<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lemos JRN</submitter><funding>Diabetes Research Institute Foundation</funding><funding>National Center for Advancing Translational Sciences</funding><funding>American Diabetes Association COVID-19 Research Award</funding><funding>National Institutes of Health awards</funding><funding>Miami Clinical and Translational Science Institute</funding><funding>US Department of Veterans Affairs Merit Review Award</funding><funding>NIMHD NIH HHS</funding><funding>Juvenile Diabetes Research Foundation International</funding><funding>National Institutes of Health</funding><funding>State of Florida</funding><funding>National Institute on Minority Health and Health Disparities</funding><funding>NIH HHS</funding><pagination>e973-e979</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8852206</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>107(3)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Islet transplantation (ITx) has proved to be effective in preventing severe hypoglycemia and improving metabolic control in selected subjects with type 1 diabetes. Long-term graft function remains a challenge. Estrogens have been shown to protect β cells from metabolic stresses and improve revascularization of transplanted human islets in the mouse. We aimed to evaluate the influence of sex in allograft survival of ITx recipients.&lt;h4>Methods&lt;/h4>We analyzed a retrospective cohort of ITx recipients (n = 56) followed-up for up to 20 years. Allograft failure was defined as a stimulated C-peptide &lt;0.3 ng/mL during a mixed-meal tolerance test. Subjects were divided into recipients of at least 1 female donor (group 1) and recipients of male donors only (group 2).&lt;h4>Results&lt;/h</pubmed_abstract><journal>The Journal of clinical endocrinology and metabolism</journal><pubmed_title>Prolonged Islet Allograft Function is Associated With Female Sex in Patients After Islet Transplantation.</pubmed_title><pmcid>PMC8852206</pmcid><funding_grant_id>R01 DK55347</funding_grant_id><funding_grant_id>7-20-COVID-051</funding_grant_id><funding_grant_id>DK070460</funding_grant_id><funding_grant_id>DK074970</funding_grant_id><funding_grant_id>17-2012-361</funding_grant_id><funding_grant_id>BX003725</funding_grant_id><funding_grant_id>UL1TR000460</funding_grant_id><funding_grant_id>4-2004-361</funding_grant_id><funding_grant_id>R01 DK056953</funding_grant_id><funding_grant_id>R01 DK025802</funding_grant_id><funding_grant_id>4-200-946</funding_grant_id><funding_grant_id>U42 RR016603</funding_grant_id><funding_grant_id>M01RR16587</funding_grant_id><funding_grant_id>DK107444</funding_grant_id><funding_grant_id>3-SRA-2017-347-M-B</funding_grant_id><pubmed_authors>Mauvais-Jarvis F</pubmed_authors><pubmed_authors>Poggioli R</pubmed_authors><pubmed_authors>Lemos JRN</pubmed_authors><pubmed_authors>Fuenmayor V</pubmed_authors><pubmed_authors>Alejandro R</pubmed_authors><pubmed_authors>Alvarez A</pubmed_authors><pubmed_authors>Linetsky E</pubmed_authors><pubmed_authors>Ricordi C</pubmed_authors><pubmed_authors>Chavez C</pubmed_authors><pubmed_authors>Baidal DA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prolonged Islet Allograft Function is Associated With Female Sex in Patients After Islet Transplantation.</name><description>&lt;h4>Background&lt;/h4>Islet transplantation (ITx) has proved to be effective in preventing severe hypoglycemia and improving metabolic control in selected subjects with type 1 diabetes. Long-term graft function remains a challenge. Estrogens have been shown to protect β cells from metabolic stresses and improve revascularization of transplanted human islets in the mouse. We aimed to evaluate the influence of sex in allograft survival of ITx recipients.&lt;h4>Methods&lt;/h4>We analyzed a retrospective cohort of ITx recipients (n = 56) followed-up for up to 20 years. Allograft failure was defined as a stimulated C-peptide &lt;0.3 ng/mL during a mixed-meal tolerance test. Subjects were divided into recipients of at least 1 female donor (group 1) and recipients of male donors only (group 2).&lt;h4>Results&lt;/h</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Feb</publication><modification>2025-04-04T22:33:57.32Z</modification><creation>2025-02-19T03:23:47.487Z</creation></dates><accession>S-EPMC8852206</accession><cross_references><pubmed>34727179</pubmed><doi>10.1210/clinem/dgab787</doi></cross_references></HashMap>