Transdiagnostic Symptom Clusters and Associations With Brain, Behavior, and Daily Function in Mood, Anxiety, and Trauma Disorders

被引:107
作者
Grisanzio, Katherine A. [1 ,2 ]
Goldstein-Piekarski, Andrea N. [1 ,2 ]
Wang, Michelle Yuyun [3 ]
Ahmed, Abdullah P. Rashed [4 ]
Samara, Zoe [1 ,2 ]
Williams, Leanne M. [1 ,2 ]
机构
[1] Stanford Univ, Dept Psychiat & Behav Sci, 401 Quarry Rd,Mail Code 5717, Stanford, CA 94305 USA
[2] Vet Affairs Palo Alto Hlth Care Syst, Sierra Pacific Mental Illness Res Educ & Clin Ctr, Palo Alto, CA USA
[3] Brain Resource Ltd, Brain Resource Int Database, Sydney, NSW, Australia
[4] SLAC Natl Accelerator Lab, Menlo Pk, CA USA
基金
澳大利亚研究理事会;
关键词
MAJOR DEPRESSIVE DISORDER; EEG ALPHA ASYMMETRY; DSM-IV; 1ST-EPISODE SCHIZOPHRENIA; MELANCHOLIC DEPRESSION; COGNITIVE IMPAIRMENT; BIPOLAR DISORDER; COMORBIDITY; CRITERIA; SUBTYPES;
D O I
10.1001/jamapsychiatry.2017.3951
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
IMPORTANCE The symptoms that define mood, anxiety, and trauma disorders are highly overlapping across disorders and heterogeneous within disorders. It is unknown whether coherent subtypes exist that span multiple diagnoses and are expressed functionally (in underlying cognition and brain function) and clinically (in daily function). The identification of cohesive subtypes would help disentangle the symptom overlap in our current diagnoses and serve as a tool for tailoring treatment choices. OBJECTIVE To propose and demonstrate 1 approach for identifying subtypes within a transdiagnostic sample. DESIGN, SETTING, AND PARTICIPANTS This cross-sectional study analyzed data from the Brain Research and Integrative Neuroscience Network Foundation Database that had been collected at the University of Sydney and University of Adelaide between 2006 and 2010 and replicated at Stanford University between 2013 and 2017. The study included 420 individuals with a primary diagnosis of major depressive disorder (n = 100), panic disorder (n = 53), posttraumatic stress disorder (n = 47), or no disorder (healthy control participants) (n = 220). Data were analyzed between October 2016 and October 2017. MAIN OUTCOMES AND MEASURES We followed a data-driven approach to achieve the primary study outcome of identifying transdiagnostic subtypes. First, machine learning with a hierarchical clustering algorithm was implemented to classify participants based on self-reported negative mood, anxiety, and stress symptoms. Second, the robustness and generalizability of the subtypes were tested in an independent sample. Third, we assessed whether symptom subtypes were expressed at behavioral and physiological levels of functioning. Fourth, we evaluated the clinically meaningful differences in functional capacity of the subtypes. Findings were interpreted relative to a complementary diagnostic frame of reference. RESULTS Four hundred twenty participants with a mean (SD) age of 39.8 (14.1) years were included in the final analysis; 256 (61.0%) were female. We identified 6 distinct subtypes characterized by tension (n=81; 19%), anxious arousal (n=55; 13%), general anxiety (n=38; 9%), anhedonia (n=29; 7%), melancholia (n=37; 9%), and normative mood (n=180; 43%), and these subtypes were replicated in an independent sample. Subtypes were expressed through differences in cognitive control (F-5,F-383 = 5.13, P < .001, eta(2)(p) = 0.063), working memory (F-5,F-401 = 3.29, P = .006, eta(2)(p) = 0.039), electroencephalography-recorded beta power in a resting paradigm (F-5,F-357 = 3.84, P = .002, eta(2)(p) = 0.051), electroencephalography-recorded beta power in an emotional paradigm (F-5,F-365 = 3.56, P = .004, eta(2)(p) = 0.047), social functional capacity (F-5,F-414 = 21.33, P < .001, eta(2)(p) = 0.205), and emotional resilience (F-5,F-376 = 15.10, P < .001, eta(2)(p) = 0.171). CONCLUSIONS AND RELEVANCE These findings offer a data-driven framework for identifying robust subtypes that signify specific, coherent, meaningful associations between symptoms, behavior, brain function, and observable real-world function, and that cut across DSM-IV-defined diagnoses of major depressive disorder, panic disorder, and posttraumatic stress disorder.
引用
收藏
页码:201 / 209
页数:9
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