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Preanalytical Variables Affecting the Quantification of Fatty Acid Ethyl Esters in Plasma and Serum Samples
Fatty acid ethyl esters (FAEEs) are cytotoxic nonoxidative ethanol metabolites produced by esterification of fatty acids and ethanol. FAEEs are detectable in blood up to 24 h after ethanol consumption. The objective of this study was to assess the impact of gender, serum or plasma triglyceride conce...
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Published in: | Clinical chemistry (Baltimore, Md.) Md.), 1999-12, Vol.45 (12), p.2183-2190 |
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container_end_page | 2190 |
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container_start_page | 2183 |
container_title | Clinical chemistry (Baltimore, Md.) |
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creator | Soderberg, Britt L Sicinska, Ewa T Blodget, Emily Cluette-Brown, Joanne E Suter, Paolo M Schuppisser, Theresa Vetter, Wilhem Laposata, Michael |
description | Fatty acid ethyl esters (FAEEs) are cytotoxic nonoxidative ethanol metabolites produced by esterification of fatty acids and ethanol. FAEEs are detectable in blood up to 24 h after ethanol consumption. The objective of this study was to assess the impact of gender, serum or plasma triglyceride concentration, time and temperature of specimen storage, type of alcoholic beverage ingested, and the rate of ethanol consumption on FAEE concentrations in plasma or serum.
For some studies, subject were recruited volunteers; in others, residual blood samples after ethanol quantification were used. FAEEs were isolated by solid-phase extraction and quantified by gas chromatography-mass spectrometry.
For weight-adjusted amounts of ethanol intake, FAEE concentrations were twofold greater for men than women (P /=24 h. The type of alcoholic beverage and rate of consumption did not affect FAEE concentrations.
These studies advance plasma and serum FAEE measurements closer to implementation as a clinical test for ethanol intake. |
doi_str_mv | 10.1093/clinchem/45.12.2183 |
format | article |
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For some studies, subject were recruited volunteers; in others, residual blood samples after ethanol quantification were used. FAEEs were isolated by solid-phase extraction and quantified by gas chromatography-mass spectrometry.
For weight-adjusted amounts of ethanol intake, FAEE concentrations were twofold greater for men than women (P </=0.05). Accounting for triglycerides improved the correlation between blood ethanol concentrations and FAEE concentrations for both men (from r = 0.640 to r = 0.874) and women (from r = 0.619 to r = 0.673). FAEE concentrations did not change when samples were stored at or below 4 degrees C, but doubled when stored at room temperature for >/=24 h. The type of alcoholic beverage and rate of consumption did not affect FAEE concentrations.
These studies advance plasma and serum FAEE measurements closer to implementation as a clinical test for ethanol intake.</description><identifier>ISSN: 0009-9147</identifier><identifier>EISSN: 1530-8561</identifier><identifier>DOI: 10.1093/clinchem/45.12.2183</identifier><identifier>PMID: 10585351</identifier><identifier>CODEN: CLCHAU</identifier><language>eng</language><publisher>Washington, DC: Am Assoc Clin Chem</publisher><subject>Alcohol Drinking - blood ; Alcoholic Beverages ; Biological and medical sciences ; Blood Preservation ; Cryopreservation ; Esters - blood ; Fatty Acids - blood ; Female ; General aspects. Methods ; Humans ; Male ; Medical sciences ; Sex Factors ; Temperature ; Time Factors ; Toxicology ; Triglycerides - blood</subject><ispartof>Clinical chemistry (Baltimore, Md.), 1999-12, Vol.45 (12), p.2183-2190</ispartof><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c407t-aefffafd4386a607c0c4f292206b49fd420e13f61cd3c25e4900838de1d92b103</citedby><cites>FETCH-LOGICAL-c407t-aefffafd4386a607c0c4f292206b49fd420e13f61cd3c25e4900838de1d92b103</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1261761$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10585351$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Soderberg, Britt L</creatorcontrib><creatorcontrib>Sicinska, Ewa T</creatorcontrib><creatorcontrib>Blodget, Emily</creatorcontrib><creatorcontrib>Cluette-Brown, Joanne E</creatorcontrib><creatorcontrib>Suter, Paolo M</creatorcontrib><creatorcontrib>Schuppisser, Theresa</creatorcontrib><creatorcontrib>Vetter, Wilhem</creatorcontrib><creatorcontrib>Laposata, Michael</creatorcontrib><title>Preanalytical Variables Affecting the Quantification of Fatty Acid Ethyl Esters in Plasma and Serum Samples</title><title>Clinical chemistry (Baltimore, Md.)</title><addtitle>Clin Chem</addtitle><description>Fatty acid ethyl esters (FAEEs) are cytotoxic nonoxidative ethanol metabolites produced by esterification of fatty acids and ethanol. FAEEs are detectable in blood up to 24 h after ethanol consumption. The objective of this study was to assess the impact of gender, serum or plasma triglyceride concentration, time and temperature of specimen storage, type of alcoholic beverage ingested, and the rate of ethanol consumption on FAEE concentrations in plasma or serum.
