Switch from Tenofovir Disoproxil Fumarate to Tenofovir Alafenamide in People Living with HIV: Lipid Changes and Statin Underutilization.


Journal

Clinical drug investigation
ISSN: 1179-1918
Titre abrégé: Clin Drug Investig
Pays: New Zealand
ID NLM: 9504817

Informations de publication

Date de publication:
Nov 2021
Historique:
accepted: 02 09 2021
pubmed: 22 9 2021
medline: 3 11 2021
entrez: 21 9 2021
Statut: ppublish

Résumé

Many people living with HIV (PLWH) on stable tenofovir disoproxil fumarate (TDF)-containing regimens have switched to tenofovir alafenamide (TAF), despite the potential lipid-lowering effect of TDF. We aimed to assess the impact of switching from TDF to TAF on lipids in real-world clinical practice. PLWH prescribed TDF for ≥ 4 weeks who switched to TAF were identified in the OPERA cohort. Patterns of dyslipidemia were compared before and after switch based on NCEP ATPIII guidelines. Elevated 10-year risk of atherosclerotic cardiovascular disease (ASCVD ≥ 7.5%) and statin use were assessed. Among 6423 PLWH switched from TDF to TAF, the proportion with dyslipidemia/severe dyslipidemia observed after switch from TDF to TAF increased statistically significantly (p < 0.0001) with total cholesterol (5-10%), low-density lipoprotein cholesterol (16-23%), and triglycerides (21-27%), but decreased statistically significantly with high-density lipoprotein cholesterol (35-30%, p < 0.0001). These patterns of dyslipidemia persisted in sensitivity analyses restricted to PLWH who maintained all other antiretrovirals (N = 4328) or stratified by pharmaco-enhancer use before and after switch. An elevated ASCVD risk was detected in 29% before and 31% after switch. As many as 59% of PLWH with an elevated ASCVD risk were not prescribed a statin after switch from TDF to TAF. In this large, diverse population of PLWH in the USA, the switch from TDF to TAF was associated with development of less favorable lipid profiles, regardless of pharmaco-enhancers or third-agent use. Statins remained underutilized after a switch from TDF to TAF.

Sections du résumé

BACKGROUND AND OBJECTIVE OBJECTIVE
Many people living with HIV (PLWH) on stable tenofovir disoproxil fumarate (TDF)-containing regimens have switched to tenofovir alafenamide (TAF), despite the potential lipid-lowering effect of TDF. We aimed to assess the impact of switching from TDF to TAF on lipids in real-world clinical practice.
METHODS METHODS
PLWH prescribed TDF for ≥ 4 weeks who switched to TAF were identified in the OPERA cohort. Patterns of dyslipidemia were compared before and after switch based on NCEP ATPIII guidelines. Elevated 10-year risk of atherosclerotic cardiovascular disease (ASCVD ≥ 7.5%) and statin use were assessed.
RESULTS RESULTS
Among 6423 PLWH switched from TDF to TAF, the proportion with dyslipidemia/severe dyslipidemia observed after switch from TDF to TAF increased statistically significantly (p < 0.0001) with total cholesterol (5-10%), low-density lipoprotein cholesterol (16-23%), and triglycerides (21-27%), but decreased statistically significantly with high-density lipoprotein cholesterol (35-30%, p < 0.0001). These patterns of dyslipidemia persisted in sensitivity analyses restricted to PLWH who maintained all other antiretrovirals (N = 4328) or stratified by pharmaco-enhancer use before and after switch. An elevated ASCVD risk was detected in 29% before and 31% after switch. As many as 59% of PLWH with an elevated ASCVD risk were not prescribed a statin after switch from TDF to TAF.
CONCLUSIONS CONCLUSIONS
In this large, diverse population of PLWH in the USA, the switch from TDF to TAF was associated with development of less favorable lipid profiles, regardless of pharmaco-enhancers or third-agent use. Statins remained underutilized after a switch from TDF to TAF.

Identifiants

pubmed: 34546533
doi: 10.1007/s40261-021-01081-y
pii: 10.1007/s40261-021-01081-y
pmc: PMC8556204
doi:

Substances chimiques

Anti-HIV Agents 0
Hydroxymethylglutaryl-CoA Reductase Inhibitors 0
Lipids 0
Tenofovir 99YXE507IL
tenofovir alafenamide EL9943AG5J
Alanine OF5P57N2ZX

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

955-965

Informations de copyright

© 2021. The Author(s).

