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Nitrous oxide as an adjunctive therapy in major depressive disorder: a randomized controlled double-blind pilot trial

OBJECTIVE: Major depressive disorder (MDD) is related to glutamatergic dysfunction. Antagonists of glutamatergic N-methyl-D-aspartate receptor (NMDAR), such as ketamine, have antidepressant properties. Nitrous oxide (N(2)O) is also a NMDAR antagonist. Thus, this study aimed to evaluate the effects o...

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Detalles Bibliográficos
Autores principales: Guimarães, Mara C., Guimarães, Tiago M., Hallak, Jaime E., Abrão, João, Machado-de-Sousa, João P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação Brasileira de Psiquiatria 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8555644/
https://www.ncbi.nlm.nih.gov/pubmed/33605397
http://dx.doi.org/10.1590/1516-4446-2020-1543
Descripción
Sumario:OBJECTIVE: Major depressive disorder (MDD) is related to glutamatergic dysfunction. Antagonists of glutamatergic N-methyl-D-aspartate receptor (NMDAR), such as ketamine, have antidepressant properties. Nitrous oxide (N(2)O) is also a NMDAR antagonist. Thus, this study aimed to evaluate the effects of augmenting antidepressant treatment with N(2)O. METHODS: This double blind, placebo-controlled randomized parallel pilot trial was conducted from June 2016 to June 2018 at the Hospital das Clínicas, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Twenty-three subjects with MDD (aged 18 to 65, on antidepressants, with a score > 17 on the 17-item-Hamilton Depression Rating Scale [HAM-D(17)]) received 50% N(2)O (n=12; 37.17±13.59 years) or placebo (100% oxygen) (n=11; 37.18±12.77 years) for 60 minutes twice a week for 4 weeks. The primary outcome was changes in HAM-D(17) from baseline to week 4. RESULTS: Depressive symptoms improved significantly in the N(2)O group (N(2)O: from 22.58±3.83 to 5.92±4.08; placebo: from 22.44±3.54 to 12.89±5.39, p < 0.005). A total of 91.7% and 75% of the N(2)O group subjects achieved response (≥ 50% reduction in HAM-D(17) score) and remission (HAM-D(17) < 7), respectively. The predominant adverse effects of N(2)O treatment were nausea, vomiting, and headache. CONCLUSION: N(2)O treatment led to a statistically significant reduction in HAM-D(17) scores compared to placebo. CLINICAL TRIAL REGISTRATION: Brazilian Register of Clinical Trials, RBR-5rz5ch