Evidence map›Paper›PMID 33350170›Full record

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

Predictive Significance of Serum Interferon-Inducible Protein Score for Response to Treatment in Systemic Sclerosis-Related Interstitial Lung Disease.

Shervin Assassi, Ning Li, Elizabeth R Volkmann, Maureen D Mayes, Dennis Rünger, Jun Ying, Michael D Roth, Monique Hinchcliff, Dinesh Khanna, Tracy Frech and 13 more

Open access · bronzeAbstract read
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. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

23 citing papers in PubMed, 39 citations in OpenAlex.

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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

23 authors at 13 institutions in 1 country.

Shervin AssassiUniversity of Texas Health Science Center at Houston.ORCID 0000-0002-8059-9978
Ning LiUniversity of California, Los Angeles.
Elizabeth R VolkmannUniversity of California, Los Angeles.ORCID 0000-0003-3750-6569
Maureen D MayesUniversity of Texas Health Science Center at Houston.
Dennis RüngerUniversity of California, Los Angeles.
Jun YingUniversity of Texas Health Science Center at Houston.
Michael D RothUniversity of California, Los Angeles.
Monique HinchcliffYale University, New Haven, Connecticut.ORCID 0000-0002-8652-9890
Dinesh KhannaUniversity of Michigan, Ann Arbor.ORCID 0000-0003-1412-4453
Tracy FrechUniversity of Utah, Salt Lake City.ORCID 0000-0002-5472-3840
Philip J ClementsUniversity of California, Los Angeles.
Daniel E FurstUniversity of California, Los Angeles.
Jonathan GoldinUniversity of California, Los Angeles.
Elana J BernsteinColumbia University, New York, New York.
Flavia V CastelinoMassachusetts General Hospital and Harvard University, Boston, Massachusetts.ORCID 0000-0001-9862-0299
Robyn T DomsicUniversity of Pittsburgh, Pittsburgh, Pennsylvania.ORCID 0000-0002-2765-0922
Jessica K GordonHospital for Special Surgery, New York, New York.ORCID 0000-0001-8068-0592
Faye N HantMedical University of South Carolina, Charleston.
Ami A ShahJohns Hopkins University School of Medicine, Baltimore, Maryland.
Victoria K ShanmugamGeorge Washington University, Washington, DC.ORCID 0000-0002-5882-4884
Virginia D SteenGeorgetown University, Washington, DC.
Robert M Elashoff
Donald P TashkinUniversity of California, Los Angeles.
University of California, Los Angeles · USThe University of Texas Health Science Center at Houston · USColumbia University · USGeorgetown University · USGeorge Washington University · USHarvard University · USHospital for Special Surgery · USJohns Hopkins University · USMedical University of South Carolina · USUniversity of Michigan · USUniversity of Pittsburgh · USUniversity of Utah · 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
MOCSLID-DCCR01HL089901 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ELASHOFF, ROBERT M · 2008 to 2012
$9.1M
Institutional Career Development CoreKL2TR003168 · NCATS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MILLER, CHARLES C · 2019 to 2023
$4.9M
MOCSLID-CCCR01HL089758 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TASHKIN, DONALD P · 2008 to 2012
$2.0M
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
Outcomes Research in Rheumatic DiseasesK24AR063120 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KHANNA, DINESH · 2012 to 2022
$1.6M
Identifying predictors of treatment response in systemic sclerosis-related interstitial lung diseaseK23HL150237 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI VOLKMANN, ELIZABETH R · 2020 to 2024
$910k
Systemic Sclerosis-Associated Interstitial Lung Disease Response IndexR01AR070470 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KHANNA, DINESH · 2017 to 2019
$642k
NCATS NIH HHS KL2 TR003168NCATS NIH HHS UL1 TR001863NHLBI NIH HHS K23 HL150237NHLBI NIH HHS R01 HL089758NHLBI NIH HHS R01 HL089901NIAMS NIH HHS K24 AR063120NIAMS NIH HHS R01 AR070470NIAMS NIH HHS R01 AR073284
6 · The paper itself

Abstract

objectiveResponse to immunosuppression is highly variable in systemic sclerosis (SSc)-related interstitial lung disease (ILD). This study was undertaken to determine whether a composite serum interferon (IFN)-inducible protein score exhibits predictive significance for the response to immunosuppression in SSc-ILD.

methodsSerum samples collected in the Scleroderma Lung Study II, a randomized controlled trial of mycophenolate mofetil (MMF) versus cyclophosphamide (CYC), were examined. Results were validated in an independent observational cohort receiving active treatment. A composite score of 6 IFN-inducible proteins IFNγ-inducible 10-kd protein, monokine induced by IFNγ, monocyte chemotactic protein 2, β

resultsHigher baseline IFN-inducible protein score predicted better response over 3 to 12 months in the MMF arm (point estimate = 0.41, P = 0.001) and CYC arm (point estimate = 0.91, P = 0.009). In contrast, higher baseline C-reactive protein (CRP) levels were predictive of a worse ILD course in both treatment arms. The predictive significance of the IFN-inducible protein score and CRP levels remained after adjustment for baseline demographic and clinical predictors. During the second year of treatment, in which patients in the CYC arm were switched to placebo, a higher IFN-inducible protein score at 12 months showed a trend toward predicting a worse ILD course (point estimate = -0.61, P = 0.068), while it remained predictive of better response to active immunosuppression in the MMF arm (point estimate = 0.28, P = 0.029). The predictive significance of baseline IFN-inducible protein score was replicated in the independent cohort (r

conclusionA higher IFN-inducible protein score in SSc-ILD is predictive of better response to immunosuppression and could potentially be used to identify patients who may derive the most benefit from MMF or CYC.

Indexed as

AdultAgedbeta 2-MicroglobulinChemokine CCL19Chemokine CCL8Chemokine CXCL10Chemokine CXCL9CyclophosphamideFemaleHumansImmunosuppressive AgentsLung Diseases, InterstitialMaleMethotrexateMiddle AgedMycophenolic Acidbeta 2-MicroglobulinChemokine CCL19Chemokine CCL8Chemokine CXCL10Chemokine CXCL9CyclophosphamideImmunosuppressive AgentsMethotrexateMycophenolic AcidReceptors, Tumor Necrosis Factor, Type II

Identifiers

PMID33350170
PMCPMC8169525
OpenAlexW3117649932

What OpenQuestion holds

Textmetadata
LicenceTDM
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.