Renal safety of coformulated tenofovir/emtricitabine vs other nucleoside analogues in combination therapy in antiretroviral-naive patients aged 50 years or older in Spain: The TRIP study. Issue 1 (February 2015)
- Record Type:
- Journal Article
- Title:
- Renal safety of coformulated tenofovir/emtricitabine vs other nucleoside analogues in combination therapy in antiretroviral-naive patients aged 50 years or older in Spain: The TRIP study. Issue 1 (February 2015)
- Main Title:
- Renal safety of coformulated tenofovir/emtricitabine vs other nucleoside analogues in combination therapy in antiretroviral-naive patients aged 50 years or older in Spain: The TRIP study
- Authors:
- Pedrol, Enric
Caro-Murillo, Ana M.
Castaño, Manuel A.
Riera, Melchor
Olalla, Julián
Domingo, Pere
Arazo, Piedad
Gómez-Sirvent, Juan L.
Pulido, Federico
Romero-Palacios, Alberto
Aguirrebengoa, Koldo
Vera, Francisco
Ferrer, Pedro
Blanco Ramos, José R. - Abstract:
- Abstract : Objectives: Our aim is to describe the impact of emtricitabine (FTC)/tenofovir (TDF) versus other nucleoside reverse transcriptase inhibitor (NRTIs)-based regimens on renal function of human immunodeficiency virus (HIV) naïve patients >50 years old who started combination antiretroviral therapy (cART). Design: National, retrospective cohort analysis of patients >50 years old when they started cART (January 1, 2006–December 31, 2009). Methods: We compared renal safety (changes in estimated glomerular filtration rate [eGFR] during the first year, and time to renal events during 4 years of follow-up) in FTC/TDF versus non-FTC/TDF users. Among FTC/TDF users, we compared protease inhibitors vs non-nucleoside reverse transcriptase inhibitors and Lopinavir/ritonavir vs Efavirenz. Results: We included 103 patients: median age: 54.9 years, 84% males, median CD4 count 247 cells/μl, median viral load 4.7 log; median follow up 18 months (max: 48 months); 73 started with FTC/TDF and 30 with other NRTIs. Change in eGFR was significantly worse for ritonavir-boosted lopinavir (LPV/r) vs efavirenz (EFV) users in the FTC/TDF group (71.2 vs 98.9 ml/min/1.73 m 2 at month 12, P < 0.05). The risk of renal events (progression to an Chronic Kidney Disease Epidemiology Collaboration value < 60 ml/min/1.73 m 2 in subjects with baseline values >60) was comparable for FTC/TDF users and non users, but was higher and almost significant for LPV/r as compared to EFV users in the FTC/TDF groupAbstract : Objectives: Our aim is to describe the impact of emtricitabine (FTC)/tenofovir (TDF) versus other nucleoside reverse transcriptase inhibitor (NRTIs)-based regimens on renal function of human immunodeficiency virus (HIV) naïve patients >50 years old who started combination antiretroviral therapy (cART). Design: National, retrospective cohort analysis of patients >50 years old when they started cART (January 1, 2006–December 31, 2009). Methods: We compared renal safety (changes in estimated glomerular filtration rate [eGFR] during the first year, and time to renal events during 4 years of follow-up) in FTC/TDF versus non-FTC/TDF users. Among FTC/TDF users, we compared protease inhibitors vs non-nucleoside reverse transcriptase inhibitors and Lopinavir/ritonavir vs Efavirenz. Results: We included 103 patients: median age: 54.9 years, 84% males, median CD4 count 247 cells/μl, median viral load 4.7 log; median follow up 18 months (max: 48 months); 73 started with FTC/TDF and 30 with other NRTIs. Change in eGFR was significantly worse for ritonavir-boosted lopinavir (LPV/r) vs efavirenz (EFV) users in the FTC/TDF group (71.2 vs 98.9 ml/min/1.73 m 2 at month 12, P < 0.05). The risk of renal events (progression to an Chronic Kidney Disease Epidemiology Collaboration value < 60 ml/min/1.73 m 2 in subjects with baseline values >60) was comparable for FTC/TDF users and non users, but was higher and almost significant for LPV/r as compared to EFV users in the FTC/TDF group (adjusted hazard ratio 6.1, 95% CI 0.8–45.5). Conclusions: In our study with a population of HIV infected subjects ≥ 50 years old, renal safety was similar for FTC/TDF and other NRTI-based regimens, but worse for LPV/r as compared to other regimens. … (more)
- Is Part Of:
- HIV clinical trials. Volume 16:Issue 1(2015)
- Journal:
- HIV clinical trials
- Issue:
- Volume 16:Issue 1(2015)
- Issue Display:
- Volume 16, Issue 1 (2015)
- Year:
- 2015
- Volume:
- 16
- Issue:
- 1
- Issue Sort Value:
- 2015-0016-0001-0000
- Page Start:
- 43
- Page End:
- 48
- Publication Date:
- 2015-02
- Subjects:
- Ageing, -- Tenofovir, -- Emtricitabine, -- Renal function, -- Antiretroviral Therapy
HIV Infections -- Chemotherapy -- Periodicals
AIDS (Disease) -- Chemotherapy -- Periodicals
HIV Infections -- Research -- Periodicals
AIDS (Disease) -- Research -- Periodicals
616.979206105 - Journal URLs:
- http://www.tandfonline.com/toc/yhct20/15/4 ↗
http://www.maneyonline.com ↗ - DOI:
- 10.1179/1528433614Z.0000000001 ↗
- Languages:
- English
- ISSNs:
- 1528-4336
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4319.044800
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