Circulating Cell-free DNA in Patients With Acute Biliary Pancreatitis: Association With Disease Markers and Prolonged Hospitalization Time—A Prospective Cohort Study
To evaluate cfDNA as an indicator of pancreatitis severity. Acute pancreatitis severity scores have limited proficiency, and are complex and challenging to use clinically. Elevation of circulating cfDNA concentration has been shown to be associated with hospital length of stay (LOS) and mortality. I...
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Veröffentlicht in: | Annals of surgery 2022-12, Vol.276 (6), p.e861-e867 |
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creator | Gibor, Udit Perry, Zvi Netz, Uri Kirshtein, Boris Mizrahi, Solly Czeiger, David Sebbag, Gilbert Douvdevani, Amos |
description | To evaluate cfDNA as an indicator of pancreatitis severity.
Acute pancreatitis severity scores have limited proficiency, and are complex and challenging to use clinically. Elevation of circulating cfDNA concentration has been shown to be associated with hospital length of stay (LOS) and mortality.
In a prospective study, cfDNA concentration was measured by a simple fluorometric test, at admission and for 2 consecutive days, in patients with acute biliary pancreatitis (ABP). Ranson and APACHE II scores were used as measures of pancreatitis severity. Hospital LOS and mortality were used as outcome measures.
Seventy-eight patients were included. Patients with severe disease according to Ranson's Criteria (n = 24) had elevated median admission cfDNA compared to patients with mild disease (n = 54, 2252ng/ml vs 1228 ng/ml, P < 0.05 ). Admission cfDNA levels correlated with Ranson and APACHE II scores and markers of bile duct obstruction. LOS did not differ between patients with mild and severe disease according to Ranson and APACHE II scores. Patients with cfDNA at 24 hours concentrations above the cutoff value of healthy patients (>850 ng/ml) had a significantly longer LOS compared to those with normal cfDNA levels ( P < 0.001 ).
cfDNA, measured by a rapid simple assay, proved a valuable early marker of severity in ABP with clear advantages for prediction of LOS over Ranson and APACHE II. Measurement of cfDNA has the potential to be an effective practical approach to predict the course of ABP and should be further evaluated in larger trials. |
doi_str_mv | 10.1097/SLA.0000000000004679 |
format | Article |
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Acute pancreatitis severity scores have limited proficiency, and are complex and challenging to use clinically. Elevation of circulating cfDNA concentration has been shown to be associated with hospital length of stay (LOS) and mortality.
In a prospective study, cfDNA concentration was measured by a simple fluorometric test, at admission and for 2 consecutive days, in patients with acute biliary pancreatitis (ABP). Ranson and APACHE II scores were used as measures of pancreatitis severity. Hospital LOS and mortality were used as outcome measures.
Seventy-eight patients were included. Patients with severe disease according to Ranson's Criteria (n = 24) had elevated median admission cfDNA compared to patients with mild disease (n = 54, 2252ng/ml vs 1228 ng/ml, P < 0.05 ). Admission cfDNA levels correlated with Ranson and APACHE II scores and markers of bile duct obstruction. LOS did not differ between patients with mild and severe disease according to Ranson and APACHE II scores. Patients with cfDNA at 24 hours concentrations above the cutoff value of healthy patients (>850 ng/ml) had a significantly longer LOS compared to those with normal cfDNA levels ( P < 0.001 ).
