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Vascular Endothelial Glycocalyx Damage in COVID-19.

作者信息

Yamaoka-Tojo Minako

机构信息

Department of Rehabilitation/Regenerative Medicine and Cell Design Research Facility, Kitasato University School of Allied Health Sciences, Sagamihara 252-0373, Japan.

Department of Cardiovascular Medicine, Kitasato University Graduate School of Medical Sciences, Sagamihara 252-0373, Japan.

出版信息

Int J Mol Sci. 2020 Dec 19;21(24):9712. doi: 10.3390/ijms21249712.


DOI:10.3390/ijms21249712
PMID:33352699
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7766512/
Abstract

The new coronavirus disease-2019 (COVID-19), which is spreading around the world and threatening people, is easily infecting a large number of people through airborne droplets; moreover, patients with hypertension, diabetes, obesity, and cardiovascular disease are more likely to experience severe conditions. Vascular endothelial dysfunction has been suggested as a common feature of high-risk patients prone to severe COVID-19, and measurement of vascular endothelial function may be recommended for predicting severe conditions in high-risk patients with COVID-19. However, fragmented vascular endothelial glycocalyx (VEGLX) is elevated in COVID-19 patients, suggesting that it may be useful as a prognostic indicator. Although the relationship between VEGLX and severe acute respiratory syndrome coronavirus 2 infections has not been well studied, some investigations into COVID-19 have clarified the relationship between VEGLX and the mechanism that leads to severe conditions. Clarifying the usefulness of VEGLX assessment as a predictive indicator of the development of severe complications is important as a strategy for confronting pandemics caused by new viruses with a high affinity for the vascular endothelium that may recur in the future.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/91a533bd1959/ijms-21-09712-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/95d90e57062c/ijms-21-09712-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/c7884e91d17d/ijms-21-09712-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/ac4d2981c7c2/ijms-21-09712-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/4befd38c4311/ijms-21-09712-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/f2d87edb19ec/ijms-21-09712-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/e5556f797c9d/ijms-21-09712-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/5b44a9c7e183/ijms-21-09712-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/81ee9439bcd8/ijms-21-09712-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/f70b086db73a/ijms-21-09712-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/fde75b242887/ijms-21-09712-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/e0a1a7621543/ijms-21-09712-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/d06868840da5/ijms-21-09712-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/0f26a04f152d/ijms-21-09712-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/91a533bd1959/ijms-21-09712-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/95d90e57062c/ijms-21-09712-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/c7884e91d17d/ijms-21-09712-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/ac4d2981c7c2/ijms-21-09712-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/4befd38c4311/ijms-21-09712-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/f2d87edb19ec/ijms-21-09712-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/e5556f797c9d/ijms-21-09712-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/5b44a9c7e183/ijms-21-09712-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/81ee9439bcd8/ijms-21-09712-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/f70b086db73a/ijms-21-09712-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/fde75b242887/ijms-21-09712-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/e0a1a7621543/ijms-21-09712-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/d06868840da5/ijms-21-09712-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/0f26a04f152d/ijms-21-09712-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbe3/7766512/91a533bd1959/ijms-21-09712-g014.jpg

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本文引用的文献

[1]
Increased Plasma Heparanase Activity in COVID-19 Patients.

Front Immunol. 2020-10-6

[2]
Endothelial dysfunction contributes to COVID-19-associated vascular inflammation and coagulopathy.

Rev Cardiovasc Med. 2020-9-30

[3]
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Angiogenesis. 2021-2

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Endothelial glycocalyx damage as a systemic inflammatory microvascular endotheliopathy in COVID-19.

Biomed J. 2020-8-24

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Microcirculatory, Endothelial, and Inflammatory Responses in Critically Ill Patients With COVID-19 Are Distinct From Those Seen in Septic Shock: A Case Control Study.

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Common cardiovascular risk factors and in-hospital mortality in 3,894 patients with COVID-19: survival analysis and machine learning-based findings from the multicentre Italian CORIST Study.

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Vascular endothelial injury exacerbates coronavirus disease 2019: The role of endothelial glycocalyx protection.

Microcirculation. 2021-4

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Tobacco, but Not Nicotine and Flavor-Less Electronic Cigarettes, Induces ACE2 and Immune Dysregulation.

Int J Mol Sci. 2020-7-31

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