The Abnormal Functional Connectivity in the Locus Coeruleus-Norepinephrine System Associated With Anxiety Symptom in Chronic Insomnia Disorder

• Published in: Frontiers in neuroscience Vol. 15; p. 678465
• Main Authors: Gong, Liang, Shi, Min, Wang, Jian, Xu, Ronghua, Yu, Siyi, Liu, Duan, Ding, Xin, Zhang, Bei, Zhang, Xingping, Xi, Chunhua
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Research Foundation 21.05.2021; Frontiers Media S.A
• Subjects: Alzheimer's disease; anterior cingulate cortex; Anxiety; Caffeine; Comorbidity; Cortex (cingulate); Cortex (frontal); Frontal gyrus; functional connectivity; Functional magnetic resonance imaging; Insomnia; locus ceruleus-norepinephrine; Locus coeruleus; Medical imaging; Mental depression; Neural networks; Neuroscience; Norepinephrine; Oligodendrocyte-myelin glycoprotein; Patients; Sleep; Sleep and wakefulness; Sleep disorders; Somatosensory cortex; Time series; locus ceruleus-norepinephrine; anxiety; functional connectivity; anterior cingulate cortex; insomnia
• ISSN: 1662-453X; 1662-4548; 1662-453X
• DOI: 10.3389/fnins.2021.678465

Mental syndromes such as anxiety and depression are common comorbidities in patients with chronic insomnia disorder (CID). The locus coeruleus noradrenergic (LC-NE) system is considered to be crucial for modulation of emotion and sleep/wake cycle. LC-NE system is also a critical mediator of the stress-induced anxiety. However, whether the LC-NE system contributes to the underlying mechanism linking insomnia and these comorbidities remain unclear. This study aimed to investigate the LC-NE system alterations in patients with insomnia and its relationship with depression and anxiety symptoms. Seventy patients with CID and 63 matched good sleep control (GSC) subjects were recruited and underwent resting-state functional MRI scan. LC-NE functional network was constructed by using seed-based functional connectivity (FC) analysis. The alterations in LC-NE FC network in patients with CID and their clinical significance was explored. Compared with GSC group, the CID group showed decreased left LC-NE FC in the left inferior frontal gyrus, while they had increased LC-NE FC in the left supramarginal gyrus and the left middle occipital gyrus (MOG). For the right LC-NE FC network, decreased FC was found in left dorsal anterior cingulate cortex (dACC). Interesting, the increased LC-NE FC was located in sensory cortex, while decreased LC-NE FC was located in frontal control cortex. In addition, the FC between the left LC and left MOG was associated with the duration of the disease, while abnormal FC between right LC and left dACC was associated with the anxiety scores in patients with CID. The present study found abnormal LC-NE functional network in patients with CID, and the altered LC-NE function in dACC was associated with anxiety symptoms in CID. The present study substantially extended our understanding of the neuropathological basis of CID and provided the potential treatment target for CID patients who also had anxiety.