Association of coagulopathy with liver dysfunction in patients with COVID‐19
Aim Liver dysfunction is sometimes observed in patients with coronavirus disease 2019 (COVID‐19), but most studies are from China, and the frequency in other countries is unclear. In addition, previous studies suggested several mechanisms of liver damage, but precise or additional mechanisms are not...
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Veröffentlicht in: | Hepatology research 2021-02, Vol.51 (2), p.227-232 |
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creator | Tsutsumi, Takeya Saito, Makoto Nagai, Hiroyuki Yamamoto, Shinya Ikeuchi, Kazuhiko Lim, Lay Ahyoung Adachi, Eisuke Koga, Michiko Okushin, Kazuya Akai, Hiroyuki Kunimatsu, Akira Yotsuyanagi, Hiroshi |
description | Aim
Liver dysfunction is sometimes observed in patients with coronavirus disease 2019 (COVID‐19), but most studies are from China, and the frequency in other countries is unclear. In addition, previous studies suggested several mechanisms of liver damage, but precise or additional mechanisms are not clearly elucidated. Therefore, we examined COVID‐19 patients to explore the proportion of patients with liver dysfunction and also the factors associated with liver dysfunction.
Methods
We retrospectively examined 60 COVID‐19 patients hospitalized at the Hospital affiliated with The Institute of Medical Science, The University of Tokyo (Tokyo, Japan). Patients who presented ≥40 U/L alanine aminotransferase (ALT) levels at least once during their hospitalization were defined as high‐ALT patients, and the others as normal‐ALT patients. The worst values of physical and laboratory findings during hospitalization for each patient were extracted for the analyses. Univariable and multivariable logistic regression models with bootstrap (for 1000 times) were carried out.
Results
Among 60 patients, there were 31 (52%) high‐ALT patients. The high‐ALT patients were obese, and had significantly higher levels of D‐dimer and fibrin/fibrinogen degradation products, as well as white blood cell count, and levels of C‐reactive protein, ferritin, and fibrinogen. Multivariable analysis showed D‐dimer and white blood cells as independent factors.
Conclusions
Considering that higher D‐dimer level and white blood cell count were independently associated with ALT elevation, liver dysfunction in COVID‐19 patients might be induced by microvascular thrombosis in addition to systemic inflammation. |
doi_str_mv | 10.1111/hepr.13577 |
format | Article |
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Liver dysfunction is sometimes observed in patients with coronavirus disease 2019 (COVID‐19), but most studies are from China, and the frequency in other countries is unclear. In addition, previous studies suggested several mechanisms of liver damage, but precise or additional mechanisms are not clearly elucidated. Therefore, we examined COVID‐19 patients to explore the proportion of patients with liver dysfunction and also the factors associated with liver dysfunction.
Methods
We retrospectively examined 60 COVID‐19 patients hospitalized at the Hospital affiliated with The Institute of Medical Science, The University of Tokyo (Tokyo, Japan). Patients who presented ≥40 U/L alanine aminotransferase (ALT) levels at least once during their hospitalization were defined as high‐ALT patients, and the others as normal‐ALT patients. The worst values of physical and laboratory findings during hospitalization for each patient were extracted for the analyses. Univariable and multivariable logistic regression models with bootstrap (for 1000 times) were carried out.
Results
Among 60 patients, there were 31 (52%) high‐ALT patients. The high‐ALT patients were obese, and had significantly higher levels of D‐dimer and fibrin/fibrinogen degradation products, as well as white blood cell count, and levels of C‐reactive protein, ferritin, and fibrinogen. Multivariable analysis showed D‐dimer and white blood cells as independent factors.
Conclusions
Considering that higher D‐dimer level and white blood cell count were independently associated with ALT elevation, liver dysfunction in COVID‐19 patients might be induced by microvascular thrombosis in addition to systemic inflammation.</description><identifier>ISSN: 1386-6346</identifier><identifier>EISSN: 1872-034X</identifier><identifier>DOI: 10.1111/hepr.13577</identifier><identifier>PMID: 33047431</identifier><language>eng</language><publisher>Netherlands: Wiley Subscription Services, Inc</publisher><subject>Alanine ; Alanine transaminase ; Blood ; Coronaviruses ; COVID-19 ; Degradation products ; D‐dimer ; Ferritin ; Fibrin ; Fibrinogen ; Leukocytes ; Liver ; Liver diseases ; liver dysfunction ; Microvasculature ; Patients ; Regression analysis ; Short Communication ; Short Communications ; Thrombosis</subject><ispartof>Hepatology research, 2021-02, Vol.51 (2), p.227-232</ispartof><rights>2020 The Japan Society of Hepatology</rights><rights>2020 The Japan Society of Hepatology.</rights><rights>2021 The Japan Society of Hepatology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5007-6db18ccf8ea797c6bbca02015bf62af0003c42ca1688502f6986ca0ba839b4333</citedby><cites>FETCH-LOGICAL-c5007-6db18ccf8ea797c6bbca02015bf62af0003c42ca1688502f6986ca0ba839b4333</cites><orcidid>0000-0003-0851-1887</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fhepr.13577$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fhepr.13577$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33047431$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tsutsumi, Takeya</creatorcontrib><creatorcontrib>Saito, Makoto</creatorcontrib><creatorcontrib>Nagai, Hiroyuki</creatorcontrib><creatorcontrib>Yamamoto, Shinya</creatorcontrib><creatorcontrib>Ikeuchi, Kazuhiko</creatorcontrib><creatorcontrib>Lim, Lay Ahyoung</creatorcontrib><creatorcontrib>Adachi, Eisuke</creatorcontrib><creatorcontrib>Koga, Michiko</creatorcontrib><creatorcontrib>Okushin, Kazuya</creatorcontrib><creatorcontrib>Akai, Hiroyuki</creatorcontrib><creatorcontrib>Kunimatsu, Akira</creatorcontrib><creatorcontrib>Yotsuyanagi, Hiroshi</creatorcontrib><title>Association of coagulopathy with liver dysfunction in patients with COVID‐19</title><title>Hepatology research</title><addtitle>Hepatol Res</addtitle><description>Aim
Liver dysfunction is sometimes observed in patients with coronavirus disease 2019 (COVID‐19), but most studies are from China, and the frequency in other countries is unclear. In addition, previous studies suggested several mechanisms of liver damage, but precise or additional mechanisms are not clearly elucidated. Therefore, we examined COVID‐19 patients to explore the proportion of patients with liver dysfunction and also the factors associated with liver dysfunction.
