Karina Moisieienko, Ruth H Asch, Margaret T Davis, Robert H Pietrzak, Irina Esterlis
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引用次数: 0
Abstract
Background: Structural and functional brain alterations may be associated with pain and anxiety. We hypothesized that synaptic density (measured in vivo with [11C]UCB-J and positron emission tomography quantification of synaptic vesicle SV2A) alterations may play a role in higher pain sensitivity, and that this relationship may be mediated by anxiety symptoms.
Methods: Twenty-one mentally and medically healthy subjects (11 males, 10 females; age 45.1 ± 16.9 years) participated in imaging, acute pain [cold pressor test (CPT)] and anxiety (State-Trait Anxiety Inventory) assessments. SV2A density was quantified as regional volumes of distribution (VT) using a one-tissue compartment model with a plasma input function. SV2A density was assessed in five regions of interest (ROIs) that were previously shown to be associated with pain: dorsolateral prefrontal cortex (DLPFC), amygdala, anterior cingulate cortex (ACC), fusiform gyrus, and cerebellum.
Results: State anxiety was positively correlated with pain sensitivity (r = 0.60, p=.004). Significant negative correlations were observed between pain sensitivity and SV2A density in cerebellum (r = -0.67, p=.001), fusiform gyrus (r = -0.66, p=.001), DLPFC (r = -0.63, p=.002), and ACC (r = -0.58, p=.006). Mediation analysis revealed a significant indirect effect of cerebellar synaptic density on pain sensitivity through state anxiety symptoms (B = -0.77, 95% CI [-1.89, -0.04]), accounting for 33% of the total effect. For the fusiform gyrus, the direct effect on pain sensitivity remained significant after controlling for anxiety symptoms (B = -1.67, p=.020), while the indirect effect through anxiety symptoms was not significant (B = -0.43, 95% CI [-1.44, 0.37]).
Conclusion: Results provide the first known in vivo evidence that lower synaptic (SV2A) density is associated with greater pain sensitivity, particularly in the fusiform gyrus and cerebellum. Mediation analyses revealed that state anxiety partially mediated the relationship between cerebellar synaptic density and pain sensitivity, while having an additive - but not mediating - effect on the relationship between fusiform synaptic density and pain sensitivity.
期刊介绍:
The central focus of the journal is on research that advances understanding of existing and new neuropsychopharmacological agents including their mode of action and clinical application or provides insights into the biological basis of psychiatric disorders and thereby advances their pharmacological treatment. Such research may derive from the full spectrum of biological and psychological fields of inquiry encompassing classical and novel techniques in neuropsychopharmacology as well as strategies such as neuroimaging, genetics, psychoneuroendocrinology and neuropsychology.