Biological differences between melancholic and nonmelancholic depression subtyped by the CORE measure

Detalhes bibliográficos
Autor(a) principal: Spanemberg, Lucas
Data de Publicação: 2014
Outros Autores: Caldieraro, Marco Antonio Knob, Vares, Edgar Arrua, Aguiar, Bianca Wollenhaupt de, Kauer-Sant'Anna, Márcia, Kawamoto, Sheila Yuri, Galvão, Emily, Parker, Gordon, Fleck, Marcelo Pio de Almeida
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/181496
Resumo: Background: The purpose of this study was to compare melancholic patients rated by the CORE measure of observable psychomotor disturbance with nonmelancholic and control subjects across a set of biomarkers. Methods: Depressed patients were classified as melancholic or nonmelancholic by using the CORE measure. Both groups of patients, as well as control subjects, were compared for a set of clinical and laboratory measures. Serum levels of brain-derived neurotrophic factor, of two markers of oxidative stress (protein carbonyl content [PCC] and thiobarbituric acid reactive substances [TBARS]), and of several immunity markers (interleukin [IL]-2, IL-4, IL-6, IL-10, IL-17, tumor necrosis factor-alpha, and interferon-gamma) were analyzed. Results: Thirty-three depressed patients and 54 healthy controls were studied. Depressive patients showed higher IL-4, IL-6, and PCC values than healthy controls. Thirteen (39%) of the depressed patients were assigned as melancholic by the CORE measure. They generated lower interferon-gamma (compared with nonmelancholic depressed patients) and TBARS (compared with both the nonmelancholic subset and controls) and returned higher IL-6 levels than controls. Both depressive groups generated higher PCC scores than controls, with no difference between melancholic and nonmelancholic subsets. Conclusion: A sign-based measure to rate melancholia was able to replicate and extend biological findings discriminating melancholic depression. Signs of psychomotor disturbance may be a useful diagnostic measure of melancholia.
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spelling Spanemberg, LucasCaldieraro, Marco Antonio KnobVares, Edgar ArruaAguiar, Bianca Wollenhaupt deKauer-Sant'Anna, MárciaKawamoto, Sheila YuriGalvão, EmilyParker, GordonFleck, Marcelo Pio de Almeida2018-08-28T02:29:22Z20141178-2021http://hdl.handle.net/10183/181496000964772Background: The purpose of this study was to compare melancholic patients rated by the CORE measure of observable psychomotor disturbance with nonmelancholic and control subjects across a set of biomarkers. Methods: Depressed patients were classified as melancholic or nonmelancholic by using the CORE measure. Both groups of patients, as well as control subjects, were compared for a set of clinical and laboratory measures. Serum levels of brain-derived neurotrophic factor, of two markers of oxidative stress (protein carbonyl content [PCC] and thiobarbituric acid reactive substances [TBARS]), and of several immunity markers (interleukin [IL]-2, IL-4, IL-6, IL-10, IL-17, tumor necrosis factor-alpha, and interferon-gamma) were analyzed. Results: Thirty-three depressed patients and 54 healthy controls were studied. Depressive patients showed higher IL-4, IL-6, and PCC values than healthy controls. Thirteen (39%) of the depressed patients were assigned as melancholic by the CORE measure. They generated lower interferon-gamma (compared with nonmelancholic depressed patients) and TBARS (compared with both the nonmelancholic subset and controls) and returned higher IL-6 levels than controls. Both depressive groups generated higher PCC scores than controls, with no difference between melancholic and nonmelancholic subsets. Conclusion: A sign-based measure to rate melancholia was able to replicate and extend biological findings discriminating melancholic depression. Signs of psychomotor disturbance may be a useful diagnostic measure of melancholia.application/pdfengNeuropsychiatric disease and treatment. Auckland. Vol. 10 (2014), p. 1523-1531DepressãoEstresse oxidativoCitocinasFator neurotrófico derivado do encéfaloBrain-derived neurotrophic factorMelancholic depressionInflammatory cytokinesOxidative stressBiological differences between melancholic and nonmelancholic depression subtyped by the CORE measureEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSORIGINAL000964772.pdfTexto completo (inglês)application/pdf266666http://www.lume.ufrgs.br/bitstream/10183/181496/1/000964772.pdfda02721c737d2df5e044776f8e30fc79MD51TEXT000964772.pdf.txt000964772.pdf.txtExtracted Texttext/plain47267http://www.lume.ufrgs.br/bitstream/10183/181496/2/000964772.pdf.txtaf9f2ccfe8b8d6cd32a2001abdc6b814MD52THUMBNAIL000964772.pdf.jpg000964772.pdf.jpgGenerated Thumbnailimage/jpeg2007http://www.lume.ufrgs.br/bitstream/10183/181496/3/000964772.pdf.jpg1c3369157c6ca5308445cd96bdf9b4d8MD5310183/1814962023-04-13 03:26:38.576324oai:www.lume.ufrgs.br:10183/181496Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2023-04-13T06:26:38Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Biological differences between melancholic and nonmelancholic depression subtyped by the CORE measure
