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海洛因使用障碍患者成瘾渴求的功能神经解剖:基于体素的功能磁共振成像(fMRI)药物线索反应性研究的荟萃分析。

Functional neuroanatomy of craving in heroin use disorder: voxel-based meta-analysis of functional magnetic resonance imaging (fMRI) drug cue reactivity studies.

机构信息

California School of Professional Psychology, Clinical Psychology PhD Program, San Diego, CA, USA.

Institute of Brain Research and Integrated Neuropsychological Services (iBRAINS.org), San Diego, CA, USA.

出版信息

Am J Drug Alcohol Abuse. 2023 Jul 4;49(4):418-430. doi: 10.1080/00952990.2023.2172423. Epub 2023 Mar 7.

Abstract

The neuroanatomy of craving, typically investigated using the functional magnetic resonance imaging (fMRI) drug cue reactivity (FDCR) paradigm, has been shown to involve the mesocorticolimbic, nigrostriatal, and corticocerebellar systems in several substances. However, the neuroanatomy of craving in heroin use disorder is still unclear. The current meta-analysis examines previous research on the neuroanatomy of craving in abstinent individuals with opioid use disorder (OUD). Seven databases were searched for studies comparing abstinent OUD versus healthy controls on drug > neutral contrast interaction at the whole-brain level. Voxel-based meta-analysis was performed using seed-based d mapping with permuted subject images (SDM-PSI). Thresholds were set at a family-wise error rate of less than 5% with the default pre-processing parameters of SDM-PSI. A total of 10 studies were included (296 OUD and 187 controls). Four hyperactivated clusters were identified with Hedge of peaks that ranged from 0.51 to 0.82. These peaks and their associated clusters correspond to the three systems identified in the previous literature: a) mesocorticolimbic, b) nigrostriatal, and c) corticocerebellar. There were also newly revealed hyperactivation regions including the bilateral cingulate, precuneus, fusiform gyrus, pons, lingual gyrus, and inferior occipital gyrus. The meta-analysis did not reveal areas of hypoactivation. Recommendations based on the functional neuroanatomical findings of this meta-analysis include pharmacological interventions such as buprenorphine/naloxone and cognitive-behavioral treatments such as cue-exposure combined with HRV biofeedback. In addition, research should utilize FDCR as pre- and post-measurement to determine the effectiveness and mechanism of action of such interventions.

摘要

成瘾的神经解剖结构,通常使用功能磁共振成像 (fMRI) 药物线索反应性 (FDCR) 范式进行研究,已被证明涉及几种物质的中脑边缘皮质、黑质纹状体和皮质小脑系统。然而,海洛因使用障碍患者的成瘾神经解剖结构仍不清楚。目前的荟萃分析检查了以前关于阿片类药物使用障碍 (OUD) 患者戒断后成瘾神经解剖结构的研究。在七个数据库中搜索了比较阿片类药物使用障碍患者与健康对照者在药物 > 中性对比交互作用的全脑水平的研究。使用基于种子的 d 映射和置换的受试者图像 (SDM-PSI) 进行基于体素的荟萃分析。使用 SDM-PSI 的默认预处理参数,将阈值设置为错误发现率小于 5%。共纳入 10 项研究 (296 例 OUD 和 187 例对照)。确定了四个超激活簇,峰值 Hedge 值范围为 0.51 至 0.82。这些峰值及其相关的簇与以前文献中确定的三个系统相对应:a) 中脑边缘皮质,b) 黑质纹状体,和 c) 皮质小脑。还有新发现的超激活区域,包括双侧扣带回、楔前叶、梭状回、脑桥、舌回和枕下回。荟萃分析未发现激活减少的区域。基于该荟萃分析的功能神经解剖学发现,建议进行药物干预,如丁丙诺啡/纳洛酮,以及认知行为治疗,如线索暴露结合 HRV 生物反馈。此外,研究应利用 FDCR 作为预测量和后测量,以确定这些干预措施的有效性和作用机制。

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