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Development and characterization of dried blood spot materials for the measurement of immunoreactive trypsinogen
Objectives: In response to increasing numbers of states in the US that test newborn babies for cystic fibrosis (CF), the Newborn Screening Quality Assurance Programme initiated a pilot proficiency testing programme for immunoreactive trypsinogen (IRT), the biomarker for CF. Dried blood spot specimen...
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Published in: | Journal of medical screening 2006-06, Vol.13 (2), p.79-84 |
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creator | Li, Lixia Zhou, Yingtao Bell, Carol J Earley, Marie C Hannon, W Harry Mei, Joanne V |
description | Objectives: In response to increasing numbers of states in the US that test newborn babies for cystic fibrosis (CF), the Newborn Screening Quality Assurance Programme initiated a pilot proficiency testing programme for immunoreactive trypsinogen (IRT), the biomarker for CF. Dried blood spot specimens (DBS) were used to evaluate the performance of laboratories that screen babies for CF.
Methods: DBS were prepared from human whole blood enriched with physiologically relevant levels of IRT. Various methods of making IRT-enriched DBS were used to optimize the recovery and stability of the biomarker, including preparation of DBS from either intact or lysed red blood cells, varying the timing of IRT addition to blood before dispensing onto filter paper, adding a protease inhibitor cocktail, and treating serum with charcoal before IRT enrichment. The recovery and stability of IRT in DBS were assessed. Newborn screening laboratories were offered the opportunity to test blind-coded DBS in the pilot PT programme.
Results: IRT was stable in the filter paper matrix when stored for one year at either −20°C or 4°C. Fifty percent more IRT was recovered from DBS prepared with lysed red blood cells where the IRT was added to blood just before dispensing; however, protease inhibitors did not improve IRT recovery.
Conclusions: IRT in the DBS matrix is stable and can be shipped worldwide under ambient conditions. Optimal IRT recovery was achieved by adjustment of DBS production practices. Laboratories receiving specimens accurately measured IRT by a variety of commercial and in-house methods. |
doi_str_mv | 10.1258/096914106777589623 |
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Methods: DBS were prepared from human whole blood enriched with physiologically relevant levels of IRT. Various methods of making IRT-enriched DBS were used to optimize the recovery and stability of the biomarker, including preparation of DBS from either intact or lysed red blood cells, varying the timing of IRT addition to blood before dispensing onto filter paper, adding a protease inhibitor cocktail, and treating serum with charcoal before IRT enrichment. The recovery and stability of IRT in DBS were assessed. Newborn screening laboratories were offered the opportunity to test blind-coded DBS in the pilot PT programme.
Results: IRT was stable in the filter paper matrix when stored for one year at either −20°C or 4°C. Fifty percent more IRT was recovered from DBS prepared with lysed red blood cells where the IRT was added to blood just before dispensing; however, protease inhibitors did not improve IRT recovery.
Conclusions: IRT in the DBS matrix is stable and can be shipped worldwide under ambient conditions. Optimal IRT recovery was achieved by adjustment of DBS production practices. Laboratories receiving specimens accurately measured IRT by a variety of commercial and in-house methods.</description><identifier>ISSN: 0969-1413</identifier><identifier>EISSN: 1475-5793</identifier><identifier>DOI: 10.1258/096914106777589623</identifier><identifier>PMID: 16792830</identifier><identifier>CODEN: JMSCFE</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Charcoal - pharmacology ; Cystic Fibrosis - blood ; Cystic Fibrosis - diagnosis ; Humans ; Infant, Newborn ; Mass Screening - methods ; Mutation ; Neonatal Screening - instrumentation ; Neonatal Screening - methods ; Pilot Projects ; Protease Inhibitors - pharmacology ; Quality Control ; Specimen Handling ; Temperature ; Trypsinogen - chemistry ; Trypsinogen - immunology ; United States</subject><ispartof>Journal of medical screening, 2006-06, Vol.13 (2), p.79-84</ispartof><rights>2006 Royal Society of Medicine Press</rights><rights>Copyright Royal Society of Medicine Press Ltd. 2006</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-3fc76bdcd02e0bb1eaf9d2f9a0c78ba096f47b514a9a15939e59be4ef30be3cf3</citedby></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/16792830$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Lixia</creatorcontrib><creatorcontrib>Zhou, Yingtao</creatorcontrib><creatorcontrib>Bell, Carol J</creatorcontrib><creatorcontrib>Earley, Marie C</creatorcontrib><creatorcontrib>Hannon, W Harry</creatorcontrib><creatorcontrib>Mei, Joanne V</creatorcontrib><title>Development and characterization of dried blood spot materials for the measurement of immunoreactive trypsinogen</title><title>Journal of medical screening</title><addtitle>J Med Screen</addtitle><description>Objectives: In response to increasing numbers of states in the US that test newborn babies for cystic fibrosis (CF), the Newborn Screening Quality Assurance Programme initiated a pilot proficiency testing programme for immunoreactive trypsinogen (IRT), the biomarker for CF. Dried blood spot specimens (DBS) were used to evaluate the performance of laboratories that screen babies for CF.
