Altered connectivity patterns of medial and lateral orbitofrontal cortex underlie the severity of bulimic symptoms

被引:3
作者
Li, Wei [1 ,2 ]
Chen, Ximei [1 ,2 ]
Luo, Yijun [1 ,2 ]
Xiao, Mingyue [1 ,2 ]
Liu, Yong [1 ,2 ]
Chen, Hong [1 ,2 ,3 ,4 ]
机构
[1] Southwest Univ, Fac Psychol, Key Lab Cognit & Personal, Minist Educ, Chongqing 400715, Peoples R China
[2] Southwest Univ, Fac Psychol, Chongqing 400715, Peoples R China
[3] Southwest Univ, Fac Psychol, Res Ctr Psychol & Social Dev, Chongqing 400715, Peoples R China
[4] Southwest Univ, Fac Psychol, 2 Tiansheng Rd, Chongqing 400715, Peoples R China
关键词
Bulimia navosa; Orbitofrontal cortex; Functional connectivity; Effective connectivity; Spectral dynamic casual modeling; EATING-DISORDER SYMPTOMS; FUNCTIONAL CONNECTIVITY; FOOD-INTAKE; REWARD; ADOLESCENTS; IMPULSIVITY; PREVALENCE; RESPONSES; NETWORKS; ANOREXIA;
D O I
10.1016/j.ijchp.2024.100439
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Objective: Compared to clinical bulimia nervosa, sub-threshold bulimic symptoms are becoming more prevalent in non-clinical or general population, which is repeatedly linked with the connectivity in orbitofrontal cortex (OFC), including functionally heterogeneous the medial and lateral OFC (mOFC; lOFC). However, the specific connectivity patterns of the mOFC and lOFC in individuals with severe or mild bulimic symptoms (SB; MB) remain poorly understood. Methods: We first utilized resting-state functional connectivity (FC) and spectral dynamic causal modeling (spDCM) to investigate abnormal functional and effective connectivity (EC) of OFC subregions in adults with different severity of bulimic. The SB group (n = 21), MB group (n = 114), and healthy controls (HC, n = 91) underwent rs-fMRI scans. A generalized linear model was applied to determine the OFC-seeded whole-brain FC across the three groups. Subsequently, spDCM was used to estimate differences in EC among the three groups based on the FC results. Results: We observed a shared neural basis for SB and MB groups (i.e., weaker lOFC-superior parietal lobule connectivity), which may support the role of dysfunctional inhibitory control in general bulimic symptomatology. Whereas, SB group displayed greater lOFC-occipital pole connectivity than MB group, suggesting the specificity of the neural correlates of full-threshold/severe bulimia. The directional links from the mOFC to lOFC and amygdala could further explain the aberrant interactions of reward sensitivity with inhibitory control and homeostatic energy in sub-threshold/mild condition. Conclusion: The current study provides novel evidence that divergent connectivity patterns of the lOFC and mOFC may contribute to different severities of bulimia, which will expands our understanding of the neurobiological substrates underlying bulimia across a spectrum from healthy to unhealthy.
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页数:10
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