Cortical Thickness Alterations in Chronic Pain Disorder: An Exploratory MRI Study.

Psychosom Med

From the Neurologische Klinik und Poliklinik (Magon, Sprenger, Papadopoulou), Universitaet Basel, Universitaetsspital Basel, Switzerland; Medical Image Analysis Center AG (Magon), Basel, Switzerland; Fachbereich Neurologie (Sprenger), DKD HELIOS Klinik Wiesbaden, Germany; Abteilung fuer Neuroradiologie (Otti), Klinikum rechts der Isar, Technische Universitaet Muenchen, Germany; Klinik fuer Psychosomatische Medizin und Psychotherapie (Otti), Klinikum rechts der Isar, Technische Universitaet Muenchen, Germany; Klinik fuer Psychosomatische Medizin und Psychotherapie (Gündel), Universitaetsklinikum Ulm, University of Ulm, Germany; and Klinik fuer Psychiatrie und Psychotherapie (Noll-Hussong), Sektion Psychosomatische Medizin und Psychotherapie, Universitaetsklinikum des Saarlandes, Homburg, Germany.

Published: September 2018

Objective: Chronic pain disorder (CPD) has been associated with brain changes, especially in limbic circuits. However, in most patients with chronic pain, depression or anxiety is a common comorbidity. In this exploratory and naturalistic study, we investigated brain cortical thickness (CTh) differences between patients with CPD and healthy controls, with consideration of concurrent psychiatric symptoms.

Methods: Twenty-three patients with CPD and 23 age- and sex-matched healthy volunteers were included in this study. CTh was estimated using Freesurfer on high-resolution three-dimensional T1-weighted images acquired with a 3T scanner. Group differences were investigated using an analysis of covariance model that included age, sex, and Beck Depression Inventory I and Trait Anxiety Inventory scores as covariates. The relationship between CTh and Toronto Alexithymia Scale (TAS-20) scores was also investigated in patients. Data were corrected for multiplicity using the False Discovery Rate approach (q < .05).

Results: The comparison between groups using demographics and Beck Depression Inventory I scores as covariates showed thinner cortex in patients compared with controls, after correction for multiplicity in the left precentral (F(1,42) = 21.9, p < .05) and postcentral gyri (F(1,42) = 26.9, p < .05) and in the left inferior temporal sulcus (F(1,42) = 19.6, p < .05). Moreover, using the Trait Anxiety Inventory as covariate, a trend toward significance (p < .001 uncorrected) was seen for the left precentral gyrus (F(1,42) = 13.8), right middle frontal (F(1,42) = 14.3) and inferior parietal gyri (F(1,42) = 13.4), and right anterior temporal pole (F(1,42) = 15.9).

Conclusions: The results indicate that brain morphological differences between patients with chronic pain disorder and healthy controls are localized to regions that correspond to sensory as well as affective dimensions of pain processing.

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Source
http://dx.doi.org/10.1097/PSY.0000000000000605DOI Listing

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