Cargando…
The Impact of N-acetylcysteine on Major Depression: Qualitative Observation and Mixed Methods Analysis of Participant Change during a 12-week Randomised Controlled Trial
OBJECTIVE: N-acetylcysteine (NAC) is a novel therapeutic agent with multiple mechanisms of action in the central nervous system and a favourable side effect profile. Clinical evidence indicates that adjunctive NAC may reduce the severity of depressive symptoms in individuals with major depressive di...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean College of Neuropsychopharmacology
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10157003/ https://www.ncbi.nlm.nih.gov/pubmed/37119225 http://dx.doi.org/10.9758/cpn.2023.21.2.320 |
_version_ | 1785036652218941440 |
---|---|
author | Russell, Samantha E. Skvarc, David R. Mohebbi, Mohammadreza Camfield, David Byrne, Linda K. Turner, Alyna Ashton, Melanie M. Berk, Michael Dodd, Seetal Malhi, Gin S. Cotton, Sue M. Bush, Ashley I. Dean, Olivia M. |
author_facet | Russell, Samantha E. Skvarc, David R. Mohebbi, Mohammadreza Camfield, David Byrne, Linda K. Turner, Alyna Ashton, Melanie M. Berk, Michael Dodd, Seetal Malhi, Gin S. Cotton, Sue M. Bush, Ashley I. Dean, Olivia M. |
author_sort | Russell, Samantha E. |
collection | PubMed |
description | OBJECTIVE: N-acetylcysteine (NAC) is a novel therapeutic agent with multiple mechanisms of action in the central nervous system and a favourable side effect profile. Clinical evidence indicates that adjunctive NAC may reduce the severity of depressive symptoms in individuals with major depressive disorder (MDD). METHODS: A 12-week randomised controlled trial of 2,000 mg/day adjunctive NAC for MDD found no significant improvement at the primary endpoint (week 12) but did see improvements at the post-discontinuation interview (week 16). Within the context of patient-centered treatment, mixed-methods qualitative analysis was also included to explore factors that may determine individual responses to adjunctive NAC treatment. These data were drawn, under blinded conditions, from clinician notes recorded in the case report form. Using the DSM-5 symptom profile for MDD as the initial framework, themes were developed and explored. Frequencies were compared between placebo and NAC groups. RESULTS: Per protocol analysis of individual themes across the six interviews revealed group differences in favour of NAC for overall depressive affect, optimism, relationships and reduced functional impairment. CONCLUSION: This study provides further evidence for the utility of the mixed methods approach complimenting the primary findings using traditional quantitative analyses, as well as being able to capture additional, often more subtle, evidence of individual symptom-level change that reflects improvement in functional abilities in response to NAC supplementation. The use of mixed methods to explore outcomes from psychiatric studies should be considered in future to work towards improved patient-centred care and both confirm quantitative findings and generate novel hypotheses. |
format | Online Article Text |
id | pubmed-10157003 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Korean College of Neuropsychopharmacology |
record_format | MEDLINE/PubMed |
spelling | pubmed-101570032023-05-30 The Impact of N-acetylcysteine on Major Depression: Qualitative Observation and Mixed Methods Analysis of Participant Change during a 12-week Randomised Controlled Trial Russell, Samantha E. Skvarc, David R. Mohebbi, Mohammadreza Camfield, David Byrne, Linda K. Turner, Alyna Ashton, Melanie M. Berk, Michael Dodd, Seetal Malhi, Gin S. Cotton, Sue M. Bush, Ashley I. Dean, Olivia M. Clin Psychopharmacol Neurosci Original Article OBJECTIVE: N-acetylcysteine (NAC) is a novel therapeutic agent with multiple mechanisms of action in the central nervous system and a favourable side effect profile. Clinical evidence indicates that adjunctive NAC may reduce the severity of depressive symptoms in individuals with major depressive disorder (MDD). METHODS: A 12-week randomised controlled trial of 2,000 mg/day adjunctive NAC for MDD found no significant improvement at the primary endpoint (week 12) but did see improvements at the post-discontinuation interview (week 16). Within the context of patient-centered treatment, mixed-methods qualitative analysis was also included to explore factors that may determine individual responses to adjunctive NAC treatment. These data were drawn, under blinded conditions, from clinician notes recorded in the case report form. Using the DSM-5 symptom profile for MDD as the initial framework, themes were developed and explored. Frequencies were compared between placebo and NAC groups. RESULTS: Per protocol analysis