<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Binari LA</submitter><funding>NCATS NIH HHS</funding><pagination>e14213</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10922352</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>26(1)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Utilization of hepatitis C viremic (HCV+) deceased donor kidneys (DDKT) for aviremic recipients increases opportunities for transplantation with excellent short-term outcomes. Our primary aim was to understand longer-term outcomes, specifically assessing kidney and liver function in the first year posttransplant.&lt;h4>Methods&lt;/h4>This was a retrospective single-center study of adult DDKT recipients of HCV+ kidneys (cases) matched 1:1 to recipients of HCV- kidneys (comparators). Between-group outcomes were analyzed using comparisons of means and proportions, survival analysis methods, and multivariable mixed effects models.&lt;h4>Results&lt;/h4>Sixty-five cases and 65 comparators had statistically comparable demographic and clinical characteristics. There were no between-group differences in serum creatinine or estimated glomerular filtration rate at month 12 (p = .662) or in their trajectories over months 1-12 (p > .292). Within the first 60 days, rates of liver function values >3 times upper limit of normal among cases were comparable to comparators for aspartate aminotransferase (AST) (14% vs. 6%, p = .242) and higher for alanine transaminase (ALT) (23% vs. 6%, p = .011). AST declined during the first 8 weeks (p = .005) and stabilized for both groups (p = .406) during the following 10 months. ALT declined during the first 8 weeks (p &lt; .001), continued to decline over months 3-12 (p = .016), and the trajectory was unrelated to antiviral therapy initiation among cases.&lt;h4>Conclusions&lt;/h4>Aviremic recipients of HCV+ kidneys had comparable kidney outcomes to matched recipients of HCV- kidneys. Despite more HCV+ recipients having an elevation in ALT within the first 60 days, ALT values normalized with no identified liver complications attributed to HCV.</pubmed_abstract><journal>Transplant infectious disease : an official journal of the Transplantation Society</journal><pubmed_title>Twelve-month kidney and liver outcomes of kidney transplantation from Hepatitis C Viremic deceased donors to aviremic recipients.</pubmed_title><pmcid>PMC10922352</pmcid><funding_grant_id>UL1 TR000445</funding_grant_id><pubmed_authors>Feurer ID</pubmed_authors><pubmed_authors>Shawar S</pubmed_authors><pubmed_authors>Naik R</pubmed_authors><pubmed_authors>DuBray BJ</pubmed_authors><pubmed_authors>Helderman JH</pubmed_authors><pubmed_authors>Birdwell KA</pubmed_authors><pubmed_authors>Binari LA</pubmed_authors><pubmed_authors>Sarrell BA</pubmed_authors><pubmed_authors>Thorne P</pubmed_authors><pubmed_authors>Rega SA</pubmed_authors><pubmed_authors>Forbes RC</pubmed_authors><pubmed_authors>Eid K</pubmed_authors><pubmed_authors>Concepcion BP</pubmed_authors><pubmed_authors>Langone A</pubmed_authors><pubmed_authors>Hickman L</pubmed_authors><pubmed_authors>Schaefer H</pubmed_authors><pubmed_authors>Shaffer D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Twelve-month kidney and liver outcomes of kidney transplantation from Hepatitis C Viremic deceased donors to aviremic recipients.</name><description>&lt;h4>Introduction&lt;/h4>Utilization of hepatitis C viremic (HCV+) deceased donor kidneys (DDKT) for aviremic recipients increases opportunities for transplantation with excellent short-term outcomes. Our primary aim was to understand longer-term outcomes, specifically assessing kidney and liver function in the first year posttransplant.&lt;h4>Methods&lt;/h4>This was a retrospective single-center study of adult DDKT recipients of HCV+ kidneys (cases) matched 1:1 to recipients of HCV- kidneys (comparators). Between-group outcomes were analyzed using comparisons of means and proportions, survival analysis methods, and multivariable mixed effects models.&lt;h4>Results&lt;/h4>Sixty-five cases and 65 comparators had statistically comparable demographic and clinical characteristics. There were no between-group differences in serum creatinine or estimated glomerular filtration rate at month 12 (p = .662) or in their trajectories over months 1-12 (p > .292). Within the first 60 days, rates of liver function values >3 times upper limit of normal among cases were comparable to comparators for aspartate aminotransferase (AST) (14% vs. 6%, p = .242) and higher for alanine transaminase (ALT) (23% vs. 6%, p = .011). AST declined during the first 8 weeks (p = .005) and stabilized for both groups (p = .406) during the following 10 months. ALT declined during the first 8 weeks (p &lt; .001), continued to decline over months 3-12 (p = .016), and the trajectory was unrelated to antiviral therapy initiation among cases.&lt;h4>Conclusions&lt;/h4>Aviremic recipients of HCV+ kidneys had comparable kidney outcomes to matched recipients of HCV- kidneys. Despite more HCV+ recipients having an elevation in ALT within the first 60 days, ALT values normalized with no identified liver complications attributed to HCV.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Feb</publication><modification>2025-04-04T22:07:12.124Z</modification><creation>2025-04-04T22:07:12.124Z</creation></dates><accession>S-EPMC10922352</accession><cross_references><pubmed>38112078</pubmed><doi>10.1111/tid.14213</doi></cross_references></HashMap>