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Abnormal liver-related biomarkers in COVID-19 patients and the role of prealbumin.

Identifieur interne : 000010 ( Main/Exploration ); précédent : 000009; suivant : 000011

Abnormal liver-related biomarkers in COVID-19 patients and the role of prealbumin.

Auteurs : Tao Li [République populaire de Chine] ; Ying Guo [République populaire de Chine] ; Xianghua Zhuang [République populaire de Chine] ; Laigang Huang [République populaire de Chine] ; Xingqian Zhang [République populaire de Chine] ; Fengtao Wei [République populaire de Chine] ; Baohua Yang [République populaire de Chine]

Source :

RBID : pubmed:32769260

Descripteurs français

English descriptors

Abstract

Background/Aims

We aimed to evaluate the distribution of abnormal liver-related biomarkers in patients with coronavirus disease (COVID-19) and explore the prognostic value of elevated liver enzymes and abnormal liver synthetic capacity with regards to patient mortality.

Patients and Methods

This retrospective observational study included 80 laboratory-confirmed COVID-19 cases. Data were collected from the electronic medical record system by a trained team of physicians. Alanine aminotransferase (ALT), aspartate aminotransferase (AST), total bilirubin (TB), albumin, and prealbumin levels at admission and on day 7 after admission were collected. The primary outcome of the current study was patient mortality.

Results

Abnormal ALT, AST, TB, albumin, and prealbumin levels were observed in 11 (13.8%), 15 (18.8%), 5 (6.3%), 22 (27.5%), and 31 (38.8%) patients, respectively. Male gender correlated with elevated ALT and AST levels (p = 0.027 and 0.036, respectively). Higher levels of AST and lower levels of albumin and prealbumin were associated with patient mortality (p = 0.009, 0.002, and 0.003, respectively). Multivariate Cox regression analysis identified patient age (p = 0.013, HR 1.108) and prealbumin levels (p = 0.015, HR 0.986) as independent predictors for patient mortality. However, changes in liver-related biomarkers were not associated with poor outcome in multivariate analysis (p > 0.05).

Conclusions

Abnormalities in albumin and prealbumin levels are common among COVID-19 patients and hypoprealbuminemia independently predicts adverse outcome and should be carefully considered in clinical practice. Moreover, changes in liver-related biomarkers is not a salient feature of COVID-19.


DOI: 10.4103/sjg.SJG_239_20
PubMed: 32769260


Affiliations:


