Evidence map›Paper›PMID 42014856›Full record

Trial reportNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2026

Target engagement in a head-to-head clinical trial of dysphoric versus anxiosomatic transcranial magnetic stimulation targets.

Samantha Baldi, Christopher Lin, Jing Li, Summer Frandsen, Emma Jones, Stephan Palm, Abigail S Greene, Joseph J Taylor, Michael D Fox, Shan H Siddiqi

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2026. 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

10 authors.

Samantha BaldiCenter for Brain Circuit Therapeutics, Brigham and Women's Hospital, Boston, MA, USA. sbaldi@bwh.harvard.edu.ORCID http://orcid.org/0000-0002-3384-247X
Christopher LinCenter for Brain Circuit Therapeutics, Brigham and Women's Hospital, Boston, MA, USA.
Jing LiCenter for Brain Circuit Therapeutics, Brigham and Women's Hospital, Boston, MA, USA.
Summer FrandsenCenter for Brain Circuit Therapeutics, Brigham and Women's Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0003-0306-3018
Emma JonesCenter for Brain Circuit Therapeutics, Brigham and Women's Hospital, Boston, MA, USA.
Stephan PalmCenter for Brain Circuit Therapeutics, Brigham and Women's Hospital, Boston, MA, USA.ORCID http://orcid.org/0009-0000-8345-5470
Abigail S GreeneCenter for Brain Circuit Therapeutics, Brigham and Women's Hospital, Boston, MA, USA.
Joseph J TaylorCenter for Brain Circuit Therapeutics, Brigham and Women's Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0002-9185-0427
Michael D FoxCenter for Brain Circuit Therapeutics, Brigham and Women's Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0001-8848-6399
Shan H SiddiqiCenter for Brain Circuit Therapeutics, Brigham and Women's Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0002-0967-9289

Funding

Personalized circuit-based neuromodulation targets for depressionK23MH121657 · NIMH · BRIGHAM AND WOMEN'S HOSPITAL · PI SIDDIQI, SHAN · 2020 to 2024
$978k
Targeted modulation of symptom-specific brain circuits with transcranial magnetic stimulationR21MH126271 · NIMH · BRIGHAM AND WOMEN'S HOSPITAL · PI FOX, MICHAEL D · 2021 to 2022
$492k
U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) K23MH121657U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) R21MH126271
6 · The paper itself

Abstract

Resting-state functional connectivity is increasingly used to measure neural engagement following transcranial magnetic stimulation (TMS), but whether connectivity changes are specific to the stimulation target and clinically meaningful remains unclear. In a head-to-head trial, thirty-six patients with depression and anxiety were randomized to 30 TMS sessions at one of two circuit-based targets: a dorsolateral prefrontal target hypothesized to improve "dysphoric" symptoms, and a dorsomedial prefrontal target hypothesized to improve "anxiosomatic" symptoms. We tested whether: (1) TMS selectively engaged the targeted circuit; (2) baseline TMS site connectivity to the targeted circuit predicted circuit engagement; (3) either metric correlated with improvement on the Beck Depression and Beck Anxiety Inventories. Twenty-nine participants with pre- and post-treatment MRI were included. Target engagement was defined as change in average connectivity within each circuit and compared between target groups; associations were measured using Spearman's partial correlation, controlling for relevant covariates. While connectivity decreased within both circuits, the effects were not clearly target-specific and did not predict symptom improvement. In contrast, stronger baseline TMS site connectivity to the targeted circuit predicted greater connectivity change (r = -0.61, p < 0.001) and anxiety improvement (r

Indexed as

AnxietyPrefrontal CortexTranscranial Magnetic StimulationAdultFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedTreatment Outcome

Identifiers

PMID42014856
PMCPMC13486470

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.