Evidence map›Paper›PMID 40475538›Full record

ArticlebioRxiv : the preprint server for biology2025

Network-based Near-Scalp Personalized Brain Stimulation Targets.

Ru Kong, Aihuiping Xue, Leon Qi Rong Ooi, Christopher Asplund, Xiao Wei Tan, Shih Ee Goh, Jonathan Jie Lee, Jovi Zheng Jie Koh, Rachel Si Yun Tan, Hasvinjit Kaur Gulwant Singh and 6 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Ru KongCentre for Sleep and Cognition & Centre for Translational MR Research, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.ORCID 0000-0001-7842-0329
Aihuiping XueCentre for Sleep and Cognition & Centre for Translational MR Research, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.ORCID 0009-0008-7907-8594
Leon Qi Rong OoiCentre for Sleep and Cognition & Centre for Translational MR Research, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.ORCID 0000-0002-3546-4580
Christopher AsplundCentre for Sleep and Cognition & Centre for Translational MR Research, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.ORCID 0000-0001-5708-6966
Xiao Wei TanInstitute of Mental Health, Singapore.
Shih Ee GohInstitute of Mental Health, Singapore.
Jonathan Jie LeeInstitute of Mental Health, Singapore.
Jovi Zheng Jie KohInstitute of Mental Health, Singapore.
Rachel Si Yun TanInstitute of Mental Health, Singapore.
Hasvinjit Kaur Gulwant SinghInstitute of Mental Health, Singapore.
Trevor Wei Kiat TanCentre for Sleep and Cognition & Centre for Translational MR Research, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Ryan D WeblerDepartment of Psychiatry, Mass General Brigham, Harvard Medical School, Boston, USA.ORCID 0000-0002-3861-3393
Michael D FoxDepartment of Psychiatry, Mass General Brigham, Harvard Medical School, Boston, USA.ORCID 0000-0001-8848-6399
Shan SiddiqiDepartment of Psychiatry, Mass General Brigham, Harvard Medical School, Boston, USA.ORCID 0000-0002-0967-9289
Phern-Chern TorInstitute of Mental Health, Singapore.ORCID 0000-0001-7972-3030
B T Thomas YeoCentre for Sleep and Cognition & Centre for Translational MR Research, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.ORCID 0000-0002-0119-3276

Funding

A mega-analysis framework for delineating autism neurosubtypesR01MH133334 · NIMH · CHILD MIND INSTITUTE, INC. · PI Adriana Di Martino · 2023 to 2026
$2.9M
NIMH NIH HHS R01 MH133334
6 · The paper itself

Abstract

Background: Functional connectivity (FC) is often used to identify personalized targets for transcranial magnetic stimulation (TMS). However, existing methods often overlook individual differences in whole-cortex network organization. Furthermore, in some personalized TMS protocols, a lower stimulation intensity is used for targets closer to the scalp. Therefore, near-scalp targets might improve patient tolerance. Objective: We develop an algorithm to simultaneously optimize FC and scalp proximity for personalized target localization. Methods: We use the multi-session hierarchical Bayesian model (MS-HBM) to estimate high-quality individual-specific cortical networks. A tree-based algorithm is then used to select the optimal target location. By essentially having no parameter to tune, our framework might improve generalizability across populations. We compare our approach to existing "cluster" and "cone" algorithms in terms of scalp proximity, test-retest reliability, and FC to brain regions implicated in depression. Results: In two test-retest datasets of healthy individuals from the United States and Singapore, tree-based MS-HBM reliably identifies personalized TMS targets for depression in close proximity to the scalp. These targets compare favorably with cone and cluster targets in terms of reliability, scalp proximity, and FC to the subgenual anterior cingulate cortex in new out-of-sample MRI sessions from the same individuals. Compared with the cluster algorithm, tree-based MS-HBM targets hypothetically reduce stimulation intensity by 12% using a linear intensity adjustment protocol. To demonstrate versatility, we apply the same algorithm, without having to tune any parameter, to identify personalized TMS targets for anxiety. Conclusion: The tree-based MS-HBM algorithm provides a robust, generalizable framework to estimate near-scalp personalized targets across different populations.

Identifiers

PMID40475538
PMCPMC12139747

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.