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Tenofovir-Related Fanconi Syndrome with Nephrogenic Diabetes Insipidus in a Patient with Acquired Immunodeficiency Syndrome: The Role of Lopinavir-Ritonavir-Didanosine
Author(s) -
Florence Rollot,
E.-M. Nazal,
Laurence ChauvelotMoachon,
Charikleia Kelaïdi,
Nathalie Daniel,
Magdi Saba,
S. Abad,
P. Blanche
Publication year - 2003
Publication title -
clinical infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.44
H-Index - 336
eISSN - 1537-6591
pISSN - 1058-4838
DOI - 10.1086/379829
Subject(s) - didanosine , nephrogenic diabetes insipidus , lopinavir , medicine , ritonavir , fanconi syndrome , tenofovir , lopinavir/ritonavir , virology , protease inhibitor (pharmacology) , gastroenterology , pharmacology , diabetes insipidus , kidney , human immunodeficiency virus (hiv) , viral load , antiretroviral therapy
Tenofovir-related tubular damage, like all other recently reported cases, occurred in patients receiving the protease inhibitor (PI) ritonavir, often with lopinavir. Increased plasma concentrations of didanosine were also observed after the addition of tenofovir. It was suspected that tenofovir with PIs interacted with renal organic anion transporters, leading to nephrotoxic tubular concentrations of tenofovir and systemic accumulation of didanosine. Until there is a better understanding of these interactions, close monitoring is recommended for patients receiving tenofovir, PIs, and didanosine.

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