Cargando…
Efficacy of eicosapentaenoic acid in inflammatory depression: study protocol for a match-mismatch trial
BACKGROUND: Most antidepressant treatment studies have included patients strictly based on the Diagnostic and Statistical Manual of Mental Disorders definition of Major Depressive Disorder (MDD). Given the heterogeneity of MDD, this approach may have obscured inter-patient differences and hampered t...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9761617/ https://www.ncbi.nlm.nih.gov/pubmed/36536364 http://dx.doi.org/10.1186/s12888-022-04430-z |
_version_ | 1784852715357077504 |
---|---|
author | Suneson, Klara Ängeby, Filip Lindahl, Jesper Söderberg, Gustav Tjernberg, Johanna Lindqvist, Daniel |
author_facet | Suneson, Klara Ängeby, Filip Lindahl, Jesper Söderberg, Gustav Tjernberg, Johanna Lindqvist, Daniel |
author_sort | Suneson, Klara |
collection | PubMed |
description | BACKGROUND: Most antidepressant treatment studies have included patients strictly based on the Diagnostic and Statistical Manual of Mental Disorders definition of Major Depressive Disorder (MDD). Given the heterogeneity of MDD, this approach may have obscured inter-patient differences and hampered the development of novel and targeted treatment strategies. An alternative strategy is to use biomarkers to delineate endophenotypes of depression and test if these can be targeted via mechanism-based interventions. Several lines of evidence suggest that “inflammatory depression” is a clinically meaningful subtype of depression. Preliminary data indicate that omega-3 fatty acids, with their anti-inflammatory and neuroprotective properties, may be efficacious in this subtype of depression, and this study aims to test this hypothesis. METHOD: We conduct a match-mismatch-trial to test if add-on omega-3 fatty acid eicosapentaenoic acid (EPA) reduces depressive symptoms in patients with MDD and systemic low-grade inflammation. MDD patients on a stable antidepressant treatment are stratified at baseline on high sensitivity-C-reactive protein (hs-CRP) levels to a high-inflammation group (hs-CRP ≥ 3 mg/L) or a low-inflammation group (hs-CRP < 3 mg/L). Both groups receive add-on EPA (2 g per day) for 8 weeks with three study visits, all including blood draws. Patients and raters are blind to inflammation status. Primary outcome measure is change in Hamilton Depression Rating Scale score between baseline and week 8. We hypothesize that the inflammation group has a superior antidepressant response to EPA compared to the non-inflammation group. Secondary outcomes include a composite score of “inflammatory depressive symptoms”, quality of life, anxiety, anhedonia, sleep disturbances, fatigue, cognitive performance and change in biomarkers relating to inflammation, oxidative stress, metabolomics and cellular aging. DISCUSSION: In this study we will, for the first time using a match-mismatch trial design, test if omega-3 is an efficacious treatment for inflammatory depression. If our study is successful, it could add to the field of precision psychiatry. TRIAL REGISTRATION: This trial was registered May 8, 2017 on clinicaltrials.gov under the reference number NCT03143075 |
format | Online Article Text |
id | pubmed-9761617 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97616172022-12-19 Efficacy of eicosapentaenoic acid in inflammatory depression: study protocol for a match-mismatch trial Suneson, Klara Ängeby, Filip Lindahl, Jesper Söderberg, Gustav Tjernberg, Johanna Lindqvist, Daniel BMC Psychiatry Study Protocol BACKGROUND: Most antidepressant treatment studies have included patients strictly based on the Diagnostic and Statistical Manual of Mental Disorders definition of Major Depressive Disorder (MDD). Given the heterogeneity of MDD, this approach may have obscured inter-patient differences and hampered the development of novel and targeted treatment strategies. An alternative strategy is to use biomarkers to delineate endophenotypes of depression and test if these can be targeted via mechanism-based interventions. Several lines of evidence suggest that “inflammatory depression” is a clinically meaningful subtype of depression. Preliminary data indicate that omega-3 fatty acids, with their anti-inflammatory and neuroprotective properties, may be efficacious in this subtype of depression, and this study aims to test this hypothesis. METHOD: We conduct a match-mismatch-trial to test if add-on omega-3 fatty acid eicosapentaenoic acid (EPA) reduces depressive symptoms in patients with MDD and systemic low-grade inflammation. MDD patients on a stable antidepressant treatment are stratified at baseline on high sensitivity-C-reactive protein (hs-CRP) levels to a high-inflammation group (hs-CRP ≥ 3 mg/L) or a low-inflammation group (hs-CRP < 3 mg/L). Both groups receive add-on EPA (2 g per day) for 8 weeks with three study visits, all including blood draws. Patients and raters are blind to inflammation status. Primary outcome measure is change in Hamilton Depression Rating Scale score between baseline and week 8. We hypothesize that the inflammation group has a superior antidepressant response to EPA compared to the non-inflammation group. Secondary outcomes include a composite score of “inflammatory depressive symptoms”, quality of life, anxiety, anhedonia, sleep disturbances, fatigue, cognitive performance and change in biomarkers relating to inflammation, oxidative stress, metabolomics and cellular aging. DISCUSSION: In this study we will, for the first time using a match-mismatch trial design, test if omega-3 is an efficacious treatment for inflammatory depression. If our study is successful, it could add to the field of precision psychiatry. TRIAL REGISTRATION: This trial was registered May 8, 2017 on clinicaltrials.gov under the reference number NCT03143075 BioMed Central 2022-12-19 /pmc/articles/PMC9761617/ /pubmed/36536364 http://dx.doi.org/10.1186/s12888-022-04430-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Study Protocol Suneson, Klara Ängeby, Filip Lindahl, Jesper Söderberg, Gustav Tjernberg, Johanna Lindqvist, Daniel Efficacy of eicosapentaenoic acid in inflammatory depression: study protocol for a match-mismatch trial |
title | Efficacy of eicosapentaenoic acid in inflammatory depression: study protocol for a match-mismatch trial |
title_full | Efficacy of eicosapentaenoic acid in inflammatory depression: study protocol for a match-mismatch trial |
title_fullStr | Efficacy of eicosapentaenoic acid in inflammatory depression: study protocol for a match-mismatch trial |
title_full_unstemmed | Efficacy of eicosapentaenoic acid in inflammatory depression: study protocol for a match-mismatch trial |
title_short | Efficacy of eicosapentaenoic acid in inflammatory depression: study protocol for a match-mismatch trial |
title_sort | efficacy of eicosapentaenoic acid in inflammatory depression: study protocol for a match-mismatch trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9761617/ https://www.ncbi.nlm.nih.gov/pubmed/36536364 http://dx.doi.org/10.1186/s12888-022-04430-z |
work_keys_str_mv | AT sunesonklara efficacyofeicosapentaenoicacidininflammatorydepressionstudyprotocolforamatchmismatchtrial AT angebyfilip efficacyofeicosapentaenoicacidininflammatorydepressionstudyprotocolforamatchmismatchtrial AT lindahljesper efficacyofeicosapentaenoicacidininflammatorydepressionstudyprotocolforamatchmismatchtrial AT soderberggustav efficacyofeicosapentaenoicacidininflammatorydepressionstudyprotocolforamatchmismatchtrial AT tjernbergjohanna efficacyofeicosapentaenoicacidininflammatorydepressionstudyprotocolforamatchmismatchtrial AT lindqvistdaniel efficacyofeicosapentaenoicacidininflammatorydepressionstudyprotocolforamatchmismatchtrial |