Persistent alterations in gray matter in COVID-19 patients experiencing sleep disturbances: a 3-month longitudinal study.

IF 5.9 2区 医学 Q2 CELL BIOLOGY Neural Regeneration Research Pub Date : 2025-10-01 Epub Date: 2024-06-26 DOI:10.4103/NRR.NRR-D-23-01651
Kaixuan Zhou, Gaoxiong Duan, Ying Liu, Bei Peng, Xiaoyan Zhou, Lixia Qin, Lingyan Liang, Yichen Wei, Qingping Zhang, Xiaocheng Li, Haixia Qin, Yinqi Lai, Yian Lu, Yan Zhang, Jiazhu Huang, Jinli Huang, Yinfei Ouyang, Bolin Bin, Mingming Zhao, Jun Liu, Jianrong Yang, Demao Deng
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Abstract

JOURNAL/nrgr/04.03/01300535-202510000-00030/figure1/v/2024-11-26T163120Z/r/image-tiff Sleep disturbances are among the most prevalent neuropsychiatric symptoms in individuals who have recovered from severe acute respiratory syndrome coronavirus 2 infections. Previous studies have demonstrated abnormal brain structures in patients with sleep disturbances who have recovered from coronavirus disease 2019 (COVID-19). However, neuroimaging studies on sleep disturbances caused by COVID-19 are scarce, and existing studies have primarily focused on the long-term effects of the virus, with minimal acute phase data. As a result, little is known about the pathophysiology of sleep disturbances in the acute phase of COVID-19. To address this issue, we designed a longitudinal study to investigate whether alterations in brain structure occur during the acute phase of infection, and verified the results using 3-month follow-up data. A total of 26 COVID-19 patients with sleep disturbances (aged 51.5 ± 13.57 years, 8 women and 18 men), 27 COVID-19 patients without sleep disturbances (aged 47.33 ± 15.98 years, 9 women and 18 men), and 31 age- and gender-matched healthy controls (aged 49.19 ± 17.51 years, 9 women and 22 men) were included in this study. Eleven COVID-19 patients with sleep disturbances were included in a longitudinal analysis. We found that COVID-19 patients with sleep disturbances exhibited brain structural changes in almost all brain lobes. The cortical thicknesses of the left pars opercularis and left precuneus were significantly negatively correlated with Pittsburgh Sleep Quality Index scores. Additionally, we observed changes in the volume of the hippocampus and its subfield regions in COVID-19 patients compared with the healthy controls. The 3-month follow-up data revealed indices of altered cerebral structure (cortical thickness, cortical grey matter volume, and cortical surface area) in the frontal-parietal cortex compared with the baseline in COVID-19 patients with sleep disturbances. Our findings indicate that the sleep disturbances patients had altered morphology in the cortical and hippocampal structures during the acute phase of infection and persistent changes in cortical regions at 3 months post-infection. These data improve our understanding of the pathophysiology of sleep disturbances caused by COVID-19.

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COVID-19 睡眠障碍患者灰质的持续改变:一项为期 3 个月的纵向研究。
摘要:睡眠障碍是严重急性呼吸系统综合征冠状病毒2型感染康复者最常见的神经精神症状之一。以往的研究表明,2019 年冠状病毒病(COVID-19)康复后的睡眠障碍患者大脑结构异常。然而,有关 COVID-19 引起的睡眠障碍的神经影像学研究很少,现有研究主要集中于病毒的长期影响,急性期数据极少。因此,人们对 COVID-19 急性期睡眠障碍的病理生理学知之甚少。为了解决这个问题,我们设计了一项纵向研究,以调查在感染的急性期是否会出现大脑结构的改变,并利用 3 个月的随访数据对结果进行验证。本研究共纳入了 26 名有睡眠障碍的 COVID-19 患者(年龄为 51.5 ± 13.57 岁,8 名女性和 18 名男性)、27 名无睡眠障碍的 COVID-19 患者(年龄为 47.33 ± 15.98 岁,9 名女性和 18 名男性)以及 31 名年龄与性别匹配的健康对照组(年龄为 49.19 ± 17.51 岁,9 名女性和 22 名男性)。11名患有睡眠障碍的 COVID-19 患者被纳入纵向分析。我们发现,COVID-19 睡眠障碍患者几乎所有脑叶的大脑结构都发生了变化。左侧小脑旁和左侧楔前叶的皮质厚度与匹兹堡睡眠质量指数评分呈显著负相关。此外,我们还观察到,与健康对照组相比,COVID-19 患者的海马及其子场区的体积发生了变化。3个月的随访数据显示,与基线相比,COVID-19睡眠障碍患者额顶叶皮层的大脑结构(皮层厚度、皮层灰质体积和皮层表面积)发生了改变。这些数据加深了我们对COVID-19引起的睡眠障碍的病理生理学的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neural Regeneration Research
Neural Regeneration Research CELL BIOLOGY-NEUROSCIENCES
CiteScore
8.00
自引率
9.80%
发文量
515
审稿时长
1.0 months
期刊介绍: Neural Regeneration Research (NRR) is the Open Access journal specializing in neural regeneration and indexed by SCI-E and PubMed. The journal is committed to publishing articles on basic pathobiology of injury, repair and protection to the nervous system, while considering preclinical and clinical trials targeted at improving traumatically injuried patients and patients with neurodegenerative diseases.
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