Wang Tongtong, Jackson Todd, Lock Matthew, Li Hui, Yan Jin, Zhuang Qian, Chen Shuaiyu
Center for Cognition and Brain Disorders, The Affiliated Hospital of Hangzhou Normal University, Hangzhou, Zhejiang, China.
Department of Psychology, University of Macau, Macau, Macao SAR, China.
Front Nutr. 2025 May 29;12:1559325. doi: 10.3389/fnut.2025.1559325. eCollection 2025.
Obesity, particularly in high-risk groups for food addiction, adversely impacts the brain's functional characteristics. However, its underlying neurobiological and molecular mechanisms remain elusive. The current study adopted a data-driven approach to investigate obesity-associated intrinsic functional architecture and neurotransmitter receptor patterns.
Resting-state fMRI data were acquired from 198 obese and 291 healthy weight individuals from the Human Connectome Project. Intrinsic connectivity contrast (ICC) and fractional amplitude of low-frequency fluctuations (fALFF) analyses were performed to identify the common altered brain regions and then seeds to whole brain functional connectivity (FC) analyses were conducted to determine obesity-related FC features. Additionally, the relationship between intrinsic functional characteristics and molecular imaging features was assessed to examine neurotransmitter-receptor distribution patterns underlying obesity.
Obese individuals, compared to healthy weight individuals, showed aberrant ICC and fALFF in both the right dorsolateral prefrontal cortex (DLPFC) and left insula. For the FC results, the obese group displayed increased FC between the right DLPFC and precuneus, left insula and left inferior parietal lobule, right DLPFC as well as decreased FC between right DLPFC and left precentral, left postcentral gyrus, and bilateral paracentral lobule. Additionally, the fALFF alterations in insula/temploral pole and also the rDLPFC-PCL FC partially mediated the relationship between body mass index and the executive function. Furthermore, cross-modal correlation analyses indicated that ICC and fALFF alterations were related to noradrenaline transporter and dopamine receptor distributions, respectively.
Together our findings suggested that obesity is associated with atypical neurotransmitter systems and dysfunctional architecture especially in the prefrontal cortex, insula, sensorimotor cortex, and default mode circuits. These may deepen our understanding the neurobiological basis of obesity and provide novel insights into neuroimaging-based treatment and intervention.
肥胖,尤其是在食物成瘾高危人群中,会对大脑的功能特征产生不利影响。然而,其潜在的神经生物学和分子机制仍不清楚。本研究采用数据驱动方法来探究与肥胖相关的内在功能结构和神经递质受体模式。
从人类连接组计划中获取了198名肥胖个体和291名健康体重个体的静息态功能磁共振成像数据。进行内在连接性对比(ICC)和低频波动分数幅值(fALFF)分析以识别常见的脑区改变,然后进行种子到全脑功能连接(FC)分析以确定与肥胖相关的FC特征。此外,评估了内在功能特征与分子成像特征之间的关系,以检查肥胖背后的神经递质 - 受体分布模式。
与健康体重个体相比,肥胖个体在右侧背外侧前额叶皮质(DLPFC)和左侧脑岛均表现出异常的ICC和fALFF。对于FC结果,肥胖组在右侧DLPFC与楔前叶、左侧脑岛和左侧顶下小叶、右侧DLPFC之间显示出增强的FC,而在右侧DLPFC与左侧中央前回、左侧中央后回以及双侧旁中央小叶之间显示出减弱的FC。此外,脑岛/颞极的fALFF改变以及右侧DLPFC - 楔前叶的FC部分介导了体重指数与执行功能之间的关系。此外,跨模态相关性分析表明,ICC和fALFF改变分别与去甲肾上腺素转运体和多巴胺受体分布有关。
我们的研究结果共同表明,肥胖与非典型神经递质系统和功能失调的结构有关,尤其是在前额叶皮质、脑岛、感觉运动皮质和默认模式回路中。这些可能会加深我们对肥胖神经生物学基础的理解,并为基于神经影像学的治疗和干预提供新的见解。