Plasma elimination of cholyl-lysyl-fluorescein (CLF): a pilot study in patients with liver cirrhosis

: Background: Cholyl‐lysyl‐fluorescein (CLF) is a fluorescein‐labelled bile acid whose biological behaviour closely resembles that of naturally occurring cholyl glycine. Aim: The aim of this study was to analyze the CLF plasma elimination in patients with liver cirrhosis. Methods: A dose of CLF at 0...

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Veröffentlicht in:Liver (Copenhagen) 2000-08, Vol.20 (4), p.330-334
Hauptverfasser: Milkiewicz, Piotr, Saksena, Sushma, Cardenas, Teresa, Mills, Charles O., Elias, Elwyn
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container_end_page 334
container_issue 4
container_start_page 330
container_title Liver (Copenhagen)
container_volume 20
creator Milkiewicz, Piotr
Saksena, Sushma
Cardenas, Teresa
Mills, Charles O.
Elias, Elwyn
description : Background: Cholyl‐lysyl‐fluorescein (CLF) is a fluorescein‐labelled bile acid whose biological behaviour closely resembles that of naturally occurring cholyl glycine. Aim: The aim of this study was to analyze the CLF plasma elimination in patients with liver cirrhosis. Methods: A dose of CLF at 0.02 mg/kg b.w. was administered i.v. in 26 patients with liver cirrhosis and 9 healthy volunteers. Blood samples were collected before injection and then at 10 min intervals over 60 min. Plasma fluorescence was measured by a luminescence spectrometer and residual fluorescence over the time of the study was compared in each group. Routine liver function tests (rLFTs) were performed before each injection. Results: Plasma elimination of CLF was significantly impaired in patients with cirrhosis compared to healthy subjects with p values
doi_str_mv 10.1034/j.1600-0676.2000.020004330.x
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Aim: The aim of this study was to analyze the CLF plasma elimination in patients with liver cirrhosis. Methods: A dose of CLF at 0.02 mg/kg b.w. was administered i.v. in 26 patients with liver cirrhosis and 9 healthy volunteers. Blood samples were collected before injection and then at 10 min intervals over 60 min. Plasma fluorescence was measured by a luminescence spectrometer and residual fluorescence over the time of the study was compared in each group. Routine liver function tests (rLFTs) were performed before each injection. Results: Plasma elimination of CLF was significantly impaired in patients with cirrhosis compared to healthy subjects with p values &lt;0.0001 at each analyzed time point. CLF test showed 100% sensitivity for liver cirrhosis when residual fluorescence was measured 30, 40, 50 and 60 min after injection. Routine LFTs showed 85% sensitivity for bilirubin, 84% for total bile acids, 69% for aspartate aminotransferase 62% for albumin and 50% for alkaline phosphatase. CLF elimination measured 60 min after injection correlated with Child‐Pugh score (r=0.3945; p&lt;0.05) and albumin (rs=0.6451; p&lt;0.001). No adverse reaction or side effects of CLF were observed. Conclusions: CLF test clearly distinguished between the two analyzed groups and was more sensitive than routine liver function tests. The test appears safe, simple to perform and analyze and after validation in larger cohorts of patients may have the potential to become a useful dynamic test of liver function.</description><identifier>ISSN: 0106-9543</identifier><identifier>EISSN: 1600-0676</identifier><identifier>DOI: 10.1034/j.1600-0676.2000.020004330.x</identifier><identifier>PMID: 10959812</identifier><identifier>CODEN: LIVEDR</identifier><language>eng</language><publisher>Copenhagen: Munksgaard International Publishers</publisher><subject>Adult ; Biological and medical sciences ; Cholic Acids - administration &amp; dosage ; Cholic Acids - pharmacokinetics ; cholyl-lysyl-fluorescein ; Female ; Fluoresceins - administration &amp; dosage ; Fluoresceins - pharmacokinetics ; Fluorescent Dyes - administration &amp; dosage ; Fluorescent Dyes - pharmacokinetics ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Injections, Intravenous ; Liver - metabolism ; Liver - pathology ; Liver Cirrhosis - diagnosis ; Liver Cirrhosis - metabolism ; liver disease ; Liver Function Tests ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Male ; Medical sciences ; Middle Aged ; Other diseases. Semiology ; Pilot Projects ; plasma elimination ; Reference Values ; Sensitivity and Specificity</subject><ispartof>Liver (Copenhagen), 2000-08, Vol.20 (4), p.330-334</ispartof><rights>2000 INIST-CNRS</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4480-d618af854a266e4da7774cca9d957383b05aa5149a3f04a41376f5002f4f632c3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1034%2Fj.1600-0676.2000.020004330.