Long-term microstructure and cerebral blood flow changes in patients recovered from COVID-19 without neurological manifestations

BACKGROUNDThe coronavirus disease 2019 (COVID-19) rapidly progressed to a global pandemic. Although some patients totally recover from COVID-19 pneumonia, the disease's long-term effects on the brain still need to be explored.METHODSWe recruited 51 patients with 2 subtypes of COVID-19 (19 mild...

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Veröffentlicht in:The Journal of clinical investigation 2021-04, Vol.131 (8)
Hauptverfasser: Qin, Yuanyuan, Wu, Jinfeng, Chen, Tao, Li, Jia, Zhang, Guiling, Wu, Di, Zhou, Yiran, Zheng, Ning, Cai, Aoling, Ning, Qin, Manyande, Anne, Xu, Fuqiang, Wang, Jie, Zhu, Wenzhen
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container_issue 8
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container_title The Journal of clinical investigation
container_volume 131
creator Qin, Yuanyuan
Wu, Jinfeng
Chen, Tao
Li, Jia
Zhang, Guiling
Wu, Di
Zhou, Yiran
Zheng, Ning
Cai, Aoling
Ning, Qin
Manyande, Anne
Xu, Fuqiang
Wang, Jie
Zhu, Wenzhen
description BACKGROUNDThe coronavirus disease 2019 (COVID-19) rapidly progressed to a global pandemic. Although some patients totally recover from COVID-19 pneumonia, the disease's long-term effects on the brain still need to be explored.METHODSWe recruited 51 patients with 2 subtypes of COVID-19 (19 mild and 32 severe) with no specific neurological manifestations at the acute stage and no obvious lesions on the conventional MRI 3 months after discharge. Changes in gray matter morphometry, cerebral blood flow (CBF), and white matter (WM) microstructure were investigated using MRI. The relationship between brain imaging measurements and inflammation markers was further analyzed.RESULTSCompared with healthy controls, the decrease in cortical thickness/CBF and the changes in WM microstructure were more severe in patients with severe disease than in those with mild disease, especially in the frontal and limbic systems. Furthermore, changes in brain microstructure, CBF, and tract parameters were significantly correlated (P < 0.05) with the inflammatory markers C-reactive protein, procalcitonin, and interleukin 6.CONCLUSIONIndirect injury related to inflammatory storm may damage the brain, altering cerebral volume, CBF, and WM tracts. COVID-19-related hypoxemia and dysfunction of vascular endothelium may also contribute to neurological changes. The abnormalities in these brain areas need to be monitored during recovery, which could help clinicians understand the potential neurological sequelae of COVID-19.FUNDINGNatural Science Foundation of China.
doi_str_mv 10.1172/JCI147329
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Although some patients totally recover from COVID-19 pneumonia, the disease's long-term effects on the brain still need to be explored.METHODSWe recruited 51 patients with 2 subtypes of COVID-19 (19 mild and 32 severe) with no specific neurological manifestations at the acute stage and no obvious lesions on the conventional MRI 3 months after discharge. Changes in gray matter morphometry, cerebral blood flow (CBF), and white matter (WM) microstructure were investigated using MRI. The relationship between brain imaging measurements and inflammation markers was further analyzed.RESULTSCompared with healthy controls, the decrease in cortical thickness/CBF and the changes in WM microstructure were more severe in patients with severe disease than in those with mild disease, especially in the frontal and limbic systems. Furthermore, changes in brain microstructure, CBF, and tract parameters were significantly correlated (P &lt; 0.05) with the inflammatory markers C-reactive protein, procalcitonin, and interleukin 6.CONCLUSIONIndirect injury related to inflammatory storm may damage the brain, altering cerebral volume, CBF, and WM tracts. COVID-19-related hypoxemia and dysfunction of vascular endothelium may also contribute to neurological changes. The abnormalities in these brain areas need to be monitored during recovery, which could help clinicians understand the potential neurological sequelae of COVID-19.FUNDINGNatural Science Foundation of China.