Endothelial Function in Human Immunodeficiency Virus-Infected Antiretroviral-Naive Subjects Before and After Starting Potent Antiretroviral Therapy : The ACTG (AIDS Clinical Trials Group) Study 5152s
This study evaluated the effects of 3 class-sparing antiretroviral therapy (ART) regimens on endothelial function in human immunodeficiency virus (HIV)-infected subjects participating in a randomized trial. Endothelial dysfunction has been observed in patients receiving ART for HIV infection. This w...
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Published in | Journal of the American College of Cardiology Vol. 52; no. 7; pp. 569 - 576 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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New York, NY
Elsevier Science
12.08.2008
Elsevier Limited |
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Abstract | This study evaluated the effects of 3 class-sparing antiretroviral therapy (ART) regimens on endothelial function in human immunodeficiency virus (HIV)-infected subjects participating in a randomized trial.
Endothelial dysfunction has been observed in patients receiving ART for HIV infection.
This was a prospective, multicenter study of treatment-naive subjects who were randomly assigned to receive a protease inhibitor-sparing regimen of nucleoside reverse transcriptase inhibitors (NRTIs) + efavirenz, a non-nucleoside reverse transcriptase inhibitor-sparing regimen of NRTIs + lopinavir/ritonavir, or a NRTI-sparing regimen of efavirenz + lopinavir/ritonavir. The NRTIs were lamivudine + stavudine, zidovudine, or tenofovir. Brachial artery flow-mediated dilation (FMD) was determined by B-mode ultrasound before starting on ART, then after 4 and 24 weeks.
There were 82 subjects (median age 35 years, 91% men, 54% white). Baseline CD4 cell counts and plasma HIV ribonucleic acid (RNA) values were 245 cells/mm(3) and 4.8 log(10) copies/ml, respectively. At baseline, FMD was 3.68% (interquartile range [IQR] 1.98% to 5.51%). After 4 and 24 weeks of ART, plasma HIV RNA decreased by 2.1 and 3.0 log(10) copies/ml, respectively. FMD increased by 0.74% (IQR -0.62% to +2.74%, p = 0.003) and 1.48% (IQR -0.20% to +4.30%, p < 0.001), respectively, with similar changes in each arm (Kruskal-Wallis p value >0.600). The decrease in plasma HIV RNA at 24 weeks was associated with greater FMD (r(s) = -0.30, p = 0.017).
Among treatment-naive individuals with HIV, 3 different ART regimens rapidly improved endothelial function. Benefits were similar for all ART regimens, appeared quickly, and persisted at 24 weeks. |
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AbstractList | This study evaluated the effects of 3 class-sparing antiretroviral therapy (ART) regimens on endothelial function in human immunodeficiency virus (HIV)-infected subjects participating in a randomized trial.
Endothelial dysfunction has been observed in patients receiving ART for HIV infection.
This was a prospective, multicenter study of treatment-naive subjects who were randomly assigned to receive a protease inhibitor-sparing regimen of nucleoside reverse transcriptase inhibitors (NRTIs) + efavirenz, a non-nucleoside reverse transcriptase inhibitor-sparing regimen of NRTIs + lopinavir/ritonavir, or a NRTI-sparing regimen of efavirenz + lopinavir/ritonavir. The NRTIs were lamivudine + stavudine, zidovudine, or tenofovir. Brachial artery flow-mediated dilation (FMD) was determined by B-mode ultrasound before starting on ART, then after 4 and 24 weeks.
There were 82 subjects (median age 35 years, 91% men, 54% white). Baseline CD4 cell counts and plasma HIV ribonucleic acid (RNA) values were 245 cells/mm(3) and 4.8 log(10) copies/ml, respectively. At baseline, FMD was 3.68% (interquartile range [IQR] 1.98% to 5.51%). After 4 and 24 weeks of ART, plasma HIV RNA decreased by 2.1 and 3.0 log(10) copies/ml, respectively. FMD increased by 0.74% (IQR -0.62% to +2.74%, p = 0.003) and 1.48% (IQR -0.20% to +4.30%, p < 0.001), respectively, with similar changes in each arm (Kruskal-Wallis p value >0.600). The decrease in plasma HIV RNA at 24 weeks was associated with greater FMD (r(s) = -0.30, p = 0.017).