Methods
We retrospectively examined 60 COVID‐19 patients hospitalized at the Hospital affiliated with The Institute of Medical Science, The University of Tokyo (Tokyo, Japan). Patients who presented ≥40 U/L alanine aminotransferase (ALT) levels at least once during their hospitalization were defined as high‐ALT patients, and the others as normal‐ALT patients. The worst values of physical and laboratory findings during hospitalization for each patient were extracted for the analyses. Univariable and multivariable logistic regression models with bootstrap (for 1000 times) were carried out.
Results
Among 60 patients, there were 31 (52%) high‐ALT patients. The high‐ALT patients were obese, and had significantly higher levels of D‐dimer and fibrin/fibrinogen degradation products, as well as white blood cell count, and levels of C‐reactive protein, ferritin, and fibrinogen. Multivariable analysis showed D‐dimer and white blood cells as independent factors.
Conclusions
Considering that higher D‐dimer level and white blood cell count were independently associated with ALT elevation, liver dysfunction in COVID‐19 patients might be induced by microvascular thrombosis in addition to systemic inflammation.</description><subject>Alanine</subject><subject>Alanine transaminase</subject><subject>Blood</subject><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>Degradation products</subject><subject>D‐dimer</subject><subject>Ferritin</subject><subject>Fibrin</subject><subject>Fibrinogen</subject><subject>Leukocytes</subject><subject>Liver</subject><subject>Liver diseases</subject><subject>liver dysfunction</subject><subject>Microvasculature</subject><subject>Patients</subject><subject>Regression analysis</subject><subject>Short Communication</subject><subject>Short Communications</subject><subject>Thrombosis</subject><issn>1386-6346</issn><issn>1872-034X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp90d1KHDEYBuAgFf9PegFloCdFGP3yM0nmpCDr1hVERVR6FjLZjBuZnWyTGWXPvIReo1di1lFpe9CcJPA9vHzhRegzhgOczuHMLsIBpoUQa2gLS0FyoOznp_SmkuecMr6JtmO8B8ACCNtAm5QCE4ziLXR-FKM3TnfOt5mvM-P1Xd_4he5my-zRdbOscQ82ZNNlrPvWvDLXZmnubNvFgYwubk-Pn59-43IXrde6iXbv7d5BNz_G16NJfnZxcjo6OstNASByPq2wNKaWVotSGF5VRgMBXFQ1J7oGAGoYMRpzKQsgNS8lT6LSkpYVo5TuoO9D7qKv5nZq0i5BN2oR3FyHpfLaqb8nrZupO_-gBBcF4SwFfHsLCP5Xb2On5i4a2zS6tb6PirACeAEFW9Gv_9B734c2fS8pWTImgJKk9gdlgo8x2PpjGQxqVZNa1aRea0r4y5_rf9D3XhLAA3h0jV3-J0pNxpdXQ-gLENOeng</recordid><startdate>202102</startdate><enddate>202102</enddate><creator>Tsutsumi, Takeya</creator><creator>Saito, Makoto</creator><creator>Nagai, Hiroyuki</creator><creator>Yamamoto, Shinya</creator><creator>Ikeuchi, Kazuhiko</creator><creator>Lim, Lay Ahyoung</creator><creator>Adachi, Eisuke</creator><creator>Koga, Michiko</creator><creator>Okushin, Kazuya</creator><creator>Akai, Hiroyuki</creator><creator>Kunimatsu, Akira</creator><creator>Yotsuyanagi, Hiroshi</creator><general>Wiley Subscription Services, Inc</general><general>John Wiley and Sons Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TM</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-0851-1887</orcidid></search><sort><creationdate>202102</creationdate><title>Association of coagulopathy with liver dysfunction in patients with COVID‐19</title><author>Tsutsumi, Takeya ; Saito, Makoto ; Nagai, Hiroyuki ; Yamamoto, Shinya ; Ikeuchi, Kazuhiko ; Lim, Lay Ahyoung ; Adachi, Eisuke ; Koga, Michiko ; Okushin, Kazuya ; Akai, Hiroyuki ; Kunimatsu, Akira ; Yotsuyanagi, Hiroshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5007-6db18ccf8ea797c6bbca02015bf62af0003c42ca1688502f6986ca0ba839b4333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Alanine</topic><topic>Alanine transaminase</topic><topic>Blood</topic><topic>Coronaviruses</topic><topic>COVID-19</topic><topic>Degradation products</topic><topic>D‐dimer</topic><topic>Ferritin</topic><topic>Fibrin</topic><topic>Fibrinogen</topic><topic>Leukocytes</topic><topic>Liver</topic><topic>Liver diseases</topic><topic>liver