of individual themes across the six interviews revealed group differences in favour of NAC for overall depressive affect, optimism, relationships and reduced functional impairment. CONCLUSION: This study provides further evidence for the utility of the mixed methods approach complimenting the primary findings using traditional quantitative analyses, as well as being able to capture additional, often more subtle, evidence of individual symptom-level change that reflects improvement in functional abilities in response to NAC supplementation. The use of mixed methods to explore outcomes from psychiatric studies should be considered in future to work towards improved patient-centred care and both confirm quantitative findings and generate novel hypotheses. Korean College of Neuropsychopharmacology 2023-05-30 2023-05-30 /pmc/articles/PMC10157003/ /pubmed/37119225 http://dx.doi.org/10.9758/cpn.2023.21.2.320 Text en Copyright© 2023, Korean College of Neuropsychopharmacology https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Russell, Samantha E. Skvarc, David R. Mohebbi, Mohammadreza Camfield, David Byrne, Linda K. Turner, Alyna Ashton, Melanie M. Berk, Michael Dodd, Seetal Malhi, Gin S. Cotton, Sue M. Bush, Ashley I. Dean, Olivia M. The Impact of N-acetylcysteine on Major Depression: Qualitative Observation and Mixed Methods Analysis of Participant Change during a 12-week Randomised Controlled Trial |
title | The Impact of N-acetylcysteine on Major Depression: Qualitative Observation and Mixed Methods Analysis of Participant Change during a 12-week Randomised Controlled Trial |
title_full | The Impact of N-acetylcysteine on Major Depression: Qualitative Observation and Mixed Methods Analysis of Participant Change during a 12-week Randomised Controlled Trial |
title_fullStr | The Impact of N-acetylcysteine on Major Depression: Qualitative Observation and Mixed Methods Analysis of Participant Change during a 12-week Randomised Controlled Trial |
title_full_unstemmed | The Impact of N-acetylcysteine on Major Depression: Qualitative Observation and Mixed Methods Analysis of Participant Change during a 12-week Randomised Controlled Trial |
title_short | The Impact of N-acetylcysteine on Major Depression: Qualitative Observation and Mixed Methods Analysis of Participant Change during a 12-week Randomised Controlled Trial |
title_sort | impact of n-acetylcysteine on major depression: qualitative observation and mixed methods analysis of participant change during a 12-week randomised controlled trial |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10157003/ https://www.ncbi.nlm.nih.gov/pubmed/37119225 http://dx.doi.org/10.9758/cpn.2023.21.2.320 |
work_keys_str_mv | AT russellsamanthae theimpactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT skvarcdavidr theimpactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT mohebbimohammadreza theimpactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT camfielddavid theimpactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT byrnelindak theimpactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT turneralyna theimpactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT ashtonmelaniem theimpactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT berkmichael theimpactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT doddseetal theimpactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT malhigins theimpactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT cottonsuem theimpactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT bushashleyi theimpactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT deanoliviam theimpactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT russellsamanthae impactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT skvarcdavidr impactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT mohebbimohammadreza impactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT camfielddavid impactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT byrnelindak impactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT turneralyna impactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT ashtonmelaniem impactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT berkmichael impactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT doddseetal impactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT malhigins impactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT cottonsuem impactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT bushashleyi impactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial AT deanoliviam impactofnacetylcysteineonmajordepressionqualitativeobservationandmixedmethodsanalysisofparticipantchangeduringa12weekrandomisedcontrolledtrial |