Melatonin is a biomarker of circadian dysregulation and is correlated with major depression and fibromyalgia symptom severity
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , |
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. |
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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 |
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info:eu-repo/semantics/publishedVersion |
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1178-7090 |
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001087615 |
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eng |
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dc.relation.ispartof.pt_BR.fl_str_mv |
Journal of pain research. Auckland. Vol. 2019, no. 12 (Jan. 2019), p. 545-556 |
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