TY - JOUR
T1 - Poor Insight in Obsessive-Compulsive Disorder as a Multifaceted Phenomenon
T2 - Evidence From Brain Activation During Symptom Provocation
AU - Broekhuizen, Aniek
AU - Vriend, Chris
AU - Wolf, Nadja
AU - Koenen, Emma H.
AU - van Oppen, Patricia
AU - van Balkom, Anton J. L. M.
AU - Visser, Henny A. D.
AU - van den Heuvel, Odile A.
N1 - Funding Information: This work was supported by ZonMW (Grant No. 636310004 [to HADV]). Publisher Copyright: © 2023 Society of Biological Psychiatry
PY - 2023/11
Y1 - 2023/11
N2 - Background: Poor insight in obsessive-compulsive disorder (OCD) is associated with higher symptom severity, more comorbidities, and worse response to treatment. This study aimed to elucidate underlying mechanisms of poor insight in OCD by exploring its neurobiological correlates. Methods: Using a symptom provocation task during functional magnetic resonance imaging, we compared brain activation of patients with poor insight (n = 19; 14 female, 5 male), good/fair insight (n = 63; 31 female, 32 male), and healthy control participants (n = 42; 22 female, 20 male) using a Bayesian region-of-interest and a general linear model whole-brain approach. Insight was assessed using the Overvalued Ideas Scale. Results: Compared with patients with good/fair insight and healthy control participants, patients with OCD and poor insight showed widespread lower task-related activation in frontal areas (subgenual anterior cingulate cortex, ventromedial prefrontal cortex, dorsolateral prefrontal cortex, ventrolateral prefrontal cortex, supplementary motor area, precentral gyrus), parietal areas (posterior parietal cortex, precuneus), and the middle temporal gyrus and insula. Results were not driven by interindividual differences in OCD symptom severity, medication usage, age of disorder onset, or state distress levels. Conclusions: During symptom provocation, patients with OCD and poor insight show altered activation in brain circuits that are involved in emotional processing, sensory processing, and cognitive control. Future research should focus on longitudinal correlates of insight and/or use tasks that probe emotional and sensory processing and cognitive control.
AB - Background: Poor insight in obsessive-compulsive disorder (OCD) is associated with higher symptom severity, more comorbidities, and worse response to treatment. This study aimed to elucidate underlying mechanisms of poor insight in OCD by exploring its neurobiological correlates. Methods: Using a symptom provocation task during functional magnetic resonance imaging, we compared brain activation of patients with poor insight (n = 19; 14 female, 5 male), good/fair insight (n = 63; 31 female, 32 male), and healthy control participants (n = 42; 22 female, 20 male) using a Bayesian region-of-interest and a general linear model whole-brain approach. Insight was assessed using the Overvalued Ideas Scale. Results: Compared with patients with good/fair insight and healthy control participants, patients with OCD and poor insight showed widespread lower task-related activation in frontal areas (subgenual anterior cingulate cortex, ventromedial prefrontal cortex, dorsolateral prefrontal cortex, ventrolateral prefrontal cortex, supplementary motor area, precentral gyrus), parietal areas (posterior parietal cortex, precuneus), and the middle temporal gyrus and insula. Results were not driven by interindividual differences in OCD symptom severity, medication usage, age of disorder onset, or state distress levels. Conclusions: During symptom provocation, patients with OCD and poor insight show altered activation in brain circuits that are involved in emotional processing, sensory processing, and cognitive control. Future research should focus on longitudinal correlates of insight and/or use tasks that probe emotional and sensory processing and cognitive control.
KW - Bayesian analysis
KW - Neurobiological correlates
KW - Obsessive-compulsive disorder
KW - Poor insight
KW - Symptom provocation
KW - Task-based fMRI
UR - http://www.scopus.com/inward/record.url?scp=85165238762&partnerID=8YFLogxK
U2 - https://doi.org/10.1016/j.bpsc.2023.04.006
DO - https://doi.org/10.1016/j.bpsc.2023.04.006
M3 - Article
C2 - 37121397
SN - 2451-9022
VL - 8
SP - 1135
EP - 1144
JO - Biological Psychiatry: Cognitive Neuroscience and Neuroimaging
JF - Biological Psychiatry: Cognitive Neuroscience and Neuroimaging
IS - 11
ER -