Modeling red blood cell survival data
Anaemia of chronic kidney disease (CKD) is a common complication in patients with renal impairment, especially in end-stage renal failure. As well as erythropoietin deficiency, decreased red blood cell survival is a contributing factor. However, it remains unclear which mechanism underlies the alter...
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Veröffentlicht in: | Journal of pharmacokinetics and pharmacodynamics 2011-12, Vol.38 (6), p.787-801 |
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creator | Korell, Julia Vos, Frederiek E. Coulter, Carolyn V. Schollum, John B. Walker, Robert J. Duffull, Stephen B. |
description | Anaemia of chronic kidney disease (CKD) is a common complication in patients with renal impairment, especially in end-stage renal failure. As well as erythropoietin deficiency, decreased red blood cell survival is a contributing factor. However, it remains unclear which mechanism underlies the altered survival of red blood cells (RBCs). In this work a previously developed statistical model for RBC survival was applied to clinical data obtained from 14 patients with CKD undergoing hemodialysis as well as 14 healthy controls using radioactive chromium (
51
Cr) as random labelling method. A classical two-stage approach and a full population analysis were applied to estimate the key parameters controlling random destruction and senescence in the model. Estimating random destruction was preferred over estimating an accelerated senescence in both approaches and both groups as it provided the better fit to the data. Due to significant nonspecific random loss of the label from the cells that cannot be quantified directly only a relative RBC survival can be obtained from data using
51
Cr as labelling method. Nevertheless, RBC survival was found to be significantly reduced in CKD patients compared to the controls with a relative reduction of 20–30% depending on the analysis method used. |
doi_str_mv | 10.1007/s10928-011-9220-6 |
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51
Cr) as random labelling method. A classical two-stage approach and a full population analysis were applied to estimate the key parameters controlling random destruction and senescence in the model. Estimating random destruction was preferred over estimating an accelerated senescence in both approaches and both groups as it provided the better fit to the data. Due to significant nonspecific random loss of the label from the cells that cannot be quantified directly only a relative RBC survival can be obtained from data using
51
Cr as labelling method. Nevertheless, RBC survival was found to be significantly reduced in CKD patients compared to the controls with a relative reduction of 20–30% depending on the analysis method used.</description><identifier>ISSN: 1567-567X</identifier><identifier>EISSN: 1573-8744</identifier><identifier>DOI: 10.1007/s10928-011-9220-6</identifier><identifier>PMID: 21997468</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Anemia - blood ; Anemia - complications ; Anemia - diagnostic imaging ; Anemia - physiopathology ; Biochemistry ; Biomedical and Life Sciences ; Biomedical Engineering and Bioengineering ; Biomedicine ; Case-Control Studies ; Cell Survival - physiology ; Chromium Radioisotopes ; Erythrocytes - diagnostic imaging ; Erythrocytes - physiology ; Female ; Humans ; Kidney Failure, Chronic - blood ; Kidney Failure, Chronic - complications ; Kidney Failure, Chronic - diagnostic imaging ; Kidney Failure, Chronic - physiopathology ; Male ; Middle Aged ; Models, Biological ; Pharmacology/Toxicology ; Pharmacy ; Radionuclide Imaging ; Renal Dialysis ; Veterinary Medicine/Veterinary Science</subject><ispartof>Journal of pharmacokinetics and pharmacodynamics, 2011-12, Vol.38 (6), p.787-801</ispartof><rights>Springer Science+Business Media, LLC 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c370t-b39768be95fa5bc02d8873a59352e8c7a92e9dd535ed53555c70f0216a7ffa163</citedby><cites>FETCH-LOGICAL-c370t-b39768be95fa5bc02d8873a59352e8c7a92e9dd535ed53555c70f0216a7ffa163</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10928-011-9220-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10928-011-9220-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51298</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21997468$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Korell, Julia</creatorcontrib><creatorcontrib>Vos, Frederiek E.