<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Havens PL</submitter><funding>NICHD NIH HHS</funding><funding>NCATS NIH HHS</funding><funding>NCRR NIH HHS</funding><funding>PHS HHS</funding><pagination>5619-28</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3811269</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>57(11)</volume><pubmed_abstract>Tenofovir disoproxil fumarate (TDF) causes bone, endocrine, and renal changes by an unknown mechanism(s). Data are limited on tenofovir pharmacokinetics and these effects. Using baseline data from a multicenter study of HIV-infected youth on stable treatment with regimens containing TDF (n = 118) or lacking TDF (n = 85), we measured cross-sectional associations of TDF use with markers of renal function, vitamin D-calcium-parathyroid hormone balance, phosphate metabolism (tubular reabsorption of phosphate and fibroblast growth factor 23 [FGF23]), and bone turnover. Pharmacokinetic-pharmacodynamic associations with plasma tenofovir and intracellular tenofovir diphosphate concentrations were explored among those receiving TDF. The mean age was 20.9 (standard deviation [SD], 2.0) years; 63% we</pubmed_abstract><journal>Antimicrobial agents and chemotherapy</journal><pubmed_title>Association of higher plasma vitamin D binding protein and lower free calcitriol levels with tenofovir disoproxil fumarate use and plasma and intracellular tenofovir pharmacokinetics: cause of a functional vitamin D deficiency?</pubmed_title><pmcid>PMC3811269</pmcid><funding_grant_id>M01 RR010710</funding_grant_id><funding_grant_id>U01 HD 040474</funding_grant_id><funding_grant_id>U01 A1068632</funding_grant_id><funding_grant_id>UL1 TR002319</funding_grant_id><funding_grant_id>M01 RR020359</funding_grant_id><funding_grant_id>U01 HD 040533</funding_grant_id><funding_grant_id>UL1 RR024134</funding_grant_id><funding_grant_id>UL1 RR025014</funding_grant_id><funding_grant_id>U01 HD040474</funding_grant_id><funding_grant_id>M01 RR000188</funding_grant_id><funding_grant_id>U01 HD040533</funding_grant_id><funding_grant_id>UL1 RR024131</funding_grant_id><funding_grant_id>U01 HD040497</funding_grant_id><funding_grant_id>UL1 TR001082</funding_grant_id><pubmed_authors>Kapogiannis BG</pubmed_authors><pubmed_authors>Havens PL</pubmed_authors><pubmed_authors>Flynn PM</pubmed_authors><pubmed_authors>Liu N</pubmed_authors><pubmed_authors>Woodhouse LR</pubmed_authors><pubmed_authors>Gordon CM</pubmed_authors><pubmed_authors>Van Loan MD</pubmed_authors><pubmed_authors>Lujan-Zilbermann J</pubmed_authors><pubmed_authors>Pan CG</pubmed_authors><pubmed_authors>Stephensen CB</pubmed_authors><pubmed_authors>Baker A</pubmed_authors><pubmed_authors>Hazra R</pubmed_authors><pubmed_authors>Bethel J</pubmed_authors><pubmed_authors>Wilson CM</pubmed_authors><pubmed_authors>Kiser JJ</pubmed_authors><pubmed_authors>Rutledge B</pubmed_authors><pubmed_authors>Mulligan K</pubmed_authors><pubmed_authors>Adolescent Medicine Trials Network for HIV/AIDS Interventions (ATN) 063 Study Team</pubmed_authors></additional><is_claimable>false</is_claimable><name>Association of higher plasma vitamin D binding protein and lower free calcitriol levels with tenofovir disoproxil fumarate use and plasma and intracellular tenofovir pharmacokinetics: cause of a functional vitamin D deficiency?</name><description>Tenofovir disoproxil fumarate (TDF) causes bone, endocrine, and renal changes by an unknown mechanism(s). Data are limited on tenofovir pharmacokinetics and these effects. Using baseline data from a multicenter study of HIV-infected youth on stable treatment with regimens containing TDF (n = 118) or lacking TDF (n = 85), we measured cross-sectional associations of TDF use with markers of renal function, vitamin D-calcium-parathyroid hormone balance, phosphate metabolism (tubular reabsorption of phosphate and fibroblast growth factor 23 [FGF23]), and bone turnover. Pharmacokinetic-pharmacodynamic associations with plasma tenofovir and intracellular tenofovir diphosphate concentrations were explored among those receiving TDF. The mean age was 20.9 (standard deviation [SD], 2.0) years; 63% we</description><dates><release>2013-01-01T00:00:00Z</release><publication>2013 Nov</publication><modification>2025-04-22T04:48:31.726Z</modification><creation>2019-03-27T01:17:45Z</creation></dates><accession>S-EPMC3811269</accession><cross_references><pubmed>24002093</pubmed><doi>10.1128/AAC.01096-13</doi><doi>10.1128/aac.01096-13</doi></cross_references></HashMap>