Evidence map›Paper›PMID 40060043›Full record

ArticleResearch square2025

A Stratified Precision Medicine Trial Targeting Selective Mechanisms of Alpha 2A Agonism as a Treatment for the Cognitive Biotype of Depression: The BIomarker Guided (BIG) Study for Depression.

Leanne Williams, Laura Hack, Jenna Jubeir, Rachel Hilton, Leonardo Tozzi, Leyla Boyar, Xue Zhang, Timothy Lyons, Booil Jo, Ruth O'Hara and 1 more

Abstract readPreprint
In one paragraph

Article in Research square, 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

11 authors.

Leanne WilliamsStanford University School of Medicine.ORCID 0000-0001-9987-7360
Laura HackDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine Stanford, CA 94305, USA.
Jenna JubeirDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine Stanford, CA 94305, USA.
Rachel HiltonStanford University.ORCID 0000-0002-7943-2206
Leonardo TozziDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine Stanford, CA 94305, USA.ORCID 0000-0002-9429-6476
Leyla BoyarDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine Stanford, CA 94305, USA.
Xue ZhangDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine Stanford, CA 94305, USA.
Timothy LyonsDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine Stanford, CA 94305, USA.
Booil JoStanford University.
Ruth O'HaraDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine Stanford, CA 94305, USA.
Alan SchatzbergStanford University.ORCID 0000-0001-9421-8278

Funding

ACE-D: Accelerating Cognition-guided signatures to Enhance translation in DepressionU01MH136062 · NIMH · STANFORD UNIVERSITY · PI AJILORE, OLUSOLA A., MA, JUN · 2024 to 2025
$7.6M
NIMH NIH HHS U01 MH136062
6 · The paper itself

Abstract

Cognitive impairments contribute significantly to psychosocial dysfunction in major depressive disorder (MDD), yet mechanistically selective treatments targeted to these impairments are lacking. We evaluated guanfacine immediate release (GIR), an alpha 2A receptor agonist, as a novel treatment for selectively improving cognitive control circuit function and behavioral performance in a subtype of depression, the cognitive biotype. Seventeen MDD participants of this biotype completed 6-8 weeks of GIR treatment (target dose: 2mg/night), meeting our per protocol criteria. GIR significantly increased activation and connectivity within the cognitive control circuit. The clinical response rate was 76.5% (defined by ≥ 50% improvement on the 17-item Hamilton Rating Scale for Depression (HRSD-17), exceeding conventional antidepressant rates, and 64.7% achieved remission (HRSD-17 score of ≤ 7). GIR significantly improved cognitive control performance, quality of life, and global life satisfaction. This study is the first to demonstrate both efficacy and target engagement of GIR as a mechanistically selective treatment specifically for the cognitive biotype of depression.

Identifiers

PMID40060043
PMCPMC11888545

What OpenQuestion holds

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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.