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Clinical Profile and Prognostic Markers of Acute on Chronic Liver Failure (ACLF): A Single-center Experience from East India
The aim of the study was to study the clinical profile of acute on chronic liver failure (ACLF) and establish Cell-free DNA (Cf DNA) as a predictor of the outcome of ACLF. In this prospective study, those patients who fulfilled EASL criteria were included. Cf DNA was estimated in 30 patients and com...
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Published in: | Journal of clinical and experimental hepatology 2023-11, Vol.13 (6), p.1017-1024 |
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description | The aim of the study was to study the clinical profile of acute on chronic liver failure (ACLF) and establish Cell-free DNA (Cf DNA) as a predictor of the outcome of ACLF.
In this prospective study, those patients who fulfilled EASL criteria were included. Cf DNA was estimated in 30 patients and compared with the CLIF-C ACLF score.
The median age of 132 consecutive ACLF patients was 40 years. The most common acute insult were sepsis (30.3%) and alcohol (22%). While alcohol (35.6%) and chronic HBV (14.3%) were the most common etiologies of cirrhosis. The overall mortality was 45.5% and 71.2% at 28 days and 90 days, respectively. Multiple regression analysis using the Cox proportional hazard model showed that heart rate (HR 1.06, 95% CI 1.04–1.08 P = 0.001), lung failure (HR 2.82, 95% CI 1.24–6.44, P = 0.02), and cell-free DNA (HR 2.70, 95% CI 1.17–6.24, P = 0.02) were independent predictors of mortality When Cf DNA was used to predict 28-day mortality, Cf DNA was found to have a higher AUC (AUROC 0.84, 95% CI 0.70-0.98, P = 0.001) than the CLIF-C-ACLF score (AUROC 0.81, 95% 0.66–0.97, P = 0.003). However, when 90-day mortality was compared, CLIF-C-ACLF score had a higher area under the curve (AUROC 0.93, 95% CI 0.83–1.00, P = 0.0001) than Cf DNA (AUROC 0.89, 95% CI 0.77–1.00, P = 0.0001).
Alcohol and sepsis remain the most common causes of acute insult. Cf DNA is a better predictor of 28-day mortality, whereas CLIF-C ACLF is more accurate to predict 90-day mortality. |
doi_str_mv | 10.1016/j.jceh.2023.06.010 |
format | article |
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In this prospective study, those patients who fulfilled EASL criteria were included. Cf DNA was estimated in 30 patients and compared with the CLIF-C ACLF score.
The median age of 132 consecutive ACLF patients was 40 years. The most common acute insult were sepsis (30.3%) and alcohol (22%). While alcohol (35.6%) and chronic HBV (14.3%) were the most common etiologies of cirrhosis. The overall mortality was 45.5% and 71.2% at 28 days and 90 days, respectively. Multiple regression analysis using the Cox proportional hazard model showed that heart rate (HR 1.06, 95% CI 1.04–1.08 P = 0.001), lung failure (HR 2.82, 95% CI 1.24–6.44, P = 0.02), and cell-free DNA (HR 2.70, 95% CI 1.17–6.24, P = 0.02) were independent predictors of mortality When Cf DNA was used to predict 28-day mortality, Cf DNA was found to have a higher AUC (AUROC 0.84, 95% CI 0.70-0.98, P = 0.001) than the CLIF-C-ACLF score (AUROC 0.81, 95% 0.66–0.97, P = 0.003). However, when 90-day mortality was compared, CLIF-C-ACLF score had a higher area under the curve (AUROC 0.93, 95% CI 0.83–1.00, P = 0.0001) than Cf DNA (AUROC 0.89, 95% CI 0.77–1.00, P = 0.0001).
