Differences in LipidMeasurements by Antiretroviral Regimen Exposure in Cohorts fromAsia and Australia

被引:6
作者
Achhra, Amit C. [1 ]
Amin, Janaki [1 ]
Hoy, Jennifer [2 ,3 ]
Tanuma, Junko [4 ]
Sirisanthana, Thira [5 ]
Nolan, David [6 ,7 ]
Merati, Tuti [8 ,9 ]
Giles, Michelle [2 ,3 ]
机构
[1] Univ New South Wales, Fac Med, Kirby Inst Infect & Immun Soc, Natl Ctr HIV Epidemiol & Clin Res, Sydney, NSW 2052, Australia
[2] Alfred Hosp, Infect Dis Unit, Melbourne, Vic 3004, Australia
[3] Monash Univ, Melbourne, Vic 3004, Australia
[4] Natl Ctr Global Hlth & Med, AIDS Clin Ctr, Tokyo 1628655, Japan
[5] Chiang Mai Univ, Res Inst Hlth Sci, Chiang Mai 50200, Thailand
[6] Murdoch Univ, Ctr Clin Immunol & Biomed Stat, Perth, WA, Australia
[7] Royal Perth Hosp, Perth, WA, Australia
[8] Udayana Univ, Fac Med, Bali 80233, Indonesia
[9] Sanglah Hosp, Bali 80233, Indonesia
基金
美国国家卫生研究院;
关键词
D O I
10.1155/2012/246280
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
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 nucleosidereverse 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 (P for interaction between regimen and cohort: <0.001) but not in case of other lipids (P for 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.
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页数:9
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