Structural and functional characterization of nucleus accumbens as a potential biomarker of the transition from acute to chronic pain after thoracoscopic surgery

IF 7.5
Yangzi Zhu, Yan Zhang, Shengjie Bai, Meiyan Zhou, Miao Zhang, Xuefeng Pan, Yibing Shi, Liwei Wang, Jun-Li Cao
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Abstract

Purpose

Chronic postsurgical pain (CPSP) poses substantial therapeutic and preventive challenges as a common postoperative complication. Identifying predictive biomarkers could enable early intervention in high-risk patients. Preclinical evidence indicates that the nucleus accumbens (NAc) plays a key role in pain chronification, yet human neuroimaging data for CPSP are scarce. This prospective cohort study characterized longitudinal structural and functional alterations in NAc subregions as potential biomarkers for CPSP development after thoracoscopic surgery.

Methods

Forty patients underwent multimodal magnetic resonance imaging (MRI), including resting-state fMRI, diffusion tensor imaging, T1-weighted imaging) and clinical assessments at acute (≤ 1 week) and chronic (12 weeks) postoperative phases. Based on the diagnostic criteria for CPSP, thirteen patients developed CPSP at 12 weeks.

Results

CPSP group patients displayed elevated pain catastrophizing scores despite comparable acute pain intensity, indicating maladaptive affective processing. Compared to non-CPSP controls, CPSP patients exhibited significantly reduced slow-5 band fractional amplitude of low-frequency fluctuation (fALFF) in bilateral NAc shell and core subregions during both phases. Decreased functional connectivity between shell and core emerged specifically at 12 weeks. Reduced gray matter density (GMD) and inferomedial atrophy were observed in bilateral NAc of CPSP patients at both timepoints. Early postoperative bilateral NAc GMD and NAc shell fALFF correlated with subsequent pain intensity and predicted CPSP development with high discriminative accuracy, particularly when combined.

Conclusions

These findings establish NAc structural and functional alterations as promising neuroimaging biomarkers for CPSP susceptibility, revealing a unified neurobiological mechanism underlying affective dysregulation and pain chronification.

Trial registration

Registered at the Chinese Clinical Trial Registry (https://www.chictr.org.cn/showproj.html?proj=131606) with No. ChiCTR2100049631, on August 7, 2021.

作为胸腔镜手术后急性疼痛向慢性疼痛转变的潜在生物标志物的伏隔核的结构和功能特征
目的:慢性术后疼痛(CPSP)作为一种常见的术后并发症,给治疗和预防带来了巨大的挑战。识别预测性生物标志物可以对高危患者进行早期干预。临床前证据表明伏隔核(NAc)在疼痛慢性化中起着关键作用,但人类神经影像学数据缺乏。这项前瞻性队列研究将NAc亚区纵向结构和功能改变作为胸腔镜手术后CPSP发展的潜在生物标志物。方法对40例患者进行多模态磁共振成像(MRI)检查,包括静息态fMRI、弥散张量成像、t1加权成像,并在术后急性期(≤1周)和慢性期(12周)进行临床评估。根据CPSP的诊断标准,13例患者在12周发生CPSP。结果scpsp组患者在急性疼痛强度相当的情况下,疼痛灾难化评分升高,提示情感加工适应不良。与非CPSP对照组相比,CPSP患者在两个阶段均表现出双侧NAc壳区和核心亚区低频波动慢-5波段分数振幅(fALFF)显著降低。在12周时,外壳和核心之间的功能连通性明显下降。在两个时间点,CPSP患者的双侧NAc均观察到灰质密度(GMD)降低和内侧间质萎缩。术后早期双侧NAc GMD和NAc外壳fALFF与随后的疼痛强度相关,并预测CPSP的发展具有很高的判别准确性,特别是当两者结合时。结论NAc结构和功能改变可作为CPSP易感性的神经成像生物标志物,揭示了情感失调和疼痛慢性化的统一神经生物学机制。在中国临床试验注册中心(https://www.chictr.org.cn/showproj.html?proj=131606)注册,注册号:ChiCTR2100049631,于2021年8月7日发布。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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