Perceptual insensitivity to the modulation of interoceptive signals in depression, anxiety, and substance use disorders

Author: Ryan Smith1, Justin S Feinstein1,2, Rayus Kuplicki1, Katherine L Forthman1, Jennifer L Stewart1,2, Martin P Paulus1,2, Tulsa 1000 Investigators; Sahib S Khalsa3,4
Affiliation: <sup>1</sup> Laureate Institute for Brain Research, 6655 S Yale Ave, Tulsa, OK, 74136, USA. <sup>2</sup> Oxley College of Health Sciences, University of Tulsa, Tulsa, OK, USA. <sup>3</sup> Laureate Institute for Brain Research, 6655 S Yale Ave, Tulsa, OK, 74136, USA. skhalsa@laureateinstitute.org. <sup>4</sup> Oxley College of Health Sciences, University of Tulsa, Tulsa, OK, USA. skhalsa@laureateinstitute.org.
Conference/Journal: Sci Rep
Date published: 2021 Jan 22
Other: Volume ID: 11 , Issue ID: 1 , Pages: 2108 , Special Notes: doi: 10.1038/s41598-021-81307-3. , Word Count: 159


This study employed a series of heartbeat perception tasks to assess the hypothesis that cardiac interoceptive processing in individuals with depression/anxiety (N = 221), and substance use disorders (N = 136) is less flexible than that of healthy individuals (N = 53) in the context of physiological perturbation. Cardiac interoception was assessed via heartbeat tapping when: (1) guessing was allowed; (2) guessing was not allowed; and (3) experiencing an interoceptive perturbation (inspiratory breath hold) expected to amplify cardiac sensation. Healthy participants showed performance improvements across the three conditions, whereas those with depression/anxiety and/or substance use disorder showed minimal improvement. Machine learning analyses suggested that individual differences in these improvements were negatively related to anxiety sensitivity, but explained relatively little variance in performance. These results reveal a perceptual insensitivity to the modulation of interoceptive signals that was evident across several common psychiatric disorders, suggesting that interoceptive deficits in the realm of psychopathology manifest most prominently during states of homeostatic perturbation.


PMID: 33483527 DOI: 10.1038/s41598-021-81307-3