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
Hauptverfasser: 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
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container_issue 2
container_start_page 227
container_title Hepatology research
container_volume 51
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
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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 ; 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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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