Among treatment-naive individuals with HIV, 3 different ART regimens rapidly improved endothelial function. Benefits were similar for all ART regimens, appeared quickly, and persisted at 24 weeks. This study evaluated the effects of 3 class-sparing antiretroviral therapy (ART) regimens on endothelial function in human immunodeficiency virus (HIV)-infected subjects participating in a randomized trial.OBJECTIVESThis study evaluated the effects of 3 class-sparing antiretroviral therapy (ART) regimens on endothelial function in human immunodeficiency virus (HIV)-infected subjects participating in a randomized trial.Endothelial dysfunction has been observed in patients receiving ART for HIV infection.BACKGROUNDEndothelial dysfunction has been observed in patients receiving ART for HIV infection.This was a prospective, multicenter study of treatment-naive subjects who were randomly assigned to receive a protease inhibitor-sparing regimen of nucleoside reverse transcriptase inhibitors (NRTIs) + efavirenz, a non-nucleoside reverse transcriptase inhibitor-sparing regimen of NRTIs + lopinavir/ritonavir, or a NRTI-sparing regimen of efavirenz + lopinavir/ritonavir. The NRTIs were lamivudine + stavudine, zidovudine, or tenofovir. Brachial artery flow-mediated dilation (FMD) was determined by B-mode ultrasound before starting on ART, then after 4 and 24 weeks.METHODSThis was a prospective, multicenter study of treatment-naive subjects who were randomly assigned to receive a protease inhibitor-sparing regimen of nucleoside reverse transcriptase inhibitors (NRTIs) + efavirenz, a non-nucleoside reverse transcriptase inhibitor-sparing regimen of NRTIs + lopinavir/ritonavir, or a NRTI-sparing regimen of efavirenz + lopinavir/ritonavir. The NRTIs were lamivudine + stavudine, zidovudine, or tenofovir. Brachial artery flow-mediated dilation (FMD) was determined by B-mode ultrasound before starting on ART, then after 4 and 24 weeks.There were 82 subjects (median age 35 years, 91% men, 54% white). Baseline CD4 cell counts and plasma HIV ribonucleic acid (RNA) values were 245 cells/mm(3) and 4.8 log(10) copies/ml, respectively. At baseline, FMD was 3.68% (interquartile range [IQR] 1.98% to 5.51%). After 4 and 24 weeks of ART, plasma HIV RNA decreased by 2.1 and 3.0 log(10) copies/ml, respectively. FMD increased by 0.74% (IQR -0.62% to +2.74%, p = 0.003) and 1.48% (IQR -0.20% to +4.30%, p < 0.001), respectively, with similar changes in each arm (Kruskal-Wallis p value >0.600). The decrease in plasma HIV RNA at 24 weeks was associated with greater FMD (r(s) = -0.30, p = 0.017).RESULTSThere were 82 subjects (median age 35 years, 91% men, 54% white). Baseline CD4 cell counts and plasma HIV ribonucleic acid (RNA) values were 245 cells/mm(3) and 4.8 log(10) copies/ml, respectively. At baseline, FMD was 3.68% (interquartile range [IQR] 1.98% to 5.51%). After 4 and 24 weeks of ART, plasma HIV RNA decreased by 2.1 and 3.0 log(10) copies/ml, respectively. FMD increased by 0.74% (IQR -0.62% to +2.74%, p = 0.003) and 1.48% (IQR -0.20% to +4.30%, p < 0.001), respectively, with similar changes in each arm (Kruskal-Wallis p value >0.600). The decrease in plasma HIV RNA at 24 weeks was associated with greater FMD (r(s) = -0.30, p = 0.017).Among treatment-naive individuals with HIV, 3 different ART regimens rapidly improved endothelial function. Benefits were similar for all ART regimens, appeared quickly, and persisted at 24 weeks.CONCLUSIONSAmong treatment-naive individuals with HIV, 3 different