Predicting non-response to ketamine for depression: An exploratory symptom-level analysis of real-world data among military veterans

被引:2
|
作者
Miller, Eric A. [1 ,2 ,8 ]
Afshar, Houtan Totonchi [1 ,2 ]
Mishra, Jyoti [2 ,3 ]
McIntyre, Roger S. [4 ,5 ,6 ]
Ramanathan, Dhakshin [1 ,2 ,3 ,7 ]
机构
[1] VA San Diego Med Ctr, Dept Mental Hlth, San Diego, CA 92161 USA
[2] Dept Psychiat, UC San Diego, La Jolla, CA 92093 USA
[3] Ctr Excellence Stress & Mental Hlth, VA San Diego Med Ctr, San Diego, CA USA
[4] Univ Toronto, Dept Psychiat, Toronto, ON, Canada
[5] Univ Toronto, Dept Pharmacol, Toronto, ON, Canada
[6] Brain & Cognit Discovery Fdn, Toronto, ON, Canada
[7] Univ Calif San Diego, Dept Psychiat, 9500 Gilman Dr, La Jolla, CA 92093 USA
[8] Univ Arizona, Coll Med Tucson, Dept Psychiat, 1501N Campbell Ave, Tucson, AZ 85724 USA
关键词
Ketamine; Esketamine; Treatment resistant depression; Predictive modeling; Symptom trajectories; TREATMENT RESPONSE; METAANALYSIS; SEVERITY; EFFICACY; THERAPY;
D O I
10.1016/j.psychres.2024.115858
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Ketamine helps some patients with treatment resistant depression (TRD), but reliable methods for predicting which patients will, or will not, respond to treatment are lacking. Herein, we aim to inform prediction models of non-response to ketamine/esketamine in adults with TRD. This is a retrospective analysis of PHQ-9 item response data from 120 patients with TRD who received repeated doses of intravenous racemic ketamine or intranasal eskatamine in a real-world clinic. Regression models were fit to patients' symptom trajectories, showing that all symptoms improved on average, but depressed mood improved relatively faster than low energy. Principal component analysis revealed a first principal component (PC) representing overall treatment response, and a second PC that reflects variance across affective versus somatic symptom subdomains. We then trained logistic regression classifiers to predict overall response (improvement on PC1) better than chance using patients' baseline symptoms alone. Finally, by parametrically adjusting the classifier decision thresholds, we identified optimal models for predicting non-response with a negative predictive value of over 96 %, while retaining a specificity of 22 %. Thus, we could identify 22 % of patients who would not respond based purely on their baseline symptoms. This approach could inform rational treatment recommendations to avoid additional treatment failures.
引用
收藏
页数:9
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