Melatonin is a biomarker of circadian dysregulation and is correlated with major depression and fibromyalgia symptom severity

Detalhes bibliográficos
Autor(a) principal: Caumo, Wolnei
Data de Publicação: 2019
Outros Autores: Hidalgo, Maria Paz Loayza, Souza, Andressa de, Torres, Iraci Lucena da Silva, Antunes, Luciana da Conceição
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/188808
Resumo: Objective: This study compared urinary 6-sulfatoxymelatonin (aMT6s) over 24 hours among fibromyalgia (FM), major depression disorder (MDD), and healthy control (HC) groups, and examined whether rhythm is correlated with depressive symptoms. To answer this question we compared the rhythm of urinary aMT6s secretion among each group in four time series: morning (06:00–12:00 hours), afternoon (12:00–18:00 hours), evening (18:00–24:00 hours), and night (24:00–06:00 hours). In the FM subjects, we assessed if the rhythm of urinary aMT6s secretion is associated with pain severity, sleep quality, number of trigger points (NTPs), and the pain pressure threshold (PPT). Patients and methods: We included 54 women, aged 18–60 years with diagnosis of FM (n=18), MDD (n=19), and HC (n =17). The 24-hour urinary aMT6s was evaluated according to four standardized periods. The assessment instruments were the Hamilton Depression Rating Scale (HDRS), Pittsburgh Sleep Quality Index, and Fibromyalgia Impact Questionnaire Results: A generalized estimating equation revealed no difference in the daily load of aMT6s secretion among the three groups (P=0.49). However, at the daily time (06:00–18:00 hours), the load secretion of aMT6s reached 41.54% and 60.71% in the FM and MDD, respectively, as compared to 20.73% in the HC (P<0.05). A higher score in the HDRS was positively correlated with the amount of aMT6s secretion during daytime (06:00–18:00 hours). Also, multivariate linear regression revealed that in FM subjects, the aMT6s secretion during daytime (06:00–18:00 hours) was negatively correlated with the PPTlog (partial η2=0.531, P=0.001). However, it was positively correlated with depressive symptoms (partial η2=0.317, P=0.01); PQSI (partial η2=0.306, P=0.017), and NTPs (partial η2=0.23, P=0.04). Conclusion: A more significant load of aMT6s secretion during daytime hours was observed in MDD and FM subjects compared to HC. These findings help to comprehend the biological basis of these disorders and show how disruption in melatonin secretion is positively correlated with clinical symptoms.
id UFRGS-2_4837f840b6a9e63c7b966f09dff9b511
oai_identifier_str oai:www.lume.ufrgs.br:10183/188808
network_acronym_str UFRGS-2
network_name_str Repositório Institucional da UFRGS
repository_id_str
spelling Caumo, WolneiHidalgo, Maria Paz LoayzaSouza, Andressa deTorres, Iraci Lucena da SilvaAntunes, Luciana da Conceição2019-02-15T02:33:40Z20191178-7090http://hdl.handle.net/10183/188808001087615Objective: This study compared urinary 6-sulfatoxymelatonin (aMT6s) over 24 hours among fibromyalgia (FM), major depression disorder (MDD), and healthy control (HC) groups, and examined whether rhythm is correlated with depressive symptoms. To answer this question we compared the rhythm of urinary aMT6s secretion among each group in four time series: morning (06:00–12:00 hours), afternoon (12:00–18:00 hours), evening (18:00–24:00 hours), and night (24:00–06:00 hours). In the FM subjects, we assessed if the rhythm of urinary aMT6s secretion is associated with pain severity, sleep quality, number of trigger points (NTPs), and the pain pressure threshold (PPT). Patients and methods: We included 54 women, aged 18–60 years with diagnosis of FM (n=18), MDD (n=19), and HC (n =17). The 24-hour urinary aMT6s was evaluated according to four standardized periods. The assessment