</description><identifier>ISSN: 0021-9738</identifier><identifier>EISSN: 1558-8238</identifier><identifier>DOI: 10.1172/JCI147329</identifier><identifier>PMID: 33630760</identifier><language>eng</language><publisher>United States: American Society for Clinical Investigation</publisher><subject>Aged ; Blood flow ; Brain - blood supply ; Brain - diagnostic imaging ; Brain - pathology ; C-Reactive Protein - metabolism ; Case-Control Studies ; Cerebrovascular Circulation - physiology ; China - epidemiology ; Clinical Medicine ; COVID-19 - diagnostic imaging ; COVID-19 - epidemiology ; COVID-19 - physiopathology ; Diffusion Tensor Imaging ; Echo-Planar Imaging ; Evaluation ; Female ; Follow-Up Studies ; Gray Matter - diagnostic imaging ; Gray Matter - pathology ; Health aspects ; Humans ; Imaging, Three-Dimensional ; Inflammation Mediators - blood ; Interleukin-6 - blood ; Male ; Middle Aged ; Neuroimaging ; Pandemics ; Procalcitonin - blood ; Prognosis ; SARS-CoV-2 ; Severity of Illness Index ; Time Factors ; White Matter - diagnostic imaging ; White Matter - pathology</subject><ispartof>The Journal of clinical investigation, 2021-04, Vol.131 (8)</ispartof><rights>COPYRIGHT 2021 American Society for Clinical Investigation</rights><rights>2021 American Society for Clinical Investigation 2021 American Society for Clinical Investigation</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c406t-4255e82ef4711c91de4d3fbf96748d7aeea70047b82a65a275f8b0ead14316f83</citedby><cites>FETCH-LOGICAL-c406t-4255e82ef4711c91de4d3fbf96748d7aeea70047b82a65a275f8b0ead14316f83</cites><orcidid>0000-0002-0673-3200</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8262559/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8262559/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33630760$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Qin, Yuanyuan</creatorcontrib><creatorcontrib>Wu, Jinfeng</creatorcontrib><creatorcontrib>Chen, Tao</creatorcontrib><creatorcontrib>Li, Jia</creatorcontrib><creatorcontrib>Zhang, Guiling</creatorcontrib><creatorcontrib>Wu, Di</creatorcontrib><creatorcontrib>Zhou, Yiran</creatorcontrib><creatorcontrib>Zheng, Ning</creatorcontrib><creatorcontrib>Cai, Aoling</creatorcontrib><creatorcontrib>Ning, Qin</creatorcontrib><creatorcontrib>Manyande, Anne</creatorcontrib><creatorcontrib>Xu, Fuqiang</creatorcontrib><creatorcontrib>Wang, Jie</creatorcontrib><creatorcontrib>Zhu, Wenzhen</creatorcontrib><title>Long-term microstructure and cerebral blood flow changes in patients recovered from COVID-19 without neurological manifestations</title><title>The Journal of clinical investigation</title><addtitle>J Clin Invest</addtitle><description>BACKGROUNDThe coronavirus disease 2019 (COVID-19) rapidly progressed to a global pandemic. Although some patients totally recover from COVID-19 pneumonia, the disease's long-term effects on the brain still need to be explored.METHODSWe recruited 51 patients with 2 subtypes of COVID-19 (19 mild and 32 severe) with no specific neurological manifestations at the acute stage and no obvious lesions on the conventional MRI 3 months after discharge. Changes in gray matter morphometry, cerebral blood flow (CBF), and white matter (WM) microstructure were investigated using MRI. The relationship between brain imaging measurements and inflammation markers was further analyzed.RESULTSCompared with healthy controls, the decrease in cortical thickness/CBF and the changes in WM microstructure were more severe in patients with severe disease than in those with mild disease, especially in the frontal and limbic systems. Furthermore, changes in brain microstructure, CBF, and tract parameters were significantly correlated (P &lt; 0.05) with the inflammatory markers C-reactive protein, procalcitonin, and interleukin 6.CONCLUSIONIndirect injury related to inflammatory storm may damage the brain, altering cerebral volume, CBF, and WM tracts. COVID-19-related hypoxemia and dysfunction of vascular endothelium may also contribute to neurological changes. The abnormalities in these brain areas need to be monitored during recovery, which could help clinicians understand the potential neurological sequelae of COVID-19.FUNDINGNatural Science Foundation of China.