Literature DB >> 16185091

COX-2 inhibitors as adjunctive therapy in schizophrenia: rationale for use and evidence to date.

Michael Riedel1, Martin Strassnig, Markus J Schwarz, Norbert Müller.   

Abstract

A better understanding of the human immune system and its complex interactions has resulted in new insights into the pathoaetiological mechanisms of psychiatric disorders. As a result, new treatment options are being explored. Several findings suggest that an imbalanced immune response is involved in the pathophysiology of schizophrenia. COX-2 inhibitors are known to influence the immune system in a way that may redirect this imbalance. Based on these suggestions, the COX-2 inhibitor celecoxib has been tested as a possible adjunctive therapeutic approach in the treatment of schizophrenia. While the first trial using celecoxib as add-on therapy to an atypical antipsychotic showed a significant beneficial effect, recent studies demonstrated that this effect may be limited to patients with recent-onset schizophrenia.

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Year:  2005        PMID: 16185091     DOI: 10.2165/00023210-200519100-00001

Source DB:  PubMed          Journal:  CNS Drugs        ISSN: 1172-7047            Impact factor:   5.749


  142 in total

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Journal:  FASEB J       Date:  2001-07       Impact factor: 5.191

Review 2.  Pharmacologic agents associated with a preventive effect on Alzheimer's disease: a review of the epidemiologic evidence.

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Journal:  Gut       Date:  2002-05       Impact factor: 23.059

5.  The Th2-hypothesis of schizophrenia: a strategy to identify a subgroup of schizophrenia caused by immune mechanisms.

Authors:  M J Schwarz; N Müller; M Riedel; M Ackenheil
Journal:  Med Hypotheses       Date:  2001-04       Impact factor: 1.538

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Journal:  Cell       Date:  1995-11-03       Impact factor: 41.582

8.  Effect of the selective COX-2 inhibitors, celecoxib and rofecoxib in rat acute models of inflammation.

Authors:  R M Pinheiro; J B Calixto
Journal:  Inflamm Res       Date:  2002-12       Impact factor: 4.575

9.  Immunological dysfunction in schizophrenia: a systematic approach.

Authors:  M Rothermundt; V Arolt; C Weitzsch; D Eckhoff; H Kirchner
Journal:  Neuropsychobiology       Date:  1998       Impact factor: 2.328

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Authors:  R Ganguli; J S Brar; W Solomon; K N Chengappa; B S Rabin
Journal:  Psychiatry Res       Date:  1992-11       Impact factor: 3.222

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  5 in total

1.  Differential age- and disease-related effects on the expression of genes related to the arachidonic acid signaling pathway in schizophrenia.

Authors:  Bin Tang; Cristina Capitao; Brian Dean; Elizabeth A Thomas
Journal:  Psychiatry Res       Date:  2012-03-06       Impact factor: 3.222

2.  Caspase 1 deficiency reduces inflammation-induced brain transcription.

Authors:  Claudio Mastronardi; Fiona Whelan; Ozlem A Yildiz; Jonas Hannestad; David Elashoff; Samuel M McCann; Julio Licinio; Ma-Li Wong
Journal:  Proc Natl Acad Sci U S A       Date:  2007-04-04       Impact factor: 11.205

3.  Does Systemic Inflammation Play a Role in Pediatric Psychosis?

Authors:  Tatiana Falcone; Erin Carlton; Catherine Lee; Mattia Janigro; Vince Fazio; Fernando Espi Forcen; Kathleen Franco; Damir Janigro
Journal:  Clin Schizophr Relat Psychoses       Date:  2013-03-14

4.  Antipsychotic combinations vs monotherapy in schizophrenia: a meta-analysis of randomized controlled trials.

Authors:  Christoph U Correll; Christine Rummel-Kluge; Caroline Corves; John M Kane; Stefan Leucht
Journal:  Schizophr Bull       Date:  2008-04-15       Impact factor: 9.306

Review 5.  Eicosanoids Derived From Arachidonic Acid and Their Family Prostaglandins and Cyclooxygenase in Psychiatric Disorders.

Authors:  Kunio Yui; George Imataka; Hiroyuki Nakamura; Naoki Ohara; Yukiko Naito
Journal:  Curr Neuropharmacol       Date:  2015       Impact factor: 7.363

  5 in total

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