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Le document en format XML

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<term>Aged (MeSH)</term>
<term>Alanine Transaminase (blood)</term>
<term>Aspartate Aminotransferases (blood)</term>
<term>Betacoronavirus (MeSH)</term>
<term>Bilirubin (blood)</term>
<term>Biomarkers (blood)</term>
<term>Comorbidity (MeSH)</term>
<term>Coronavirus Infections (blood)</term>
<term>Coronavirus Infections (epidemiology)</term>
<term>Female (MeSH)</term>
<term>Follow-Up Studies (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Liver Diseases (blood)</term>
<term>Liver Diseases (epidemiology)</term>
<term>Liver Function Tests (MeSH)</term>
<term>Male (MeSH)</term>
<term>Middle Aged (MeSH)</term>
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<term>Pneumonia, Viral (blood)</term>
<term>Pneumonia, Viral (epidemiology)</term>
<term>Prealbumin (metabolism)</term>
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<term>Adulte d'âge moyen (MeSH)</term>
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<term>Aspartate aminotransferases (sang)</term>
<term>Betacoronavirus (MeSH)</term>
<term>Bilirubine (sang)</term>
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<term>Pneumopathie virale (épidémiologie)</term>
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<term>Préalbumine (métabolisme)</term>
<term>Sujet âgé (MeSH)</term>
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<term>Aspartate Aminotransferases</term>
<term>Bilirubin</term>
<term>Biomarkers</term>
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<term>Alanine transaminase</term>
<term>Aspartate aminotransferases</term>
<term>Bilirubine</term>
<term>Infections à coronavirus</term>
<term>Maladies du foie</term>
<term>Marqueurs biologiques</term>
<term>Pneumopathie virale</term>
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<term>Infections à coronavirus</term>
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<term>Pneumopathie virale</term>
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<term>Aged</term>
<term>Betacoronavirus</term>
<term>Comorbidity</term>
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<term>Follow-Up Studies</term>
<term>Humans</term>
<term>Liver Function Tests</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Pandemics</term>
<term>Prognosis</term>
<term>Retrospective Studies</term>
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<term>Adulte d'âge moyen</term>
<term>Betacoronavirus</term>
<term>Comorbidité</term>
<term>Femelle</term>
<term>Humains</term>
<term>Mâle</term>
<term>Pandémies</term>
<term>Pronostic</term>
<term>Sujet âgé</term>
<term>Tests de la fonction hépatique</term>
<term>Études de suivi</term>
<term>Études rétrospectives</term>
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<p>
<b>Background/Aims</b>
</p>
<p>We aimed to evaluate the distribution of abnormal liver-related biomarkers in patients with coronavirus disease (COVID-19) and explore the prognostic value of elevated liver enzymes and abnormal liver synthetic capacity with regards to patient mortality.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>Patients and Methods</b>
</p>
<p>This retrospective observational study included 80 laboratory-confirmed COVID-19 cases. Data were collected from the electronic medical record system by a trained team of physicians. Alanine aminotransferase (ALT), aspartate aminotransferase (AST), total bilirubin (TB), albumin, and prealbumin levels at admission and on day 7 after admission were collected. The primary outcome of the current study was patient mortality.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>Results</b>
</p>
<p>Abnormal ALT, AST, TB, albumin, and prealbumin levels were observed in 11 (13.8%), 15 (18.8%), 5 (6.3%), 22 (27.5%), and 31 (38.8%) patients, respectively. Male gender correlated with elevated ALT and AST levels (p = 0.027 and 0.036, respectively). Higher levels of AST and lower levels of albumin and prealbumin were associated with patient mortality (p = 0.009, 0.002, and 0.003, respectively). Multivariate Cox regression analysis identified patient age (p = 0.013, HR 1.108) and prealbumin levels (p = 0.015, HR 0.986) as independent predictors for patient mortality. However, changes in liver-related biomarkers were not associated with poor outcome in multivariate analysis (p > 0.05).</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>Conclusions</b>
</p>
<p>Abnormalities in albumin and prealbumin levels are common among COVID-19 patients and hypoprealbuminemia independently predicts adverse outcome and should be carefully considered in clinical practice. Moreover, changes in liver-related biomarkers is not a salient feature of COVID-19.</p>
</div>
</front>
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<AbstractText Label="Background/Aims">We aimed to evaluate the distribution of abnormal liver-related biomarkers in patients with coronavirus disease (COVID-19) and explore the prognostic value of elevated liver enzymes and abnormal liver synthetic capacity with regards to patient mortality.</AbstractText>
<AbstractText Label="Patients and Methods">This retrospective observational study included 80 laboratory-confirmed COVID-19 cases. Data were collected from the electronic medical record system by a trained team of physicians. Alanine aminotransferase (ALT), aspartate aminotransferase (AST), total bilirubin (TB), albumin, and prealbumin levels at admission and on day 7 after admission were collected. The primary outcome of the current study was patient mortality.</AbstractText>
<AbstractText Label="Results">Abnormal ALT, AST, TB, albumin, and prealbumin levels were observed in 11 (13.8%), 15 (18.8%), 5 (6.3%), 22 (27.5%), and 31 (38.8%) patients, respectively. Male gender correlated with elevated ALT and AST levels (p = 0.027 and 0.036, respectively). Higher levels of AST and lower levels of albumin and prealbumin were associated with patient mortality (p = 0.009, 0.002, and 0.003, respectively). Multivariate Cox regression analysis identified patient age (p = 0.013, HR 1.108) and prealbumin levels (p = 0.015, HR 0.986) as independent predictors for patient mortality. However, changes in liver-related biomarkers were not associated with poor outcome in multivariate analysis (p > 0.05).</AbstractText>
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<MeshHeading>
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<MeshHeading>
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<DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
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<MeshHeading>
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<DescriptorName UI="D012529" MajorTopicYN="N" Type="Geographic">Saudi Arabia</DescriptorName>
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<Keyword MajorTopicYN="Y">COVID-19</Keyword>
<Keyword MajorTopicYN="Y">hypoprealbuminemia</Keyword>
<Keyword MajorTopicYN="Y">liver impairment</Keyword>
<Keyword MajorTopicYN="Y">prognosis</Keyword>
</KeywordList>
<CoiStatement>None</CoiStatement>
</MedlineCitation>
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<Month>8</Month>
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<Hour>6</Hour>
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<Year>2020</Year>
<Month>10</Month>
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<Year>2020</Year>
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<ArticleId IdType="pubmed">32769260</ArticleId>
<ArticleId IdType="pii">291474</ArticleId>
<ArticleId IdType="doi">10.4103/sjg.SJG_239_20</ArticleId>
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<list>
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<li>République populaire de Chine</li>
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<name sortKey="Li, Tao" sort="Li, Tao" uniqKey="Li T" first="Tao" last="Li">Tao Li</name>
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<name sortKey="Huang, Laigang" sort="Huang, Laigang" uniqKey="Huang L" first="Laigang" last="Huang">Laigang Huang</name>
<name sortKey="Wei, Fengtao" sort="Wei, Fengtao" uniqKey="Wei F" first="Fengtao" last="Wei">Fengtao Wei</name>
<name sortKey="Yang, Baohua" sort="Yang, Baohua" uniqKey="Yang B" first="Baohua" last="Yang">Baohua Yang</name>
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<name sortKey="Zhuang, Xianghua" sort="Zhuang, Xianghua" uniqKey="Zhuang X" first="Xianghua" last="Zhuang">Xianghua Zhuang</name>
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