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. 2018 Feb 1;75(2):201-209.
doi: 10.1001/jamapsychiatry.2017.3951.

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

Affiliations

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

Katherine A Grisanzio et al. JAMA Psychiatry. .

Erratum in

  • Error in Data Presentation in Figure.
    [No authors listed] [No authors listed] JAMA Psychiatry. 2018 Feb 1;75(2):215. doi: 10.1001/jamapsychiatry.2017.4400. JAMA Psychiatry. 2018. PMID: 29417151 Free PMC article. No abstract available.
  • Error in Table 2.
    [No authors listed] [No authors listed] JAMA Psychiatry. 2018 Dec 1;75(12):1304. doi: 10.1001/jamapsychiatry.2018.3460. JAMA Psychiatry. 2018. PMID: 30422154 Free PMC article. No abstract available.

Abstract

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 (F5,383 = 5.13, P < .001, ηp2 = 0.063), working memory (F5,401 = 3.29, P = .006, ηp2 = 0.039), electroencephalography-recorded β power in a resting paradigm (F5,357 = 3.84, P = .002, ηp2 = 0.051), electroencephalography-recorded β power in an emotional paradigm (F5,365 = 3.56, P = .004, ηp2 = 0.047), social functional capacity (F5,414 = 21.33, P < .001, ηp2 = 0.205), and emotional resilience (F5,376 = 15.10, P < .001, ηp2 = 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.

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Conflict of interest statement

Conflict of Interest Disclosures: Dr Williams has previously received consultant fees from Brain Resource and Humana and is currently on the Scientific Advisory Board for Psyberguide, a project of the One Mind Institute. Dr Wang is an employee of Brain Resource. No other disclosures were reported.

Figures

Figure 1.
Figure 1.. Visual Demonstration of Clustering of Subtypes in 3-Dimensional Space
Each symptom component is a spatial dimension on the x-axis, y-axis, and z-axis.
Figure 2.
Figure 2.. Clinical-Behavioral-Brain Profiles for Each Subtype
Cognitive control is measured by the go/no-go paradigm; working memory is measured by the digit span paradigm; emotion electroencephalographic (EEG) β is β power in the parietal/occipital region for the happy condition during the conscious emotion paradigm; frontal electroencephalographic β is mean β power in the frontal region during the eyes-open resting condition; social function is self-reported daily functional capacity in the domain of social skills; and resilience is daily functional capacity in the domain of emotional resilience. All values are expressed in standardized units to facilitate interpretation of profiles across measures. Error bars represent 1 SD from the mean.

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References

    1. Kessler RC, Gruber M, Hettema JM, Hwang I, Sampson N, Yonkers KA. Co-morbid major depression and generalized anxiety disorders in the National Comorbidity Survey follow-up. Psychol Med. 2008;38(3):365-374. - PMC - PubMed
    1. Goldstein-Piekarski AN, Williams LM, Humphreys K. A trans-diagnostic review of anxiety disorder comorbidity and the impact of multiple exclusion criteria on studying clinical outcomes in anxiety disorders. Transl Psychiatry. 2016;6(6):e847. - PMC - PubMed
    1. Somers JM, Goldner EM, Waraich P, Hsu L. Prevalence and incidence studies of anxiety disorders: a systematic review of the literature. Can J Psychiatry. 2006;51(2):100-113. - PubMed
    1. Substance Abuse and Mental Health Services Administration HHS Publication No. (SMA) 13-4805: Results From the 2012 National Survey on Drug Use and Health: Mental Health Findings. Rockville, MD: US Department of Health and Human Services, 2013: 1-136.
    1. Weissman MM, Bland RC, Canino GJ, et al. . The cross-national epidemiology of panic disorder. Arch Gen Psychiatry. 1997;54(4):305-309. - PubMed

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