Transcranial Magnetic Stimulation and Transcranial Direct Current Stimulation Across Mental Disorders: A Systematic Review and Dose-Response Meta-Analysis.


Journal

JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235

Informations de publication

Date de publication:
01 May 2024
Historique:
medline: 22 5 2024
pubmed: 22 5 2024
entrez: 22 5 2024
Statut: epublish

Résumé

Noninvasive brain stimulation (NIBS) interventions have been shown to be efficacious in several mental disorders, but the optimal dose stimulation parameters for each disorder are unknown. To define NIBS dose stimulation parameters associated with the greatest efficacy in symptom improvement across mental disorders. Studies were drawn from an updated (to April 30, 2023) previous systematic review based on a search of PubMed, OVID, and Web of Knowledge. Randomized clinical trials were selected that tested transcranial magnetic stimulation (TMS) or transcranial direct current stimulation (tDCS) for any mental disorder in adults aged 18 years or older. Two authors independently extracted the data. A 1-stage dose-response meta-analysis using a random-effects model was performed. Sensitivity analyses were conducted to test robustness of the findings. This study followed the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) reporting guideline. The main outcome was the near-maximal effective doses of total pulses received for TMS and total current dose in coulombs for tDCS. A total of 110 studies with 4820 participants (2659 men [61.4%]; mean [SD] age, 42.3 [8.8] years) were included. The following significant dose-response associations emerged with bell-shaped curves: (1) in schizophrenia, high-frequency (HF) TMS on the left dorsolateral prefrontal cortex (LDLPFC) for negative symptoms (χ2 = 9.35; df = 2; P = .009) and TMS on the left temporoparietal junction for resistant hallucinations (χ2 = 36.52; df = 2; P < .001); (2) in depression, HF-DLPFC TMS (χ2 = 14.49; df = 2; P < .001); (3) in treatment-resistant depression, LDLPFC tDCS (χ2 = 14.56; df = 2; P < .001); and (4) in substance use disorder, LDLPFC tDCS (χ2 = 33.63; df = 2; P < .001). The following significant dose-response associations emerged with plateaued or ascending curves: (1) in depression, low-frequency (LF) TMS on the right DLPFC (RDLPFC) with ascending curve (χ2 = 25.67; df = 2; P = .001); (2) for treatment-resistant depression, LF TMS on the bilateral DLPFC with ascending curve (χ2 = 5.86; df = 2; P = .004); (3) in obsessive-compulsive disorder, LF-RDLPFC TMS with ascending curve (χ2 = 20.65; df = 2; P < .001) and LF TMS on the orbitofrontal cortex with a plateaued curve (χ2 = 15.19; df = 2; P < .001); and (4) in posttraumatic stress disorder, LF-RDLPFC TMS with ascending curve (χ2 = 54.15; df = 2; P < .001). Sensitivity analyses confirmed the main findings. The study findings suggest that NIBS yields specific outcomes based on dose parameters across various mental disorders and brain regions. Clinicians should consider these dose parameters when prescribing NIBS. Additional research is needed to prospectively validate the findings in randomized, sham-controlled trials and explore how other parameters contribute to the observed dose-response association.

Identifiants

pubmed: 38776083
pii: 2818884
doi: 10.1001/jamanetworkopen.2024.12616
doi:

Types de publication

Journal Article Systematic Review Meta-Analysis

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2412616

Auteurs

Michel Sabé (M)

Centre for Innovation in Mental Health, School of Psychology, University of Southampton, United Kingdom.
Clinic of Psychiatry, Social Psychiatry and Psychotherapy, Hannover Medical School, Hanover, Germany.

Joshua Hyde (J)

Centre for Innovation in Mental Health, School of Psychology, University of Southampton, United Kingdom.

Catharina Cramer (C)

Clinic of Psychiatry, Social Psychiatry and Psychotherapy, Hannover Medical School, Hanover, Germany.

Antonia Eberhard (A)

Clinic of Psychiatry, Social Psychiatry and Psychotherapy, Hannover Medical School, Hanover, Germany.

Alessio Crippa (A)

Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.

André Russowsky Brunoni (AR)

Departamento e Instituto de Psiquiatria da Faculdade de Medicina da Universidade de São Paulo, Universidade de São Paulo, Brazil.

André Aleman (A)

Department of Biomedical Sciences of Cells and Systems, Section Cognitive Neurosciences, University Medical Center Groningen, University of Groningen, the Netherlands.

Stefan Kaiser (S)

Division of Adult Psychiatry, Department of Psychiatry, University Hospitals of Geneva, Thonex, Switzerland.

David S Baldwin (DS)

Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, United Kingdom.
University Department of Psychiatry and Mental Health, University of Cape Town, South Africa.

Matthew Garner (M)

The Ottawa Hospital and Ottawa Hospital Research Institute, Ontario, Canada.

Othman Sentissi (O)

Division of Adult Psychiatry, Department of Psychiatry, University Hospitals of Geneva, Thonex, Switzerland.
Faculty of Medicine, University of Geneva, Geneva, Switzerland.

Jess G Fiedorowicz (JG)

The Ottawa Hospital and Ottawa Hospital Research Institute, Ontario, Canada.
Department of Psychiatry, University of Ottawa, Ontario, Canada.

Valerie Brandt (V)

Centre for Innovation in Mental Health, School of Psychology, University of Southampton, United Kingdom.
Clinic of Psychiatry, Social Psychiatry and Psychotherapy, Hannover Medical School, Hanover, Germany.

Samuele Cortese (S)

Centre for Innovation in Mental Health, School of Psychology, University of Southampton, United Kingdom.
Clinical and Experimental Sciences (CNS and Psychiatry), Faculty of Medicine, University of Southampton, United Kingdom.
Hassenfeld Children's Hospital at New York University Langone, New York University Child Study Center, New York, New York.
Division of Psychiatry and Applied Psychology, School of Medicine, University of Nottingham, United Kingdom.
DiMePRe-J-Department of Precision and Regenerative Medicine-Jonic Area, University of Bari "Aldo Moro", Bari, Italy.

Marco Solmi (M)

The Ottawa Hospital and Ottawa Hospital Research Institute, Ontario, Canada.
School of Epidemiology and Public Health, Faculty of Medicine, University of Ottawa, Ontario, Canada.
Department of Child and Adolescent Psychiatry, Charité Universitätsmedizin, Berlin, Germany.
Department of Mental Health, The Ottawa Hospital, Ontario, Canada.
SIENCES Laboratory, Department of Psychiatry, University of Ottawa, Ontario, Canada.

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