ART regimens rapidly improved endothelial function. Benefits were similar for all ART regimens, appeared quickly, and persisted at 24 weeks. Endothelial Function in Human Immunodeficiency Virus-Infected Antiretroviral-Naive Subjects Before and After Starting Potent Antiretroviral Therapy: The ACTG (AIDS Clinical Trials Group) Study 5152s Francesca J. Torriani, Lauren Komarow, Robert A. Parker, Bruno R. Cotter, Judith S. Currier, Michael P. Dubé, Carl J. Fichtenbaum, Mariana Gerschenson, Carol K. C. Mitchell, Robert L. Murphy, Kathleen Squires, James H. Stein, for the ACTG 5152s Study Team Among 82 treatment-naive human immunodeficiency virus-infected subjects participating in a prospective, multicenter study of 3 class-sparing antiretroviral therapy regimens, flow-mediated dilation of the brachial artery improved after 4 (+0.74%, p = 0.003) and 24 weeks (+1.48%, p < 0.001), with similar changes in each arm (Kruskal-Wallis p value >0.600). |
Author | KOMAROW, Lauren PARKER, Robert A FICHTENBAUM, Carl J TORRIANI, Francesca J STEIN, James H GERSCHENSON, Mariana DUBE, Michael P MURPHY, Robert L COTTER, Bruno R CURRIER, Judith S SQUIRES, Kathleen MITCHELL, Carol K. C |
Author_xml | – sequence: 1 givenname: Francesca J surname: TORRIANI fullname: TORRIANI, Francesca J organization: University of California-San Diego, San Diego, California, United States – sequence: 2 givenname: Lauren surname: KOMAROW fullname: KOMAROW, Lauren organization: Harvard School of Public Health, Boston, Massachusetts, United States – sequence: 3 givenname: Kathleen surname: SQUIRES fullname: SQUIRES, Kathleen organization: University of Southern California, Los Angeles, California, United States – sequence: 4 givenname: James H surname: STEIN fullname: STEIN, James H organization: University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, United States – sequence: 5 givenname: Robert A surname: PARKER fullname: PARKER, Robert A organization: Harvard School of Public Health, Boston, Massachusetts, United States – sequence: 6 givenname: Bruno R surname: COTTER fullname: COTTER, Bruno R organization: University of California-San Diego, San Diego, California, United States – sequence: 7 givenname: Judith S surname: CURRIER fullname: CURRIER, Judith S organization: University of California-Los Angeles, Los Angeles, California, United States – sequence: 8 givenname: Michael P surname: DUBE fullname: DUBE, Michael P organization: Indiana University School of Medicine, Indianapolis, Indiana, United States – sequence: 9 givenname: Carl J surname: FICHTENBAUM fullname: FICHTENBAUM, Carl J organization: University of Cincinnati Medical Center, Cincinnati, Ohio, United States – sequence: 10 givenname: Mariana surname: GERSCHENSON fullname: GERSCHENSON, Mariana organization: University of Hawaii, Honolulu, Hawaii, United States – sequence: 11 givenname: Carol K. C surname: MITCHELL fullname: MITCHELL, Carol K. C organization: University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, United States – sequence: 12 givenname: Robert L surname: MURPHY fullname: MURPHY, Robert L organization: Northwestern University Feinberg School of Medicine, Chicago, Illinois, United States |
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Title | Endothelial Function in Human Immunodeficiency Virus-Infected Antiretroviral-Naive Subjects Before and After Starting Potent Antiretroviral Therapy : The ACTG (AIDS Clinical Trials Group) Study 5152s |
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