Douaud Gwenaëlle, Lee Soojin, Alfaro-Almagro Fidel, Arthofer Christoph, Wang Chaoyue, McCarthy Paul, Lange Frederik, Andersson Jesper L R, Griffanti Ludovica, Duff Eugene, Jbabdi Saad, Taschler Bernd, Keating Peter, Winkler Anderson M, Collins Rory, Matthews Paul M, Allen Naomi, Miller Karla L, Nichols Thomas E, Smith Stephen M
medRxiv. 2022 Mar 2:2021.06.11.21258690. doi: 10.1101/2021.06.11.21258690.
There is strong evidence for brain-related abnormalities in COVID-19 . It remains unknown however whether the impact of SARS-CoV-2 infection can be detected in milder cases, and whether this can reveal possible mechanisms contributing to brain pathology. Here, we investigated brain changes in 785 UK Biobank participants (aged 51-81) imaged twice, including 401 cases who tested positive for infection with SARS-CoV-2 between their two scans, with 141 days on average separating their diagnosis and second scan, and 384 controls. The availability of pre-infection imaging data reduces the likelihood of pre-existing risk factors being misinterpreted as disease effects. We identified significant longitudinal effects when comparing the two groups, including: (i) greater reduction in grey matter thickness and tissue-contrast in the orbitofrontal cortex and parahippocampal gyrus, (ii) greater changes in markers of tissue damage in regions functionally-connected to the primary olfactory cortex, and (iii) greater reduction in global brain size. The infected participants also showed on average larger cognitive decline between the two timepoints. Importantly, these imaging and cognitive longitudinal effects were still seen after excluding the 15 cases who had been hospitalised. These mainly limbic brain imaging results may be the in vivo hallmarks of a degenerative spread of the disease via olfactory pathways, of neuroinflammatory events, or of the loss of sensory input due to anosmia. Whether this deleterious impact can be partially reversed, or whether these effects will persist in the long term, remains to be investigated with additional follow up.
有强有力的证据表明新冠病毒感染存在与大脑相关的异常情况。然而,在症状较轻的病例中是否能检测到严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染的影响,以及这是否能揭示导致脑部病变的可能机制,目前仍不清楚。在此,我们对英国生物银行的785名参与者(年龄在51 - 81岁之间)进行了脑部变化调查,这些参与者接受了两次成像扫描,其中包括401例在两次扫描期间检测出SARS-CoV-2感染呈阳性的病例,其诊断与第二次扫描之间平均间隔141天,还有384名对照者。感染前成像数据的可用性降低了将预先存在的风险因素误解为疾病影响的可能性。在比较两组时,我们发现了显著的纵向影响,包括:(i)眶额皮质和海马旁回的灰质厚度和组织对比度有更大程度的降低;(ii)与初级嗅觉皮质功能相连区域的组织损伤标志物有更大变化;(iii)全脑体积有更大程度的减小。受感染的参与者在两个时间点之间平均还表现出更大的认知能力下降。重要的是,在排除15例曾住院的病例后,这些成像和认知方面的纵向影响仍然存在。这些主要涉及边缘系统的脑部成像结果可能是该疾病通过嗅觉途径发生退行性传播、神经炎症事件或因嗅觉丧失导致感觉输入缺失在体内的标志。这种有害影响是否能部分逆转,或者这些影响是否会长期持续,仍有待通过进一步随访进行研究。