Inflammation markers after randomization to abacavir/lamivudine or tenofovir/emtricitabine with efavirenz or atazanavir/ritonavir

被引:89
作者
McComsey, Grace A. [1 ,2 ]
Kitch, Douglas [3 ]
Daar, Eric S. [4 ]
Tierney, Camlin [3 ]
Jahed, Nasreen C. [5 ]
Melbourne, Kathleen [6 ]
Ha, Belinda [7 ]
Brown, Todd T. [8 ]
Bloom, Anthony [9 ]
Fedarko, Neal [8 ]
Sax, Paul E. [10 ,11 ]
机构
[1] Case Western Reserve Univ, Cleveland, OH 44106 USA
[2] Rainbow Babies & Childrens Hosp, Cleveland, OH 44106 USA
[3] Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
[4] Harbor UCLA Med Ctr, Los Angeles Biomed Res Inst, Torrance, CA 90509 USA
[5] Social & Sci Syst Inc, Silver Spring, MD USA
[6] Gilead Sci, Foster City, CA USA
[7] GlaxoSmithKline, Res Triangle Pk, NC USA
[8] Johns Hopkins, Baltimore, MD USA
[9] Frontier Sci & Technol Res Fdn Inc, Amherst, NY USA
[10] Brigham & Womens Hosp, Boston, MA 02115 USA
[11] Harvard Univ, Sch Med, Boston, MA USA
关键词
abacavir; C-reactive protein; endothelial activation markers; inflammation markers; interleukin-6; TNF alpha; C-REACTIVE PROTEIN; HIV-INFECTED PATIENTS; INTIMA-MEDIA THICKNESS; INDIVIDUAL ANTIRETROVIRAL DRUGS; ENDOTHELIAL ACTIVATION MARKERS; BONE-MINERAL DENSITY; MYOCARDIAL-INFARCTION; ABACAVIR-LAMIVUDINE; CLINICAL-TRIALS; TENOFOVIR-EMTRICITABINE;
D O I
10.1097/QAD.0b013e328354f4fb
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: The effect of specific antiretrovirals on inflammation is unclear. Methods: A5224s was a substudy of A5202, which randomized HIV-infected treatment-naive patients to blinded abacavir/lamivudine (ABC/3TC) or tenofovir/emtricitabine (TDF/FTC) with open-label efavirenz (EFV) or atazanavir/ritonavir (ATV/r) in a factorial design. Our analysis compared changes in inflammation markers from baseline to week 24 between ABC/3TC and TDF/FTC. Secondary analyses included changes at week 96 and comparisons of EFV vs. ATV/r. Results: Analyses included 244 patients (85% male, 48% white non-Hispanic), median age 39 years, HIV-1 RNA 4.6 log(10) copies/ml, CD4 240 cells/mu l. TNF-alpha, soluble receptors of TNF-alpha (sTNFR)-I and II, soluble vascular cellular adhesion molecule (sVCAM)-1 and soluble intercellular adhesion molecule (sICAM)-1 decreased significantly at weeks 24 and 96, without significant differences between components (P >= 0.44). At week 24, ABC/3TC had a greater high-sensitivity C-reactive protein (hsCRP) mean fold change than TDF/FTC {1.43 vs. 0.88, estimated mean fold change percentage difference [Delta] 61.5% [95% confidence interval (CI) 13.6%, 129.5%]; P = 0.008}. Similar results were seen at week 96 (P = 0.021). At week 24 (but not 96), EFV had a greater hsCRP mean fold change than ATV/r [1.41 vs. 0.88; Delta 60.2% (12.6%, 127.7%); P = 0.009]. IL-6 decreased significantly at week 24 with TDF/FTC but not with ABC/3TC (between-components P = 0.019). At week 96, IL-6 decreased significantly in both nucleoside reverse transcriptase inhibitor components (between-components P = 0.11). IL-6 changes were not significantly different between ATV/r and EFV at either time point (P >= 0.89). Conclusions: Soluble TNF-receptors and adhesion molecules decreased following treatment initiation and did not differ by regimens. Differences were seen on hsCRP and IL-6 changes with ABC/3TC vs. TDF/FTC and on hsCRP with EFV vs. ATV/r. (C) 2012 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins
引用
收藏
页码:1371 / 1385
页数:15
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