instruments were the Hamilton Depression Rating Scale (HDRS), Pittsburgh Sleep Quality Index, and Fibromyalgia Impact Questionnaire Results: A generalized estimating equation revealed no difference in the daily load of aMT6s secretion among the three groups (P=0.49). However, at the daily time (06:00–18:00 hours), the load secretion of aMT6s reached 41.54% and 60.71% in the FM and MDD, respectively, as compared to 20.73% in the HC (P<0.05). A higher score in the HDRS was positively correlated with the amount of aMT6s secretion during daytime (06:00–18:00 hours). Also, multivariate linear regression revealed that in FM subjects, the aMT6s secretion during daytime (06:00–18:00 hours) was negatively correlated with the PPTlog (partial η2=0.531, P=0.001). However, it was positively correlated with depressive symptoms (partial η2=0.317, P=0.01); PQSI (partial η2=0.306, P=0.017), and NTPs (partial η2=0.23, P=0.04). Conclusion: A more significant load of aMT6s secretion during daytime hours was observed in MDD and FM subjects compared to HC. These findings help to comprehend the biological basis of these disorders and show how disruption in melatonin secretion is positively correlated with clinical symptoms.application/pdfengJournal of pain research. Auckland. Vol. 2019, no. 12 (Jan. 2019), p. 545-556Ritmo circadianoFibromialgiaDor crônicaDepressãoMelatoninaFibromyalgiaDepressionPainMelatonin6 sulfatoxymelatonin (aMT6s)Melatonin is a biomarker of circadian dysregulation and is correlated with major depression and fibromyalgia symptom severityEstrangeiroinfo: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:UFRGSTEXT001087615.pdf.txt001087615.pdf.txtExtracted Texttext/plain61334http://www.lume.ufrgs.br/bitstream/10183/188808/2/001087615.pdf.txtf59be0ab65abbed787b7178fb1fcf088MD52ORIGINAL001087615.pdfTexto completo (inglês)application/pdf470873http://www.lume.ufrgs.br/bitstream/10183/188808/1/001087615.pdf493e14f6f9cb335520b937c9df84f113MD5110183/1888082019-02-16 02:34:26.946071oai:www.lume.ufrgs.br:10183/188808Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2019-02-16T04:34:26Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Melatonin is a biomarker of circadian dysregulation and is correlated with major depression and fibromyalgia symptom severity
title Melatonin is a biomarker of circadian dysregulation and is correlated with major depression and fibromyalgia symptom severity
spellingShingle Melatonin is a biomarker of circadian dysregulation and is correlated with major depression and fibromyalgia symptom severity
Caumo, Wolnei
Ritmo circadiano
Fibromialgia
Dor crônica
Depressão
Melatonina
Fibromyalgia
Depression
Pain
Melatonin
6 sulfatoxymelatonin (aMT6s)
title_short Melatonin is a biomarker of circadian dysregulation and is correlated with major depression and fibromyalgia symptom severity
title_full Melatonin is a biomarker of circadian dysregulation and is correlated with major depression and fibromyalgia symptom severity
title_fullStr Melatonin is a biomarker of circadian dysregulation and is correlated with major depression and fibromyalgia symptom severity
title_full_unstemmed Melatonin is a biomarker of circadian dysregulation and is correlated with major depression and fibromyalgia symptom severity
title_sort Melatonin is a biomarker of circadian dysregulation and is correlated with major depression and fibromyalgia symptom severity
author Caumo, Wolnei
author_facet Caumo, Wolnei
Hidalgo, Maria Paz Loayza
Souza, Andressa de
Torres, Iraci Lucena da Silva
Antunes, Luciana da Conceição
author_role author
author2 Hidalgo, Maria Paz Loayza
Souza, Andressa de
Torres, Iraci Lucena da Silva
Antunes, Luciana da Conceição
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Caumo, Wolnei
Hidalgo, Maria Paz Loayza
