Abstract
Repetitive transcranial magnetic stimulation (rTMS) is a promising alternative therapy for treatment-resistant depression, although its limited remission rate indicates room for improvement. As depression is a phenomenological construction, the biological heterogeneity within this syndrome needs to be considered to improve the existing therapies. Whole-brain modeling provides an integrative multi-modal framework for capturing disease heterogeneity in a holistic manner. Computational modelling combined with probabilistic nonparametric fitting was applied to the resting-state fMRI data from 42 patients (21 women), to parametrize baseline brain dynamics in depression. All patients were randomly assigned to two treatment groups, namely active (i.e., rTMS, n = 22) or sham (n = 20). The active treatment group received rTMS treatment with an accelerated intermittent theta burst protocol over the dorsomedial prefrontal cortex. The sham treatment group underwent the identical procedure but with the magnetically shielded side of the coil. We stratified the depression sample into distinct covert subtypes based on their baseline attractor dynamics captured by different model parameters. Notably, the two detected depression subtypes exhibited different phenotypic behaviors at baseline. Our stratification could predict the diverse response to the active treatment that could not be explained by the sham treatment. Critically, we further found that one group exhibited more distinct improvement in certain affective and negative symptoms. The subgroup of patients with higher responsiveness to treatment exhibited blunted frequency dynamics for intrinsic activity at baseline, as indexed by lower global metastability and synchrony. Our findings suggested that whole-brain modeling of intrinsic dynamics may constitute a determinant for stratifying patients into treatment groups and bringing us closer towards precision medicine.
Original language | English |
---|---|
Article number | e1010958 |
Pages (from-to) | 1-21 |
Number of pages | 21 |
Journal | PLoS Computational Biology |
Volume | 19 |
Issue number | 3 |
Early online date | 6 Mar 2023 |
DOIs | |
Publication status | Published - Mar 2023 |
Bibliographical note
Publisher Copyright:Copyright: © 2023 Kaboodvand et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding
N.K, B.I. and R.B. were financially supported by the Swedish Research Council (https://www.vr.se/), with the grant numbers: 2020-00724, 2021-06645 and 2016-02362. Data preprocessing was enabled by resources provided by the Swedish National Infrastructure for Computing (SNIC) at Uppsala Multidisciplinary Center for Advanced Computational Science (UPPMAX) partially funded by the Swedish Research Council through grant agreement no. 2018-05973. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. We appreciate the Human Connectome Project for providing the open access data used in this study.
Funders | Funder number |
---|---|
Vetenskapsrådet | 2021-06645, 2018-05973, 2016-02362, 2020-00724 |