A randomised double-blind placebo-controlled 12- week feasibility trial of methotrexate added to treatment as usual in early schizophrenia: study protocol for a randomised controlled trial

Imran B Chaudhry, Nusrat Husain, Raza ur Rahman, Mohammed Omair Husain, Mohammed M Hamirani, Ajmal Kazmi, Shakeel Baig, Peter M Haddad, Maya H Buch, Inti Qureshi, Nasir Mehmood, Tayyeba Kiran, Bo Fu, Salahuddin Afsar, Bill Deakin, Imran B Chaudhry, Nusrat Husain, Raza ur Rahman, Mohammed Omair Husain, Mohammed M Hamirani, Ajmal Kazmi, Shakeel Baig, Peter M Haddad, Maya H Buch, Inti Qureshi, Nasir Mehmood, Tayyeba Kiran, Bo Fu, Salahuddin Afsar, Bill Deakin

Abstract

Background: Methotrexate is a commonly used anti-inflammatory and immunosuppressive drug. There is growing evidence that inflammatory processes are involved in the pathogenesis of schizophrenia. In our recent randomised double-blind placebo-controlled clinical trial in Pakistan and Brazil, the addition of minocycline (antibiotic and anti-inflammatory drug) for 1 year to treatment as usual reduced negative symptoms and improved some cognitive measures. A meta-analysis of cytokine changes in the peripheral blood has identified IL-2, IFN-gamma, TNF-alpha and soluble IL-2 receptor as trait markers of schizophrenia because their levels were elevated during acute exacerbations and reduced in remission. This suggests immune activation and an inflammatory syndrome in schizophrenia. Based on the evidence of the strong anti-inflammatory properties of methotrexate, we propose that low-dose methotrexate may be an effective therapy in early schizophrenia.

Methods/design: This is a double-blind placebo-controlled study of methotrexate added to treatment as usual for patients suffering from schizophrenia, schizoaffective disorder, psychosis not otherwise specified or schizophreniform disorder. This will be with 72 patients, 36 in each arm over 3 months. There will be screening, randomisation and follow-up visits. Full clinical assessments will be carried out at baseline, 2, 4, 8 and 12 weeks. Social and cognitive assessments will be carried out at baseline and 12 weeks. Methotrexate will be given at a dose of 10 mgs orally once a week for a 3-month period.

Discussion: Evidence suggests inflammatory processes are involved in the pathogenesis of schizophrenia and anti-inflammatory treatments have shown to have some beneficial effects. Methotrexate is a known immunosuppressant and anti-inflammatory drug. The aim of this study is to establish the degree of improvement in positive and negative symptoms, as well as cognitive functioning with the addition of methotrexate to treatment as usual.ClinicalTrials.gov identifier: NCT02074319 (24 February 2014).

