Does Islet Size Really Influence Graft Function After Clinical Islet Transplantation?
BACKGROUNDIt has been proposed that islet transplants comprised primarily of small rather than large islets may provide better graft function, due to their lower susceptibility to hypoxic damage. Our aim was to determine whether islet size correlated with in vivo graft function in islet transplant r...
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Veröffentlicht in: | Transplantation 2018-11, Vol.102 (11), p.1857-1863 |
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container_title | Transplantation |
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creator | Hughes, Stephen J Bateman, Paul A Cross, Sarah E Brandhorst, Daniel Brandhorst, Heide Spiliotis, Ioannis Ballav, Chitrabhanu Rosenthal, Miranda Rutter, Martin K Shaw, James Gough, Stephen Johnson, Paul R.V |
description | BACKGROUNDIt has been proposed that islet transplants comprised primarily of small rather than large islets may provide better graft function, due to their lower susceptibility to hypoxic damage. Our aim was to determine whether islet size correlated with in vivo graft function in islet transplant recipients with C peptide–negative type 1 diabetes when islets have undergone pretransplant islet culture.
METHODSHuman pancreatic islets were isolated, cultured for 24 hours and infused by standardized protocols. Ninety-minute stimulated C-peptide concentrations were determined during a standard meal tolerance test 3 months posttransplant. The islet isolation index (IEq/islet number) was determined immediately after isolation and again before transplantation (after tissue culture). This was correlated with patient insulin requirement or stimulated C-peptide.
RESULTSChanges in insulin requirement did not significantly correlate with islet isolation index. Stimulated C-peptide correlated weakly with IEq at isolation (P = 0.40) and significantly with IEq at transplantation (P = 0.018). Stimulated C-peptide correlated with islet number at isolation (P = 0.013) and more strongly with the islet number at transplantation (P = 0.001). In contrast, the correlation of stimulated C-peptide and islet isolation index was weaker (P = 0.018), and this was poorer at transplantation (P = 0.034). Using linear regression, the strongest association with graft function was islet number (r = 0.722, P = 0.001). Islet size was not related to graft function after adjusting for islet volume or number.
CONCLUSIONSThese data show no clear correlation between islet isolation index and graft function; both small and large islets are suitable for transplantation, provided the islets have survived a short culture period postisolation. |
doi_str_mv | 10.1097/TP.0000000000002392 |
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METHODSHuman pancreatic islets were isolated, cultured for 24 hours and infused by standardized protocols. Ninety-minute stimulated C-peptide concentrations were determined during a standard meal tolerance test 3 months posttransplant. The islet isolation index (IEq/islet number) was determined immediately after isolation and again before transplantation (after tissue culture). This was correlated with patient insulin requirement or stimulated C-peptide.
RESULTSChanges in insulin requirement did not significantly correlate with islet isolation index. Stimulated C-peptide correlated weakly with IEq at isolation (P = 0.40) and significantly with IEq at transplantation (P = 0.018). Stimulated C-peptide correlated with islet number at isolation (P = 0.013) and more strongly with the islet number at transplantation (P = 0.001). In contrast, the correlation of stimulated C-peptide and islet isolation index was weaker (P = 0.018), and this was poorer at transplantation (P = 0.034). Using linear regression, the strongest association with graft function was islet number (r = 0.722, P = 0.001). Islet size was not related to graft function after adjusting for islet volume or number.