Alcohol and sepsis remain the most common causes of acute insult. Cf DNA is a better predictor of 28-day mortality, whereas CLIF-C ACLF is more accurate to predict 90-day mortality.</description><identifier>ISSN: 0973-6883</identifier><identifier>EISSN: 2213-3453</identifier><identifier>DOI: 10.1016/j.jceh.2023.06.010</identifier><identifier>PMID: 37975045</identifier><language>eng</language><publisher>India: Elsevier B.V</publisher><subject>ACLF ; acute on chronic liver failure ; cell free DNA ; Original ; prognostic marker</subject><ispartof>Journal of clinical and experimental hepatology, 2023-11, Vol.13 (6), p.1017-1024</ispartof><rights>2023 Indian National Association for Study of the Liver</rights><rights>2023 Indian National Association for Study of the Liver. Published by Elsevier B.V. All rights reserved.</rights><rights>2023 Indian National Association for Study of the Liver. Published by Elsevier B.V. All rights reserved. 2023 Indian National Association for Study of the Liver</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c456t-ec8c57419dfc5aeada3d7a4a506254efebadbc58a1bd3bd24abe0d56ee492b0e3</citedby><cites>FETCH-LOGICAL-c456t-ec8c57419dfc5aeada3d7a4a506254efebadbc58a1bd3bd24abe0d56ee492b0e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10643518/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10643518/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,725,778,782,883,27911,27912,53778,53780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37975045$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Halder, Prasenjit</creatorcontrib><creatorcontrib>Roy, Susree</creatorcontrib><creatorcontrib>Banerjee, Soma</creatorcontrib><creatorcontrib>Mandal, Syamsundar</creatorcontrib><creatorcontrib>Das, Kausik</creatorcontrib><creatorcontrib>Chowdhury, Abhijit</creatorcontrib><creatorcontrib>Mahiuddin Ahammed, Sk</creatorcontrib><title>Clinical Profile and Prognostic Markers of Acute on Chronic Liver Failure (ACLF): A Single-center Experience from East India</title><title>Journal of clinical and experimental hepatology</title><addtitle>J Clin Exp Hepatol</addtitle><description>The aim of the study was to study the clinical profile of acute on chronic liver failure (ACLF) and establish Cell-free DNA (Cf DNA) as a predictor of the outcome of ACLF.
In this prospective study, those patients who fulfilled EASL criteria were included. Cf DNA was estimated in 30 patients and compared with the CLIF-C ACLF score.
The median age of 132 consecutive ACLF patients was 40 years. The most common acute insult were sepsis (30.3%) and alcohol (22%). While alcohol (35.6%) and chronic HBV (14.3%) were the most common etiologies of cirrhosis. The overall mortality was 45.5% and 71.2% at 28 days and 90 days, respectively. Multiple regression analysis using the Cox proportional hazard model showed that heart rate (HR 1.06, 95% CI 1.04–1.08 P = 0.001), lung failure (HR 2.82, 95% CI 1.24–6.44, P = 0.02), and cell-free DNA (HR 2.70, 95% CI 1.17–6.24, P = 0.02) were independent predictors of mortality When Cf DNA was used to predict 28-day mortality, Cf DNA was found to have a higher AUC (AUROC 0.84, 95% CI 0.70-0.98, P = 0.001) than the CLIF-C-ACLF score (AUROC 0.81, 95% 0.66–0.97, P = 0.003). However, when 90-day mortality was compared, CLIF-C-ACLF score had a higher area under the curve (AUROC 0.93, 95% CI 0.83–1.00, P = 0.0001) than Cf DNA (AUROC 0.89, 95% CI 0.77–1.00, P = 0.0001).
Alcohol and sepsis remain the most common causes of acute insult. Cf DNA is a better predictor of 28-day mortality, whereas CLIF-C ACLF is more accurate to predict 90-day mortality.</description><subject>ACLF</subject><subject>acute on chronic liver failure</subject><subject>cell free DNA</subject><subject>Original</subject><subject>prognostic marker</subject><issn>0973-6883</issn><issn>2213-3453</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kU2LFDEQhoMo7rDuH_AgOa6H7s1nf4ggQzOjCyMK6jmkk-qZjD3JmHQPK_jj7XZ2F72YSwXqfd8q6kHoJSU5JbS42ed7A7ucEcZzUuSEkidowRjlGReSP0ULUpc8K6qKX6CrlPZkegVhgrDn6IKXdSmJkAv0q-mdd0b3-HMMnesBa2_n_9aHNDiDP-r4HWLCocNLMw6Ag8fNLobJhDfuBBGvtevHCPh62WzWr9_gJf7i_LaHzIAfpv7q7gjRgTeAuxgOeKXTgG-9dfoFetbpPsHVfb1E39arr82HbPPp_W2z3GRGyGLIwFRGloLWtjNSg7aa21ILLUnBpIAOWm1bIytNW8tby4RugVhZAIiatQT4JXp3zj2O7QHsvFfUvTpGd9DxpwraqX873u3UNpwUJYXgklZTwvV9Qgw_RkiDOrhkoO-1hzAmxaqallKQmk9SdpaaGFKK0D3OoUTN6NRezejUjE6RQk3oJtOrvzd8tDyAmgRvzwKY7nRyEFUyf25qXQQzKBvc__J_A17erE8</recordid><startdate>20231101</startdate><enddate>20231101</enddate><creator>Halder, Prasenjit</creator><creator>Roy, Susree</creator><creator>Banerjee, Soma</creator><creator>Mandal, Syamsundar</creator><creator>Das, Kausik</creator><creator>Chowdhury, Abhijit</creator><creator>Mahiuddin Ahammed, Sk</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20231101</creationdate><title>Clinical Profile and Prognostic Markers of Acute on Chronic Liver Failure (ACLF): A Single-center Experience from East India</title><author>Halder, Prasenjit ; Roy, Susree ; Banerjee, Soma ; Mandal, Syamsundar ; Das, Kausik ; Chowdhury, Abhijit ; Mahiuddin Ahammed, Sk</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c456t-ec8c57419dfc5aeada3d7a4a506254efebadbc58a1bd3bd24abe0d56ee492b0e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>ACLF</topic><topic>acute on chronic liver failure</topic><topic>cell free DNA</topic><topic>Original</topic><topic>prognostic marker</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Halder, Prasenjit</creatorcontrib><creatorcontrib>Roy, Susree</creatorcontrib><creatorcontrib>Banerjee, Soma</creatorcontrib><creatorcontrib>Mandal, Syamsundar</creatorcontrib><creatorcontrib>Das, Kausik</creatorcontrib><creatorcontrib>Chowdhury, Abhijit</creatorcontrib><creatorcontrib>Mahiuddin Ahammed, Sk</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical and experimental hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Halder, Prasenjit</au><au>Roy, Susree</au><au>Banerjee, Soma</au><au>Mandal, Syamsundar</au><au>Das, Kausik</au><au>Chowdhury, Abhijit</au><au>Mahiuddin Ahammed, Sk</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical Profile and Prognostic Markers of Acute on Chronic Liver Failure (ACLF): A Single-center Experience from East India</atitle><jtitle>Journal of clinical and experimental hepatology</jtitle><addtitle>J Clin Exp Hepatol</addtitle><date>2023-11-01</date><risdate>2023</risdate><volume>13</volume><issue>6</issue><spage>1017</spage><epage>1024</epage><pages>1017-1024</pages><issn>0973-6883</issn><eissn>2213-3453</eissn><abstract>The aim of the study was to study the clinical profile of acute on chronic liver failure (ACLF) and establish Cell-free DNA (Cf DNA) as a predictor of the outcome of ACLF.
In this prospective study, those patients who fulfilled EASL criteria were included. Cf DNA was estimated in 30 patients and compared with the CLIF-C ACLF score.
The median age of 132 consecutive ACLF patients was 40 years. The most common acute insult were sepsis (30.3%) and alcohol (22%). While alcohol (35.6%) and chronic HBV (14.3%) were the most common etiologies of cirrhosis. The overall mortality was 45.5% and 71.2% at 28 days and 90 days, respectively. Multiple regression analysis using the Cox proportional hazard model showed that heart rate (HR 1.06, 95% CI 1.04–1.08 P = 0.001), lung failure (HR 2.82, 95% CI 1.24–6.44, P = 0.02), and cell-free DNA (HR 2.70, 95% CI 1.17–6.24, P = 0.02) were independent predictors of mortality When Cf DNA was used to predict 28-day mortality, Cf DNA was found to have a higher AUC (AUROC 0.84, 95% CI 0.70-0.98, P = 0.001) than the CLIF-C-ACLF score (AUROC 0.81, 95% 0.66–0.97, P = 0.003). However, when 90-day mortality was compared, CLIF-C-ACLF score had a higher area under the curve (AUROC 0.93, 95% CI 0.83–1.00, P = 0.0001) than Cf DNA (AUROC 0.89, 95% CI 0.77–1.00, P = 0.0001).
Alcohol and sepsis remain the most common causes of acute insult. Cf DNA is a better predictor of 28-day mortality, whereas CLIF-C ACLF is more accurate to predict 90-day mortality.</abstract><cop>India</cop><pub>Elsevier B.V</pub><pmid>37975045</pmid><doi>10.1016/j.jceh.2023.06.010</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | ACLF acute on chronic liver failure cell free DNA Original prognostic marker |
title | Clinical Profile and Prognostic Markers of Acute on Chronic Liver Failure (ACLF): A Single-center Experience from East India |
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