References

    1. Cronstein BN. Low-dose methotrexate: a mainstay in the treatment of rheumatoid arthritis. Pharmacol Rev. 2005;57(2):163–72. doi: 10.1124/pr.57.2.3.
    1. Ravi Rajagopalan PT, Zhang Z, McCourt L, Dwyer M, Benkovic SJ, Hammes G. Interaction of dihydrofolate reductase with methotrexate: ensemble and single-molecule kinetics. Proc Natl Acad Sci. 2002;99(21):13481–6. doi: 10.1073/pnas.172501499.
    1. Johnston A, Gudjonsson JE, Sigmundsdottir H, Runar Ludviksson B, Valdimarsson H. The anti-inflammatory action of methotrexate is not mediated by lymphocyte apoptosis, but by the suppression of activation and adhesion molecules. Clin Immunol. 2005;114(2):154–63. doi: 10.1016/j.clim.2004.09.001.
    1. Gong K, Zhang Z, Sun X, Zhang X, Li A, Yan J, Luo Q, Gao Y, Feng Y. The nonspecific anti-inflammatory therapy with methotrexate for patients with chronic heart failure. Am Heart J. 2006;151(1):62–8. doi: 10.1016/j.ahj.2005.02.040.
    1. Zhang Z, Zhao P, Li A, Lv X, Gao Y, Sun H, Ding Y, Liu J. Mediators Inflamm. 2009. Effects of methotrexate on plasma cytokines and cardiac remodeling and function in postmyocarditis rats.
    1. Busse S, Busse M, Schiltz K, Bielau H, Gos T, Brisch R, Mawrin C, Schmitt A, Jordan W, Müller UJ, Bernstein HG, Bogerts B, Steiner J. Different distribution patterns of lymphocytes and microglia in the hippocampus of patients with residual versus paranoid schizophrenia: further evidence for disease course-related immune alterations? Brain Behav Immun. 2012;26(8):1273–9. doi: 10.1016/j.bbi.2012.08.005.
    1. Chaudhry IB, Hallak J, Husain N, Minhas F, Stirling J, Richardson P, Dursun S, Dunn G, Deakin B. Minocycline benefits negative symptoms in early schizophrenia: a randomised double-blind placebo-controlled clinical trial in patients on standard treatment. J Psychopharmacol. 2012;26(9):1185–93. doi: 10.1177/0269881112444941.
    1. Potvin S, Stip E, Sepehry AA, Gendron A, Bah R, Kouassi E. Inflammatory cytokine alterations in schizophrenia: a systematic quantitative review. Biol Psychiatry. 2008;63(8):801–8. doi: 10.1016/j.biopsych.2007.09.024.
    1. Mansur RB, Zugman A, Asevedo EM, da Cunha GR, Bressan RA, Brietzke E. Cytokines in schizophrenia: possible role of anti-inflammatory medications in clinical and preclinical stages. Psychiatry Clin Neurosci. 2012;66(4):247–60. doi: 10.1111/j.1440-1819.2012.02354.x.
    1. Miller BJ, Buckley P, Seabolt W, Mellor A, Kirkpatrick B. Meta-analysis of cytokine alterations in schizophrenia: clinical status and antipsychotic effects. Biol Psychiatry. 2011;70:663–71. doi: 10.1016/j.biopsych.2011.04.013.
    1. Behrens MM, Ali SS, Dugan LL. Interleukin-6 mediates the increase in NADPH-oxidase in the ketamine model of schizophrenia. J Neurosci. 2008;28:13957–66. doi: 10.1523/JNEUROSCI.4457-08.2008.
    1. Schulte-Herbruggen O, Nassenstein C, Lommatzsch M, Quarcoo D, Renz H, Braun A. Tumor necrosis factor-alpha and interleukin-6 regulate secretion of brain derived neurotrophic factor in human monocytes. J Neuroimmunol. 2005;160:204–9. doi: 10.1016/j.jneuroim.2004.10.026.
    1. Drzyzga L, Obuchowicz E, Marcinowska A, Herman ZS. Cytokines in schizophrenia and the effects of antipsychotic drugs. Brain Behav Immun. 2006;20(6):532–45. doi: 10.1016/j.bbi.2006.02.002.
    1. Bernstein HG, Steiner J, Bogerts B. Glial cells in schizophrenia: pathophysiological significance and possible consequences for therapy. Expert Rev Neurother. 2009;9:1059–71. doi: 10.1586/ern.09.59.
    1. Monji A, Kato T, Kanba S. Cytokines and schizophrenia: microglia hypothesis of schizophrenia. Psychiatry Clin Neurosci. 2009;63:257–65. doi: 10.1111/j.1440-1819.2009.01945.x.
    1. Myint AM. Kynurenines: from the perspective of major psychiatric disorders. FEBS J. 2012;2009(279):1375–85. doi: 10.1111/j.1742-4658.2012.08551.x.
    1. Doorduin J, de Vries EF, Willemsen AT, de Groot JC, Dierckx RA, Klein HC. Neuroinflammation in schizophrenia-related psychosis: a PET study. J Nucl Med. 2009;50:1801–7. doi: 10.2967/jnumed.109.066647.
    1. van Berckel BN, Bossong MG, Boellaard R, Kloet R, Schuitemaker A, Caspers E, Luurtsema G, Windhorst AD, Cahn W, Lammertsma AA, Kahn RS. Microglia activation in recent-onset schizophrenia: a quantitative (R)-[11C]PK11195 positron emission tomography study. Biol Psychiatry. 2008;64:820–2. doi: 10.1016/j.biopsych.2008.04.025.
    1. Kay SR, Fiszbein A, Opler LA. The positive and negative syndrome scale (PANSS) for schizophrenia. Schizophr Bull. 1987;13:261–76. doi: 10.1093/schbul/13.2.261.
    1. American Psychiatric Association . Diagnostic and statistical manual of mental disorders. 4. Washington, DC: American Psychiatric Association; 2000.
    1. Birchwood M, The Social Functioning Scale The development and validation of a new scale of social adjustment for use in family intervention programmes with schizophrenic patients. Br J Psychiatry. 1990;157:853–9. doi: 10.1192/bjp.157.6.853.
    1. Heinrichs DW, Hanlon TE, Carpenter WT. The quality of life scale: an instrument for rating the schizophrenic deficit syndrome. Schizophr Bull. 1984;10:388–98. doi: 10.1093/schbul/10.3.388.
    1. Yusufi BZ, Mukherjee S, Aitchison K, Dunn G, Page E, Barnes TR. Abstracts of the XX International Congress on Schizophrenia Research, April 2 – April 6, 2005, Volume 31. Savannah, Georgia: Schizophr Bull; 2005. Inter-rater reliability of the antipsychotic non-neurological side-effects rating scale (ANNSERS) p. 574.
    1. Whittle SL, Hughes RA. Folate supplementation and methotrexate treatment in rheumatoid arthritis: a review. Rheumatology. 2004;43:267–71. doi: 10.1093/rheumatology/keh088.
    1. Ortiz Z, Shea B, Suarez-Almazor ME, Moher D, Wells GA, Tugwell P. The efficacy of folic acid and folinic acid in reducing methotrexate gastrointestinal toxicity in rheumatoid arthritis: a meta-analysis of randomised controlled trials. J Rheumatol. 1998;25:36–43.
    1. Morgan SL, Baggott JE, Vaughn WH, Austin JS, Veitch TA, Lee JY, Koopman WJ, Krumdieck CL, Alarcón GS. Supplementation with folic acid during methotrexate therapy for rheumatoid arthritis: a double-blind placebo-controlled trial. Ann Intern Med. 1994;121:833–41. doi: 10.7326/0003-4819-121-11-199412010-00002.
    1. Procter A. Enhancement of recovery from psychiatric illness by methylfolate. Br J Psychiatry. 1991;159:271–2. doi: 10.1192/bjp.159.2.271.
    1. Harmonised Tripartite Guideline for Good Clinical Practice 1996 Geneva: International Federation of the Pharmaceutical Manufacturers Association; 1996.

Source: PubMed

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