Souza, Andressa de
Torres, Iraci Lucena da Silva
Antunes, Luciana da Conceição
dc.subject.por.fl_str_mv Ritmo circadiano
Fibromialgia
Dor crônica
Depressão
Melatonina
topic Ritmo circadiano
Fibromialgia
Dor crônica
Depressão
Melatonina
Fibromyalgia
Depression
Pain
Melatonin
6 sulfatoxymelatonin (aMT6s)
dc.subject.eng.fl_str_mv Fibromyalgia
Depression
Pain
Melatonin
6 sulfatoxymelatonin (aMT6s)
description Objective: This study compared urinary 6-sulfatoxymelatonin (aMT6s) over 24 hours among fibromyalgia (FM), major depression disorder (MDD), and healthy control (HC) groups, and examined whether rhythm is correlated with depressive symptoms. To answer this question we compared the rhythm of urinary aMT6s secretion among each group in four time series: morning (06:00–12:00 hours), afternoon (12:00–18:00 hours), evening (18:00–24:00 hours), and night (24:00–06:00 hours). In the FM subjects, we assessed if the rhythm of urinary aMT6s secretion is associated with pain severity, sleep quality, number of trigger points (NTPs), and the pain pressure threshold (PPT). Patients and methods: We included 54 women, aged 18–60 years with diagnosis of FM (n=18), MDD (n=19), and HC (n =17). The 24-hour urinary aMT6s was evaluated according to four standardized periods. The assessment instruments were the Hamilton Depression Rating Scale (HDRS), Pittsburgh Sleep Quality Index, and Fibromyalgia Impact Questionnaire Results: A generalized estimating equation revealed no difference in the daily load of aMT6s secretion among the three groups (P=0.49). However, at the daily time (06:00–18:00 hours), the load secretion of aMT6s reached 41.54% and 60.71% in the FM and MDD, respectively, as compared to 20.73% in the HC (P<0.05). A higher score in the HDRS was positively correlated with the amount of aMT6s secretion during daytime (06:00–18:00 hours). Also, multivariate linear regression revealed that in FM subjects, the aMT6s secretion during daytime (06:00–18:00 hours) was negatively correlated with the PPTlog (partial η2=0.531, P=0.001). However, it was positively correlated with depressive symptoms (partial η2=0.317, P=0.01); PQSI (partial η2=0.306, P=0.017), and NTPs (partial η2=0.23, P=0.04). Conclusion: A more significant load of aMT6s secretion during daytime hours was observed in MDD and FM subjects compared to HC. These findings help to comprehend the biological basis of these disorders and show how disruption in melatonin secretion is positively correlated with clinical symptoms.
publishDate 2019
dc.date.accessioned.fl_str_mv 2019-02-15T02:33:40Z
dc.date.issued.fl_str_mv 2019
dc.type.driver.fl_str_mv Estrangeiro
info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10183/188808
dc.identifier.issn.pt_BR.fl_str_mv 1178-7090
dc.identifier.nrb.pt_BR.fl_str_mv 001087615
identifier_str_mv 1178-7090
001087615
url http://hdl.handle.net/10183/188808
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.pt_BR.fl_str_mv Journal of pain research. Auckland. Vol. 2019, no. 12 (Jan. 2019), p. 545-556
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFRGS
instname:Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
instname_str Universidade Federal do Rio Grande do Sul (UFRGS)
instacron_str UFRGS
institution UFRGS
reponame_str Repositório Institucional da UFRGS
collection Repositório Institucional da UFRGS
bitstream.url.fl_str_mv http://www.lume.ufrgs.br/bitstream/10183/188808/2/001087615.pdf.txt
http://www.lume.ufrgs.br/bitstream/10183/188808/1/001087615.pdf
bitstream.checksum.fl_str_mv f59be0ab65abbed787b7178fb1fcf088
493e14f6f9cb335520b937c9df84f113
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
repository.name.fl_str_mv Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)
repository.mail.fl_str_mv
_version_ 1815447682495283200