Evidence map›Paper›PMID 20974172›Full record

ReviewNeuroscience and biobehavioral reviews2011

Oxidative stress in schizophrenia: an integrated approach.

Byron K Y Bitanihirwe, Tsung-Ung W Woo

2 registry-linked trialsAbstract readReview
In one paragraph

Review in Neuroscience and biobehavioral reviews, 2011. 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 201 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
201citing papers in PubMed, 4 pooled it
7.8field-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.

NCT02880462 phase2completednot on this mapstarted 2016, after this paper: background citation

Phase 2 Study of the Effect of add-on Sulforaphane in Treatment of Schizophrenia

TypeinterventionalSponsorCentral South UniversityRan2016 to 2019Enrolled172ConditionsSchizophreniaArmssulforaphane, placebo
NCT03788759 phase2 / phase3completednot on this mapstarted 2019, after this paper: background citation

Alpha-lipoic Acid Adjunctive Therapy in Schizophrenia: A Randomized, Double-blind, Placebo-controlled Trial

TypeinterventionalSponsorNucleo De Pesquisa E Desenvolvimento De Medicamentos Da Universidade Federal Do CearaRan2019 to 2021Enrolled48ConditionsSchizophrenia, Oxidative StressArmsAlpha-lipoic acid, Placebo Oral Tablet
3 · Its place in the literature

Who cites it

201 citing papers in PubMed, 4 syntheses or guidelines pooled it, 469 citations in OpenAlex.

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141 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

2 authors at 2 institutions in 2 countries.

Byron K Y BitanihirweLaboratory of Behavioural Neurobiology, Swiss Federal Institute of Technology, Zurich, Schorenstrasse 16, Schwerzenbach CH 8603, Switzerland. byron.bitanihirwe@behav.biol.ethz.ch
Tsung-Ung W Woo
École Polytechnique Fédérale de Lausanne · CHHarvard University · US

Funding

Vulnerability to Progression SchizophreniaP50MH080272 · NIMH · BETH ISRAEL DEACONESS MEDICAL CENTER · PI WOO, TSUNGUNG · 2007 to 2011
$9.9M
Parvalbumin-Containing Neurons in SchizophreniaR01MH076060 · NIMH · MCLEAN HOSPITAL · PI WOO, TSUNG-UNG W. · 2006 to 2014
$2.6M
GABA and Early Intervention of SchizophreniaR21MH082235 · NIMH · BETH ISRAEL DEACONESS MEDICAL CENTER · PI WOO, TSUNG-UNG W. · 2009 to 2010
$468k
NIMH NIH HHS MH076060NIMH NIH HHS MH080272NIMH NIH HHS MH082235NIMH NIH HHS R01 MH076060NIMH NIH HHS R21 MH082235
6 · The paper itself

Abstract

Oxidative stress has been suggested to contribute to the pathophysiology of schizophrenia. In particular, oxidative damage to lipids, proteins, and DNA as observed in schizophrenia is known to impair cell viability and function, which may subsequently account for the deteriorating course of the illness. Currently available evidence points towards an alteration in the activities of enzymatic and nonenzymatic antioxidant systems in schizophrenia. In fact, experimental models have demonstrated that oxidative stress induces behavioral and molecular anomalies strikingly similar to those observed in schizophrenia. These findings suggest that oxidative stress is intimately linked to a variety of pathophysiological processes, such as inflammation, oligodendrocyte abnormalities, mitochondrial dysfunction, hypoactive N-methyl-d-aspartate receptors and the impairment of fast-spiking gamma-aminobutyric acid interneurons. Such self-sustaining mechanisms may progressively worsen producing the functional and structural consequences associated with schizophrenia. Recent clinical studies have shown antioxidant treatment to be effective in ameliorating schizophrenic symptoms. Hence, identifying viable therapeutic strategies to tackle oxidative stress and the resulting physiological disturbances provide an exciting opportunity for the treatment and ultimately prevention of schizophrenia.

Indexed as

AnimalsAntioxidantsGenetic Predisposition to DiseaseHomocystineHumansNeurotransmitter AgentsNitric OxideOxidative StressSchizophreniaAntioxidantsHomocystineNeurotransmitter AgentsNitric Oxide

Identifiers

PMID20974172
PMCPMC3021756
OpenAlexW1965707086

What OpenQuestion holds

Textmetadata
LicenceTDM
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.