Evidence map›Paper›PMID 31242264›Full record

ArticlePloS one2019

The antipsychotic medication, risperidone, causes global immunosuppression in healthy mice.

Meghan May, Megan Beauchemin, Calvin Vary, Deborah Barlow, Karen L Houseknecht

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

21 citing papers in PubMed, 51 citations in OpenAlex.

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  5. Modifiable contributing factors to COVID-19: A comprehensive review.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2023
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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

5 authors at 2 institutions in 1 country.

Meghan MayDepartment of Biomedical Sciences, College of Osteopathic Medicine, University of New England, Biddeford, ME, United States of America.ORCID 0000-0002-5230-1281
Megan BeaucheminDepartment of Biomedical Sciences, College of Osteopathic Medicine, University of New England, Biddeford, ME, United States of America.
Calvin VaryCenter for Molecular Medicine, Maine Medical Center Research Institute, Scarborough, ME, United States of America.
Deborah BarlowDepartment of Biomedical Sciences, College of Osteopathic Medicine, University of New England, Biddeford, ME, United States of America.
Karen L HouseknechtDepartment of Biomedical Sciences, College of Osteopathic Medicine, University of New England, Biddeford, ME, United States of America.ORCID 0000-0002-6967-9299
University of New England · USMaine Medical Center · US

Funding

Understanding Factors Influencing COVID-19 Testing and Vaccination in Immigrant Low-income and Homeless Populations and Testing Targeted InterventionsU54GM115516 · NIGMS · MAINEHEALTH · PI Kimberly Luebbers · 2017 to 2026
$51.6M
The role of night shift work in metabolic disorders during and after pregnancyP20GM121301 · NIGMS · MAINEHEALTH · PI CLIFFORD JAMES ROSEN · 2017 to 2026
$25.1M
Pharmacology of Risperidone Effects on Bone Remodeling and Energy MetabolismR01DK095413 · NIDDK · UNIVERSITY OF NEW ENGLAND · PI HOUSEKNECHT, KAREN L. · 2013 to 2016
$1.2M
NIDDK NIH HHS R01 DK095413NIGMS NIH HHS P20 GM121301NIGMS NIH HHS U54 GM115516
6 · The paper itself

Abstract

Atypical antipsychotic medications such as risperidone are widely prescribed for diverse psychiatric indications including schizophrenia, bipolar disorder and depression. These medications have complex pharmacology and are associated with significant endocrine and metabolic side effects. This class of medications also carries FDA black box warnings due to increased risk of death in elderly patients. Clinical reports indicate that patients treated with these medications are more susceptible to infections; however, the underlying mechanisms/pharmacology are unclear. We have previously reported that risperidone and it's active metabolite distributes to the bone marrow in clinically relevant concentrations in preclinical species, leading us to hypothesize that the hematopoietic system may be impacted by these medications. To test this hypothesis, using proteomic and cytokine array technology, we evaluated the expression of genes involved in inflammatory and immune function following short term (5 days) and longer term (4 weeks) treatment in healthy animals. We report that low-dose risperidone treatment results in global immunosuppression in mice, observed following 5 days of dosing and exacerbated with longer term drug treatment (4 weeks). These data are consistent with increased susceptibility to infection in patients administered these medications and have profound implications for the increasing off-label prescribing to vulnerable patient populations including children and the elderly.

Indexed as

AnimalsAntipsychotic AgentsHumansImmunosuppressive AgentsInflammationMaleMiceMice, Inbred C57BLProteomicsPsychotic DisordersRisperidoneSoftwareAntipsychotic AgentsImmunosuppressive AgentsRisperidone

Identifiers

PMID31242264
PMCPMC6594635
OpenAlexW2955732908

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.