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1034%2Fj.1600-0676.2000.020004330.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1430756$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10959812$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Milkiewicz, Piotr</creatorcontrib><creatorcontrib>Saksena, Sushma</creatorcontrib><creatorcontrib>Cardenas, Teresa</creatorcontrib><creatorcontrib>Mills, Charles O.</creatorcontrib><creatorcontrib>Elias, Elwyn</creatorcontrib><title>Plasma elimination of cholyl-lysyl-fluorescein (CLF): a pilot study in patients with liver cirrhosis</title><title>Liver (Copenhagen)</title><addtitle>Liver</addtitle><description>: Background: Cholyl‐lysyl‐fluorescein (CLF) is a fluorescein‐labelled bile acid whose biological behaviour closely resembles that of naturally occurring cholyl glycine. Aim: The aim of this study was to analyze the CLF plasma elimination in patients with liver cirrhosis. Methods: A dose of CLF at 0.02 mg/kg b.w. was administered i.v. in 26 patients with liver cirrhosis and 9 healthy volunteers. Blood samples were collected before injection and then at 10 min intervals over 60 min. Plasma fluorescence was measured by a luminescence spectrometer and residual fluorescence over the time of the study was compared in each group. Routine liver function tests (rLFTs) were performed before each injection. Results: Plasma elimination of CLF was significantly impaired in patients with cirrhosis compared to healthy subjects with p values &lt;0.0001 at each analyzed time point. CLF test showed 100% sensitivity for liver cirrhosis when residual fluorescence was measured 30, 40, 50 and 60 min after injection. Routine LFTs showed 85% sensitivity for bilirubin, 84% for total bile acids, 69% for aspartate aminotransferase 62% for albumin and 50% for alkaline phosphatase. CLF elimination measured 60 min after injection correlated with Child‐Pugh score (r=0.3945; p&lt;0.05) and albumin (rs=0.6451; p&lt;0.001). No adverse reaction or side effects of CLF were observed. Conclusions: CLF test clearly distinguished between the two analyzed groups and was more sensitive than routine liver function tests. The test appears safe, simple to perform and analyze and after validation in larger cohorts of patients may have the potential to become a useful dynamic test of liver function.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Cholic Acids - administration &amp; dosage</subject><subject>Cholic Acids - pharmacokinetics</subject><subject>cholyl-lysyl-fluorescein</subject><subject>Female</subject><subject>Fluoresceins - administration &amp; dosage</subject><subject>Fluoresceins - pharmacokinetics</subject><subject>Fluorescent Dyes - administration &amp; dosage</subject><subject>Fluorescent Dyes - pharmacokinetics</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Injections, Intravenous</subject><subject>Liver - metabolism</subject><subject>Liver - pathology</subject><subject>Liver Cirrhosis - diagnosis</subject><subject>Liver Cirrhosis - metabolism</subject><subject>liver disease</subject><subject>Liver Function Tests</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Other diseases. Semiology</subject><subject>Pilot Projects</subject><subject>plasma elimination</subject><subject>Reference Values</subject><subject>Sensitivity and Specificity</subject><issn>0106-9543</issn><issn>1600-0676</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkE2P0zAQhi0EYkvhLyAfVggOCeP4K0FcULW7rKgKSHwcLa9jqy5uUuyEbf49iVIKVy5j2X7mndGD0CWBnABlr3c5EQAZCCnyAgBymCqjFPLjA7Q4fz5ECyAgsoozeoGepLQDIIJJ_hhdEKh4VZJigepPQae9xjb4vW9059sGtw6bbRuGkIUhjdWFvo02Gesb_HK1vn71Bmt88KHtcOr6esDj-2FstU2X8L3vtjj4XzZi42Pctsmnp-iR0yHZZ6dzib5eX31Zvc_WH29uV-_WmWGshKwWpNSu5EwXQlhWayklM0ZXdcUlLekdcK05YZWmDphmhErhOEDhmBO0MHSJXsy5h9j-7G3q1N6Pa4egG9v2ScmigFKMSUv0dgZNbFOK1qlD9HsdB0VATZbVTk0i1SRSTX7V2bI6ju3PT3P6u72t_2metY7A5QnQyejgom6MT385RkFyMWJXM3bvgx3-awe1vv325zbmZHOOT509nnN0_KGEpJKr75sbxWTxebOqNuoD_Q0Tn6hE</recordid><startdate>200008</startdate><enddate>200008</enddate><creator>Milkiewicz, Piotr</creator><creator>Saksena, Sushma</creator><creator>Cardenas, Teresa</creator><creator>Mills, Charles O.