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Kidney function and daily emtricitabine/tenofovir disoproxil fumarate pre-exposure prophylaxis against HIV: results from the real-life multicentric demonstrative project PrEP Brazil
BACKGROUND: Pre-Exposure Prophylaxis (PrEP) has demonstrated efficacy in the reduction of sexually transmitted HIV infections. The prolonged use of tenofovir disoproxil fumarate (TDF) and emtricitabine (FTC) co-formulation (TDF/FTC), however, may result in augmented risk of renal toxicity. We aimed...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8867642/ https://www.ncbi.nlm.nih.gov/pubmed/35209929 http://dx.doi.org/10.1186/s12981-022-00437-4 |
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author | Petruccelli, Karla Cristina Silva Baía-da-Silva, Djane Clarys Val, Fernando Valões, Monica Santos Cubas-Vega, Nadia Silva-Neto, Alexandre Vilhena Sampaio, Vanderson Alencar, Aline Pecoits-Filho, Roberto Moreira, Rodrigo Carvalho Cardoso, Sandra Wagner Moreira, Ronaldo I. Leite, Iuri Costa Madruga, José Valdez Kallas, Esper G. Alencastro, Paulo R. Hoagland, Brenda Grinsztejn, Beatriz Santos, Valdiléa Gonçalves Veloso Lacerda, Marcus Vinícius Guimarães |
author_facet | Petruccelli, Karla Cristina Silva Baía-da-Silva, Djane Clarys Val, Fernando Valões, Monica Santos Cubas-Vega, Nadia Silva-Neto, Alexandre Vilhena Sampaio, Vanderson Alencar, Aline Pecoits-Filho, Roberto Moreira, Rodrigo Carvalho Cardoso, Sandra Wagner Moreira, Ronaldo I. Leite, Iuri Costa Madruga, José Valdez Kallas, Esper G. Alencastro, Paulo R. Hoagland, Brenda Grinsztejn, Beatriz Santos, Valdiléa Gonçalves Veloso Lacerda, Marcus Vinícius Guimarães |
author_sort | Petruccelli, Karla Cristina Silva |
collection | PubMed |
description | BACKGROUND: Pre-Exposure Prophylaxis (PrEP) has demonstrated efficacy in the reduction of sexually transmitted HIV infections. The prolonged use of tenofovir disoproxil fumarate (TDF) and emtricitabine (FTC) co-formulation (TDF/FTC), however, may result in augmented risk of renal toxicity. We aimed to evaluate changes in the estimated Glomerular Filtration Rate (eGFR) in a real-world population setting of participants enrolled in PrEP Brazil, a 48-week prospective, open-label, demonstration study to assess the feasibility of daily oral TDF/FTC used by men who have sex with men and transgender women at high-risk of HIV infection, all over 18 years old. METHODS: Kidney function was assessed by serial measurement of serum creatinine and eGFR with the Modification of Diet in Renal Disease Study (MDRD) formula on weeks 4, 12, 24, 36 and 48. Adherence to PrEP was assessed by dosing TDF concentration in dried blood spots at weeks 4 and 48, measured by liquid chromatography-mass spectrometry or mass spectrometry. RESULTS: Of 392 participants completing the 48-week follow-up protocol with TDF blood detectable levels and eGFR measures, 43.1% were young adults, of Caucasian ethnic background (57.9%), with BMI below 30 kg/m(2), without arterial hypertension. At screening, median eGFR was 93.0 mL/min/1.73 m(2). At week 4 follow-up, 90 (23% of the study population) participants presented reductions in eGFR greater than 10 mL/min/1.73 m(2) as compared to baseline eGFR, some as large as 59 mL/min/1.73 m(2), but with no clinical outcomes (adverse events and renal adverse events) severe enough to demand TDF/FTC discontinuation. A negative relationship was observed between TDF blood levels and eGFR at weeks 4 (r = − 0.005; p < 0.01) and 48 (r = − 0.006; p < 0.01). CONCLUSIONS: These results suggest that the renal function profile in individuals on TDF/FTC may be assessed on week 4 and then only annually, allowing a more flexible medical follow-up in primary care centers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12981-022-00437-4. |
format | Online Article Text |
