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The B-VITAGE trial: A randomized trial of homocysteine lowering treatment of depression in later life
BACKGROUND: Depression is a leading cause of disability worldwide and depressive symptoms are common in later life. Observational evidence suggests that depression is more prevalent among people with high plasma homocysteine (tHcy), but the results of randomized trials to date have been unable to sh...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2822769/ https://www.ncbi.nlm.nih.gov/pubmed/20096138 http://dx.doi.org/10.1186/1745-6215-11-8 |
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author | Ford, Andrew H Flicker, Leon McCaul, Kieran van Bockxmeer, Frank Hegarty, Sarah Hirani, Varsha Fenner, Stephen Almeida, Osvaldo P |
author_facet | Ford, Andrew H Flicker, Leon McCaul, Kieran van Bockxmeer, Frank Hegarty, Sarah Hirani, Varsha Fenner, Stephen Almeida, Osvaldo P |
author_sort | Ford, Andrew H |
collection | PubMed |
description | BACKGROUND: Depression is a leading cause of disability worldwide and depressive symptoms are common in later life. Observational evidence suggests that depression is more prevalent among people with high plasma homocysteine (tHcy), but the results of randomized trials to date have been unable to show that lowering tHcy through the supplementation of vitamins B(6), B(12 )and folate benefits depressive symptoms. We designed the B-VITAGE trial to determine whether adjunctive treatment with vitamins B(6), B(12 )and folate increases the efficacy of standard antidepressant treatment. METHODS/DESIGN: The B-VITAGE trial is a 12-month randomized, double-blind, placebo-controlled trial of daily citalopram (20 to 40 mg) plus B(12)(0.4 mg), B(6 )(25 mg) and folic acid (2 mg) or citalopram (20 to 40 mg) plus placebo for the treatment of depression in later life. The trial aims to recruit over 300 older adults with major depression (DSM-IV) and has been powered to detect the impact of an intervention associated with moderate effect size. Depressive symptoms will be rated with the Montgomery-Åsberg Depression Rating Scale (MADRS). The trial has two main outcomes of interest: a reduction of 50% or more in the MADRS total score between baseline and week 12 and the remission of the depressive episode at weeks 12, 26 and 52 according to DSM-IV criteria. We hypothesize that subjects randomly allocated to the vitamin arm of the study will be more likely to show a clinically significant improvement and achieve and maintain remission of symptoms at 12, 26 and 52 weeks. Secondary outcomes of interest include compliance with treatment, reduction in the severity of depressive symptoms, switching to different antidepressants, the use of non-pharmacological antidepressant treatments, response to treatment according to MTHFRC677T genotype, and changes in cognitive function over 52 weeks. CONCLUSIONS: The results of this trial will clarify whether the systematic use of B-vitamins improves the response of older adults to standard antidepressant treatment. We anticipate that our findings will have implications for clinical practice and health policy development. TRIAL REGISTRATION: The trial is registered with the Australian Clinical Trials Registry, trial number (())ACTRN12609000256279. |
format | Text |
id | pubmed-2822769 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28227692010-02-17 The B-VITAGE trial: A randomized trial of homocysteine lowering treatment of depression in later life Ford, Andrew H Flicker, Leon McCaul, Kieran van Bockxmeer, Frank Hegarty, Sarah Hirani, Varsha Fenner, Stephen Almeida, Osvaldo P Trials Study protocol BACKGROUND: Depression is a leading cause of disability worldwide and depressive symptoms are common in later life. Observational evidence suggests that depression is more prevalent among people with high plasma homocysteine (tHcy), but the results of randomized trials to date have been unable to show that lowering tHcy through the supplementation of vitamins B(6), B(12 )and folate benefits depressive symptoms. We designed the B-VITAGE trial to determine whether adjunctive treatment with vitamins B(6), B(12 )and folate increases the efficacy of standard antidepressant treatment. METHODS/DESIGN: The B-VITAGE trial is a 12-month randomized, double-blind, placebo-controlled trial of daily citalopram (20 to 40 mg) plus B(12)(0.4 mg), B(6 )(25 mg) and folic acid (2 mg) or citalopram (20 to 40 mg) plus placebo for the treatment of depression in later life. The trial aims to recruit over 300 older adults with major depression (DSM-IV) and has been powered to detect the impact of an intervention associated with moderate effect size. Depressive symptoms will be rated with the Montgomery-Åsberg Depression Rating Scale (MADRS). The trial has two main outcomes of interest: a reduction of 50% or more in the MADRS total score between baseline and week 12 and the remission of the depressive episode at weeks 12, 26 and 52 according to DSM-IV criteria. We hypothesize that subjects randomly allocated to the vitamin arm of the study will be more likely to show a clinically significant improvement and achieve and maintain remission of symptoms at 12, 26 and 52 weeks. Secondary outcomes of interest include compliance with treatment, reduction in the severity of depressive symptoms, switching to different antidepressants, the use of non-pharmacological antidepressant treatments, response to treatment according to MTHFRC677T genotype, and changes in cognitive function over 52 weeks. CONCLUSIONS: The results of this trial will clarify whether the systematic use of B-vitamins improves the response of older adults to standard antidepressant treatment. We anticipate that our findings will have implications for clinical practice and health policy development. TRIAL REGISTRATION: The trial is registered with the Australian Clinical Trials Registry, trial number (())ACTRN12609000256279. BioMed Central 2010-01-25 /pmc/articles/PMC2822769/ /pubmed/20096138 http://dx.doi.org/10.1186/1745-6215-11-8 Text en Copyright ©2010 Ford et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Study protocol Ford, Andrew H Flicker, Leon McCaul, Kieran van Bockxmeer, Frank Hegarty, Sarah Hirani, Varsha Fenner, Stephen Almeida, Osvaldo P The B-VITAGE trial: A randomized trial of homocysteine lowering treatment of depression in later life |
title | The B-VITAGE trial: A randomized trial of homocysteine lowering treatment of depression in later life |
title_full | The B-VITAGE trial: A randomized trial of homocysteine lowering treatment of depression in later life |
title_fullStr | The B-VITAGE trial: A randomized trial of homocysteine lowering treatment of depression in later life |
title_full_unstemmed | The B-VITAGE trial: A randomized trial of homocysteine lowering treatment of depression in later life |
title_short | The B-VITAGE trial: A randomized trial of homocysteine lowering treatment of depression in later life |
title_sort | b-vitage trial: a randomized trial of homocysteine lowering treatment of depression in later life |
topic | Study protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2822769/ https://www.ncbi.nlm.nih.gov/pubmed/20096138 http://dx.doi.org/10.1186/1745-6215-11-8 |
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