For some studies, subject were recruited volunteers; in others, residual blood samples after ethanol quantification were used. FAEEs were isolated by solid-phase extraction and quantified by gas chromatography-mass spectrometry.
For weight-adjusted amounts of ethanol intake, FAEE concentrations were twofold greater for men than women (P </=0.05). Accounting for triglycerides improved the correlation between blood ethanol concentrations and FAEE concentrations for both men (from r = 0.640 to r = 0.874) and women (from r = 0.619 to r = 0.673). FAEE concentrations did not change when samples were stored at or below 4 degrees C, but doubled when stored at room temperature for >/=24 h. The type of alcoholic beverage and rate of consumption did not affect FAEE concentrations.
These studies advance plasma and serum FAEE measurements closer to implementation as a clinical test for ethanol intake.</description><subject>Alcohol Drinking - blood</subject><subject>Alcoholic Beverages</subject><subject>Biological and medical sciences</subject><subject>Blood Preservation</subject><subject>Cryopreservation</subject><subject>Esters - blood</subject><subject>Fatty Acids - blood</subject><subject>Female</subject><subject>General aspects. Methods</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Sex Factors</subject><subject>Temperature</subject><subject>Time Factors</subject><subject>Toxicology</subject><subject>Triglycerides - blood</subject><issn>0009-9147</issn><issn>1530-8561</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNpNkE1rGzEQhkVpaNykv6BQdCjtaR19rXb3aILTFAJJSdqrGGulrFqt1pW0GP_7ytihOQ0zPO878CD0kZIlJR2_0t4FPZjxStRLypaMtvwNWtCak6qtJX2LFoSQruqoaM7R-5R-l1U0rXyHzimp25rXdIH-PEQDAfw-Ow0e_4LoYONNwitrjc4uPOM8GPxjhpCdLUx2U8CTxTeQ8x6vtOvxOg97j9cpm5iwC_jBQxoBQ-jxo4nziB9h3JbOS3RmwSfz4TQv0M-b9dP1bXV3_-379equ0oI0uQJjrQXbC95KkKTRRAvLOsaI3Iiu3BkxlFtJdc81q43oCGl52xvad2xDCb9AX4692zj9nU3KanRJG-8hmGlOSnZcSEJYAfkR1HFKKRqrttGNEPeKEnVwrF4cK1ErytTBcUl9OtXPm9H0rzJHqQX4fAIgFak2QtAu_eeYpI08YF-P2OCeh52LRhVr3pdWqna73auP_wA6vpTA</recordid><startdate>19991201</startdate><enddate>19991201</enddate><creator>Soderberg, Britt L</creator><creator>Sicinska, Ewa T</creator><creator>Blodget, Emily</creator><creator>Cluette-Brown, Joanne E</creator><creator>Suter, Paolo M</creator><creator>Schuppisser, Theresa</creator><creator>Vetter, Wilhem</creator><creator>Laposata, Michael</creator><general>Am Assoc Clin Chem</general><general>American Association for Clinical Chemistry</general><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>19991201</creationdate><title>Preanalytical Variables Affecting the Quantification of Fatty Acid Ethyl Esters in Plasma and Serum Samples</title><author>Soderberg, Britt L ; Sicinska, Ewa T ; Blodget, Emily ; Cluette-Brown, Joanne E ; Suter, Paolo M ; Schuppisser, Theresa ; Vetter, Wilhem ; Laposata, Michael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c407t-aefffafd4386a607c0c4f292206b49fd420e13f61cd3c25e4900838de1d92b103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Alcohol Drinking - blood</topic><topic>Alcoholic Beverages</topic><topic>Biological and medical sciences</topic><topic>Blood Preservation</topic><topic>Cryopreservation</topic><topic>Esters - blood</topic><topic>Fatty Acids - blood</topic><topic>Female</topic><topic>General aspects. Methods</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Sex Factors</topic><topic>Temperature</topic><topic>Time