title Biological differences between melancholic and nonmelancholic depression subtyped by the CORE measure
spellingShingle Biological differences between melancholic and nonmelancholic depression subtyped by the CORE measure
Spanemberg, Lucas
Depressão
Estresse oxidativo
Citocinas
Fator neurotrófico derivado do encéfalo
Brain-derived neurotrophic factor
Melancholic depression
Inflammatory cytokines
Oxidative stress
title_short Biological differences between melancholic and nonmelancholic depression subtyped by the CORE measure
title_full Biological differences between melancholic and nonmelancholic depression subtyped by the CORE measure
title_fullStr Biological differences between melancholic and nonmelancholic depression subtyped by the CORE measure
title_full_unstemmed Biological differences between melancholic and nonmelancholic depression subtyped by the CORE measure
title_sort Biological differences between melancholic and nonmelancholic depression subtyped by the CORE measure
author Spanemberg, Lucas
author_facet Spanemberg, Lucas
Caldieraro, Marco Antonio Knob
Vares, Edgar Arrua
Aguiar, Bianca Wollenhaupt de
Kauer-Sant'Anna, Márcia
Kawamoto, Sheila Yuri
Galvão, Emily
Parker, Gordon
Fleck, Marcelo Pio de Almeida
author_role author
author2 Caldieraro, Marco Antonio Knob
Vares, Edgar Arrua
Aguiar, Bianca Wollenhaupt de
Kauer-Sant'Anna, Márcia
Kawamoto, Sheila Yuri
Galvão, Emily
Parker, Gordon
Fleck, Marcelo Pio de Almeida
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Spanemberg, Lucas
Caldieraro, Marco Antonio Knob
Vares, Edgar Arrua
Aguiar, Bianca Wollenhaupt de
Kauer-Sant'Anna, Márcia
Kawamoto, Sheila Yuri
Galvão, Emily
Parker, Gordon
Fleck, Marcelo Pio de Almeida
dc.subject.por.fl_str_mv Depressão
Estresse oxidativo
Citocinas
Fator neurotrófico derivado do encéfalo
topic Depressão
Estresse oxidativo
Citocinas
Fator neurotrófico derivado do encéfalo
Brain-derived neurotrophic factor
Melancholic depression
Inflammatory cytokines
Oxidative stress
dc.subject.eng.fl_str_mv Brain-derived neurotrophic factor
Melancholic depression
Inflammatory cytokines
Oxidative stress
description Background: The purpose of this study was to compare melancholic patients rated by the CORE measure of observable psychomotor disturbance with nonmelancholic and control subjects across a set of biomarkers. Methods: Depressed patients were classified as melancholic or nonmelancholic by using the CORE measure. Both groups of patients, as well as control subjects, were compared for a set of clinical and laboratory measures. Serum levels of brain-derived neurotrophic factor, of two markers of oxidative stress (protein carbonyl content [PCC] and thiobarbituric acid reactive substances [TBARS]), and of several immunity markers (interleukin [IL]-2, IL-4, IL-6, IL-10, IL-17, tumor necrosis factor-alpha, and interferon-gamma) were analyzed. Results: Thirty-three depressed patients and 54 healthy controls were studied. Depressive patients showed higher IL-4, IL-6, and PCC values than healthy controls. Thirteen (39%) of the depressed patients were assigned as melancholic by the CORE measure. They generated lower interferon-gamma (compared with nonmelancholic depressed patients) and TBARS (compared with both the nonmelancholic subset and controls) and returned higher IL-6 levels than controls. Both depressive groups generated higher PCC scores than controls, with no difference between melancholic and nonmelancholic subsets. Conclusion: A sign-based measure to rate melancholia was able to replicate and extend biological findings discriminating melancholic depression. Signs of psychomotor disturbance may be a useful diagnostic measure of melancholia.
publishDate 2014
dc.date.issued.fl_str_mv 2014
dc.date.accessioned.fl_str_mv 2018-08-28T02:29:22Z
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dc.identifier.issn.pt_BR.fl_str_mv 1178-2021
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dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.pt_BR.fl_str_mv Neuropsychiatric disease and treatment. Auckland. Vol. 10 (2014), p. 1523-1531
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