基于种子的静息状态连通性作为纤维肌痛和抑郁症的神经特征:叙述系统综述。

IF 2.4 3区 医学 Q3 NEUROSCIENCES
Frontiers in Human Neuroscience Pub Date : 2025-04-28 eCollection Date: 2025-01-01 DOI:10.3389/fnhum.2025.1548617
Betina Franceschini Tocchetto, Andrea Cristiane Janz Moreira, Álvaro de Oliveira Franco, Iraci L S Torres, Felipe Fregni, Wolnei Caumo
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引用次数: 0

摘要

背景:重度抑郁障碍(MDD)常与纤维肌痛(FM)共同发生,这两种情况都与静息状态功能连接受损(rs-FC)有关。本系统综述旨在总结与健康对照比较MDD和FM个体rs-FC的证据,并探讨重叠连接模式及其与临床症状的关系。方法:按照PRISMA指南系统检索EMBASE、PubMed、Scopus和ScienceDirect数据库。纳入了与HC相比,MDD和FM患者使用基于种子的分析来解决rs-FC的研究。方法学质量和偏倚风险的评估采用了13点检查表,该检查表改编自之前的神经影像学荟萃分析。结果:共纳入33篇文献(MDD 17篇,FM 16篇)。样本包括1877个人,包括947名患者和930名对照组,平均年龄为39.83岁。这些种子被分成6个神经网络。在MDD和FM研究中,在关键回路中发现了共同的中断,包括岛与前扣带皮层(ACC)、额叶中回(MFG)、额叶上回(SFG)和壳核之间的连通性下降。背外侧前额叶皮层(DLPFC)和ACC之间以及丘脑和楔前叶之间的FC增加。脑岛-前扣带连接减少与FM患者更大的疼痛强度和灾难化以及MDD患者更严重的抑郁症状相关。rs-FC的独特模式也被观察到:fm特异性的变化涉及到导水管周围灰质、下丘脑和丘脑,表明疼痛调节和情绪处理受损。相比之下,mdd特异性的变化主要在奖励、突出和默认模式网络中观察到,反映了受损的情绪调节。这些研究表明,在种子选择和研究设计方面存在相当大的异质性,这限制了meta分析的可行性,并强调了标准化方法的必要性。研究结果:该研究提供了FM和MDD中重叠和不同的神经机制的信息,表明潜在的潜在神经特征的存在,反映了疼痛和情绪调节网络的共同中断,同时突出了各自病理生理背后的独特途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Seed-based resting-state connectivity as a neurosignature in fibromyalgia and depression: a narrative systematic review.

Background: Major depressive disorder (MDD) often co-occur with fibromyalgia (FM), and both conditions have been associated with impaired resting state functional connectivity (rs-FC). The present systematic review aims to summarize the evidence on rs-FC in individuals with MDD and FM compared with healthy controls and explore overlapping connectivity patterns and their relationships with clinical symptoms.

Methods: A systematic search of the EMBASE, PubMed, Scopus and ScienceDirect databases was conducted according to PRISMA guidelines. Studies were included that addressed rs-FC using seed-based analysis in MDD and FM patients compared to HC. Methodological quality and risk of bias were assessed using a 13-point checklist adapted from previous neuroimaging meta-analyzes.

Results: A total of 33 articles were included in the analysis (17 with MDD and 16 with FM). The sample comprised 1,877 individuals, including 947 patients and 930 controls, with a mean age of 39.83 years. The seeds were categorized into six neural networks. Shared disruptions across MDD and FM studies have been identified in key circuits, including decreased connectivity between the insula and anterior cingulate cortex (ACC), middle frontal gyrus (MFG), superior frontal gyrus (SFG), and putamen. Increased FC was observed between the dorsolateral prefrontal cortex (DLPFC) and ACC, as well as between the thalamus and precuneus. Decreased insula-ACC connectivity correlated with greater pain intensity and catastrophizing in FM and with more severe depressive symptoms in MDD. Unique patterns of rs-FC were also observed: FM-specific changes involved the periaqueductal gray, hypothalamus, and thalamus, indicating impaired pain modulation and emotional processing. In contrast, MDD-specific changes were primarily observed in the reward, salience, and default mode networks, reflecting impaired emotional regulation. The studies showed considerable heterogeneity in the selection of seeds and study designs, which limits the feasibility of meta-analyses and underlines the need for standardized methods.

Findings: This study provides information about overlapping and distinct neural mechanisms in FM and MDD, suggesting potentially the presence of a potential neurosignature that reflects shared disruptions in pain and emotion regulation networks while highlighting unique pathways underlying their respective pathophysiology.

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来源期刊
Frontiers in Human Neuroscience
Frontiers in Human Neuroscience 医学-神经科学
CiteScore
4.70
自引率
6.90%
发文量
830
审稿时长
2-4 weeks
期刊介绍: Frontiers in Human Neuroscience is a first-tier electronic journal devoted to understanding the brain mechanisms supporting cognitive and social behavior in humans, and how these mechanisms might be altered in disease states. The last 25 years have seen an explosive growth in both the methods and the theoretical constructs available to study the human brain. Advances in electrophysiological, neuroimaging, neuropsychological, psychophysical, neuropharmacological and computational approaches have provided key insights into the mechanisms of a broad range of human behaviors in both health and disease. Work in human neuroscience ranges from the cognitive domain, including areas such as memory, attention, language and perception to the social domain, with this last subject addressing topics, such as interpersonal interactions, social discourse and emotional regulation. How these processes unfold during development, mature in adulthood and often decline in aging, and how they are altered in a host of developmental, neurological and psychiatric disorders, has become increasingly amenable to human neuroscience research approaches. Work in human neuroscience has influenced many areas of inquiry ranging from social and cognitive psychology to economics, law and public policy. Accordingly, our journal will provide a forum for human research spanning all areas of human cognitive, social, developmental and translational neuroscience using any research approach.
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