S-Adenosylmethionine (SAMe) monotherapy for depression: an 8-week double-blind, randomised, controlled trial.
Antidepressant
Clinical trial
Depression
Nutraceutical
S-Adenosylmethionine
Journal
Psychopharmacology
ISSN: 1432-2072
Titre abrégé: Psychopharmacology (Berl)
Pays: Germany
ID NLM: 7608025
Informations de publication
Date de publication:
Jan 2020
Jan 2020
Historique:
received:
27
05
2019
accepted:
02
09
2019
pubmed:
13
11
2019
medline:
11
4
2020
entrez:
13
11
2019
Statut:
ppublish
Résumé
Dysregulation of the one carbon cycle is documented in depression. Thereby, S-adenosylmethionine (SAMe), a one-carbon cycle nutraceutical compound with a favourable side effect profile, has a theoretical rationale for efficacy. However, further controlled studies are required to confirm SAMe's efficacy. To test the efficacy of SAMe versus placebo in unmedicated DSM-5 diagnosed (major depressive disorder) (MDD) patients with mild-to-moderate levels of depressive symptoms. We conducted an 8-week, double-blind, randomised controlled trial testing 800 mg/day of SAMe monotherapy versus placebo in 49 patients with MDD (Montgomery-Åsberg Depression Rating Scale [MADRS] score 14-25) who were not currently taking antidepressants. One-carbon cycle biomarkers, brain-derived neurotropic factor (BDNF), and relevant single nucleotide polymorphisms (SNPs) were analysed as potential treatment moderators. A clinically relevant differential reduction from baseline to week 8 of 3.76 points occurred on the primary outcome (MADRS) in favour of SAMe. This however was not significant (p = 0.13) on an adjusted linear mixed model, notwithstanding a medium to large effect size of 0.72. A high placebo response rate of 53% occurred (> 50% reduction on MADRS). Exploratory analyses showed that SAMe was however effective in reducing depression amongst participants with milder depression severity (MADRS ≤ 22, p = 0.045). Response was not moderated by BDNF, SNPs, or one-carbon cycle biomarkers, although increased folate concentrations were correlated with improved symptoms in the SAMe group (r = - 0.57, p = 0.026). The treatment was safe and well tolerated. Although a differential reduction in depression symptoms between groups was observed in favour of SAMe, the results of this pilot study were not statistically significant. ANZCTR-Australian New Zealand Clinical Trials Registry; No.: ACTRN12613001299796; URL: https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=364900.
Identifiants
pubmed: 31712971
doi: 10.1007/s00213-019-05358-1
pii: 10.1007/s00213-019-05358-1
doi:
Substances chimiques
Antidepressive Agents
0
S-Adenosylmethionine
7LP2MPO46S
Types de publication
Journal Article
Multicenter Study
Randomized Controlled Trial
Langues
eng
Sous-ensembles de citation
IM
Pagination
209-218Subventions
Organisme : National Health and Medical Research Council
ID : APP1048222
Références
Am J Psychiatry. 1991 Jun;148(6):705-13
pubmed: 2035713
Psychopharmacol Bull. 1986;22(2):343-81
pubmed: 3774930
Am J Psychiatry. 2016 Jun 1;173(6):575-87
pubmed: 27113121
BMC Med. 2013 May 14;11:126
pubmed: 23672542
Molecules. 2017 Aug 03;22(8):null
pubmed: 28771213
Psychopharmacology (Berl). 1980;71(2):173-9
pubmed: 6777817
J Affect Disord. 2014 Aug;164:76-81
pubmed: 24856557
Eur Neuropsychopharmacol. 2011 Dec;21(12):841-60
pubmed: 21601431
Eur Neuropsychopharmacol. 2018 Oct;28(10):1126-1136
pubmed: 30115553
Curr Med Res Opin. 2008 May;24(5):1329-35
pubmed: 18377706
J Clin Psychopharmacol. 2002 Feb;22(1):40-5
pubmed: 11799341
F1000Res. 2017 May 3;6:
pubmed: 28529691
Arch Gen Psychiatry. 1961 Jun;4:561-71
pubmed: 13688369
Harv Rev Psychiatry. 2013 Sep-Oct;21(5):269-74
pubmed: 24651559
Eur Neuropsychopharmacol. 2005 Oct;15(5):533-43
pubmed: 16046102
Med Care. 1996 Mar;34(3):220-33
pubmed: 8628042
QJM. 2003 Sep;96(9):635-42
pubmed: 12925718
J Clin Psychiatry. 2017 Jun;78(6):e656-e667
pubmed: 28682528
J Clin Psychiatry. 1998;59 Suppl 20:22-33;quiz 34-57
pubmed: 9881538
Cochrane Database Syst Rev. 2016 Oct 10;10:CD011286
pubmed: 27727432
J Clin Psychiatry. 2014 Apr;75(4):370-6
pubmed: 24500245
Br J Psychiatry. 1979 Apr;134:382-9
pubmed: 444788
Pharmacopsychiatry. 2015 Jul;48(4-5):141-4
pubmed: 26011569
BMC Psychiatry. 2017 Feb 8;17(1):58
pubmed: 28178949