CONCLUSIONSThese data show no clear correlation between islet isolation index and graft function; both small and large islets are suitable for transplantation, provided the islets have survived a short culture period postisolation.</description><identifier>ISSN: 0041-1337</identifier><identifier>EISSN: 1534-6080</identifier><identifier>DOI: 10.1097/TP.0000000000002392</identifier><identifier>PMID: 30063695</identifier><language>eng</language><publisher>United States: Copyright Wolters Kluwer Health, Inc. All rights reserved</publisher><subject>Original Basic Science—General</subject><ispartof>Transplantation, 2018-11, Vol.102 (11), p.1857-1863</ispartof><rights>Copyright © 2018 Wolters Kluwer Health, Inc. All rights reserved.</rights><rights>Copyright © 2018 The Author(s). Published by Wolters Kluwer Health, Inc. 2018 Wolters Kluwer Health, Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5032-3b7ec94dfff1ae6f1c090dfde28f5ffd6b68237a64b2d637312d417244fa78133</citedby><cites>FETCH-LOGICAL-c5032-3b7ec94dfff1ae6f1c090dfde28f5ffd6b68237a64b2d637312d417244fa78133</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,778,782,883,27911,27912</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30063695$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hughes, Stephen J</creatorcontrib><creatorcontrib>Bateman, Paul A</creatorcontrib><creatorcontrib>Cross, Sarah E</creatorcontrib><creatorcontrib>Brandhorst, Daniel</creatorcontrib><creatorcontrib>Brandhorst, Heide</creatorcontrib><creatorcontrib>Spiliotis, Ioannis</creatorcontrib><creatorcontrib>Ballav, Chitrabhanu</creatorcontrib><creatorcontrib>Rosenthal, Miranda</creatorcontrib><creatorcontrib>Rutter, Martin K</creatorcontrib><creatorcontrib>Shaw, James</creatorcontrib><creatorcontrib>Gough, Stephen</creatorcontrib><creatorcontrib>Johnson, Paul R.V</creatorcontrib><title>Does Islet Size Really Influence Graft Function After Clinical Islet Transplantation?</title><title>Transplantation</title><addtitle>Transplantation</addtitle><description>BACKGROUNDIt has been proposed that islet transplants comprised primarily of small rather than large islets may provide better graft function, due to their lower susceptibility to hypoxic damage. Our aim was to determine whether islet size correlated with in vivo graft function in islet transplant recipients with C peptide–negative type 1 diabetes when islets have undergone pretransplant islet culture.
METHODSHuman pancreatic islets were isolated, cultured for 24 hours and infused by standardized protocols. Ninety-minute stimulated C-peptide concentrations were determined during a standard meal tolerance test 3 months posttransplant. The islet isolation index (IEq/islet number) was determined immediately after isolation and again before transplantation (after tissue culture). This was correlated with patient insulin requirement or stimulated C-peptide.
RESULTSChanges in insulin requirement did not significantly correlate with islet isolation index. Stimulated C-peptide correlated weakly with IEq at isolation (P = 0.40) and significantly with IEq at transplantation (P = 0.018). Stimulated C-peptide correlated with islet number at isolation (P = 0.013) and more strongly with the islet number at transplantation (P = 0.001). In contrast, the correlation of stimulated C-peptide and islet isolation index was weaker (P = 0.018), and this was poorer at transplantation (P = 0.034). Using linear regression, the strongest association with graft function was islet number (r = 0.722, P = 0.001). Islet size was not related to graft function after adjusting for islet volume or number.
CONCLUSIONSThese data show no clear correlation between islet isolation index and graft function; both small and large islets are suitable for transplantation, provided the islets have survived a short culture period postisolation.</description><subject>Original Basic Science—General</subject><issn>0041-1337</issn><issn>1534-6080</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kTtPwzAUhS0EoqXwC5BQRpYUvxInCwiVVyUkKiiz5TrXNOA6xU6oyq8nVUsFDHi5g79z7uMgdExwn-BcnI1HffzjUZbTHdQlCeNxijO8i7oYcxITxkQHHYTw2kIJE2IfdRjGKUvzpIueryoI0TBYqKOn8hOiR1DWLqOhM7YBpyG69crU0U3jdF1WLro0NfhoYEtXamU3yrFXLsytcrVaQReHaM8oG-BoU3vo-eZ6PLiL7x9uh4PL-1gnmNGYTQTonBfGGKIgNUTjHBemAJqZxJginaQZZUKlfEKLlAlGaMGJoJwbJbJ2sR46X_vOm8kMCg2u9srKuS9nyi9lpUr5-8eVU_lSfUixulDCW4PTjYGv3hsItZyVQYNtV4GqCZLijCQ8T_gKZWtU-yoED2bbhmC5CkSOR_JvIK3q5OeEW813Ai0g1sCisu1lw5ttFuDltI2hnv5r_QWKZpgJ</recordid><startdate>201811</startdate><enddate>201811</enddate><creator>Hughes, Stephen J</creator><creator>Bateman, Paul A</creator><creator>Cross, Sarah E</creator><creator>Brandhorst, Daniel</creator><creator>Brandhorst, Heide</creator><creator>Spiliotis, Ioannis</creator><creator>Ballav, Chitrabhanu</creator><creator>Rosenthal, Miranda</creator><creator>Rutter, Martin K</creator><creator>Shaw, James</creator><creator>Gough, Stephen</creator><creator>Johnson, Paul R.V</creator><general>Copyright Wolters Kluwer Health, Inc. All rights reserved</general><general>Lippincott Williams & Wilkins</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201811</creationdate><title>Does Islet Size Really Influence Graft Function After Clinical Islet Transplantation?