Evidence map›Paper›PMID 33037080›Full record

Trial reportLupus science & medicine2020

Baricitinib-associated changes in global gene expression during a 24-week phase II clinical systemic lupus erythematosus trial implicates a mechanism of action through multiple immune-related pathways.

Thomas Dörner, Yoshiya Tanaka, Michelle A Petri, Josef S Smolen, Daniel J Wallace, Ernst R Dow, Richard E Higgs, Guilherme Rocha, Brenda Crowe, Robert J Benschop and 5 more

Open access · goldAbstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in Lupus science & medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
7.2field-weighted citation impact, top 2% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 61 citations in OpenAlex.

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  8. Apoptotic body-encapsulated zinc-dopedMaterials today. Bio · 2026
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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

15 authors at 6 institutions in 4 countries.

Thomas DörnerDRFZ Berlin and Department of Rheumatology and Clinical Immunology, Charite University Hospital Berlin, Berlin, Germany thomas.doerner@charite.de.ORCID 0000-0002-6478-7725
Yoshiya TanakaThe First Department of Internal Medicine, School of Medicine, University of Occupational & Environmental Health, Kitakyushu, Japan.
Michelle A PetriDivision of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.ORCID 0000-0003-1441-5373
Josef S SmolenDivision of Rheumatology, Medical University of Vienna, Wien, Austria.
Daniel J WallaceDepartment of Rheumatology, Cedars-Sinai Medical Center, West Hollywood, California, USA.ORCID 0000-0002-2502-1372
Ernst R DowEli Lilly and Company, Indianapolis, Indiana, USA.
Richard E HiggsEli Lilly and Company, Indianapolis, Indiana, USA.
Guilherme RochaEli Lilly and Company, Indianapolis, Indiana, USA.
Brenda CroweEli Lilly and Company, Indianapolis, Indiana, USA.
Robert J BenschopEli Lilly and Company, Indianapolis, Indiana, USA.
Nicole L ByersEli Lilly and Company, Indianapolis, Indiana, USA.
Maria E SilkEli Lilly and Company, Indianapolis, Indiana, USA.
Stephanie de BonoEli Lilly and Company, Indianapolis, Indiana, USA.
Damiano Fantini *Eli Lilly and Company, Indianapolis, Indiana, USA.
Robert W Hoffman *Eli Lilly and Company, Indianapolis, Indiana, USA.
Eli Lilly (United States) · USCedars-Sinai Medical Center · USCharité - Universitätsmedizin Berlin · DEJohns Hopkins University · USMedical University of Vienna · ATUniversity of Occupational and Environmental Health Japan · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo characterise the molecular pathways impacted by the pharmacologic effects of the Janus kinase (JAK) 1 and JAK2 inhibitor baricitinib in SLE.

methodsIn a phase II, 24-week, randomised, placebo-controlled, double-blind study (JAHH), RNA was isolated from whole blood in 274 patients and analysed using Affymetrix HTA2.0 array. Serum cytokines were measured using ultrasensitive quantitative assays.

resultsGene expression profiling demonstrated an elevation of

conclusionBaricitinib treatment induced significant reduction in the RNA expression of a network of genes associated with the JAK/STAT pathway, cytokine signalling and SLE pathogenesis. Baricitinib consistently reduced serum levels of two key cytokines implicated in SLE pathogenesis, IL-12p40 and IL-6.

Indexed as

Lupus Erythematosus, SystemicAdultAzetidinesFemaleGene ExpressionHumansMaleMiddle AgedPurinesPyrazolesSulfonamidesAzetidinesbaricitinibPurinesPyrazolesSulfonamidesautoimmune diseasescytokineslupus erythematosussystemictherapeutics

Identifiers

PMID33037080
PMCPMC7549481
OpenAlexW3092452074

What OpenQuestion holds

Textmetadata
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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.