Evidence map›Paper›PMID 24106335›Full record

SynthesisSchizophrenia bulletin2014

Efficacy of anti-inflammatory agents to improve symptoms in patients with schizophrenia: an update.

Iris E Sommer, Roos van Westrhenen, Marieke J H Begemann, Lot D de Witte, Stefan Leucht, René S Kahn

2 registry-linked trialsOpen access · bronzeAbstract readMeta-Analysis
In one paragraph

Synthesis in Schizophrenia bulletin, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 160 papers, 18 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
160citing papers in PubMed, 18 pooled it
8.9field-weighted citation impact, top 1% 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.

NCT02685748 phase2 / phase3completednot on this mapstarted 2017, after this paper: background citation

Aspirin as Adjuvant Therapy in Young Psychotic Patients

TypeinterventionalSponsorClinic for Psychiatric Disorders, Dr Laza LazarevicRan2017 to 2019Enrolled60ConditionsPsychosis, Acute Psychosis, SchizophreniaArmsAspirin, Placebo, Pantoprazole
NCT02796859 phase1 / phase2unknown statusnot on this mapstarted 2016, after this paper: background citation

A Randomized Controlled Trial of Adjunctive Siltuximab in Schizophrenia

TypeinterventionalSponsorBrian MillerRan2016 to 2023Enrolled30ConditionsSchizophrenia, Psychotic DisordersArmsSiltuximab, normal saline
3 · Its place in the literature

Who cites it

160 citing papers in PubMed, 18 syntheses or guidelines pooled it, 333 citations in OpenAlex.

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  6. Interventions for prodromal stage of psychosis.The Cochrane database of systematic reviews · 2019
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  8. Acetylsalicylic acid (aspirin) for schizophrenia.The Cochrane database of systematic reviews · 2019
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  19. Trial
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100 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 2 countries.

Iris E Sommer*To whom correspondence should be addressed; Department of Psychiatry, University Medical Centre Utrecht, Room A01.161/A01.126, Heidelberglaan 100, 3508GA Utrecht, The Netherlands; tel: +31-887556365, fax: +31-887556543, e-mail: i.sommer@umcutrecht.nl.
Roos van Westrhenen
Marieke J H Begemann
Lot D de Witte
Stefan Leucht
René S Kahn
University Medical Center Utrecht · NLTechnical University of Munich · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe inflammatory hypothesis of schizophrenia is not new, but recently it has regained interest because more data suggest a role of the immune system in the pathogenesis of schizophrenia. If increased inflammation of the brain contributes to the symptoms of schizophrenia, reduction of the inflammatory status could improve the clinical picture. Lately, several trials have been conducted investigating the potential of anti-inflammatory agents to improve symptoms of schizophrenia. This study provides an update regarding the efficacy of anti-inflammatory agents on schizophrenic symptoms in clinical studies performed so far.

methodsAn electronic search was performed using PubMed, Embase, the National Institutes of Health web site http://www.clinicaltrials.gov, Cochrane Schizophrenia Group entries in PsiTri, and the Cochrane Database of Systematic Reviews. Only randomized, double-blind, placebo-controlled studies that investigated clinical outcome were included.

resultsOur search yielded 26 double-blind randomized controlled trials that provided information on the efficacy on symptom severity of the following components: aspirin, celecoxib, davunetide, fatty acids such as eicosapentaenoic acids and docosahexaenoic acids, estrogens, minocycline, and N-acetylcysteine (NAC). Of these components, aspirin (mean weighted effect size [ES]: 0.3, n = 270, 95% CI: 0.06-0.537, I(2) = 0), estrogens (ES: 0.51, n = 262, 95% CI: 0.043-0.972, I(2) = 69%), and NAC (ES: 0.45, n = 140, 95% CI: 0.112-0.779) showed significant effects. Celecoxib, minocycline, davunetide, and fatty acids showed no significant effect.

conclusionThe results of aspirin addition to antipsychotic treatment seem promising, as does the addition of NAC and estrogens. These 3 agents are all very broadly active substances, and it has to be investigated if the beneficial effects on symptom severity are indeed mediated by their anti-inflammatory aspects.

Indexed as

Anti-Inflammatory Agents, Non-SteroidalHumansSchizophreniaAnti-Inflammatory Agents, Non-Steroidaladd-on antipsychotic therapyaspirinestrogensN-acetylcysteine

Identifiers

PMID24106335
PMCPMC3885306
OpenAlexW2169079754

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.