Impact of switch from tenofovir disoproxil fumarate-based regimens to tenofovir alafenamide-based regimens on lipid profile, weight gain and cardiovascular risk score in people living with HIV.


Journal

BMC infectious diseases
ISSN: 1471-2334
Titre abrégé: BMC Infect Dis
Pays: England
ID NLM: 100968551

Informations de publication

Date de publication:
06 Sep 2021
Historique:
received: 02 02 2021
accepted: 19 07 2021
entrez: 7 9 2021
pubmed: 8 9 2021
medline: 25 9 2021
Statut: epublish

Résumé

As cardiovascular diseases represent the main cause of non-AIDS related death in people living with HIV (PLWH) with undetectable viral load, we evaluated lipid profile, weight gain and calculated cardiovascular risk change after switching from tenofovir disoproxil fumarate (TDF)-based regimens to tenofovir alafenamide (TAF)-based regimens. For this retrospective study, we selected HIV-infected patients with suppressed viral load who fitted in one of the two groups below: First group (TDF/TDF): Patients treated continuously with TDF-based regimens. Second group (TDF/TAF): Patients treated with TDF-regimens during at least 6 months then switched to TAF-regimens while maintaining other drugs unchanged. Available data included date of birth, gender, ethnicity, lymphocyte T CD4 Switching from TDF to TAF resulted in a significant increase in triglycerides levels, total cholesterol and HDL cholesterol. LDL cholesterol and total cholesterol/HDL ratio did not show significant changes. Calculated cardiovascular risk increased after switch from TDF- to TAF-based therapy. Together with favorable outcomes at the bone and kidney levels, potential negative impact of TAF on lipid profile should be included in the reflection to propose the most appropriate and tailored ARV treatment.

Sections du résumé

BACKGROUND BACKGROUND
As cardiovascular diseases represent the main cause of non-AIDS related death in people living with HIV (PLWH) with undetectable viral load, we evaluated lipid profile, weight gain and calculated cardiovascular risk change after switching from tenofovir disoproxil fumarate (TDF)-based regimens to tenofovir alafenamide (TAF)-based regimens.
METHODS METHODS
For this retrospective study, we selected HIV-infected patients with suppressed viral load who fitted in one of the two groups below: First group (TDF/TDF): Patients treated continuously with TDF-based regimens. Second group (TDF/TAF): Patients treated with TDF-regimens during at least 6 months then switched to TAF-regimens while maintaining other drugs unchanged. Available data included date of birth, gender, ethnicity, lymphocyte T CD4
RESULTS RESULTS
Switching from TDF to TAF resulted in a significant increase in triglycerides levels, total cholesterol and HDL cholesterol. LDL cholesterol and total cholesterol/HDL ratio did not show significant changes. Calculated cardiovascular risk increased after switch from TDF- to TAF-based therapy.
CONCLUSIONS CONCLUSIONS
Together with favorable outcomes at the bone and kidney levels, potential negative impact of TAF on lipid profile should be included in the reflection to propose the most appropriate and tailored ARV treatment.

Identifiants

pubmed: 34488664
doi: 10.1186/s12879-021-06479-9
pii: 10.1186/s12879-021-06479-9
pmc: PMC8420041
doi:

Substances chimiques

Anti-HIV Agents 0
Lipids 0
Tenofovir 99YXE507IL
tenofovir alafenamide EL9943AG5J
Alanine OF5P57N2ZX

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

910

Informations de copyright

© 2021. The Author(s).

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Auteurs

Pierre-Emmanuel Plum (PE)

Infectious Diseases Department, Liège University Hospital, Liège, Belgium.

Nathalie Maes (N)

Biostatistics and Medico-Economic Information Department, Liège University Hospital, Liège, Belgium.

Anne-Sophie Sauvage (AS)

Infectious Diseases Department, Liège University Hospital, Liège, Belgium.

Frédéric Frippiat (F)

Infectious Diseases Department, Liège University Hospital, Liège, Belgium.

Christelle Meuris (C)

Infectious Diseases Department, Liège University Hospital, Liège, Belgium.

Françoise Uurlings (F)

Infectious Diseases Department, Liège University Hospital, Liège, Belgium.

Marianne Lecomte (M)

Infectious Diseases Department, Liège University Hospital, Liège, Belgium.

Philippe Léonard (P)

Infectious Diseases Department, Liège University Hospital, Liège, Belgium.

Nicolas Paquot (N)

Diabetology Department, Liège University Hospital, Liège, Belgium.

Karine Fombellida (K)

Infectious Diseases Department, Liège University Hospital, Liège, Belgium.

Dolores Vaira (D)

AIDS Reference Laboratory, Liège University, Liège, Belgium.

Michel Moutschen (M)

Infectious Diseases Department, Liège University Hospital, Liège, Belgium.
AIDS Reference Laboratory, Liège University, Liège, Belgium.

Gilles Darcis (G)

Infectious Diseases Department, Liège University Hospital, Liège, Belgium. gdarcis@chuliege.be.

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