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Grace A McComsey, Douglas Kitch, Paul E Sax, Camlin Tierney, Nasreen C Jahed, Kathleen Melbourne, Belinda Ha, Todd T Brown, Anthony Bloom, Neal Fedarko,

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Presentation on theme: "Grace A McComsey, Douglas Kitch, Paul E Sax, Camlin Tierney, Nasreen C Jahed, Kathleen Melbourne, Belinda Ha, Todd T Brown, Anthony Bloom, Neal Fedarko,"— Presentation transcript:

1 Grace A McComsey, Douglas Kitch, Paul E Sax, Camlin Tierney, Nasreen C Jahed, Kathleen Melbourne, Belinda Ha, Todd T Brown, Anthony Bloom, Neal Fedarko, and Eric S Daar on behalf of the ACTG A5224s team

2  Increased inflammation persists on ART and may drive clinical events and mortality  Several studies have found associations between single measurements of selective inflammatory markers and mortality  The purpose of this presentation is to present the associations between inflammatory markers (pre-ART and after ART initiation) and clinical events in a prospective clinical trial A5224s

3 A5224s design: Metabolic substudy of A5202 A5224s

4 Significant decreases in TNF- , sTNFR-I, sTNFR-II, sVCAM-1, and sICAM-1 levels within all arms, without differences between ABC/3TC and TDF/FTC or ATV/r and EFV More favorable changes in IL-6 at week 24 and hsCRP at weeks 24 and 96 with TDF/FTC vs. ABC/3TC McComsey, AIDS 2012 A5224s

5  Exploratory analysis  To assess the association between baseline and time-updated inflammatory biomarker levels and time to first AIDS-defining and/or non-AIDS-defining events  Cox proportional hazards regression models  Only first event occurring in each category in each subject was used in analysis

6 N=244 Age years, median (Q1, Q3)39 (31, 44) Male (%)85% White non-Hispanic Race/Ethnicity (%)48% HIV-1 RNA log 10 c/mL, median (Q1, Q3)4.64 (4.26, 4.91) HIV RNA ≥ 100,000 c/mL Stratum (%)41% CD4 cells/mm 3, median (Q1, Q3)240 (106, 335) CD4 < 200 cells/mm 3 (%)43% hsCRP  g/mL, median (Q1, Q3) 1.7 (0.7, 4.0) IL-6 pg/mL, median (Q1, Q3) 0.8 (0.5, 1.4) TNF-α pg/mL, median (Q1, Q3) 11.0 (8.2, 14.7) sTNF-RI pg/mL, median (Q1, Q3) 1277 (1105, 1538) sTNFR-II pg/mL, median (Q1, Q3) 5350 (3965, 7756) sVCAM-1 ng/mL, median (Q1, Q3) 1187 (939, 1599) sICAM-1 ng/mL, median (Q1, Q3) 330 (267, 402) A5224s

7 Correlations Among Markers at Baseline A5224s Spearman’s rank correlation coefficient

8 Correlations Among Markers at Week 24 A5224s Spearman’s rank correlation coefficient

9 Description of Events  AIDS-defining events (CDC classification)  13 events: 9 OIs; 3 AIDS-cancers, 1 recurrent bacterial pneumonia  Events occurred between 2 and 133 weeks, median 16 weeks  Of these, 7 events occurred within first 24 weeks  Non-AIDS events  18 events: 6 diabetes, 4 cancers, 3 cardiovascular, 5 pneumonias  Events occurred between 3.5 and 165 weeks, median 81 weeks  Of these, 4 events occurred within first 24 weeks  AIDS- or Non-AIDS events  28 events  Events occurred between 2 and 164 weeks, median 32 weeks  Of these, 11 events occurred within first 24 weeks A5224s

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11 HR= hazard ratio from Cox Proportional Hazard model

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18 Other Results A5224s

19 HR= hazard ratio from Cox Proportional Hazard model

20  15 (traumatic) fractures occurred  Considered separate from non-AIDS events  Neither baseline nor time-updated biomarker values were significantly associated with an increased risk of fracture

21  At baseline, CD4 count correlated with IL6, sTNFR-I and II  Changes in CD4 correlated with changes in TNF- , sTNF-Rs and adhesion molecules  At baseline, HIV-1 RNA correlated with all markers except for hsCRP  Only change (0-24 w) in sTNFR-I level significantly different between suppressed subjects vs. those >50 copies/mL at week 24

22  Higher levels of several inflammatory biomarkers were associated independently of CD4 count with increased risk of AIDS and non-AIDS events.  Time-updated levels in markers of TNF-  and/or sTNF receptors were associated with clinical events whereas this was not observed for hsCRP.

23  Small number of events  Relatively short follow up  Time-updated for AIDS events driven by early events  Large number of analyses performed  Adjusted analyses to be interpreted with caution (small events n) Larger and longer studies needed to investigate the use of these markers as predictors of clinical endpoints.

24 Thank yous  Study Participants and ACTG sites  ACTG 5224s team: Douglas Kitch and Camlin Tierney (SDAC), Paul Sax, Eric Daar, Pablo Tebas, Nasreen Jahed, Laurie Myers, Belinda Ha, Kathleen Melbourne, Lynda Szczech, David Currin, Lori Mong-Kryspin  ACTG 5202 team  ACTG and NIH (NIAID) for supporting A5202/5224 studies  GSK and Gilead for supporting inflammatory markers cost A5224s


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