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Blood plasma B vitamins in depression and the therapeutic response to electroconvulsive therapy

A growing body of research has indicated a role for B vitamins in depression, with some previous studies suggesting that B vitamin status in patients with depression can impact on antidepressant response. Here we aimed to investigate B vitamin plasma concentrations in medicated patients with depress...

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Autores principales: Ryan, Karen M., Allers, Kelly A., Harkin, Andrew, McLoughlin, Declan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8474603/
https://www.ncbi.nlm.nih.gov/pubmed/34589848
http://dx.doi.org/10.1016/j.bbih.2020.100063
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author Ryan, Karen M.
Allers, Kelly A.
Harkin, Andrew
McLoughlin, Declan M.
author_facet Ryan, Karen M.
Allers, Kelly A.
Harkin, Andrew
McLoughlin, Declan M.
author_sort Ryan, Karen M.
collection PubMed
description A growing body of research has indicated a role for B vitamins in depression, with some previous studies suggesting that B vitamin status in patients with depression can impact on antidepressant response. Here we aimed to investigate B vitamin plasma concentrations in medicated patients with depression (n ​= ​94) compared to age- and sex-matched healthy controls (n ​= ​57), and in patients with depression after electroconvulsive therapy (ECT) in a real-world clinical setting. Our results show that nicotinamide (vitamin B3), N1-methylnicotinamide (vitamin B3 metabolite), and pyridoxal 5′-phosphate (PLP; vitamin B6) concentrations were significantly reduced in patients with depression compared to controls. The Cohen’s d effect sizes for nicotinamide, N1-methylnicotinamide, and PLP were moderate–large (−0.47, −0.51, and −0.59, respectively), and likely to be of clinical relevance. Functional biomarkers of vitamin B6 status (PAr index, 3-hydroxykynurenine: hydroxyanthranilic acid ratio, 3-hydroxykynurenine: xanthurenic acid ratio, and HKr) were elevated in depressed patients compared to controls, suggestive of reduced vitamin B6 function. Over 30% of the patient cohort were found to have low to deficient PLP concentrations, and exploratory analyses revealed that these patients had higher IL-6 and CRP concentrations compared to patients with PLP levels within the normal range. Treatment with ECT did not alter B vitamin concentrations, and B vitamin concentrations were not associated with depression severity or the therapeutic response to ECT. Overall, reduced plasma PLP, nicotinamide, and N1-methylnicotinamide concentrations could have wide ranging effects on pathways and systems implicated in depression. Further studies are required to understand the reasons why patients with depression present with low plasma B vitamin concentrations.
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spelling pubmed-84746032021-09-28 Blood plasma B vitamins in depression and the therapeutic response to electroconvulsive therapy Ryan, Karen M. Allers, Kelly A. Harkin, Andrew McLoughlin, Declan M. Brain Behav Immun Health Full Length Article A growing body of research has indicated a role for B vitamins in depression, with some previous studies suggesting that B vitamin status in patients with depression can impact on antidepressant response. Here we aimed to investigate B vitamin plasma concentrations in medicated patients with depression (n ​= ​94) compared to age- and sex-matched healthy controls (n ​= ​57), and in patients with depression after electroconvulsive therapy (ECT) in a real-world clinical setting. Our results show that nicotinamide (vitamin B3), N1-methylnicotinamide (vitamin B3 metabolite), and pyridoxal 5′-phosphate (PLP; vitamin B6) concentrations were significantly reduced in patients with depression compared to controls. The Cohen’s d effect sizes for nicotinamide, N1-methylnicotinamide, and PLP were moderate–large (−0.47, −0.51, and −0.59, respectively), and likely to be of clinical relevance. Functional biomarkers of vitamin B6 status (PAr index, 3-hydroxykynurenine: hydroxyanthranilic acid ratio, 3-hydroxykynurenine: xanthurenic acid ratio, and HKr) were elevated in depressed patients compared to controls, suggestive of reduced vitamin B6 function. Over 30% of the patient cohort were found to have low to deficient PLP concentrations, and exploratory analyses revealed that these patients had higher IL-6 and CRP concentrations compared to patients with PLP levels within the normal range. Treatment with ECT did not alter B vitamin concentrations, and B vitamin concentrations were not associated with depression severity or the therapeutic response to ECT. Overall, reduced plasma PLP, nicotinamide, and N1-methylnicotinamide concentrations could have wide ranging effects on pathways and systems implicated in depression. Further studies are required to understand the reasons why patients with depression present with low plasma B vitamin concentrations. Elsevier 2020-03-28 /pmc/articles/PMC8474603/ /pubmed/34589848 http://dx.doi.org/10.1016/j.bbih.2020.100063 Text en © 2020 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Full Length Article
Ryan, Karen M.
Allers, Kelly A.
Harkin, Andrew
McLoughlin, Declan M.
Blood plasma B vitamins in depression and the therapeutic response to electroconvulsive therapy
title Blood plasma B vitamins in depression and the therapeutic response to electroconvulsive therapy
title_full Blood plasma B vitamins in depression and the therapeutic response to electroconvulsive therapy
title_fullStr Blood plasma B vitamins in depression and the therapeutic response to electroconvulsive therapy
title_full_unstemmed Blood plasma B vitamins in depression and the therapeutic response to electroconvulsive therapy
title_short Blood plasma B vitamins in depression and the therapeutic response to electroconvulsive therapy
title_sort blood plasma b vitamins in depression and the therapeutic response to electroconvulsive therapy
topic Full Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8474603/
https://www.ncbi.nlm.nih.gov/pubmed/34589848
http://dx.doi.org/10.1016/j.bbih.2020.100063
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