phase II Multicenter Study of High-Dose Immunosuppressive Therapy Using Total Body Irradiation, Cyclophosphamide, ATGAM, and Autologous Transplantation With Auto-CD34+HPC Versus Intravenous Pulse Cyclophosphamide for the Treatment of Severe Systemic Sclerosis (SCSSc-01)

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2005 to 2016Enrolled75ConditionsScleroderma, Systemic, Sclerosis, Autoimmune DiseaseArmsmHSCT, cyclophosphamide
3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 14 citations in OpenAlex.

  1. Trial
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  10. Review
  11. Article
  12. Adiponectin Deregulation in Systemic Autoimmune Rheumatic Diseases.International journal of molecular sciences · 2021
    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

17 authors at 10 institutions in 2 countries.

Chiara BellocchiThe University of Texas Health Science Center at Houston and McGovern Medical School, Houston, and Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico di Milano, Milan, Italy.ORCID 0000-0001-8326-7904
Jun YingThe University of Texas Health Science Center at Houston and McGovern Medical School, Houston.
Ellen A GoldmuntzNational Institute of Allergy and Infectious Diseases, NIH, Rockville, Maryland.
Lynette Keyes-ElsteinRho Federal Systems Division, Inc., Durham, North Carolina.
John VargaNorthwestern University, Chicago, Illinois.
Monique E HinchcliffYale University School of Medicine, New Haven, Connecticut.ORCID 0000-0002-8652-9890
Marka A LyonsThe University of Texas Health Science Center at Houston and McGovern Medical School, Houston.
Peter McSweeneyColorado Blood Cancer Institute, Denver.
Daniel E FurstUniversity of California Los Angeles, University of Washington, Seattle, and University of Florence, Florence, Italy.
Richard NashColorado Blood Cancer Institute, Denver.
Leslie J CroffordVanderbilt University Medical Center, Nashville, Tennessee.
Beverly WelchNational Institute of Allergy and Infectious Diseases, NIH, Rockville, Maryland.
Jonathan G GoldinUniversity of California Los Angeles.
Ashley PinckneyRho Federal Systems Division, Inc., Durham, North Carolina.
Maureen D MayesThe University of Texas Health Science Center at Houston and McGovern Medical School, Houston.
Keith M SullivanDuke University, Durham, North Carolina.ORCID 0000-0002-1379-9216
Shervin AssassiThe University of Texas Health Science Center at Houston and McGovern Medical School, Houston.ORCID 0000-0002-8059-9978
The University of Texas Health Science Center · USColorado Blood Cancer Institute · USNational Institute of Allergy and Infectious Diseases · USRho (United States) · USUniversity of California, Los Angeles · USDuke University · USFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITNorthwestern University · USVanderbilt University Medical Center · USYale University · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Center for Clinical and Translational Sciences (CCTS)UL1TR000371 · NCATS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MCPHERSON, DAVID D · 2012 to 2016
$13.4M
STEM CELL TRANSPLANTATION FOR TX OF AUTOIMMUNE DISEASES-N01AI5419N01AI005419 · NIAID · DUKE UNIVERSITY · PI SULLIVAN, KEITH M · 2000 to 2006
$6.2M
Rheumatic Diseases Research Core CentersP30AR061271 · NIAMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI WHITFIELD, MICHAEL L · 2011 to 2015
$3.1M
CFlm25 mediated alternative polyadenylation regulates fibrosis in systemic sclerosisR01AR073284 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ASSASSI, SHERVIN, MILLS, TINGTING WENG · 2019 to 2023
$1.7M
NCATS NIH HHS UL1 TR000371NCATS NIH HHS UL1 TR001863NIAID NIH HHS HHSN272201100025CNIAID NIH HHS N01 AI005419NIAMS NIH HHS P30 AR061271NIAMS NIH HHS R01 AR073284
6 · The paper itself

Abstract

objectiveTo provide a large-scale assessment of serum protein dysregulation in diffuse cutaneous systemic sclerosis (dcSSc) and to investigate serum protein correlates of SSc fibrotic features.

methodsWe investigated serum protein profiles of 66 participants with dcSSc at baseline who were enrolled in the Scleroderma: Cyclophosphamide or Transplant Trial and 66 age- and sex-matched healthy control subjects. A panel of 230 proteins, including several cytokines and chemokines, was investigated. Whole blood gene expression profiling in concomitantly collected samples was performed.

resultsAmong the participants with dcSSc, the mean disease duration was 2.3 years. All had interstitial lung disease (ILD), and none were being treated with immunosuppressive agents at baseline. Ninety proteins were differentially expressed in participants with dcSSc compared to healthy control subjects. Similar to previous global skin transcript results, hepatic fibrosis, granulocyte and agranulocyte adhesion, and diapedesis were the top overrepresented pathways. Eighteen proteins correlated with the modified Rodnan skin thickness score (MRSS). Soluble epidermal growth factor receptor was significantly down-regulated in dcSSc and showed the strongest negative correlation with the MRSS, being predictive of the score's course over time, whereas α

conclusionDiffuse cutaneous SSc has a distinct serum protein profile with prominent dysregulation of proteins related to fibrosis and immune cell adhesion/diapedesis. The differential expression for most serum proteins in SSc is likely to originate outside the peripheral blood cells.

Indexed as

TranscriptomeAdultChemokinesCytokinesFemaleFibrosisHumansLungMaleMiddle AgedPulmonary FibrosisScleroderma, SystemicSkinSkin DiseasesChemokinesCytokines

Identifiers

PMID33131208
PMCPMC8005427
OpenAlexW3096809416

What OpenQuestion holds

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Registered trials

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.