</title><author>Hughes, Stephen J ; Bateman, Paul A ; Cross, Sarah E ; Brandhorst, Daniel ; Brandhorst, Heide ; Spiliotis, Ioannis ; Ballav, Chitrabhanu ; Rosenthal, Miranda ; Rutter, Martin K ; Shaw, James ; Gough, Stephen ; Johnson, Paul R.V</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5032-3b7ec94dfff1ae6f1c090dfde28f5ffd6b68237a64b2d637312d417244fa78133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Original Basic Science—General</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hughes, Stephen J</creatorcontrib><creatorcontrib>Bateman, Paul A</creatorcontrib><creatorcontrib>Cross, Sarah E</creatorcontrib><creatorcontrib>Brandhorst, Daniel</creatorcontrib><creatorcontrib>Brandhorst, Heide</creatorcontrib><creatorcontrib>Spiliotis, Ioannis</creatorcontrib><creatorcontrib>Ballav, Chitrabhanu</creatorcontrib><creatorcontrib>Rosenthal, Miranda</creatorcontrib><creatorcontrib>Rutter, Martin K</creatorcontrib><creatorcontrib>Shaw, James</creatorcontrib><creatorcontrib>Gough, Stephen</creatorcontrib><creatorcontrib>Johnson, Paul R.V</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hughes, Stephen J</au><au>Bateman, Paul A</au><au>Cross, Sarah E</au><au>Brandhorst, Daniel</au><au>Brandhorst, Heide</au><au>Spiliotis, Ioannis</au><au>Ballav, Chitrabhanu</au><au>Rosenthal, Miranda</au><au>Rutter, Martin K</au><au>Shaw, James</au><au>Gough, Stephen</au><au>Johnson, Paul R.V</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Does Islet Size Really Influence Graft Function After Clinical Islet Transplantation?</atitle><jtitle>Transplantation</jtitle><addtitle>Transplantation</addtitle><date>2018-11</date><risdate>2018</risdate><volume>102</volume><issue>11</issue><spage>1857</spage><epage>1863</epage><pages>1857-1863</pages><issn>0041-1337</issn><eissn>1534-6080</eissn><abstract>BACKGROUNDIt has been proposed that islet transplants comprised primarily of small rather than large islets may provide better graft function, due to their lower susceptibility to hypoxic damage. Our aim was to determine whether islet size correlated with in vivo graft function in islet transplant recipients with C peptide–negative type 1 diabetes when islets have undergone pretransplant islet culture.
METHODSHuman pancreatic islets were isolated, cultured for 24 hours and infused by standardized protocols. Ninety-minute stimulated C-peptide concentrations were determined during a standard meal tolerance test 3 months posttransplant. The islet isolation index (IEq/islet number) was determined immediately after isolation and again before transplantation (after tissue culture). This was correlated with patient insulin requirement or stimulated C-peptide.
RESULTSChanges in insulin requirement did not significantly correlate with islet isolation index. Stimulated C-peptide correlated weakly with IEq at isolation (P = 0.40) and significantly with IEq at transplantation (P = 0.018). Stimulated C-peptide correlated with islet number at isolation (P = 0.013) and more strongly with the islet number at transplantation (P = 0.001). In contrast, the correlation of stimulated C-peptide and islet isolation index was weaker (P = 0.018), and this was poorer at transplantation (P = 0.034). Using linear regression, the strongest association with graft function was islet number (r = 0.722, P = 0.001). Islet size was not related to graft function after adjusting for islet volume or number.
CONCLUSIONSThese data show no clear correlation between islet isolation index and graft function; both small and large islets are suitable for transplantation, provided the islets have survived a short culture period postisolation.</abstract><cop>United States</cop><pub>Copyright Wolters Kluwer Health, Inc. All rights reserved</pub><pmid>30063695</pmid><doi>10.1097/TP.0000000000002392</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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title | Does Islet Size Really Influence Graft Function After Clinical Islet Transplantation? |
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