Factors</topic><topic>Toxicology</topic><topic>Triglycerides - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Soderberg, Britt L</creatorcontrib><creatorcontrib>Sicinska, Ewa T</creatorcontrib><creatorcontrib>Blodget, Emily</creatorcontrib><creatorcontrib>Cluette-Brown, Joanne E</creatorcontrib><creatorcontrib>Suter, Paolo M</creatorcontrib><creatorcontrib>Schuppisser, Theresa</creatorcontrib><creatorcontrib>Vetter, Wilhem</creatorcontrib><creatorcontrib>Laposata, Michael</creatorcontrib><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>Clinical chemistry (Baltimore, Md.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Soderberg, Britt L</au><au>Sicinska, Ewa T</au><au>Blodget, Emily</au><au>Cluette-Brown, Joanne E</au><au>Suter, Paolo M</au><au>Schuppisser, Theresa</au><au>Vetter, Wilhem</au><au>Laposata, Michael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preanalytical Variables Affecting the Quantification of Fatty Acid Ethyl Esters in Plasma and Serum Samples</atitle><jtitle>Clinical chemistry (Baltimore, Md.)</jtitle><addtitle>Clin Chem</addtitle><date>1999-12-01</date><risdate>1999</risdate><volume>45</volume><issue>12</issue><spage>2183</spage><epage>2190</epage><pages>2183-2190</pages><issn>0009-9147</issn><eissn>1530-8561</eissn><coden>CLCHAU</coden><abstract>Fatty acid ethyl esters (FAEEs) are cytotoxic nonoxidative ethanol metabolites produced by esterification of fatty acids and ethanol. FAEEs are detectable in blood up to 24 h after ethanol consumption. The objective of this study was to assess the impact of gender, serum or plasma triglyceride concentration, time and temperature of specimen storage, type of alcoholic beverage ingested, and the rate of ethanol consumption on FAEE concentrations in plasma or serum.
For some studies, subject were recruited volunteers; in others, residual blood samples after ethanol quantification were used. FAEEs were isolated by solid-phase extraction and quantified by gas chromatography-mass spectrometry.
For weight-adjusted amounts of ethanol intake, FAEE concentrations were twofold greater for men than women (P </=0.05). Accounting for triglycerides improved the correlation between blood ethanol concentrations and FAEE concentrations for both men (from r = 0.640 to r = 0.874) and women (from r = 0.619 to r = 0.673). FAEE concentrations did not change when samples were stored at or below 4 degrees C, but doubled when stored at room temperature for >/=24 h. The type of alcoholic beverage and rate of consumption did not affect FAEE concentrations.
These studies advance plasma and serum FAEE measurements closer to implementation as a clinical test for ethanol intake.</abstract><cop>Washington, DC</cop><pub>Am Assoc Clin Chem</pub><pmid>10585351</pmid><doi>10.1093/clinchem/45.12.2183</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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source | Oxford University Press:Jisc Collections:OUP Read and Publish 2024-2025 (2024 collection) (Reading list) |
subjects | Alcohol Drinking - blood Alcoholic Beverages Biological and medical sciences Blood Preservation Cryopreservation Esters - blood Fatty Acids - blood Female General aspects. Methods Humans Male Medical sciences Sex Factors Temperature Time Factors Toxicology Triglycerides - blood |
title | Preanalytical Variables Affecting the Quantification of Fatty Acid Ethyl Esters in Plasma and Serum Samples |
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