Neurostimulation Methods in the Treatment of Depression: A Comparison of rTMS, tDCS, and Venlafaxine Using a Pooled Analysis of Two Studies.

MDD efficacy major depressive disorder rTMS repetitive transcranial magnetic stimulation tDCS transcranial direct-current stimulation treatment venlafaxine

Journal

Neuropsychiatric disease and treatment
ISSN: 1176-6328
Titre abrégé: Neuropsychiatr Dis Treat
Pays: New Zealand
ID NLM: 101240304

Informations de publication

Date de publication:
2021
Historique:
received: 22 01 2021
accepted: 13 04 2021
entrez: 7 6 2021
pubmed: 8 6 2021
medline: 8 6 2021
Statut: epublish

Résumé

There are no head-to-head studies comparing the antidepressant effect of transcranial direct current stimulation (tDCS) with repetitive transcranial magnetic stimulation (rTMS). This pooled analysis compared indirectly the antidepressant efficacy and acceptability of rTMS, tDCS, and the antidepressant venlafaxine (VNF) extended-release. The analysis (n=117, both patients with treatment-resistant depression (TRD) and non-TRD were included) examined pooled data from two 4-week, single-centered, two-armed, double-blind, randomized studies (EUDRACT n. 2005-000826-22 and EUDRACT n. 2015-001639-19). The antidepressant efficacy of right-sided low-frequency rTMS (n=29) vs VNF (n=31) and left-sided anodal tDCS (n=29) vs VNF (n=28) was evaluated. The primary outcome was a change in the Montgomery-Åsberg Depression Rating Scale (MADRS) score from baseline to the treatment endpoint at week 4. The response was defined as a ≥50% reduction in the MADRS score and remission as the MADRS score ≤10 points, both were calculated for the primary treatment endpoint at week 4. Mean change in total MADRS scores from baseline to week 4 was 7.0 (95% CI, 4.8-9.1) points in the rTMS group, 7.6 (95% CI, 5.5-9.8) in the tDCS group, and 8.9 (95% CI, 7.4-10.4) among patients in the VNF group, a non-significant difference (F(2111)=0.62, p=0.54). Similarly, neither the response rates nor remission rates for rTMS (response 31%; remission 17%), tDCS (24%, 17%), or VNF (41%; 27%) significantly differed among treatment groups ( Our current analysis found a comparable efficacy and acceptability in all three treatment modalities (rTMS, tDCS, and VNF) and clinical relevance for the acute treatment of major depressive disorder.

Sections du résumé

BACKGROUND BACKGROUND
There are no head-to-head studies comparing the antidepressant effect of transcranial direct current stimulation (tDCS) with repetitive transcranial magnetic stimulation (rTMS). This pooled analysis compared indirectly the antidepressant efficacy and acceptability of rTMS, tDCS, and the antidepressant venlafaxine (VNF) extended-release.
METHODS METHODS
The analysis (n=117, both patients with treatment-resistant depression (TRD) and non-TRD were included) examined pooled data from two 4-week, single-centered, two-armed, double-blind, randomized studies (EUDRACT n. 2005-000826-22 and EUDRACT n. 2015-001639-19). The antidepressant efficacy of right-sided low-frequency rTMS (n=29) vs VNF (n=31) and left-sided anodal tDCS (n=29) vs VNF (n=28) was evaluated. The primary outcome was a change in the Montgomery-Åsberg Depression Rating Scale (MADRS) score from baseline to the treatment endpoint at week 4. The response was defined as a ≥50% reduction in the MADRS score and remission as the MADRS score ≤10 points, both were calculated for the primary treatment endpoint at week 4.
RESULTS RESULTS
Mean change in total MADRS scores from baseline to week 4 was 7.0 (95% CI, 4.8-9.1) points in the rTMS group, 7.6 (95% CI, 5.5-9.8) in the tDCS group, and 8.9 (95% CI, 7.4-10.4) among patients in the VNF group, a non-significant difference (F(2111)=0.62, p=0.54). Similarly, neither the response rates nor remission rates for rTMS (response 31%; remission 17%), tDCS (24%, 17%), or VNF (41%; 27%) significantly differed among treatment groups (
CONCLUSION CONCLUSIONS
Our current analysis found a comparable efficacy and acceptability in all three treatment modalities (rTMS, tDCS, and VNF) and clinical relevance for the acute treatment of major depressive disorder.

Identifiants

pubmed: 34093015
doi: 10.2147/NDT.S303226
pii: 303226
pmc: PMC8169053
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1713-1722

Informations de copyright

© 2021 Hejzlar et al.

Déclaration de conflit d'intérêts

Dr Tomas Novak reports personal fees from Krka ČR sro, outside the submitted work. The authors report no other conflicts of interest in this work.

