Exploring the Influence of Synaptic Density and Anxiety on Pain Perception: Evidence from a [11C]UCB-J PET Imaging Study.

IF 4.5 2区 医学 Q1 CLINICAL NEUROLOGY
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.

探讨突触密度和焦虑对疼痛感知的影响:来自UCB-J PET成像研究的证据[11]。
背景:大脑结构和功能的改变可能与疼痛和焦虑有关。我们假设突触密度(体内用[11C]UCB-J和突触囊泡SV2A正电子发射断层成像定量测量)的改变可能在更高的疼痛敏感性中起作用,这种关系可能是由焦虑症状介导的。方法:21名心理健康、身体健康的受试者(男11名,女10名;年龄(45.1±16.9岁)参加影像学、急性疼痛[冷压试验(CPT)]和焦虑(状态-特质焦虑量表)评估。采用带血浆输入函数的单组织室模型将SV2A密度量化为区域分布体积(VT)。SV2A的密度在五个先前被证明与疼痛相关的感兴趣区域(roi)进行评估:背外侧前额叶皮层(DLPFC)、杏仁核、前扣带皮层(ACC)、梭状回和小脑。结果:状态焦虑与疼痛敏感性呈正相关(r = 0.60, p= 0.004)。疼痛敏感性与小脑(r = -0.67, p=.001)、梭状回(r = -0.66, p=.001)、DLPFC (r = -0.63, p=.002)、ACC (r = -0.58, p=.006) SV2A密度呈显著负相关。中介分析显示,小脑突触密度通过状态焦虑症状间接影响疼痛敏感性(B = -0.77, 95% CI[-1.89, -0.04]),占总效应的33%。在控制焦虑症状后,梭状回对疼痛敏感性的直接影响仍然显著(B = -1.67, p= 0.020),而焦虑症状对疼痛敏感性的间接影响不显著(B = -0.43, 95% CI[-1.44, 0.37])。结论:研究结果提供了第一个已知的体内证据,即较低的突触(SV2A)密度与较高的疼痛敏感性有关,特别是在梭状回和小脑中。中介分析表明,状态焦虑在小脑突触密度与疼痛敏感性之间具有部分中介作用,而在梭状回突触密度与疼痛敏感性之间具有加性作用,但不具有中介作用。
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来源期刊
CiteScore
8.40
自引率
2.10%
发文量
230
审稿时长
4-8 weeks
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.
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