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Changes in lipidomic profile by anti-retroviral treatment regimen: An ACTG 5257 ancillary study

High cardiovascular disease risk in people living with HIV is partly attributed to antiretroviral therapy (ART). Lipid response to ART has been extensively studied, yet, little is known how small molecule lipids respond to Integrase inhibitor-based (INSTI-based) compared to Protease inhibitor-based...

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Autores principales: Chaudhary, Ninad S., Kind, Tobias, Willig, Amanda L., Saag, Michael S., Shrestha, Sadeep, Funderburg, Nicholas, Wiener, Howard W., Overton, E. Turner, Irvin, Marguerite R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8322553/
https://www.ncbi.nlm.nih.gov/pubmed/34397689
http://dx.doi.org/10.1097/MD.0000000000026588
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author Chaudhary, Ninad S.
Kind, Tobias
Willig, Amanda L.
Saag, Michael S.
Shrestha, Sadeep
Funderburg, Nicholas
Wiener, Howard W.
Overton, E. Turner
Irvin, Marguerite R.
author_facet Chaudhary, Ninad S.
Kind, Tobias
Willig, Amanda L.
Saag, Michael S.
Shrestha, Sadeep
Funderburg, Nicholas
Wiener, Howard W.
Overton, E. Turner
Irvin, Marguerite R.
author_sort Chaudhary, Ninad S.
collection PubMed
description High cardiovascular disease risk in people living with HIV is partly attributed to antiretroviral therapy (ART). Lipid response to ART has been extensively studied, yet, little is known how small molecule lipids respond to Integrase inhibitor-based (INSTI-based) compared to Protease inhibitor-based (PI-based) ART regimens. Ancillary study to a phase 3, randomized, open-label trial [AIDS Clinical Trial Group A5257 Study] in treatment-naive HIV-infected patients randomized in a 1:1:1 ratio to receive ritonavir-boosted atazanavir (ATV/r), ritonavir-boosted darunavir (DRV/r) (both PI-based), or raltegravir with Tenofovir Disoproxil Fumarate-TDF plus emtricitabine (RAL, INSTI-based). We examined small molecule lipid response in a subcohort of 75 participants. Lipidomic assays of plasma samples collected pre- and post-ART treatment (48 weeks) were conducted using ultra-performance liquid chromatography coupled to time-of-flight mass spectrometry. The effect of ART regimens was regressed on lipid species response adjusting for the baseline covariates (lipids, age, sex, race, CD4 level, BMI, and smoking). Results were validated in the Centers for AIDS Research Network of Integrated Clinical Systems study (N = 16). Out of 417 annotated lipids, glycerophospholipids (P = .007) and sphingolipids (P = .028) had a higher response to ATV/r and DRV/r compared to RAL. The lysophosphatidylcholine (LPCs(16:1),(17:1),(20:3)) and phosphophatidylcholine species (PCs(40:7),(38:4)) had an opposite response to RAL versus ATV/r in the discovery and validation cohort. The INSTI-based regimen had an opposite response of ceramide species ((d38:1), (d42:2)), PCs((35:2), (38:4)), phosphatidylethanolamines (PEs(38:4), (38:6)), and sphingomyelin(SMd38:1) species compared with the PI-based regimens. There were no differences observed between 2 PI-based regimens. We observed differences in response of small molecule lipid species by ART regimens in treatment-naive people living with HIV.
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spelling pubmed-83225532021-08-02 Changes in lipidomic profile by anti-retroviral treatment regimen: An ACTG 5257 ancillary study Chaudhary, Ninad S. Kind, Tobias Willig, Amanda L. Saag, Michael S. Shrestha, Sadeep Funderburg, Nicholas Wiener, Howard W. Overton, E. Turner Irvin, Marguerite R. Medicine (Baltimore) 4400 High cardiovascular disease risk in people living with HIV is partly attributed to antiretroviral therapy (ART). Lipid response to ART has been extensively studied, yet, little is known how small molecule lipids respond to Integrase inhibitor-based (INSTI-based) compared to Protease inhibitor-based (PI-based) ART regimens. Ancillary study to a phase 3, randomized, open-label trial [AIDS Clinical Trial Group A5257 Study] in treatment-naive HIV-infected patients randomized in a 1:1:1 ratio to receive ritonavir-boosted atazanavir (ATV/r), ritonavir-boosted darunavir (DRV/r) (both PI-based), or raltegravir with Tenofovir Disoproxil Fumarate-TDF plus emtricitabine (RAL, INSTI-based). We examined small molecule lipid response in a subcohort of 75 participants. Lipidomic assays of plasma samples collected pre- and post-ART treatment (48 weeks) were conducted using ultra-performance liquid chromatography coupled to time-of-flight mass spectrometry. The effect of ART regimens was regressed on lipid species response adjusting for the baseline covariates (lipids, age, sex, race, CD4 level, BMI, and smoking). Results were validated in the Centers for AIDS Research Network of Integrated Clinical Systems study (N = 16). Out of 417 annotated lipids, glycerophospholipids (P = .007) and sphingolipids (P = .028) had a higher response to ATV/r and DRV/r compared to RAL. The lysophosphatidylcholine (LPCs(16:1),(17:1),(20:3)) and phosphophatidylcholine species (PCs(40:7),(38:4)) had an opposite response to RAL versus ATV/r in the discovery and validation cohort. The INSTI-based regimen had an opposite response of ceramide species ((d38:1), (d42:2)), PCs((35:2), (38:4)), phosphatidylethanolamines (PEs(38:4), (38:6)), and sphingomyelin(SMd38:1) species compared with the PI-based regimens. There were no differences observed between 2 PI-based regimens. We observed differences in response of small molecule lipid species by ART regimens in treatment-naive people living with HIV. Lippincott Williams & Wilkins 2021-07-30 /pmc/articles/PMC8322553/ /pubmed/34397689 http://dx.doi.org/10.1097/MD.0000000000026588 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle 4400
Chaudhary, Ninad S.
Kind, Tobias
Willig, Amanda L.
Saag, Michael S.
Shrestha, Sadeep
Funderburg, Nicholas
Wiener, Howard W.
Overton, E. Turner
Irvin, Marguerite R.
Changes in lipidomic profile by anti-retroviral treatment regimen: An ACTG 5257 ancillary study
title Changes in lipidomic profile by anti-retroviral treatment regimen: An ACTG 5257 ancillary study
title_full Changes in lipidomic profile by anti-retroviral treatment regimen: An ACTG 5257 ancillary study
title_fullStr Changes in lipidomic profile by anti-retroviral treatment regimen: An ACTG 5257 ancillary study
title_full_unstemmed Changes in lipidomic profile by anti-retroviral treatment regimen: An ACTG 5257 ancillary study
title_short Changes in lipidomic profile by anti-retroviral treatment regimen: An ACTG 5257 ancillary study
title_sort changes in lipidomic profile by anti-retroviral treatment regimen: an actg 5257 ancillary study
topic 4400
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8322553/
https://www.ncbi.nlm.nih.gov/pubmed/34397689
http://dx.doi.org/10.1097/MD.0000000000026588
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