cfDNA, measured by a rapid simple assay, proved a valuable early marker of severity in ABP with clear advantages for prediction of LOS over Ranson and APACHE II. Measurement of cfDNA has the potential to be an effective practical approach to predict the course of ABP and should be further evaluated in larger trials.</description><identifier>ISSN: 0003-4932</identifier><identifier>EISSN: 1528-1140</identifier><identifier>DOI: 10.1097/SLA.0000000000004679</identifier><identifier>PMID: 33351491</identifier><language>eng</language><publisher>United States: Lippincott Williams & Wilkins</publisher><subject>Acute Disease ; Cell-Free Nucleic Acids ; Humans ; Length of Stay ; Pancreatitis - complications ; Pancreatitis - diagnosis ; Predictive Value of Tests ; Prognosis ; Prospective Studies ; Severity of Illness Index</subject><ispartof>Annals of surgery, 2022-12, Vol.276 (6), p.e861-e867</ispartof><rights>Lippincott Williams & Wilkins</rights><rights>Copyright © 2020 Wolters Kluwer Health, Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2820-6dd4f8f5d428cd940b825a6deaa29ce56fc95ebbc4c844314d0d176bd19edd9a3</citedby><cites>FETCH-LOGICAL-c2820-6dd4f8f5d428cd940b825a6deaa29ce56fc95ebbc4c844314d0d176bd19edd9a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33351491$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gibor, Udit</creatorcontrib><creatorcontrib>Perry, Zvi</creatorcontrib><creatorcontrib>Netz, Uri</creatorcontrib><creatorcontrib>Kirshtein, Boris</creatorcontrib><creatorcontrib>Mizrahi, Solly</creatorcontrib><creatorcontrib>Czeiger, David</creatorcontrib><creatorcontrib>Sebbag, Gilbert</creatorcontrib><creatorcontrib>Douvdevani, Amos</creatorcontrib><title>Circulating Cell-free DNA in Patients With Acute Biliary Pancreatitis: Association With Disease Markers and Prolonged Hospitalization Time—A Prospective Cohort Study</title><title>Annals of surgery</title><addtitle>Ann Surg</addtitle><description>To evaluate cfDNA as an indicator of pancreatitis severity.
Acute pancreatitis severity scores have limited proficiency, and are complex and challenging to use clinically. Elevation of circulating cfDNA concentration has been shown to be associated with hospital length of stay (LOS) and mortality.
In a prospective study, cfDNA concentration was measured by a simple fluorometric test, at admission and for 2 consecutive days, in patients with acute biliary pancreatitis (ABP). Ranson and APACHE II scores were used as measures of pancreatitis severity. Hospital LOS and mortality were used as outcome measures.
Seventy-eight patients were included. Patients with severe disease according to Ranson's Criteria (n = 24) had elevated median admission cfDNA compared to patients with mild disease (n = 54, 2252ng/ml vs 1228 ng/ml, P < 0.05 ). Admission cfDNA levels correlated with Ranson and APACHE II scores and markers of bile duct obstruction. LOS did not differ between patients with mild and severe disease according to Ranson and APACHE II scores. Patients with cfDNA at 24 hours concentrations above the cutoff value of healthy patients (>850 ng/ml) had a significantly longer LOS compared to those with normal cfDNA levels ( P < 0.001 ).
cfDNA, measured by a rapid simple assay, proved a valuable early marker of severity in ABP with clear advantages for prediction of LOS over Ranson and APACHE II. Measurement of cfDNA has the potential to be an effective practical approach to predict the course of ABP and should be further evaluated in larger trials.</description><subject>Acute Disease</subject><subject>Cell-Free Nucleic Acids</subject><subject>Humans</subject><subject>Length of Stay</subject><subject>Pancreatitis - complications</subject><subject>Pancreatitis - diagnosis</subject><subject>Predictive Value of Tests</subject><subject>Prognosis</subject><subject>Prospective Studies</subject><subject>Severity of Illness Index</subject><issn>0003-4932</issn><issn>1528-1140</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdUUtuFDEUtBCITAI3QMhLNh3864_ZNR0gSANEShDLltt-nTHxtAfbTZSsOAR34F6cBI86fIQly3rPVfWeqhB6QskxJbJ-fr5uj8k_R1S1vIdWtGRNQakg99Eqd3khJGcH6DDGz4RQ0ZD6ITrgnJdUSLpCPzob9OxUstMl7sC5YgwA-OR9i-2Ez3IfphTxJ5s2uNVzAvzSOqvCTf6bdIAMSDa-wG2MXttc-WkBn9gIKgJ-p8IVhIjVZPBZ8M5Pl2DwqY87m5Sztwvlwm7h57fv7R4Sd6CT_Qq48xsfEj5Ps7l5hB6MykV4fPceoY-vX110p8X6w5u3XbsuNGsYKSpjxNiMpRGs0UYKMjSsVJUBpZjUUFajliUMgxa6EYJTYYihdTUYKsEYqfgRerbo7oL_MkNM_dZGnX1RE_g59kzUXOy9rjJULFCdd44Bxn4X7DZb01PS7yPqc0T9_xFl2tO7CfOwBfOH9DuTv7rX3qVs3ZWbryH0G1AubRa9qmwKRhijLBdFviXhvwDepZ_y</recordid><startdate>20221201</startdate><enddate>20221201</enddate><creator>Gibor, Udit</creator><creator>Perry, Zvi</creator><creator>Netz, Uri</creator><creator>Kirshtein, Boris</creator><creator>Mizrahi, Solly</creator><creator>Czeiger, David</creator><creator>Sebbag, Gilbert</creator><creator>Douvdevani, Amos</creator><general>Lippincott Williams & Wilkins</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20221201</creationdate><title>Circulating Cell-free DNA in Patients With Acute Biliary Pancreatitis: Association With Disease Markers and Prolonged Hospitalization Time—A Prospective Cohort Study</title><author>Gibor, Udit ; Perry, Zvi ; Netz, Uri ; Kirshtein, Boris ; Mizrahi, Solly ; Czeiger, David ; Sebbag, Gilbert ; Douvdevani, Amos</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2820-6dd4f8f5d428cd940b825a6deaa29ce56fc95ebbc4c844314d0d176bd19edd9a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Acute Disease</topic><topic>Cell-Free Nucleic Acids</topic><topic>Humans</topic><topic>Length of Stay</topic><topic>Pancreatitis - complications</topic><topic>Pancreatitis - diagnosis</topic><topic>Predictive Value of Tests</topic><topic>Prognosis</topic><topic>Prospective Studies</topic><topic>Severity of Illness Index</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gibor, Udit</creatorcontrib><creatorcontrib>Perry, Zvi</creatorcontrib><creatorcontrib>Netz, Uri</creatorcontrib><creatorcontrib>Kirshtein, Boris</creatorcontrib><creatorcontrib>Mizrahi, Solly</creatorcontrib><creatorcontrib>Czeiger, David</creatorcontrib><creatorcontrib>Sebbag, Gilbert</creatorcontrib><creatorcontrib>Douvdevani, Amos</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gibor, Udit</au><au>Perry, Zvi</au><au>Netz, Uri</au><au>Kirshtein, Boris</au><au>Mizrahi, Solly</au><au>Czeiger, David</au><au>Sebbag, Gilbert</au><au>Douvdevani, Amos</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Circulating Cell-free DNA in Patients With Acute Biliary Pancreatitis: Association With Disease Markers and Prolonged Hospitalization Time—A Prospective Cohort Study</atitle><jtitle>Annals of surgery</jtitle><addtitle>Ann Surg</addtitle><date>2022-12-01</date><risdate>2022</risdate><volume>276</volume><issue>6</issue><spage>e861</spage><epage>e867</epage><pages>e861-e867</pages><issn>0003-4932</issn><eissn>1528-1140</eissn><abstract>To evaluate cfDNA as an indicator of pancreatitis severity.
Acute pancreatitis severity scores have limited proficiency, and are complex and challenging to use clinically. Elevation of circulating cfDNA concentration has been shown to be associated with hospital length of stay (LOS) and mortality.
In a prospective study, cfDNA concentration was measured by a simple fluorometric test, at admission and for 2 consecutive days, in patients with acute biliary pancreatitis (ABP). Ranson and APACHE II scores were used as measures of pancreatitis severity. Hospital LOS and mortality were used as outcome measures.
Seventy-eight patients were included. Patients with severe disease according to Ranson's Criteria (n = 24) had elevated median admission cfDNA compared to patients with mild disease (n = 54, 2252ng/ml vs 1228 ng/ml, P < 0.05 ). Admission cfDNA levels correlated with Ranson and APACHE II scores and markers of bile duct obstruction. LOS did not differ between patients with mild and severe disease according to Ranson and APACHE II scores. Patients with cfDNA at 24 hours concentrations above the cutoff value of healthy patients (>850 ng/ml) had a significantly longer LOS compared to those with normal cfDNA levels ( P < 0.001 ).
cfDNA, measured by a rapid simple assay, proved a valuable early marker of severity in ABP with clear advantages for prediction of LOS over Ranson and APACHE II. Measurement of cfDNA has the potential to be an effective practical approach to predict the course of ABP and should be further evaluated in larger trials.</abstract><cop>United States</cop><pub>Lippincott Williams & Wilkins</pub><pmid>33351491</pmid><doi>10.1097/SLA.0000000000004679</doi></addata></record> |
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subjects | Acute Disease Cell-Free Nucleic Acids Humans Length of Stay Pancreatitis - complications Pancreatitis - diagnosis Predictive Value of Tests Prognosis Prospective Studies Severity of Illness Index |
title | Circulating Cell-free DNA in Patients With Acute Biliary Pancreatitis: Association With Disease Markers and Prolonged Hospitalization Time—A Prospective Cohort Study |
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