Literature DB >> 29197929

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

Katherine A Grisanzio1,2, Andrea N Goldstein-Piekarski1,2, Michelle Yuyun Wang3, Abdullah P Rashed Ahmed4, Zoe Samara1,2, Leanne M Williams1,2.   

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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Mesh:

Year:  2018        PMID: 29197929      PMCID: PMC5838569          DOI: 10.1001/jamapsychiatry.2017.3951

Source DB:  PubMed          Journal:  JAMA Psychiatry        ISSN: 2168-622X            Impact factor:   21.596


  73 in total

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4.  Data-Driven Subgroups in Depression Derived from Directed Functional Connectivity Paths at Rest.

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5.  Using brain-based cognitive measures to support clinical decisions in ADHD.

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6.  Lifetime prevalence and age-of-onset distributions of DSM-IV disorders in the National Comorbidity Survey Replication.

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7.  Polygenic dissection of major depression clinical heterogeneity.

Authors:  Y Milaneschi; F Lamers; W J Peyrot; A Abdellaoui; G Willemsen; J-J Hottenga; R Jansen; H Mbarek; A Dehghan; C Lu; D I Boomsma; B W J H Penninx
Journal:  Mol Psychiatry       Date:  2015-06-30       Impact factor: 15.992

8.  Resting-state connectivity biomarkers define neurophysiological subtypes of depression.

Authors:  Andrew T Drysdale; Logan Grosenick; Jonathan Downar; Katharine Dunlop; Farrokh Mansouri; Yue Meng; Robert N Fetcho; Benjamin Zebley; Desmond J Oathes; Amit Etkin; Alan F Schatzberg; Keith Sudheimer; Jennifer Keller; Helen S Mayberg; Faith M Gunning; George S Alexopoulos; Michael D Fox; Alvaro Pascual-Leone; Henning U Voss; B J Casey; Marc J Dubin; Conor Liston
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Review 10.  A trans-diagnostic review of anxiety disorder comorbidity and the impact of multiple exclusion criteria on studying clinical outcomes in anxiety disorders.

Authors:  A N Goldstein-Piekarski; L M Williams; K Humphreys
Journal:  Transl Psychiatry       Date:  2016-06-28       Impact factor: 6.222

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  48 in total

1.  Functional and Optogenetic Approaches to Discovering Stable Subtype-Specific Circuit Mechanisms in Depression.

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2.  Error in Table 2.

Authors: 
Journal:  JAMA Psychiatry       Date:  2018-12-01       Impact factor: 21.596

Review 3.  Deep Brain Stimulation in Psychiatry: Mechanisms, Models, and Next-Generation Therapies.

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Journal:  Psychiatr Clin North Am       Date:  2018-07-09

4.  Neurostructural Heterogeneity in Youths With Internalizing Symptoms.

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Journal:  Biol Psychiatry       Date:  2019-09-18       Impact factor: 13.382

5.  Error in Data Presentation in Figure.

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Journal:  JAMA Psychiatry       Date:  2018-02-01       Impact factor: 21.596

6.  The hidden links between mental disorders.

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Journal:  Nature       Date:  2020-05       Impact factor: 49.962

7.  Attentional control abnormalities in posttraumatic stress disorder: Functional, behavioral, and structural correlates.

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Review 8.  The Future of Digital Psychiatry.

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9.  Transdiagnostic psychiatry: a systematic review.

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Review 10.  Approaches to Defining Common and Dissociable Neurobiological Deficits Associated With Psychopathology in Youth.

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Journal:  Biol Psychiatry       Date:  2019-12-23       Impact factor: 13.382

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