</creator><creator>Elias, Elwyn</creator><general>Munksgaard International Publishers</general><general>Munksgaard</general><scope>BSCLL</scope><scope>IQODW</scope><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>200008</creationdate><title>Plasma elimination of cholyl-lysyl-fluorescein (CLF): a pilot study in patients with liver cirrhosis</title><author>Milkiewicz, Piotr ; Saksena, Sushma ; Cardenas, Teresa ; Mills, Charles O. ; Elias, Elwyn</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4480-d618af854a266e4da7774cca9d957383b05aa5149a3f04a41376f5002f4f632c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Cholic Acids - administration &amp; dosage</topic><topic>Cholic Acids - pharmacokinetics</topic><topic>cholyl-lysyl-fluorescein</topic><topic>Female</topic><topic>Fluoresceins - administration &amp; dosage</topic><topic>Fluoresceins - pharmacokinetics</topic><topic>Fluorescent Dyes - administration &amp; dosage</topic><topic>Fluorescent Dyes - pharmacokinetics</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Injections, Intravenous</topic><topic>Liver - metabolism</topic><topic>Liver - pathology</topic><topic>Liver Cirrhosis - diagnosis</topic><topic>Liver Cirrhosis - metabolism</topic><topic>liver disease</topic><topic>Liver Function Tests</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Other diseases. Semiology</topic><topic>Pilot Projects</topic><topic>plasma elimination</topic><topic>Reference Values</topic><topic>Sensitivity and Specificity</topic><toplevel>online_resources</toplevel><creatorcontrib>Milkiewicz, Piotr</creatorcontrib><creatorcontrib>Saksena, Sushma</creatorcontrib><creatorcontrib>Cardenas, Teresa</creatorcontrib><creatorcontrib>Mills, Charles O.</creatorcontrib><creatorcontrib>Elias, Elwyn</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><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>Liver (Copenhagen)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Milkiewicz, Piotr</au><au>Saksena, Sushma</au><au>Cardenas, Teresa</au><au>Mills, Charles O.</au><au>Elias, Elwyn</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plasma elimination of cholyl-lysyl-fluorescein (CLF): a pilot study in patients with liver cirrhosis</atitle><jtitle>Liver (Copenhagen)</jtitle><addtitle>Liver</addtitle><date>2000-08</date><risdate>2000</risdate><volume>20</volume><issue>4</issue><spage>330</spage><epage>334</epage><pages>330-334</pages><issn>0106-9543</issn><eissn>1600-0676</eissn><coden>LIVEDR</coden><abstract>: Background: Cholyl‐lysyl‐fluorescein (CLF) is a fluorescein‐labelled bile acid whose biological behaviour closely resembles that of naturally occurring cholyl glycine. Aim: The aim of this study was to analyze the CLF plasma elimination in patients with liver cirrhosis. Methods: A dose of CLF at 0.02 mg/kg b.w. was administered i.v. in 26 patients with liver cirrhosis and 9 healthy volunteers. Blood samples were collected before injection and then at 10 min intervals over 60 min. Plasma fluorescence was measured by a luminescence spectrometer and residual fluorescence over the time of the study was compared in each group. Routine liver function tests (rLFTs) were performed before each injection. Results: Plasma elimination of CLF was significantly impaired in patients with cirrhosis compared to healthy subjects with p values &lt;0.0001 at each analyzed time point. CLF test showed 100% sensitivity for liver cirrhosis when residual fluorescence was measured 30, 40, 50 and 60 min after injection. Routine LFTs showed 85% sensitivity for bilirubin, 84% for total bile acids, 69% for aspartate aminotransferase 62% for albumin and 50% for alkaline phosphatase. CLF elimination measured 60 min after injection correlated with Child‐Pugh score (r=0.3945; p&lt;0.05) and albumin (rs=0.6451; p&lt;0.001). No adverse reaction or side effects of CLF were observed. Conclusions: CLF test clearly distinguished between the two analyzed groups and was more sensitive than routine liver function tests. The test appears safe, simple to perform and analyze and after validation in larger cohorts of patients may have the potential to become a useful dynamic test of liver function.</abstract><cop>Copenhagen</cop><pub>Munksgaard International Publishers</pub><pmid>10959812</pmid><doi>10.1034/j.1600-0676.2000.020004330.x</doi><tpages>5</tpages></addata></record>
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subjects Adult
Biological and medical sciences
Cholic Acids - administration & dosage
Cholic Acids - pharmacokinetics
cholyl-lysyl-fluorescein
Female
Fluoresceins - administration & dosage
Fluoresceins - pharmacokinetics
Fluorescent Dyes - administration & dosage
Fluorescent Dyes - pharmacokinetics
Gastroenterology. Liver. Pancreas. Abdomen
Humans
Injections, Intravenous
Liver - metabolism
Liver - pathology
Liver Cirrhosis - diagnosis
Liver Cirrhosis - metabolism
liver disease
Liver Function Tests
Liver. Biliary tract. Portal circulation. Exocrine pancreas
Male
Medical sciences
Middle Aged
Other diseases. Semiology
Pilot Projects
plasma elimination
Reference Values
Sensitivity and Specificity
title Plasma elimination of cholyl-lysyl-fluorescein (CLF): a pilot study in patients with liver cirrhosis
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