Evidence map›Paper›PMID 41890433›Full record

ArticleFrontiers in psychiatry2026

Equivalent efficacy of left versus right hemisphere accelerated intermittent theta burst stimulation for major depressive disorder.

Davin K Quinn, Joel Upston, Thomas R Jones, Tessa A Olmstead, Justine Yang, Samuel Reyes, Samuel MacDonald, Adam Littleton, Alexander Win, Dorothy H Bowers-Wu and 19 more

Abstract read
In one paragraph

Article in Frontiers in psychiatry, 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

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

29 authors.

Davin K QuinnDepartment of Psychiatry and Behavioral Sciences, University of New Mexico School of Medicine, Albuquerque, NM, United States.
Joel UpstonDepartment of Psychiatry and Behavioral Sciences, University of New Mexico School of Medicine, Albuquerque, NM, United States.
Thomas R JonesDepartment of Psychiatry and Behavioral Sciences, University of New Mexico School of Medicine, Albuquerque, NM, United States.
Tessa A OlmsteadDepartment of Psychiatry and Behavioral Sciences, University of New Mexico School of Medicine, Albuquerque, NM, United States.
Justine YangDepartment of Psychiatry and Behavioral Sciences, University of New Mexico School of Medicine, Albuquerque, NM, United States.
Samuel ReyesDepartment of Psychiatry and Behavioral Sciences, University of New Mexico School of Medicine, Albuquerque, NM, United States.
Samuel MacDonaldDepartment of Psychiatry and Behavioral Sciences, University of New Mexico School of Medicine, Albuquerque, NM, United States.
Adam LittletonDepartment of Neurosciences, University of New Mexico, Albuquerque, NM, United States.
Alexander WinDepartment of Psychiatry and Behavioral Sciences, University of New Mexico School of Medicine, Albuquerque, NM, United States.
Dorothy H Bowers-WuDepartment of Psychiatry and Behavioral Sciences, University of New Mexico School of Medicine, Albuquerque, NM, United States.
Jordan G LeeUniversity of New Mexico School of Medicine, Albuquerque, NM, United States.
Pearl HuynhUniversity of New Mexico School of Medicine, Albuquerque, NM, United States.
Robert T DeBurloDepartment of Psychiatry and Behavioral Sciences, University of New Mexico School of Medicine, Albuquerque, NM, United States.
Alyssa VelascoDepartment of Psychiatry and Behavioral Sciences, University of New Mexico School of Medicine, Albuquerque, NM, United States.
Ali NakipDepartment of Psychiatry and Behavioral Sciences, University of New Mexico School of Medicine, Albuquerque, NM, United States.
Elizabeth R RichardsonDepartment of Psychiatry and Behavioral Sciences, University of New Mexico School of Medicine, Albuquerque, NM, United States.
Justin R DavisUniversity of New Mexico School of Medicine, Albuquerque, NM, United States.
Shawn HazlewoodDepartment of Psychiatry and Behavioral Sciences, University of New Mexico School of Medicine, Albuquerque, NM, United States.
Crystal A GarciaDepartment of Psychiatry and Behavioral Sciences, University of New Mexico School of Medicine, Albuquerque, NM, United States.
Cesar J OjedaDepartment of Psychiatry and Behavioral Sciences, University of New Mexico School of Medicine, Albuquerque, NM, United States.
Karen LuoDepartment of Neurosciences, University of New Mexico, Albuquerque, NM, United States.
Julian DavidDepartment of Neurosciences, University of New Mexico, Albuquerque, NM, United States.
Benjamin C GibsonDepartment of Psychology, University of New Mexico, Albuquerque, NM, United States.
Gregory M NikogosyanDepartment of Psychiatry and Behavioral Sciences, University of New Mexico School of Medicine, Albuquerque, NM, United States.
Brant W HagerDepartment of Psychiatry and Behavioral Sciences, University of New Mexico School of Medicine, Albuquerque, NM, United States.
Danielle FarrarDepartment of Psychiatry and Behavioral Sciences, University of New Mexico School of Medicine, Albuquerque, NM, United States.
Orrin MyersDepartment of Family and Community Medicine, University of New Mexico, Albuquerque, NM, United States.
Andrei A VakhtinMind Research Network, Albuquerque, NM, United States.
Christopher C AbbottDepartment of Psychiatry and Behavioral Sciences, University of New Mexico School of Medicine, Albuquerque, NM, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Intermittent theta burst stimulation (iTBS) to the dorsolateral prefrontal cortex (DLPFC) for major depression has been FDA-approved in the United States since 2018. Accelerated iTBS (aiTBS) protocols of multiple treatments per day have shown promising response and remission rates for major depression, especially when combined with connectivity-guided targeting. Brain networks associated with emotion regulation demonstrate significant changes in connectivity after effective iTBS. However, these findings have been confined to treatment of the left DLPFC, despite literature suggesting equivalent outcomes with right side stimulation. To date there has not been a direct comparison of clinical outcomes and connectivity changes between left and right DLPFC aiTBS for depression. Methods: Forty-four patients aged 50-79 with chronic major depressive disorder underwent open-label accelerated fMRI-guided aiTBS (45 sessions, 9 days) to the DLPFC (18 left, 26 right). Depression, anxiety, and anhedonia symptoms were assessed, and resting-state fMRI was obtained at baseline (Visit 1), after 15 sessions (Visit 2), and end of treatment (Visit 3). Patients who were not demonstrating at least 10% improvement in depression at Visit 2 were switched to contralateral stimulation for the remaining 30 sessions. Results: For the entire cohort (N = 44), mean depression (IDS-C Conclusion: Accelerated iTBS to the right DLPFC appears to have equivalent efficacy as aiTBS to the left DLPFC in terms of magnitude of reduction of depressive, anxious, and anhedonic symptoms in a late-life population. However, connectivity changes associated with treatment were asymmetric, and may reflect hemispheric lateralization of functional network responses to iTBS. Further work is needed to confirm the comparative efficacy and network dynamics of left versus right hemisphere aiTBS for depression.

Indexed as

accelerated intermittent theta burst stimulationelectric field distributionfunctional connectivityhemispheric asymmetrymajor depression (MDD)

Identifiers

PMID41890433
PMCPMC13014255

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.