Références

AIDS. 2020 Dec 1;34(15):2259-2268
pubmed: 33048869
Ann Intern Med. 2021 Jun;174(6):758-767
pubmed: 33721521
J Acquir Immune Defic Syndr. 2017 Sep 1;76(1):e26-e29
pubmed: 28520617
Antivir Ther. 2010;15(2):227-33
pubmed: 20386078
Clin Infect Dis. 2015 Aug 1;61(3):403-8
pubmed: 25870325
J Am Coll Cardiol. 2014 Jul 1;63(25 Pt B):2889-934
pubmed: 24239923
Eur J Prev Cardiol. 2012 Apr;19(2):267-74
pubmed: 21450595
Curr HIV/AIDS Rep. 2021 Aug;18(4):271-279
pubmed: 34247329
J Am Coll Cardiol. 2019 Jun 25;73(24):3168-3209
pubmed: 30423391
Aliment Pharmacol Ther. 2017 Sep;46(6):599-604
pubmed: 28707319
Lancet. 2015 Jun 27;385(9987):2606-15
pubmed: 25890673
Clin Infect Dis. 2016 Aug 1;63(3):407-13
pubmed: 27143663
HIV Med. 2017 Nov;18(10):782-786
pubmed: 28671337
J Int AIDS Soc. 2018 Oct;21 Suppl 8:e25187
pubmed: 30362663
HIV Clin Trials. 2015 Oct;16(5):178-89
pubmed: 26395328
Lancet HIV. 2017 May;4(5):e195-e204
pubmed: 28259777
J Acquir Immune Defic Syndr. 2016 Apr 15;71(5):530-7
pubmed: 26627107
AIDS. 2019 Dec 1;33(15):2387-2391
pubmed: 31764103
J Int AIDS Soc. 2021 Apr;24(4):e25702
pubmed: 33838004
Open Forum Infect Dis. 2019 Oct 04;6(10):ofz414
pubmed: 31660372
Curr Opin HIV AIDS. 2016 May;11(3):326-32
pubmed: 26859637
Croat Med J. 2015 Feb;56(1):14-23
pubmed: 25727038
Lancet Infect Dis. 2016 Jan;16(1):43-52
pubmed: 26538525
Biochem Pharmacol. 2016 Nov 1;119:1-7
pubmed: 27133890
Prev Chronic Dis. 2013;10:E10
pubmed: 23347705
AIDS. 2014 Sep 10;28(14):2061-70
pubmed: 25265074
J Acquir Immune Defic Syndr. 2017 Jun 1;75(2):211-218
pubmed: 28282300
AIDS Patient Care STDS. 2017 Nov;31(11):447-454
pubmed: 29087746
JAMA. 2004 Jul 14;292(2):191-201
pubmed: 15249568
Int J STD AIDS. 2021 May;32(6):570-577
pubmed: 33612018
Basic Clin Pharmacol Toxicol. 2019 Apr;124(4):479-490
pubmed: 30388308
AIDS. 2020 Jul 1;34(8):1161-1170
pubmed: 32310899
Clin Infect Dis. 2018 Jul 18;67(3):411-419
pubmed: 29415175
J Am Coll Cardiol. 2014 Jul 1;63(25 Pt B):2935-2959
pubmed: 24239921
Antivir Ther. 2012;17(6):1011-20
pubmed: 22910324
J Acquir Immune Defic Syndr. 2017 Jun 1;75(2):226-231
pubmed: 28272164
Drug Des Devel Ther. 2020 Dec 15;14:5515-5520
pubmed: 33364747
AIDS. 2010 Jul 17;24(11):1781-4
pubmed: 20495438
Clin Infect Dis. 2010 Sep 1;51(5):496-505
pubmed: 20673002
AIDS. 2011 Jan 14;25(2):185-95
pubmed: 21150555

Auteurs

Laurence Brunet (L)

Epividian, Inc., 4819 Emperor Blvd., Suite 400, Durham, NC, 27703, USA. laurence.brunet@epividian.com.

Patrick Mallon (P)

Centre for Experimental Pathogen Host Research, University College Dublin, Dublin, Ireland.

Jennifer S Fusco (JS)

Epividian, Inc., 4819 Emperor Blvd., Suite 400, Durham, NC, 27703, USA.

Michael B Wohlfeiler (MB)

AIDS Healthcare Foundation, Miami, FL, USA.

Girish Prajapati (G)

Merck & Co., Inc., Kenilworth, NJ, USA.

Andrew Beyer (A)

Merck & Co., Inc., Kenilworth, NJ, USA.

Gregory P Fusco (GP)

Epividian, Inc., 4819 Emperor Blvd., Suite 400, Durham, NC, 27703, USA.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH