Abstract

Posttraumatic Stress Disorder (PTSD) is a prevalent and debilitating condition with complex and variable presentation. While PTSD symptom domains (intrusion, avoidance, cognition/mood, and arousal/reactivity) correlate highly, the relative importance of these symptom subsets often differs across patients. In this study, we used machine learning to derive how PTSD symptom subsets differ based upon brain functional connectivity. We acquired resting-state magnetic resonance imaging in a sample (N = 50) of PTSD patients and characterized clinical features using the PTSD Checklist for DSM-5 (PCL-5). We compared connectivity among 100 cortical and subcortical regions within the default mode, salience, executive, and affective networks. We then used principal component analysis and least-angle regression (LARS) to identify relationships between symptom domain severity and brain networks. We found connectivity predicted PTSD symptom profiles. The goodness of fit (R2) for total PCL-5 score was 0.29 and the R2 for intrusion, avoidance, cognition/mood, and arousal/reactivity symptoms was 0.33, 0.23, −0.01, and 0.06, respectively. The model performed significantly better than chance in predicting total PCL-5 score (p = 0.030) as well as intrusion and avoidance scores (p = 0.002 and p = 0.034). It was not able to predict cognition and arousal scores (p = 0.412 and p = 0.164). While this work requires replication, these findings demonstrate that this computational approach can directly link PTSD symptom domains with neural network connectivity patterns. This line of research provides an important step toward data-driven diagnostic assessments in PTSD, and the use of computational methods to identify individual patterns of network pathology that can be leveraged toward individualized treatment.

Highlights

  • Introduction Posttraumatic StressDisorder (PTSD) is a highly prevalent and chronic psychiatric disorder, characterized by trauma exposure, followed by intrusive thoughts/recollections, avoidance of related stimuli, hyperarousal, and mood and cognitive impairment[1,2]

  • The models performed significantly better than chance in predicting total PTSD Checklist for DSM-5 (PCL-5) score (p = 0.030) as well as intrusion and avoidance subscales (p = 0.002 and p = 0.034)

  • There is an immediate need for innovations including biological markers to address the challenges that symptom heterogeneity poses for Posttraumatic Stress Disorder (PTSD) diagnosis (e.g.,41)

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Summary

Introduction

Disorder (PTSD) is a highly prevalent and chronic psychiatric disorder, characterized by trauma exposure, followed by intrusive thoughts/recollections, avoidance of related stimuli, hyperarousal, and mood and cognitive impairment[1,2]. In the USA, lifetime prevalence is estimated at 7%, with higher prevalence in military Veterans[1,2,3]. Current evidence-based treatments, including psychopharmacology and psychotherapy, are often inadequately effective[3]. As PTSD is highly comorbid with other psychiatric illnesses[7,8] and individuals may possess a myriad of symptoms. Different diagnostic and nosological models attempt to identify PTSD symptoms—this is evident in the DSM-52 criteria for PTSD, which groups symptoms in four domains: intrusion (criterion B); avoidance

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