## Abstract ## Background This study examined psychosocial and clinical predictors of depression non‐remittance among a sample of initially clinically depressed elders. ## Methods Incident and prevalent unipolar depression cases (__n__ = 166) were enrolled into the MHCRC for the Study of Depress
6-Sulfatoxymelatonin as a predictor of clinical outcome in depressive patients
✍ Scribed by Maria Paz Loayza Hidalgo; Wolnei Caumo; Giovana Dantas; Daiane Gil Franco; Iraci Lucena da Silva Torres; Julio Pezzi; Elaine Elisabetsky; Bernardo Carraro Detanico; Ângelo Piato; Regina P. Markus
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 154 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0885-6222
- DOI
- 10.1002/hup.1204
No coin nor oath required. For personal study only.
✦ Synopsis
Objectives
This study established the value of the 6‐sulfatoxymelatonin (aMT6s) urine concentration as a predictor of the therapeutic response to noradrenaline reuptake inhibitors in depressive patients.
Methods
Twenty‐two women aged 18–60 years were selected. Depressive symptoms were assessed by using the Hamilton Depression Scale. Urine samples were collected at 0600–1200 h, 1200–1800 h, 1800–2400 h, and 2400–0600 h intervals, 1 day before and 1 day after starting on the nortriptyline treatment. Urine aMT6s concentration was analyzed by a one‐way analysis of variance/Bonferroni test. Spearman's rank correlation coefficient was used to analyze the correlation between depressive symptoms after 2 weeks of antidepressant treatment and the increase in aMT6s urine concentration.
Results
Higher and lower size effect groups were compared by independent Student's t‐tests. At baseline, the 2400‐ to 0600‐h interval differed from all other intervals presenting a significantly higher aMT6s urine concentration. A significant difference in aMT6s urine concentrations was found 1 day after treatment in all four intervals. Higher size effect group had lower levels of depressive symptoms 2 weeks after the treatment. A positive correlation between depressive symptoms and the delta of aMT6s in the 2400–06 00h interval was observed.
Conclusion
Our results reinforce the hypothesis that aMT6s excretion is a predictor of clinical outcome in depression, especially in regard to noradrenaline reuptake inhibitors. Copyright © 2011 John Wiley & Sons, Ltd.
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