Références

Brain Stimul. 2018 Jan - Feb;11(1):125-133
pubmed: 29111077
Can J Psychiatry. 2016 Sep;61(9):540-60
pubmed: 27486148
Br J Psychiatry. 2016 Jun;208(6):522-31
pubmed: 27056623
Psychol Rep. 1974 Jun;34(3):1184-6
pubmed: 4424377
Depress Anxiety. 2020 Jul;37(7):594-608
pubmed: 32101631
N Engl J Med. 2006 Mar 23;354(12):1231-42
pubmed: 16554525
J Clin Psychiatry. 2010 Mar;71(3):270-9
pubmed: 20122371
Eur Psychiatry. 2008 Jan;23(1):74-6
pubmed: 18023968
BMJ. 2019 Mar 27;364:l1079
pubmed: 30917990
Brain Stimul. 2016 May-Jun;9(3):336-346
pubmed: 27090022
JAMA Psychiatry. 2013 Apr;70(4):383-91
pubmed: 23389323
Neuropsychopharmacology. 2021 Mar;46(4):774-782
pubmed: 33349674
Psychol Med. 2014 Jan;44(2):225-39
pubmed: 23507264
Arch Gen Psychiatry. 2012 Jun;69(6):572-9
pubmed: 22393205
Brain Stimul. 2014 Nov-Dec;7(6):855-63
pubmed: 25192980
Prog Neuropsychopharmacol Biol Psychiatry. 2020 Apr 20;99:109836
pubmed: 31837388
J Affect Disord. 2009 Nov;118(1-3):94-100
pubmed: 19249105
J Clin Psychiatry. 1998;59 Suppl 20:22-33;quiz 34-57
pubmed: 9881538
Lancet Psychiatry. 2016 Nov;3(11):1059-1066
pubmed: 27726982
J Clin Psychiatry. 2014 May;75(5):477-89; quiz 489
pubmed: 24922485
Neuropsychiatr Dis Treat. 2019 Oct 23;15:3003-3014
pubmed: 31695391
Psychiatry Res. 2013 Dec 30;210(3):1260-4
pubmed: 24113125
Int J Neuropsychopharmacol. 2014 Sep;17(9):1443-52
pubmed: 24713139
Curr Opin Psychiatry. 2019 Sep;32(5):409-415
pubmed: 31145145
Front Psychiatry. 2018 Sep 07;9:413
pubmed: 30245641
Clin Neurophysiol. 2020 Feb;131(2):474-528
pubmed: 31901449
N Engl J Med. 2017 Jun 29;376(26):2523-2533
pubmed: 28657871
Neurosci Biobehav Rev. 2015 Oct;57:46-62
pubmed: 26232699
Br J Psychiatry. 1979 Apr;134:382-9
pubmed: 444788
Lancet. 2018 Apr 7;391(10128):1357-1366
pubmed: 29477251
Prog Neuropsychopharmacol Biol Psychiatry. 2018 Feb 2;81:105-113
pubmed: 29111404
J Affect Disord. 2019 Jun 1;252:475-483
pubmed: 31005790
Brain Stimul. 2016 Jul-Aug;9(4):501-17
pubmed: 27160468
J Prim Health Care. 2016 Dec;8(4):325-334
pubmed: 29530157
J Clin Psychiatry. 2018 Jan/Feb;79(1):
pubmed: 28541649
Psychiatry Res. 2013 Nov 30;210(1):127-33
pubmed: 23742865
Br J Psychiatry. 2019 Aug;215(2):445-446
pubmed: 31014413
Lancet. 2015 Nov 28;386(10009):2145-91
pubmed: 26321261
Can J Psychiatry. 2016 Sep;61(9):561-75
pubmed: 27486154
Neurosci Biobehav Rev. 2018 Sep;92:291-303
pubmed: 29763711
Neuropsychopharmacology. 2013 Mar;38(4):543-51
pubmed: 23249815
J Clin Psychiatry. 2018 May/Jun;79(3):
pubmed: 29659207
J Psychiatr Res. 2013 Jan;47(1):1-7
pubmed: 23084964

Auteurs

Martin Hejzlar (M)

NIMH Clinical Center, National Institute of Mental Health Czech Republic, Klecany, Czech Republic.
Department of Psychiatry and Medical Psychology, Third Medical Faculty, Charles University, Prague, Czech Republic.

Tomas Novak (T)

NIMH Clinical Center, National Institute of Mental Health Czech Republic, Klecany, Czech Republic.
Department of Psychiatry and Medical Psychology, Third Medical Faculty, Charles University, Prague, Czech Republic.

Martin Bares (M)

NIMH Clinical Center, National Institute of Mental Health Czech Republic, Klecany, Czech Republic.
Department of Psychiatry and Medical Psychology, Third Medical Faculty, Charles University, Prague, Czech Republic.

Classifications MeSH