Why the study?
The relationship between distortions in specific brain properties, psychological and physical traits, and distinct pain dimensions in chronic pain patients remains poorly understood.
Chronic pain comprises distinct domains (magnitude, affect/disability, quality) that correlate with specific psychological traits and brain functional connectivity networks.
May support domain-specific chronic pain phenotyping; cross-sectional data leave causal brain network links open.
Chronic pain is a multidimensional pathological state. Recent evidence suggests that specific brain properties and patients' psychological and physical traits are distorted in chronic pain patients. However, the relationship between these alterations and pain dimensions remains poorly understood. Here, we first evaluated multiple dimensions of chronic pain by assessing a broad battery of pain-related questionnaire scores (23 outcomes) of 107 chronic low back pain patients and identified 3 distinct chronic pain domains: magnitude, affect & disability, and quality. Second, we investigated the pain domains relationship with measures of personality, social interaction, psychological traits, and ability traits (77 biopsychosocial & ability [biopsy&ab] outcomes). Pain magnitude (out-of-sample [OOS] ) is associated with emotional control, attention, and working memory, with higher pain scores showing lower capacity to regulate and adapt behaviorally. Pain affect & disability (OOS associated with anxiety, catastrophizing and social relationships dysfunction. Pain quality did not relate significantly to biopsy&ab variables. Third, we mapped these 3 pain domains to brain functional connectivity. Pain magnitude mainly associated with the sensorimotor and the cingulo-opercular networks (OOS ). Pain affect & disability related to frontoparietal and default mode networks (OOS . Pain quality integrated sensorimotor, auditory, and cingulo-opercular networks (OOS ). Mediation analysis could link functional connectivity and biopsy&ab models to respective pain domains. Our results provide a global overview of the complexity of chronic pain, showing how underlying distinct domains of the experience map to different biopsy&ab correlates and underlie unique brain network signatures.
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Pinto et al. (2022) studied this question.
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