PMID- 30787633 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20220331 IS - 1178-7090 (Print) IS - 1178-7090 (Electronic) IS - 1178-7090 (Linking) VI - 12 DP - 2019 TI - Melatonin is a biomarker of circadian dysregulation and is correlated with major depression and fibromyalgia symptom severity. PG - 545-556 LID - 10.2147/JPR.S176857 [doi] AB - 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 eta2=0.531, P=0.001). However, it was positively correlated with depressive symptoms (partial eta2=0.317, P=0.01); PQSI (partial eta2=0.306, P=0.017), and NTPs (partial eta2=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. FAU - Caumo, Wolnei AU - Caumo W AD - School of Medicine, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, Brazil, wcaumo@hcpa.edu.br. AD - Pain and Palliative Care Service at Hospital de Clinicas de Porto Alegre (HCPA), Laboratory of Pain and Neuromodulation at UFRGS, Porto Alegre, Brazil, wcaumo@hcpa.edu.br. AD - Pain and Anesthesia in Surgery Department, School of Medicine, UFRGS, Porto Alegre, Brazil, wcaumo@hcpa.edu.br. FAU - Hidalgo, Maria Paz AU - Hidalgo MP AD - Psychiatry Department, School of Medicine, UFRGS, Porto Alegre, Brazil. AD - Laboratorio de Cronobiologia e Sono do Hospital de Clinicas de Porto Alegre; Porto Alegre, Brazil. FAU - Souza, Andressa AU - Souza A AD - Postgraduate Program in Health and Human Development, La Salle Universitary Center, Canoas, Brazil. FAU - Torres, Iraci L S AU - Torres ILS AD - School of Medicine, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, Brazil, wcaumo@hcpa.edu.br. AD - Pharmacology Department, Instituto de Ciencias Basicas da Saude, UFRGS, Porto Alegre, Brazil. FAU - Antunes, Luciana C AU - Antunes LC AD - Centro de Ciencias da Saude - Departamento de Nutricao da Universidade Federal De Santa Catarina, Florianopolis, Brazil. LA - eng PT - Journal Article DEP - 20190131 PL - New Zealand TA - J Pain Res JT - Journal of pain research JID - 101540514 PMC - PMC6365222 OTO - NOTNLM OT - 6 sulfatoxymelatonin (aMT6s) OT - depression OT - fibromyalgia OT - melatonin OT - pain COIS- Disclosure The authors report no conflicts of interest in this work. EDAT- 2019/02/23 06:00 MHDA- 2019/02/23 06:01 PMCR- 2019/01/31 CRDT- 2019/02/22 06:00 PHST- 2019/02/22 06:00 [entrez] PHST- 2019/02/23 06:00 [pubmed] PHST- 2019/02/23 06:01 [medline] PHST- 2019/01/31 00:00 [pmc-release] AID - jpr-12-545 [pii] AID - 10.2147/JPR.S176857 [doi] PST - epublish SO - J Pain Res. 2019 Jan 31;12:545-556. doi: 10.2147/JPR.S176857. eCollection 2019.