dysfunction</topic><topic>Microvasculature</topic><topic>Patients</topic><topic>Regression analysis</topic><topic>Short Communication</topic><topic>Short Communications</topic><topic>Thrombosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tsutsumi, Takeya</creatorcontrib><creatorcontrib>Saito, Makoto</creatorcontrib><creatorcontrib>Nagai, Hiroyuki</creatorcontrib><creatorcontrib>Yamamoto, Shinya</creatorcontrib><creatorcontrib>Ikeuchi, Kazuhiko</creatorcontrib><creatorcontrib>Lim, Lay Ahyoung</creatorcontrib><creatorcontrib>Adachi, Eisuke</creatorcontrib><creatorcontrib>Koga, Michiko</creatorcontrib><creatorcontrib>Okushin, Kazuya</creatorcontrib><creatorcontrib>Akai, Hiroyuki</creatorcontrib><creatorcontrib>Kunimatsu, Akira</creatorcontrib><creatorcontrib>Yotsuyanagi, Hiroshi</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Hepatology research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tsutsumi, Takeya</au><au>Saito, Makoto</au><au>Nagai, Hiroyuki</au><au>Yamamoto, Shinya</au><au>Ikeuchi, Kazuhiko</au><au>Lim, Lay Ahyoung</au><au>Adachi, Eisuke</au><au>Koga, Michiko</au><au>Okushin, Kazuya</au><au>Akai, Hiroyuki</au><au>Kunimatsu, Akira</au><au>Yotsuyanagi, Hiroshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association of coagulopathy with liver dysfunction in patients with COVID‐19</atitle><jtitle>Hepatology research</jtitle><addtitle>Hepatol Res</addtitle><date>2021-02</date><risdate>2021</risdate><volume>51</volume><issue>2</issue><spage>227</spage><epage>232</epage><pages>227-232</pages><issn>1386-6346</issn><eissn>1872-034X</eissn><abstract>Aim
Liver dysfunction is sometimes observed in patients with coronavirus disease 2019 (COVID‐19), but most studies are from China, and the frequency in other countries is unclear. In addition, previous studies suggested several mechanisms of liver damage, but precise or additional mechanisms are not clearly elucidated. Therefore, we examined COVID‐19 patients to explore the proportion of patients with liver dysfunction and also the factors associated with liver dysfunction.
Methods
We retrospectively examined 60 COVID‐19 patients hospitalized at the Hospital affiliated with The Institute of Medical Science, The University of Tokyo (Tokyo, Japan). Patients who presented ≥40 U/L alanine aminotransferase (ALT) levels at least once during their hospitalization were defined as high‐ALT patients, and the others as normal‐ALT patients. The worst values of physical and laboratory findings during hospitalization for each patient were extracted for the analyses. Univariable and multivariable logistic regression models with bootstrap (for 1000 times) were carried out.
Results
Among 60 patients, there were 31 (52%) high‐ALT patients. The high‐ALT patients were obese, and had significantly higher levels of D‐dimer and fibrin/fibrinogen degradation products, as well as white blood cell count, and levels of C‐reactive protein, ferritin, and fibrinogen. Multivariable analysis showed D‐dimer and white blood cells as independent factors.
Conclusions
Considering that higher D‐dimer level and white blood cell count were independently associated with ALT elevation, liver dysfunction in COVID‐19 patients might be induced by microvascular thrombosis in addition to systemic inflammation.</abstract><cop>Netherlands</cop><pub>Wiley Subscription Services, Inc</pub><pmid>33047431</pmid><doi>10.1111/hepr.13577</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0003-0851-1887</orcidid><oa>free_for_read</oa></addata></record> |
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source | Wiley Online Library Journals Frontfile Complete |
subjects | Alanine Alanine transaminase Blood Coronaviruses COVID-19 Degradation products D‐dimer Ferritin Fibrin Fibrinogen Leukocytes Liver Liver diseases liver dysfunction Microvasculature Patients Regression analysis Short Communication Short Communications Thrombosis |
title | Association of coagulopathy with liver dysfunction in patients with COVID‐19 |
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