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重症新冠病毒肺炎会在人类大脑中引发衰老的分子特征。

Severe COVID-19 induces molecular signatures of aging in the human brain.

作者信息

Mavrikaki Maria, Lee Jonathan D, Solomon Isaac H, Slack Frank J

机构信息

Department of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.

These authors contributed equally: Maria Mavrikaki and Jonathan D. Lee.

出版信息

medRxiv. 2021 Nov 24:2021.11.24.21266779. doi: 10.1101/2021.11.24.21266779.

Abstract

Coronavirus disease 2019 (COVID-19) is predominantly an acute respiratory disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and remains a significant threat to public health. COVID-19 is accompanied by neurological symptoms and cognitive decline, but the molecular mechanisms underlying this effect remain unclear. As aging induces distinct molecular signatures in the brain associated with cognitive decline in healthy populations, we hypothesized that COVID-19 may induce molecular signatures of aging. Here, we performed whole transcriptomic analysis of human frontal cortex, a critical area for cognitive function, in 12 COVID-19 cases and age- and sex-matched uninfected controls. COVID-19 induces profound changes in gene expression, despite the absence of detectable virus in brain tissue. Pathway analysis shows downregulation of genes involved in synaptic function and cognition and upregulation of genes involved in immune processes. Comparison with five independent transcriptomic datasets of aging human frontal cortex reveals striking similarities between aged individuals and severe COVID-19 patients. Critically, individuals below 65 years of age exhibit profound transcriptomic changes not observed among older individuals in our patient cohort. Our data indicate that severe COVID-19 induces molecular signatures of aging in the human brain and emphasize the value of neurological follow-up in recovered individuals.

摘要

2019冠状病毒病(COVID-19)主要是一种由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的急性呼吸道疾病,仍然对公众健康构成重大威胁。COVID-19伴有神经症状和认知衰退,但其潜在的分子机制仍不清楚。由于衰老会在健康人群大脑中诱导与认知衰退相关的独特分子特征,我们推测COVID-19可能会诱导衰老的分子特征。在此,我们对12例COVID-19病例以及年龄和性别匹配的未感染对照的人类额叶皮质(认知功能的关键区域)进行了全转录组分析。尽管在脑组织中未检测到病毒,但COVID-19仍会诱导基因表达发生深刻变化。通路分析显示,参与突触功能和认知的基因下调,而参与免疫过程的基因上调。与五个独立的衰老人类额叶皮质转录组数据集进行比较后发现,老年个体与重症COVID-19患者之间存在惊人的相似之处。至关重要的是,在我们的患者队列中,65岁以下的个体表现出老年个体未观察到的深刻转录组变化。我们的数据表明,重症COVID-19会在人类大脑中诱导衰老的分子特征,并强调了对康复个体进行神经学随访的价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27e2/8629201/519a431a8c00/nihpp-2021.11.24.21266779v1-f0001.jpg

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