海洛因依赖个体的异常脑代谢和代谢连通性:大规模网络静息态PET/fMRI综合研究

IF 4.1 2区 医学 Q2 NEUROSCIENCES
Long Jin, Menghui Yuan, Jiajie Chen, Wei Zhang, Lei Wang, Yixin Wei, Yunbo Li, Zhirui Guo, Wei Wang, Longxiao Wei, Qiang Li
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引用次数: 0

摘要

背景:越来越多的证据表明,海洛因成瘾可能与脑三重网络(默认模式网络[DMN]、突出网络[SN]和执行控制网络[ECN])功能障碍有关。然而,三联脑网络核心区域之间的糖代谢特征和代谢连通性尚不清楚。因此,我们假设海洛因依赖个体会出现糖代谢异常,并伴随三联脑网络代谢连接异常。方法:对海洛因依赖者和年龄、性别相匹配的健康对照者进行正电子发射断层扫描/磁共振成像(PET/MRI)检查。基于18f -氟脱氧葡萄糖PET和静息状态fMRI数据,分析DMN、SN和ECN之间葡萄糖代谢和代谢连通性的差异。结果:我们纳入了36名海洛因依赖者和30名匹配的健康对照。海洛因依赖组双侧前叶(AI)和下顶叶(IPL)的糖代谢显著降低,右侧AI与左侧背外侧前额叶皮质(DLPFC)之间的代谢连性显著降低。每日美沙酮剂量与右侧AI和右侧IPL糖代谢呈负相关。局限性:研究结果显示,海洛因依赖者仅在三联脑网络内存在糖代谢改变和代谢连通性;在未来的研究中,应该对更多的大脑网络进行调查。虽然美沙酮是一种与海洛因具有相似神经生理机制的阿片类药物,但美沙酮对脑代谢和代谢连通性的特异性慢性影响还应在未来的研究中进一步研究。结论:长期使用阿片类药物可能在一定程度上与SN和ECN之间的协同能力降低有关,这可能与认知控制功能障碍有关。特别是右侧AI表现出代谢低下和相关的SN-ECN代谢连通性降低,在未来的研究中应该得到越来越多的关注。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Abnormal cerebral metabolism and metabolic connectivity in individuals with heroin dependence: an integrated resting-state PET/fMRI study in large-scale networks.

Abnormal cerebral metabolism and metabolic connectivity in individuals with heroin dependence: an integrated resting-state PET/fMRI study in large-scale networks.

Abnormal cerebral metabolism and metabolic connectivity in individuals with heroin dependence: an integrated resting-state PET/fMRI study in large-scale networks.

Abnormal cerebral metabolism and metabolic connectivity in individuals with heroin dependence: an integrated resting-state PET/fMRI study in large-scale networks.

Background: Increasing evidence suggests that heroin addiction may be related to the dysfunction among the triple brain network (default mode network [DMN], salience network [SN] and executive control network [ECN]). However, the characteristics of glucose metabolism and metabolic connectivity among core regions of the triple brain network remain unknown. Therefore, we hypothesized that individuals with heroin dependence would show abnormal glucose metabolism and accompanied abnormal metabolic connectivity within the triple brain network.

Methods: Individuals with heroin dependence and healthy controls matched for age and sex underwent integrated positron emission tomography/magnetic resonance imaging (PET/MRI). Differences in glucose metabolism and metabolic connectivity among the DMN, SN and ECN were analyzed based on 18F-fluorodeoxyglucose PET and resting-state fMRI data.

Results: We included 36 individuals with heroin dependence and 30 matched healthy controls in our study. The heroin dependence group showed a significant reduction of glucose metabolism in the bilateral anterior insula (AI) and inferior parietal lobule (IPL), and a significantly decreased metabolic connectivity between the right AI and the left dorsolateral prefrontal cortex (DLPFC). The daily dose of methadone was negatively correlated with glucose metabolism of the right AI and right IPL.

Limitations: The results revealed the glucose metabolism alterations and metabolic connectivity only within the triple brain network in individuals with heroin dependence; additional brain networks should be investigated in future studies. Although methadone is an opioid with a similar neurophysiological mechanism as heroin, the specific chronic effects of methadone on cerebral metabolism and metabolic connectivity should also be investigated in future studies.

Conclusion: Our findings suggest that long-term opioid use might, to some extent, be associated with reduced synergistic ability between the SN and ECN, which may be associated with the dysfunction of cognitive control. In particular, the right AI, which showed hypometabolism and related reduction in SN-ECN metabolic connectivity, should receive increasing attention in future studies.

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来源期刊
CiteScore
6.80
自引率
2.30%
发文量
51
审稿时长
2 months
期刊介绍: The Journal of Psychiatry & Neuroscience publishes papers at the intersection of psychiatry and neuroscience that advance our understanding of the neural mechanisms involved in the etiology and treatment of psychiatric disorders. This includes studies on patients with psychiatric disorders, healthy humans, and experimental animals as well as studies in vitro. Original research articles, including clinical trials with a mechanistic component, and review papers will be considered.
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