Changes in Cardiovascular Disease Risk Factors With Immediate Versus Deferred Antiretroviral Therapy Initiation Among HIV‐Positive Participants in the START (Strategic Timing of Antiretroviral Treatment) Trial

Author:

Baker Jason V.12,Sharma Shweta3,Achhra Amit C.4,Bernardino Jose Ignacio5,Bogner Johannes R.6,Duprez Daniel1,Emery Sean4,Gazzard Brian7,Gordin Jonathan8,Grandits Greg3,Phillips Andrew N.9,Schwarze Siegfried10,Soliman Elsayed Z.11,Spector Stephen A.12,Tambussi Giuseppe13,Lundgren Jens14,

Affiliation:

1. Department of Medicine, University of Minnesota, Minneapolis, MN

2. Division of Infectious Diseases, Hennepin County Medical Center, Minneapolis, MN

3. Division of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, MN

4. Kirby Institute, University of New South Wales, Sydney, Australia

5. Department of Medicine, Hospital La Paz, IdiPAZ, Madrid, Spain

6. Division of Infectious Diseases MedIV University Hospital of Munich, Germany

7. Chelsea and Westminster Hospital, London, United Kingdom

8. Division of Cardiology, David Geffen School of Medicine at University of California, Los Angeles, CA

9. HIV Epidemiology & Biostatistics Group, University College London, London, United Kingdom

10. European AIDS Treatment Group, Berlin, Germany

11. Epidemiological Cardiology Research Center, Wake Forest School of Medicine, Winston Salem, NC

12. Division of Pediatric Infectious Diseases, University of California San Diego and Rady Children's Hospital, San Diego, CA

13. San Raffaele Scientific Institute, Milano, Italy

14. CHIP, Department of Infectious Diseases, Rigshospitalet University of Copenhagen, Denmark

Abstract

Introduction HIV infection and certain antiretroviral therapy ( ART ) medications increase atherosclerotic cardiovascular disease risk, mediated, in part, through traditional cardiovascular disease risk factors. Methods and Results We studied cardiovascular disease risk factor changes in the START (Strategic Timing of Antiretroviral Treatment) trial, a randomized study of immediate versus deferred ART initiation among HIV‐positive persons with CD 4 + cell counts >500 cells/mm 3 . Mean change from baseline in risk factors and the incidence of comorbid conditions were compared between groups. The characteristics among 4685 HIV ‐positive START trial participants include a median age of 36 years, a CD4 cell count of 651 cells/mm 3 , an HIV viral load of 12 759 copies/mL, a current smoking status of 32%, a median systolic/diastolic blood pressure of 120/76 mm Hg, and median levels of total cholesterol of 168 mg/dL, low‐density lipoprotein cholesterol of 102 mg/dL, and high‐density lipoprotein cholesterol of 41 mg/dL. Mean follow‐up was 3.0 years. The immediate and deferred ART groups spent 94% and 28% of follow‐up time taking ART , respectively. Compared with patients in the deferral group, patients in the immediate ART group had increased total cholesterol and low‐density lipoprotein cholesterol and higher use of lipid‐lowering therapy (1.2%; 95% CI , 0.1–2.2). Concurrent increases in high‐density lipoprotein cholesterol with immediate ART resulted in a 0.1 lower total cholesterol to high‐density lipoprotein cholesterol ratio (95% CI , 0.1–0.2). Immediate ART resulted in 2.3% less BP ‐lowering therapy use (95% CI , 0.9–3.6), but there were no differences in new‐onset hypertension or diabetes mellitus. Conclusions Among HIV‐positive persons with preserved immunity, immediate ART led to increases in total cholesterol and low‐density lipoprotein cholesterol but also concurrent increases in high‐density lipoprotein cholesterol and decreased use of blood pressure medications. These opposing effects suggest that, in the short term, the net effect of early ART on traditional cardiovascular disease risk factors may be clinically insignificant." Clinical Trial Registration URL : http://www.clinicaltrials.gov . Unique identifier: NCT 00867048.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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