</creatorcontrib><creatorcontrib>Coulter, Carolyn V.</creatorcontrib><creatorcontrib>Schollum, John B.</creatorcontrib><creatorcontrib>Walker, Robert J.</creatorcontrib><creatorcontrib>Duffull, Stephen B.</creatorcontrib><title>Modeling red blood cell survival data</title><title>Journal of pharmacokinetics and pharmacodynamics</title><addtitle>J Pharmacokinet Pharmacodyn</addtitle><addtitle>J Pharmacokinet Pharmacodyn</addtitle><description>Anaemia of chronic kidney disease (CKD) is a common complication in patients with renal impairment, especially in end-stage renal failure. As well as erythropoietin deficiency, decreased red blood cell survival is a contributing factor. However, it remains unclear which mechanism underlies the altered survival of red blood cells (RBCs). In this work a previously developed statistical model for RBC survival was applied to clinical data obtained from 14 patients with CKD undergoing hemodialysis as well as 14 healthy controls using radioactive chromium (
51
Cr) as random labelling method. A classical two-stage approach and a full population analysis were applied to estimate the key parameters controlling random destruction and senescence in the model. Estimating random destruction was preferred over estimating an accelerated senescence in both approaches and both groups as it provided the better fit to the data. Due to significant nonspecific random loss of the label from the cells that cannot be quantified directly only a relative RBC survival can be obtained from data using
51
Cr as labelling method. Nevertheless, RBC survival was found to be significantly reduced in CKD patients compared to the controls with a relative reduction of 20–30% depending on the analysis method used.</description><subject>Anemia - blood</subject><subject>Anemia - complications</subject><subject>Anemia - diagnostic imaging</subject><subject>Anemia - physiopathology</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedical Engineering and Bioengineering</subject><subject>Biomedicine</subject><subject>Case-Control Studies</subject><subject>Cell Survival - physiology</subject><subject>Chromium Radioisotopes</subject><subject>Erythrocytes - diagnostic imaging</subject><subject>Erythrocytes - physiology</subject><subject>Female</subject><subject>Humans</subject><subject>Kidney Failure, Chronic - blood</subject><subject>Kidney Failure, Chronic - complications</subject><subject>Kidney Failure, Chronic - diagnostic imaging</subject><subject>Kidney Failure, Chronic - physiopathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Models, Biological</subject><subject>Pharmacology/Toxicology</subject><subject>Pharmacy</subject><subject>Radionuclide Imaging</subject><subject>Renal Dialysis</subject><subject>Veterinary Medicine/Veterinary Science</subject><issn>1567-567X</issn><issn>1573-8744</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1kFtLwzAYhoMoTqc_wBspgngV_ZI0p0sZnmDijYJ3IW3S0dG1M1kH_ntTOhUEL3KAPHm_lwehMwLXBEDeRAKaKgyEYE0pYLGHjgiXDCuZ5_vDXUic1vsEHce4BCCCUzhEE0q0lrlQR-jyuXO-qdtFFrzLiqbrXFb6psliH7b11jaZsxt7gg4q20R_ujun6O3-7nX2iOcvD0-z2zkumYQNLpiWQhVe88ryogTqlJLMcs049aqUVlOvneOM-2HjvJRQASXCyqqyRLApuhpz16H76H3cmFUdhzq29V0fjYacUqo4JPLiD7ns-tCmcgliSioQKkFkhMrQxRh8ZdahXtnwaQiYwaAZDZpk0AwGzVDhfBfcFyvvfn58K0sAHYGYntqFD7-T_0_9AliAeP4</recordid><startdate>20111201</startdate><enddate>20111201</enddate><creator>Korell, Julia</creator><creator>Vos, Frederiek E.</creator><creator>Coulter, Carolyn V.</creator><creator>Schollum, John B.</creator><creator>Walker, Robert J.</creator><creator>Duffull, Stephen B.</creator><general>Springer US</general><general>Springer Nature B.V</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>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20111201</creationdate><title>Modeling red blood cell survival data</title><author>Korell, Julia ; Vos, Frederiek E. ; Coulter, Carolyn V. ; Schollum, John B. ; Walker, Robert J. ; Duffull, Stephen B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c370t-b39768be95fa5bc02d8873a59352e8c7a92e9dd535ed53555c70f0216a7ffa163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Anemia - blood</topic><topic>Anemia - complications</topic><topic>Anemia - diagnostic imaging</topic><topic>Anemia - physiopathology</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedical Engineering and Bioengineering</topic><topic>Biomedicine</topic><topic>Case-Control Studies</topic><topic>Cell Survival - physiology</topic><topic>Chromium Radioisotopes</topic><topic>Erythrocytes - diagnostic imaging</topic><topic>Erythrocytes - physiology</topic><topic>Female</topic><topic>Humans</topic><topic>Kidney Failure, Chronic - blood</topic><topic>Kidney Failure, Chronic - complications</topic><topic>Kidney Failure, Chronic - diagnostic imaging</topic><topic>Kidney Failure, Chronic - physiopathology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Models, Biological</topic><topic>Pharmacology/Toxicology</topic><topic>Pharmacy</topic><topic>Radionuclide Imaging</topic><topic>Renal Dialysis</topic><topic>Veterinary Medicine/Veterinary Science</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Korell, Julia</creatorcontrib><creatorcontrib>Vos, Frederiek E.</creatorcontrib><creatorcontrib>Coulter, Carolyn V.</creatorcontrib><creatorcontrib>Schollum, John B.</creatorcontrib><creatorcontrib>Walker, Robert J.</creatorcontrib><creatorcontrib>Duffull, Stephen B.</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>Virology and AIDS Abstracts</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>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</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>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</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 pharmacokinetics and pharmacodynamics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Korell, Julia</au><au>Vos, Frederiek E.</au><au>Coulter, Carolyn V.</au><au>Schollum, John B.</au><au>Walker, Robert J.</au><au>Duffull, Stephen B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modeling red blood cell survival data</atitle><jtitle>Journal of pharmacokinetics and pharmacodynamics</jtitle><stitle>J Pharmacokinet Pharmacodyn</stitle><addtitle>J Pharmacokinet Pharmacodyn</addtitle><date>2011-12-01</date><risdate>2011</risdate><volume>38</volume><issue>6</issue><spage>787</spage><epage>801</epage><pages>787-801</pages><issn>1567-567X</issn><eissn>1573-8744</eissn><abstract>Anaemia of chronic kidney disease (CKD) is a common complication in patients with renal impairment, especially in end-stage renal failure. As well as erythropoietin deficiency, decreased red blood cell survival is a contributing factor. However, it remains unclear which mechanism underlies the altered survival of red blood cells (RBCs). In this work a previously developed statistical model for RBC survival was applied to clinical data obtained from 14 patients with CKD undergoing hemodialysis as well as 14 healthy controls using radioactive chromium (
51
Cr) as random labelling method. A classical two-stage approach and a full population analysis were applied to estimate the key parameters controlling random destruction and senescence in the model. Estimating random destruction was preferred over estimating an accelerated senescence in both approaches and both groups as it provided the better fit to the data. Due to significant nonspecific random loss of the label from the cells that cannot be quantified directly only a relative RBC survival can be obtained from data using
51
Cr as labelling method. Nevertheless, RBC survival was found to be significantly reduced in CKD patients compared to the controls with a relative reduction of 20–30% depending on the analysis method used.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>21997468</pmid><doi>10.1007/s10928-011-9220-6</doi><tpages>15</tpages></addata></record> |
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subjects | Anemia - blood Anemia - complications Anemia - diagnostic imaging Anemia - physiopathology Biochemistry Biomedical and Life Sciences Biomedical Engineering and Bioengineering Biomedicine Case-Control Studies Cell Survival - physiology Chromium Radioisotopes Erythrocytes - diagnostic imaging Erythrocytes - physiology Female Humans Kidney Failure, Chronic - blood Kidney Failure, Chronic - complications Kidney Failure, Chronic - diagnostic imaging Kidney Failure, Chronic - physiopathology Male Middle Aged Models, Biological Pharmacology/Toxicology Pharmacy Radionuclide Imaging Renal Dialysis Veterinary Medicine/Veterinary Science |
title | Modeling red blood cell survival data |
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