Methods: DBS were prepared from human whole blood enriched with physiologically relevant levels of IRT. Various methods of making IRT-enriched DBS were used to optimize the recovery and stability of the biomarker, including preparation of DBS from either intact or lysed red blood cells, varying the timing of IRT addition to blood before dispensing onto filter paper, adding a protease inhibitor cocktail, and treating serum with charcoal before IRT enrichment. The recovery and stability of IRT in DBS were assessed. Newborn screening laboratories were offered the opportunity to test blind-coded DBS in the pilot PT programme.
Results: IRT was stable in the filter paper matrix when stored for one year at either −20°C or 4°C. Fifty percent more IRT was recovered from DBS prepared with lysed red blood cells where the IRT was added to blood just before dispensing; however, protease inhibitors did not improve IRT recovery.
Conclusions: IRT in the DBS matrix is stable and can be shipped worldwide under ambient conditions. Optimal IRT recovery was achieved by adjustment of DBS production practices. Laboratories receiving specimens accurately measured IRT by a variety of commercial and in-house methods.</description><subject>Charcoal - pharmacology</subject><subject>Cystic Fibrosis - blood</subject><subject>Cystic Fibrosis - diagnosis</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Mass Screening - methods</subject><subject>Mutation</subject><subject>Neonatal Screening - instrumentation</subject><subject>Neonatal Screening - methods</subject><subject>Pilot Projects</subject><subject>Protease Inhibitors - pharmacology</subject><subject>Quality Control</subject><subject>Specimen Handling</subject><subject>Temperature</subject><subject>Trypsinogen - chemistry</subject><subject>Trypsinogen - immunology</subject><subject>United States</subject><issn>0969-1413</issn><issn>1475-5793</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNp9kctKxDAUhoMoznh5ARcSXLirJk3TJEvxDoIbXZckPdEObVOTdkCf3owzMKDg6my-_zs3hE4ouaA5l5dElYoWlJRCCC5VmbMdNKeF4BkXiu2i-QrIEsFm6CDGBSGEUSr30YyWQuWSkTkabmAJrR866Ees-xrbdx20HSE0X3psfI-9w3VooMam9b7GcfAj7vQK0G3Ezgc8vgPuQMcpwI8mJZqum3ofIJmaJeAxfA6x6f0b9Edoz6UgHG_qIXq9u325fsienu8fr6-eMlvQfMyYs6I0ta1JDsQYCtqpOndKEyuk0WkzVwjDaaGVplwxBVwZKMAxYoBZxw7R-do7BP8xQRyrrokW2lb34KdYlZKXJWM0gWe_wIWfQp9mq3JaSCElLxKUryEbfIwBXDWEptPhs6KkWj2j-vuMFDrdmCfTQb2NbK6fgMs1EPUbbNv-o_wGWZOVKQ</recordid><startdate>200606</startdate><enddate>200606</enddate><creator>Li, Lixia</creator><creator>Zhou, Yingtao</creator><creator>Bell, Carol J</creator><creator>Earley, Marie C</creator><creator>Hannon, W Harry</creator><creator>Mei, Joanne V</creator><general>SAGE Publications</general><general>Sage Publications Ltd</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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>200606</creationdate><title>Development and characterization of dried blood spot materials for the measurement of immunoreactive trypsinogen</title><author>Li, Lixia ; Zhou, Yingtao ; Bell, Carol J ; Earley, Marie C ; Hannon, W Harry ; Mei, Joanne V</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c412t-3fc76bdcd02e0bb1eaf9d2f9a0c78ba096f47b514a9a15939e59be4ef30be3cf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Charcoal - pharmacology</topic><topic>Cystic Fibrosis - blood</topic><topic>Cystic Fibrosis - diagnosis</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Mass Screening - methods</topic><topic>Mutation</topic><topic>Neonatal Screening - instrumentation</topic><topic>Neonatal Screening - methods</topic><topic>Pilot Projects</topic><topic>Protease Inhibitors - pharmacology</topic><topic>Quality Control</topic><topic>Specimen Handling</topic><topic>Temperature</topic><topic>Trypsinogen - chemistry</topic><topic>Trypsinogen - immunology</topic><topic>United States</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Lixia</creatorcontrib><creatorcontrib>Zhou, Yingtao</creatorcontrib><creatorcontrib>Bell, Carol J</creatorcontrib><creatorcontrib>Earley, Marie C</creatorcontrib><creatorcontrib>Hannon, W Harry</creatorcontrib><creatorcontrib>Mei, Joanne V</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>Health Medical collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Consumer Health Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of medical screening</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Lixia</au><au>Zhou, Yingtao</au><au>Bell, Carol J</au><au>Earley, Marie C</au><au>Hannon, W Harry</au><au>Mei, Joanne V</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development and characterization of dried blood spot materials for the measurement of immunoreactive trypsinogen</atitle><jtitle>Journal of medical screening</jtitle><addtitle>J Med Screen</addtitle><date>2006-06</date><risdate>2006</risdate><volume>13</volume><issue>2</issue><spage>79</spage><epage>84</epage><pages>79-84</pages><issn>0969-1413</issn><eissn>1475-5793</eissn><coden>JMSCFE</coden><abstract>Objectives: In response to increasing numbers of states in the US that test newborn babies for cystic fibrosis (CF), the Newborn Screening Quality Assurance Programme initiated a pilot proficiency testing programme for immunoreactive trypsinogen (IRT), the biomarker for CF. Dried blood spot specimens (DBS) were used to evaluate the performance of laboratories that screen babies for CF.
Methods: DBS were prepared from human whole blood enriched with physiologically relevant levels of IRT. Various methods of making IRT-enriched DBS were used to optimize the recovery and stability of the biomarker, including preparation of DBS from either intact or lysed red blood cells, varying the timing of IRT addition to blood before dispensing onto filter paper, adding a protease inhibitor cocktail, and treating serum with charcoal before IRT enrichment. The recovery and stability of IRT in DBS were assessed. Newborn screening laboratories were offered the opportunity to test blind-coded DBS in the pilot PT programme.
Results: IRT was stable in the filter paper matrix when stored for one year at either −20°C or 4°C. Fifty percent more IRT was recovered from DBS prepared with lysed red blood cells where the IRT was added to blood just before dispensing; however, protease inhibitors did not improve IRT recovery.
Conclusions: IRT in the DBS matrix is stable and can be shipped worldwide under ambient conditions. Optimal IRT recovery was achieved by adjustment of DBS production practices. Laboratories receiving specimens accurately measured IRT by a variety of commercial and in-house methods.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>16792830</pmid><doi>10.1258/096914106777589623</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Charcoal - pharmacology Cystic Fibrosis - blood Cystic Fibrosis - diagnosis Humans Infant, Newborn Mass Screening - methods Mutation Neonatal Screening - instrumentation Neonatal Screening - methods Pilot Projects Protease Inhibitors - pharmacology Quality Control Specimen Handling Temperature Trypsinogen - chemistry Trypsinogen - immunology United States |
title | Development and characterization of dried blood spot materials for the measurement of immunoreactive trypsinogen |
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