id | pubmed-8867642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-88676422022-02-28 Kidney function and daily emtricitabine/tenofovir disoproxil fumarate pre-exposure prophylaxis against HIV: results from the real-life multicentric demonstrative project PrEP Brazil Petruccelli, Karla Cristina Silva Baía-da-Silva, Djane Clarys Val, Fernando Valões, Monica Santos Cubas-Vega, Nadia Silva-Neto, Alexandre Vilhena Sampaio, Vanderson Alencar, Aline Pecoits-Filho, Roberto Moreira, Rodrigo Carvalho Cardoso, Sandra Wagner Moreira, Ronaldo I. Leite, Iuri Costa Madruga, José Valdez Kallas, Esper G. Alencastro, Paulo R. Hoagland, Brenda Grinsztejn, Beatriz Santos, Valdiléa Gonçalves Veloso Lacerda, Marcus Vinícius Guimarães AIDS Res Ther Research BACKGROUND: Pre-Exposure Prophylaxis (PrEP) has demonstrated efficacy in the reduction of sexually transmitted HIV infections. The prolonged use of tenofovir disoproxil fumarate (TDF) and emtricitabine (FTC) co-formulation (TDF/FTC), however, may result in augmented risk of renal toxicity. We aimed to evaluate changes in the estimated Glomerular Filtration Rate (eGFR) in a real-world population setting of participants enrolled in PrEP Brazil, a 48-week prospective, open-label, demonstration study to assess the feasibility of daily oral TDF/FTC used by men who have sex with men and transgender women at high-risk of HIV infection, all over 18 years old. METHODS: Kidney function was assessed by serial measurement of serum creatinine and eGFR with the Modification of Diet in Renal Disease Study (MDRD) formula on weeks 4, 12, 24, 36 and 48. Adherence to PrEP was assessed by dosing TDF concentration in dried blood spots at weeks 4 and 48, measured by liquid chromatography-mass spectrometry or mass spectrometry. RESULTS: Of 392 participants completing the 48-week follow-up protocol with TDF blood detectable levels and eGFR measures, 43.1% were young adults, of Caucasian ethnic background (57.9%), with BMI below 30 kg/m(2), without arterial hypertension. At screening, median eGFR was 93.0 mL/min/1.73 m(2). At week 4 follow-up, 90 (23% of the study population) participants presented reductions in eGFR greater than 10 mL/min/1.73 m(2) as compared to baseline eGFR, some as large as 59 mL/min/1.73 m(2), but with no clinical outcomes (adverse events and renal adverse events) severe enough to demand TDF/FTC discontinuation. A negative relationship was observed between TDF blood levels and eGFR at weeks 4 (r = − 0.005; p < 0.01) and 48 (r = − 0.006; p < 0.01). CONCLUSIONS: These results suggest that the renal function profile in individuals on TDF/FTC may be assessed on week 4 and then only annually, allowing a more flexible medical follow-up in primary care centers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12981-022-00437-4. BioMed Central 2022-02-24 /pmc/articles/PMC8867642/ /pubmed/35209929 http://dx.doi.org/10.1186/s12981-022-00437-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Petruccelli, Karla Cristina Silva Baía-da-Silva, Djane Clarys Val, Fernando Valões, Monica Santos Cubas-Vega, Nadia Silva-Neto, Alexandre Vilhena Sampaio, Vanderson Alencar, Aline Pecoits-Filho, Roberto Moreira, Rodrigo Carvalho Cardoso, Sandra Wagner Moreira, Ronaldo I. Leite, Iuri Costa Madruga, José Valdez Kallas, Esper G. Alencastro, Paulo R. Hoagland, Brenda Grinsztejn, Beatriz Santos, Valdiléa Gonçalves Veloso Lacerda, Marcus Vinícius Guimarães Kidney function and daily emtricitabine/tenofovir disoproxil fumarate pre-exposure prophylaxis against HIV: results from the real-life multicentric demonstrative project PrEP Brazil |
title | Kidney function and daily emtricitabine/tenofovir disoproxil fumarate pre-exposure prophylaxis against HIV: results from the real-life multicentric demonstrative project PrEP Brazil |
title_full | Kidney function and daily emtricitabine/tenofovir disoproxil fumarate pre-exposure prophylaxis against HIV: results from the real-life multicentric demonstrative project PrEP Brazil |
title_fullStr | Kidney function and daily emtricitabine/tenofovir disoproxil fumarate pre-exposure prophylaxis against HIV: results from the real-life multicentric demonstrative project PrEP Brazil |
title_full_unstemmed | Kidney function and daily emtricitabine/tenofovir disoproxil fumarate pre-exposure prophylaxis against HIV: results from the real-life multicentric demonstrative project PrEP Brazil |
title_short | Kidney function and daily emtricitabine/tenofovir disoproxil fumarate pre-exposure prophylaxis against HIV: results from the real-life multicentric demonstrative project PrEP Brazil |
title_sort | kidney function and daily emtricitabine/tenofovir disoproxil fumarate pre-exposure prophylaxis against hiv: results from the real-life multicentric demonstrative project prep brazil |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8867642/ https://www.ncbi.nlm.nih.gov/pubmed/35209929 http://dx.doi.org/10.1186/s12981-022-00437-4 |
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