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      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

      research-article
      , MD, MS 1 , 2 , , , MS 3 , , MD, PhD, MPH 4 , , MD 5 , , MD 6 , , MD, PhD 1 , , PhD 4 , , MD 7 , , MD 8 , , MS 3 , , PhD 9 , , Dipl Bio 10 , , MD, PhD 11 , , MD 12 , , MD 13 , , MD 14 , the INSIGHT (International Network for Strategic Initiatives in Global HIV Trials) START (Strategic Timing of Antiretroviral Treatment) Study Group
      Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
      John Wiley and Sons Inc.
      antiretroviral therapy, cholesterol, HIV, risk factor, Lipids and Cholesterol, Cardiovascular Disease, Risk Factors

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          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 CD4 + 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: NCT00867048.

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          Most cited references45

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          2013 ACC/AHA Guideline on the Assessment of Cardiovascular Risk

          Supplemental Digital Content is available in the text.
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            Initiation of Antiretroviral Therapy in Early Asymptomatic HIV Infection

            New England Journal of Medicine, 373(9), 795-807
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              Cardiovascular disease risk profiles.

              This article presents prediction equations for several cardiovascular disease endpoints, which are based on measurements of several known risk factors. Subjects (n = 5573) were original and offspring subjects in the Framingham Heart Study, aged 30 to 74 years, and initially free of cardiovascular disease. Equations to predict risk for the following were developed: myocardial infarction, coronary heart disease (CHD), death from CHD, stroke, cardiovascular disease, and death from cardiovascular disease. The equations demonstrated the potential importance of controlling multiple risk factors (blood pressure, total cholesterol, high-density lipoprotein cholesterol, smoking, glucose intolerance, and left ventricular hypertrophy) as opposed to focusing on one single risk factor. The parametric model used was seen to have several advantages over existing standard regression models. Unlike logistic regression, it can provide predictions for different lengths of time, and probabilities can be expressed in a more straightforward way than the Cox proportional hazards model.
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                Author and article information

                Contributors
                baker@umn.edu
                Journal
                J Am Heart Assoc
                J Am Heart Assoc
                10.1002/(ISSN)2047-9980
                JAH3
                ahaoa
                Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
                John Wiley and Sons Inc. (Hoboken )
                2047-9980
                22 May 2017
                May 2017
                : 6
                : 5 ( doiID: 10.1002/jah3.2017.6.issue-5 )
                : e004987
                Affiliations
                [ 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
                Author notes
                [*] [* ] Correspondence to: Jason V. Baker, MD, MS, 701 Park Avenue, MC G5, Minneapolis, MN 55417. E‐mail: baker@ 123456umn.edu
                [†]

                A complete list of the INSIGHT (International Network for Strategic Initiatives in Global HIV Trials) START (Strategic Timing of Antiretroviral Treatment) Study Group members are given in Appendix  S1.

                Article
                JAH32237
                10.1161/JAHA.116.004987
                5524070
                28533305
                c157fa71-ba8b-4360-b672-ceede8ce718f
                © 2017 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley.

                This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 22 November 2016
                : 30 March 2017
                Page count
                Figures: 3, Tables: 2, Pages: 23, Words: 7732
                Funding
                Funded by: National Institute of Allergy and Infectious Diseases (NIAID) of the National Institutes of Health
                Award ID: UM1‐AI068641
                Award ID: UMN1‐AI120197
                Funded by: National Heart, Lung, and Blood Institute
                Funded by: Eunice Kennedy Shriver National Institute of Child Health and Human Development
                Funded by: National Institute of Mental Health
                Funded by: National Institute of Neurological Disorders and Stroke
                Funded by: National Institute of Arthritis and Musculoskeletal and Skin Diseases
                Funded by: Agence Nationale de Recherches sur le SIDA et les Hépatites Virales (France)
                Funded by: National Health and Medical Research Council (Australia)
                Funded by: National Research Foundation (Denmark)
                Funded by: Bundesministerium für Bildung und Forschung (Germany)
                Funded by: European AIDS Treatment Network
                Funded by: Medical Research Council (United Kingdom)
                Funded by: National Institute for Health Research
                Funded by: National Health Service (United Kingdom)
                Funded by: University of Minnesota
                Funded by: NIH Cardiovascular Scientist Training Program
                Award ID: T32 HL007895
                Categories
                Original Research
                Original Research
                Preventive Cardiology
                Custom metadata
                2.0
                jah32237
                May 2017
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.1.3 mode:remove_FC converted:11.07.2017

                Cardiovascular Medicine
                antiretroviral therapy,cholesterol,hiv,risk factor,lipids and cholesterol,cardiovascular disease,risk factors

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