Evidence map›Paper›PMID 40926834›Full record

ArticleAlpha psychiatry2025

Artificial Intelligence for Management of Major Depression: Initial Design, Progress, and Research Plans.

Farrokh Alemi, Janusz Wojtusiak, Aneel Ursani, K Pierre Eklou, Kevin Lybarger

Abstract read
In one paragraph

Article in Alpha psychiatry, 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

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

5 authors.

Farrokh AlemiHealth Administration and Policy, George Mason University, Fairfax, VA 22030, USA.ORCID https://orcid.org/0000-0002-7402-9063
Janusz WojtusiakHealth Administration and Policy, George Mason University, Fairfax, VA 22030, USA.
Aneel UrsaniKlinic Inc., Seattle, WA 98101, USA.
K Pierre EklouSchool of Nursing, George Mason University, Fairfax, VA 22030, USA.ORCID https://orcid.org/0000-0001-5242-2991
Kevin LybargerInformation Sciences and Technology, George Mason University, Fairfax, VA 22030, USA.ORCID https://orcid.org/0000-0001-5798-2664

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Herein, we report on the initial development, progress, and future plans for an autonomous artificial intelligence (AI) system designed to manage major depressive disorder (MDD). The system is a web-based, patient-facing conversational AI that collects medical history, provides presumed diagnosis, recommends treatment, and coordinates care for patients with MDD. Methods: The system includes seven components, five of which are complete and two are in development. The first component is the AI's knowledgebase, which was constructed using Least Absolute Shrinkage and Selection Operator (LASSO) logistic regression to analyze extensive patient medical histories and identify factors influencing response to antidepressants. The second component is a series of adjustments to the knowledgebase designed to correct algorithm bias in patient subgroups. The third component is a conversational Large Language Model (LLM) that efficiently gathers patients' medical histories. The fourth component is a dialogue management system that minimizes digressions in the LLM conversations, using a topic network statistically derived from the AI's own knowledgebase. The fifth component is planned to enable real-time, human-in-the-loop monitoring. The sixth component is an existing analytical, non-generative module that provides and explains treatment advice. The seventh component is planned to coordinate care with clinicians via closed-loop referrals. Results: In component 1, the AI's knowledgebase correctly predicted 69.2% to 78.5% of the variation in response to 15 oral antidepressants. Patients treated by AI-concordant clinicians were 17.5% more likely to benefit from their treatment than patients of AI-discordant clinicians. In component 2, the use of the system required adjustments to improve accuracy for predicting the responses of African Americans to four antidepressants and no adjustments were required for the remaining 10 antidepressants. In component 3, the conversational intake efficiently covered 1499 relevant medical history events (including 700 diagnoses, 550 medications, 151 procedures, and 98 prior antidepressant responses). In the fourth component, the dialogue management system was effective in maintaining a long dialogue with many turns in the conversation. In the sixth component, the advice system was able to rely exclusively on pre-set text. An online ad campaign attracted 1536 residents of Virginia to use the advice system. Initially, a focus group of clinicians was skeptical of the value of the advice system and requested more prospective studies before they would implement the system in their clinics. When the system was redesigned to advise patients at home, clinicians were willing to receive referrals from the system and discuss the advice of the system with their patients. Conclusions: Further research is needed to refine and evaluate the system. We outline our plans for a prospective randomized trial to assess the system's impact on prescription patterns and patient outcomes.

Indexed as

antidepressantantidepressant-resistant depressiondepressionmajor depressive disorder

Identifiers

PMID40926834
PMCPMC12416039

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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.