Differences in Lipid Measurements by Antiretroviral Regimen Exposure in Cohorts from Asia and Australia

Author:

Achhra Amit C.1,Amin Janaki1,Hoy Jennifer2,Tanuma Junko3,Sirisanthana Thira4,Nolan David5,Merati Tuti6,Giles Michelle2

Affiliation:

1. The Kirby Institute for Infection and Immunity in Society (Formerly the National Centre in HIV Epidemiology and Clinical Research), Faculty of Medicine, University of New South Wales, Sydney, NSW 2052, Australia

2. Infectious Diseases Unit, Alfred Hospital and Monash University, Melbourne, VIC 3004, Australia

3. AIDS Clinical Center, National Center for Global Health and Medicine, Tokyo 162-8655, Japan

4. Research Institute for Health Sciences, Chiang Mai University, Chiang Mai 50200, Thailand

5. Centre for Clinical Immunology and Biomedical Statistics, Murdoch University and Royal Perth Hospital, Perth, Australia

6. Faculty of Medicine, Udayana University and Sanglah Hospital, Bali 80233, Indonesia

Abstract

We explored the mean differences in routinely measured lipids (total cholesterol, triglycerides, and high-density lipoprotein cholesterol) according to exposure to different combination antiretroviral regimens in Asian (n=2051) and Australian (predominantly Caucasian,n=794) cohorts. The regimen was defined as at least 3 antiretroviral drugs with at least 2 nucleoside-reverse transcriptases (NRTIs) and either of at least one protease inhibitor (PI) or non-nucleoside-reverse transcriptases (NNRTIs). We categorised cART regimens as: NRTIs as tenofovir based or not; NNRTIs as nevirapine or efavirenz (but not both); and PI as atazanavir based or not. We found that the impact of various antiretroviral regimens on lipids in Asian and Australian cohorts was only different by cohort for total cholesterol (Pfor interaction between regimen and cohort: <0.001) but not in case of other lipids (Pfor interaction: >0.05). The differences in total cholesterol were however small and unlikely to be of clinical significance. Overall, tenofovir with nevirapine or atazanavir was associated with the most favorable lipids, while the PI regimens without tenofovir and atazanavir were associated with least favorable lipids. We conclude that the impact of various ART regimens on lipids is largely similar in Asian and Australian cohorts and that the newer drugs such as tenofovir and atazanavir are likely to provide similar benefit in terms of lipid profiles in both populations.

Publisher

Hindawi Limited

Subject

Infectious Diseases,Public Health, Environmental and Occupational Health,Dermatology,Immunology and Allergy

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