</description><subject>Aged</subject><subject>Blood flow</subject><subject>Brain - blood supply</subject><subject>Brain - diagnostic imaging</subject><subject>Brain - pathology</subject><subject>C-Reactive Protein - metabolism</subject><subject>Case-Control Studies</subject><subject>Cerebrovascular Circulation - physiology</subject><subject>China - epidemiology</subject><subject>Clinical Medicine</subject><subject>COVID-19 - diagnostic imaging</subject><subject>COVID-19 - epidemiology</subject><subject>COVID-19 - physiopathology</subject><subject>Diffusion Tensor Imaging</subject><subject>Echo-Planar Imaging</subject><subject>Evaluation</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Gray Matter - diagnostic imaging</subject><subject>Gray Matter - pathology</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Imaging, Three-Dimensional</subject><subject>Inflammation Mediators - blood</subject><subject>Interleukin-6 - blood</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neuroimaging</subject><subject>Pandemics</subject><subject>Procalcitonin - blood</subject><subject>Prognosis</subject><subject>SARS-CoV-2</subject><subject>Severity of Illness Index</subject><subject>Time Factors</subject><subject>White Matter - diagnostic imaging</subject><subject>White Matter - pathology</subject><issn>0021-9738</issn><issn>1558-8238</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkTuP1DAUhSMEYoeFgj-AXKGlCPgZ2w3SangNGmkboLWc5OaBHHuwnV3R8dPxMMsIqlv487nn3FNVzwl-TYikbz5vd4RLRvWDakOEULWiTD2sNhhTUmvJ1EX1JKXvGBPOBX9cXTDWMCwbvKl-7YMf6wxxQcvcxZByXLu8RkDW96iDCG20DrUuhB4NLtyhbrJ-hIRmjw42z-BzQhG6cFvYgsSwoO3Nt927mmh0N-cprBl5WGNwYZy7orVYPw-QcvkcfHpaPRqsS_Dsfl5WXz-8_7L9VO9vPu621_u647jJNadCgKIwcElIp0kPvGdDO-hGctVLC2Alxly2itpGWCrFoFoMtieckWZQ7LJ6e9I9rO0CfVd8l2DmEOfFxp8m2Nn8_-LnyYzh1ijalN26CFzdC8TwYy3-zTKnDpyzHsKaDOWaUy2pPqIvT-hoHZgJrMtTCm79E9hcN0JToQQTBXx1Ao-XTxGGsx-CzbFac662sC_-DXAm_3bJfgOQiaEL</recordid><startdate>20210415</startdate><enddate>20210415</enddate><creator>Qin, Yuanyuan</creator><creator>Wu, Jinfeng</creator><creator>Chen, Tao</creator><creator>Li, Jia</creator><creator>Zhang, Guiling</creator><creator>Wu, Di</creator><creator>Zhou, Yiran</creator><creator>Zheng, Ning</creator><creator>Cai, Aoling</creator><creator>Ning, Qin</creator><creator>Manyande, Anne</creator><creator>Xu, Fuqiang</creator><creator>Wang, Jie</creator><creator>Zhu, Wenzhen</creator><general>American Society for Clinical Investigation</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-0673-3200</orcidid></search><sort><creationdate>20210415</creationdate><title>Long-term microstructure and cerebral blood flow changes in patients recovered from COVID-19 without neurological manifestations</title><author>Qin, Yuanyuan ; Wu, Jinfeng ; Chen, Tao ; Li, Jia ; Zhang, Guiling ; Wu, Di ; Zhou, Yiran ; Zheng, Ning ; Cai, Aoling ; Ning, Qin ; Manyande, Anne ; Xu, Fuqiang ; Wang, Jie ; Zhu, Wenzhen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c406t-4255e82ef4711c91de4d3fbf96748d7aeea70047b82a65a275f8b0ead14316f83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Aged</topic><topic>Blood flow</topic><topic>Brain - blood supply</topic><topic>Brain - diagnostic imaging</topic><topic>Brain - pathology</topic><topic>C-Reactive Protein - metabolism</topic><topic>Case-Control Studies</topic><topic>Cerebrovascular Circulation - physiology</topic><topic>China - epidemiology</topic><topic>Clinical Medicine</topic><topic>COVID-19 - diagnostic imaging</topic><topic>COVID-19 - epidemiology</topic><topic>COVID-19 - physiopathology</topic><topic>Diffusion Tensor Imaging</topic><topic>Echo-Planar Imaging</topic><topic>Evaluation</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Gray Matter - diagnostic imaging</topic><topic>Gray Matter - pathology</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Imaging, Three-Dimensional</topic><topic>Inflammation Mediators - blood</topic><topic>Interleukin-6 - blood</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neuroimaging</topic><topic>Pandemics</topic><topic>Procalcitonin - blood</topic><topic>Prognosis</topic><topic>SARS-CoV-2</topic><topic>Severity of Illness Index</topic><topic>Time Factors</topic><topic>White Matter - diagnostic imaging</topic><topic>White Matter - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Qin, Yuanyuan</creatorcontrib><creatorcontrib>Wu, Jinfeng</creatorcontrib><creatorcontrib>Chen, Tao</creatorcontrib><creatorcontrib>Li, Jia</creatorcontrib><creatorcontrib>Zhang, Guiling</creatorcontrib><creatorcontrib>Wu, Di</creatorcontrib><creatorcontrib>Zhou, Yiran</creatorcontrib><creatorcontrib>Zheng, Ning</creatorcontrib><creatorcontrib>Cai, Aoling</creatorcontrib><creatorcontrib>Ning, Qin</creatorcontrib><creatorcontrib>Manyande, Anne</creatorcontrib><creatorcontrib>Xu, Fuqiang</creatorcontrib><creatorcontrib>Wang, Jie</creatorcontrib><creatorcontrib>Zhu, Wenzhen</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of clinical investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Qin, Yuanyuan</au><au>Wu, Jinfeng</au><au>Chen, Tao</au><au>Li, Jia</au><au>Zhang, Guiling</au><au>Wu, Di</au><au>Zhou, Yiran</au><au>Zheng, Ning</au><au>Cai, Aoling</au><au>Ning, Qin</au><au>Manyande, Anne</au><au>Xu, Fuqiang</au><au>Wang, Jie</au><au>Zhu, Wenzhen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long-term microstructure and cerebral blood flow changes in patients recovered from COVID-19 without neurological manifestations</atitle><jtitle>The Journal of clinical investigation</jtitle><addtitle>J Clin Invest</addtitle><date>2021-04-15</date><risdate>2021</risdate><volume>131</volume><issue>8</issue><issn>0021-9738</issn><eissn>1558-8238</eissn><abstract>BACKGROUNDThe coronavirus disease 2019 (COVID-19) rapidly progressed to a global pandemic. Although some patients totally recover from COVID-19 pneumonia, the disease's long-term effects on the brain still need to be explored.METHODSWe recruited 51 patients with 2 subtypes of COVID-19 (19 mild and 32 severe) with no specific neurological manifestations at the acute stage and no obvious lesions on the conventional MRI 3 months after discharge. Changes in gray matter morphometry, cerebral blood flow (CBF), and white matter (WM) microstructure were investigated using MRI. The relationship between brain imaging measurements and inflammation markers was further analyzed.RESULTSCompared with healthy controls, the decrease in cortical thickness/CBF and the changes in WM microstructure were more severe in patients with severe disease than in those with mild disease, especially in the frontal and limbic systems. Furthermore, changes in brain microstructure, CBF, and tract parameters were significantly correlated (P &lt; 0.05) with the inflammatory markers C-reactive protein, procalcitonin, and interleukin 6.CONCLUSIONIndirect injury related to inflammatory storm may damage the brain, altering cerebral volume, CBF, and WM tracts. COVID-19-related hypoxemia and dysfunction of vascular endothelium may also contribute to neurological changes. The abnormalities in these brain areas need to be monitored during recovery, which could help clinicians understand the potential neurological sequelae of COVID-19.FUNDINGNatural Science Foundation of China.</abstract><cop>United States</cop><pub>American Society for Clinical Investigation</pub><pmid>33630760</pmid><doi>10.1172/JCI147329</doi><orcidid>https://orcid.org/0000-0002-0673-3200</orcidid><oa>free_for_read</oa></addata></record>
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subjects Aged
Blood flow
Brain - blood supply
Brain - diagnostic imaging
Brain - pathology
C-Reactive Protein - metabolism
Case-Control Studies
Cerebrovascular Circulation - physiology
China - epidemiology
Clinical Medicine
COVID-19 - diagnostic imaging
COVID-19 - epidemiology
COVID-19 - physiopathology
Diffusion Tensor Imaging
Echo-Planar Imaging
Evaluation
Female
Follow-Up Studies
Gray Matter - diagnostic imaging
Gray Matter - pathology
Health aspects
Humans
Imaging, Three-Dimensional
Inflammation Mediators - blood
Interleukin-6 - blood
Male
Middle Aged
Neuroimaging
Pandemics
Procalcitonin - blood
Prognosis
SARS-CoV-2
Severity of Illness Index
Time Factors
White Matter - diagnostic imaging
White Matter - pathology
title Long-term microstructure and cerebral blood flow changes in patients recovered from COVID-19 without neurological manifestations
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