Personalizing Repetitive Transcranial Magnetic Stimulation Parameters for Depression Treatment Using Multimodal Neuroimaging

Deborah C.W. Klooster (Corresponding author), Michael A. Ferguson, Paul A.J.M. Boon, Chris Baeken

Onderzoeksoutput: Bijdrage aan tijdschriftArtikel recenserenpeer review

29 Citaten (Scopus)
103 Downloads (Pure)

Samenvatting

Repetitive transcranial magnetic stimulation (rTMS) is a tool that can be used to administer treatment for neuropsychiatric disorders such as major depressive disorder, although the clinical efficacy is still rather modest. Overly general stimulation protocols that consider neither patient-specific depression symptomology nor individualized brain characteristics, such as anatomy or structural and functional connections, may be the cause of the high inter- and intraindividual variability in rTMS clinical responses. Multimodal neuroimaging can provide the necessary insights into individual brain characteristics and can therefore be used to personalize rTMS parameters. Optimal coil positioning should include a three-step process: 1) identify the optimal (indirect) target area based on the exact symptom pattern of the patient; 2) derive the cortical (direct) target location based on functional and/or structural connectomes derived from functional and diffusion magnetic resonance imaging data; and 3) determine the ideal coil position by computational modeling, such that the electric field distribution overlaps with the cortical target. These TMS-induced electric field simulations, derived from anatomical and diffusion magnetic resonance imaging data, can be further applied to compute optimal stimulation intensities. In addition to magnetic resonance imaging, electroencephalography can provide complementary information regarding the ongoing brain oscillations. This information can be used to determine the optimal timing and frequency of the stimuli. The heightened benefits of these personalized stimulation approaches are logically reasoned, but speculative. Randomized clinical trials will be required to compare clinical responses from standard rTMS protocols to personalized protocols. Ultimately, an optimized clinical response may result from precision protocols derived from combinations of personalized stimulation parameters.

Originele taal-2Engels
Pagina's (van-tot)536-545
Aantal pagina's10
TijdschriftBiological Psychiatry. Cognitive Neuroscience and Neuroimaging
Volume7
Nummer van het tijdschrift6
Vroegere onlinedatum2022
DOI's
StatusGepubliceerd - jun. 2022

Bibliografische nota

Funding Information:
This study was supported by a grants from Fonds Wetenschappelijk Onderzoek (FWO), Vlaanderen, Belgium (Grant No. 1259121N [to DCWK]); funds from FWO Vlaanderen , BOF UGent , Geneeskundige Stichting Koningin Elisabeth (GSKE-FMRE), and Health Holland (PerStim grant [to PAJMB]); by grants from FWO, including the grant for Applied Biomedical Research PrevenD 2.0 (to CB); GSKE-FMRE; and a Strategic Research Program (SRP 57) from the Free University Brussels.

Publisher Copyright:
© 2022 Society of Biological Psychiatry

Financiering

This study was supported by a grants from Fonds Wetenschappelijk Onderzoek (FWO), Vlaanderen, Belgium (Grant No. 1259121N [to DCWK]); funds from FWO Vlaanderen , BOF UGent , Geneeskundige Stichting Koningin Elisabeth (GSKE-FMRE), and Health Holland (PerStim grant [to PAJMB]); by grants from FWO, including the grant for Applied Biomedical Research PrevenD 2.0 (to CB); GSKE-FMRE; and a Strategic Research Program (SRP 57) from the Free University Brussels.

FinanciersFinanciernummer
GSKE-FMRESRP 57
Health~Holland
Health~Holland
Fonds Wetenschappelijk Onderzoek1259121N
Vrije Universiteit Brussel

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