Evidence map›Paper›PMID 33462203›Full record

ArticleTranslational psychiatry2021

The IL-6 antagonist tocilizumab is associated with worse depression and related symptoms in the medically ill.

Jennifer M Knight, Erin S Costanzo, Suraj Singh, Ziyan Yin, Aniko Szabo, Deepa S Pawar, Cecilia J Hillard, J Douglas Rizzo, Anita D'Souza, Marcelo Pasquini and 4 more

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 2 pooled it
4.0field-weighted citation impact, top 5% 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

41 citing papers in PubMed, 2 syntheses or guidelines pooled it, 72 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

14 authors at 3 institutions in 1 country.

Jennifer M KnightDepartment of Psychiatry and Behavioral Medicine, Medical College of Wisconsin, Milwaukee, WI, USA. jmknight@mcw.edu.ORCID 0000-0002-9140-3109
Erin S CostanzoDepartment of Psychiatry, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Suraj SinghDepartment of Psychiatry and Behavioral Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
Ziyan YinDivision of Biostatistics, Institute for Health & Society; Medical College of Wisconsin, Milwaukee, WI, USA.
Aniko SzaboDivision of Biostatistics, Institute for Health & Society; Medical College of Wisconsin, Milwaukee, WI, USA.ORCID 0000-0002-8129-0614
Deepa S PawarDepartment of Psychiatry and Behavioral Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
Cecilia J HillardDepartment of Pharmacology and Toxicology and Neuroscience Research Center, Medical College of Wisconsin, Milwaukee, WI, USA.
J Douglas RizzoSection of BMT & Cellular Therapies; Division of Hematology/Oncology, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
Anita D'SouzaSection of BMT & Cellular Therapies; Division of Hematology/Oncology, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
Marcelo PasquiniSection of BMT & Cellular Therapies; Division of Hematology/Oncology, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
Christopher L CoeDepartment of Psychiatry, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Michael R IrwinNorman Cousins Center for Psychoneuroimmunology at the Jane and Terry Semel Institute for Neuroscience, and the Department of Psychiatry and Biobehavioral Sciences; David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.
Charles L RaisonDepartment of Psychiatry, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.ORCID 0000-0001-6687-0066
William R DrobyskiSection of BMT & Cellular Therapies; Division of Hematology/Oncology, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
Medical College of Wisconsin · USUniversity of Wisconsin–Madison · USUniversity of California, Los Angeles · US

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Justine Yang Bruce · 1985 to 2026
$142.6M
Clinical and Translational Science AwardUL1TR001436 · NCATS · MEDICAL COLLEGE OF WISCONSIN · PI FREED, JULIE K · 2015 to 2025
$47.5M
INSTITUTIONAL CTSA (UW-MADISON): CLINICAL TRIALSUL1RR025011 · NCRR · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2007 to 2011
$29.5M
Institutional Career Development CoreKL2TR001438 · NCATS · MEDICAL COLLEGE OF WISCONSIN · PI WIDLANSKY, MICHAEL E · 2015 to 2024
$2.9M
Mechanistic Inflammatory Pathways in Graft Versus Host DiseaseR01HL154579 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI DROBYSKI, WILLIAM R., HILLARD, CECILIA J · 2020 to 2023
$2.8M
Biobehavioral Mechanisms Facilitating Recovery From Stem Cell TransplantationK07CA136966 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI COSTANZO, ERIN · 2011 to 2015
$744k
Predictors of Optimal Immune Reconstitution in Stem Cell Transplant PatientsR21CA133343 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI COSTANZO, ERIN · 2010 to 2011
$350k
NCATS NIH HHS KL2 TR001438NCATS NIH HHS UL1 TR001436NCI NIH HHS K07 CA136966NCI NIH HHS P30 CA014520NCI NIH HHS R21 CA133343NCRR NIH HHS UL1 RR025011NHLBI NIH HHS R01 HL154579
6 · The paper itself

Abstract

Because medical illness is associated with increased inflammation and an increased risk for treatment-resistant major depressive disorder, anti-cytokine therapy may represent a novel, and especially efficacious, treatment for depression. We hypothesized that blockade of the interleukin (IL)-6 signaling pathway with tocilizumab would decrease depression and related symptomatology in a longitudinal cohort of allogeneic hematopoietic stem cell transplantation (HCT) patients, a medically ill population with a significant inflammation and psychopathology. Patients undergoing allogeneic HCT received either a single dose of tocilizumab one day prior to HCT (n = 25), or HCT alone (n = 62). The primary outcome included depressive symptoms at 28 days post HCT; anxiety, fatigue, sleep, and pain were assessed at pretreatment baseline and days +28, +100, and +180 post HCT as secondary outcomes. Multivariate regression demonstrated that preemptive treatment with tocilizumab was associated with significantly higher depression scores at D28 vs. the comparison group (β = 5.74; 95% CI 0.75, 10.73; P = 0.03). Even after adjustment for baseline depressive symptoms, propensity score, and presence of acute graft-versus-host disease (grades II-IV) and other baseline covariates, the tocilizumab-exposed group continued to have significantly higher depression scores compared to the nonexposed group at D28 (β = 4.73; 95% CI 0.64, 8.81; P = 0.02). Despite evidence that IL-6 antagonism would be beneficial, blockade of the IL-6 receptor with tocilizumab among medically ill patients resulted in significantly more-not less-depressive symptoms.

Indexed as

Graft vs Host DiseaseAntibodies, Monoclonal, HumanizedDepressionHematopoietic Stem Cell TransplantationHumansInterleukin-6 InhibitorsTransplant RecipientsAntibodies, Monoclonal, HumanizedInterleukin-6 Inhibitorstocilizumab

Identifiers

PMID33462203
PMCPMC7812704
OpenAlexW3121782720

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.