Treatment with tenofovir alafenamide fumarate worsens the lipid profile of HIV-infected patients versus treatment with tenofovir disoproxil fumarate, each coformulated with elvitegravir, cobicistat, and emtricitabine

被引:37
|
作者
Cid-Silva, Purificacion [1 ,2 ]
Fernandez-Bargiela, Noelia [2 ]
Margusino-Framinan, Luis [1 ,2 ]
Balboa-Barreiro, Vanesa [3 ]
Mena-De-Cea, Alvaro [1 ,4 ]
Lopez-Calvo, Soledad [4 ]
Vazquez-Rodriguez, Pilar [4 ]
Martin-Herranz, Isabel [2 ]
Miguez-Rey, Enrique [1 ]
Poveda, Eva [5 ]
Castro-Iglesias, Angeles [1 ,4 ]
机构
[1] Univ A Coruna UDC, SERGAS, Univ Hosp A Coruna CHUAC, Div Clin Virol,Biomed Res Inst,A Coruna INIBIC, La Coruna, Spain
[2] Univ Hosp A Coruna CHUAC, SERGAS, Serv Pharm, La Coruna, Spain
[3] Univ A Coruna UDC, SERGAS, Univ Hosp A Coruna CHUAC, Clin Epidemiol & Biostat Unit,Biomed Res Inst,A C, La Coruna, Spain
[4] Univ Hosp A Coruna CHUAC, SERGAS, Serv Infect Internal Med, La Coruna, Spain
[5] Complexo Hosp Univ Vigo, SERGAS UVigo, Galicia Hlth Res Inst IIS Galicia Sur, Grp Virol & Pathogenesis, Vigo, Spain
关键词
adverse events; dyslipidemia; HIV; tenofovir alafenamide furamate; tenofovir disoproxil fumarate; VIROLOGICALLY SUPPRESSED ADULTS; DOUBLE-BLIND; ANTIRETROVIRAL THERAPY; INITIAL TREATMENT; NAIVE PATIENTS; PHASE-3; EFFICACY; SAFETY; DYSLIPIDEMIA; MULTICENTER;
D O I
10.1111/bcpt.13161
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Two elvitegravir/cobicistat-based therapies combined with emtricitabine/tenofovir disoproxil fumarate (EVG/c/FTC/TDF) or emtricitabine/tenofovir alafenamide fumarate (EVG/c/FTC/TAF) are currently available for HIV patients. This study evaluated the modifications in the lipid profile of patients who received these treatments in the last three years at our institution. A retrospective observational study in HIV-infected patients who received EVG/c/FTC/TDF or EVG/c/FTC/TAF from January 2015 to January 2018 at a reference hospital in northwestern Spain was carried out. Epidemiological, clinical and immunovirological data were recorded. A statistical analysis was performed using SPSS software. A total of 384 EVG/c-based therapies were initiated during the study period, 151 EVG/c/FTC/TDF and 233 EVG/c/FTC/TAF. A significantly negative influence in all the lipid profile parameters in experienced patients and total cholesterol (TC), and LDL-C in naive patients were observed after 48 weeks of treatment with EVG/c/FTC/TAF, while these parameters remained stable in the EVG/c/FTC/TDF group. During follow-up, a greater proportion of patients had lipid levels above the normal range (63.1% TC, 56.2% LDL-C) and new lipid-modifying drugs were prescribed (11.9%) in the EVG/c/FTC/TAF group. The number of cardiovascular risk factors (OR 1.66 [95% CI 1.01-2.72]; P = 0.043) was recognised as an independent predictor of lipid-lowering prescription for patients treated with both EVG/c/FTC/TDF and EVG/c/FTC/TAF. For patients treated with EVG/c/FTC/TAF, the mean total cholesterol to HDL ratio in the first 48 weeks of the study treatment was associated with a higher likelihood of lipid-lowering prescription in multivariate analysis (OR 1.6 [95% CI 1.12-2.52]; P = 0.011). Significant changes in lipid profile have been observed in patients who have received EVG/c/FTC/TAF. It was necessary to prescribe almost twice the number of lipid-lowering drugs to patients who received EVG/c/FTC/TAF (11.9%) vs EVG/c/FTC/TDF (4.7%).
引用
收藏
页码:479 / 490
页数:12
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