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      Cardiovascular Risk and Health Among People With Human Immunodeficiency Virus (HIV) Eligible for Primary Prevention: Insights From the REPRIEVE Trial

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          Abstract

          Background

          In addition to traditional cardiovascular (CV) risk factors, antiretroviral therapy, lifestyle, and human immunodeficiency virus (HIV)-related factors may contribute to future CV events in persons with HIV (PWH).

          Methods

          Among participants in the global REPRIEVE randomized trial, we characterized demographics and HIV characteristics relative to ACC/AHA pooled cohort equations (PCE) for atherosclerotic CV disease predicted risk and CV health evaluated by Life’s Simple 7 (LS7; includes smoking, diet, physical activity, body mass index, blood pressure, total cholesterol, and glucose).

          Results

          Among 7382 REPRIEVE participants (31% women, 45% Black), the median PCE risk score was 4.5% (lower and upper quartiles Q1, Q3: 2.2, 7.2); 29% had a PCE score <2.5%, and 9% scored above 10%. PCE score was related closely to known CV risk factors and modestly (<1% difference in risk score) to immune function and HIV parameters. The median LS7 score was 9 (Q1, Q3: 7, 10) of a possible 14. Only 24 participants (0.3%) had 7/7 ideal components, and 36% had ≤2 ideal components; 90% had <5 ideal components. The distribution of LS7 did not vary by age or natal sex, although ideal health was more common in low sociodemographic index countries and among Asians. Poor dietary and physical activity patterns on LS7 were seen across all PCE scores, including the lowest risk categories.

          Conclusions

          Poor CV health by LS7 was common among REPRIEVE participants, regardless of PCE. This suggests a critical and independent role for lifestyle interventions in conjunction with conventional treatment to improve CV outcomes in PWH.

          Clinical Trials Registration: NCT02344290.

          AIDS Clinical Trials Group study number: A5332.

          Abstract

          Measures of cardiovascular (CV) risk and health are not closely related in persons with human immunodeficiency virus (HIV) in the REPRIEVE trial. Poor health scores among low-CV-risk persons with HIV suggest a critical role for lifestyle interventions regardless of CV risk prediction.

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          Most cited references30

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          Defining and setting national goals for cardiovascular health promotion and disease reduction: the American Heart Association's strategic Impact Goal through 2020 and beyond.

          This document details the procedures and recommendations of the Goals and Metrics Committee of the Strategic Planning Task Force of the American Heart Association, which developed the 2020 Impact Goals for the organization. The committee was charged with defining a new concept, cardiovascular health, and determining the metrics needed to monitor it over time. Ideal cardiovascular health, a concept well supported in the literature, is defined by the presence of both ideal health behaviors (nonsmoking, body mass index <25 kg/m(2), physical activity at goal levels, and pursuit of a diet consistent with current guideline recommendations) and ideal health factors (untreated total cholesterol <200 mg/dL, untreated blood pressure <120/<80 mm Hg, and fasting blood glucose <100 mg/dL). Appropriate levels for children are also provided. With the use of levels that span the entire range of the same metrics, cardiovascular health status for the whole population is defined as poor, intermediate, or ideal. These metrics will be monitored to determine the changing prevalence of cardiovascular health status and define achievement of the Impact Goal. In addition, the committee recommends goals for further reductions in cardiovascular disease and stroke mortality. Thus, the committee recommends the following Impact Goals: "By 2020, to improve the cardiovascular health of all Americans by 20% while reducing deaths from cardiovascular diseases and stroke by 20%." These goals will require new strategic directions for the American Heart Association in its research, clinical, public health, and advocacy programs for cardiovascular health promotion and disease prevention in the next decade and beyond.
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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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              2019 ACC/AHA Guideline on the Primary Prevention of Cardiovascular Disease: Executive Summary

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                Author and article information

                Journal
                Clin Infect Dis
                Clin Infect Dis
                cid
                Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America
                Oxford University Press (US )
                1058-4838
                1537-6591
                01 December 2021
                16 June 2021
                16 June 2021
                : 73
                : 11
                : 2009-2022
                Affiliations
                [1 ] Duke Clinical Research Institute, Duke University School of Medicine , Durham, North Carolina, USA
                [2 ] Center for Biostatistics in AIDS Research, Harvard T.H. Chan School of Public Health , Boston, Massachusetts, USA
                [3 ] University of Cincinnati , Cincinnati, Ohio, USA
                [4 ] Massachusetts General Hospital , Boston, Massachusetts, USA
                [5 ] University of Alabama at Birmingham , Birmingham, Alabama, USA
                [6 ] Icahn School of Medicine at Mount Sinai , New York, New York, USA
                [7 ] University of California at Los Angeles , Los Angeles, California, USA
                [8 ] Kowa Pharmaceuticals America, Inc. , Montgomery, Alabama, USA
                [9 ] Gilead Sciences, Inc. , Foster City, California, USA
                [10 ] HIV Netherlands Australia Thailand Research Collaboration, Thai Red Cross AIDS Research Centre, and Tuberculosis Research Unit, Faculty of Medicine, Chulalongkorn University , Thailand
                [11 ] Hospital Geral de Nova Iguacu , Rio de Janeiro,Brazil
                [12 ] Hospital San Carlos , Madrid, Spain
                [13 ] Hospital de Bellvitge, l’Hospitalet de Llobregat , Spain
                [14 ] University of Texas Southwestern Medical Center , Dallas, Texas, USA
                Author notes
                Correspondence: P. S. Douglas, Duke University School of Medicine, Duke Clinical Research Institute, PO Box 17969, 200 Morris St, Rm 7710, Durham, NC 27715 ( pamela.douglas@ 123456duke.edu ).
                Author information
                https://orcid.org/0000-0001-9876-4049
                Article
                ciab552
                10.1093/cid/ciab552
                8664454
                34134131
                80cbc497-dfc2-4b76-812c-7891031e7696
                © The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence ( https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                : 15 April 2021
                : 05 June 2021
                : 22 October 2021
                Page count
                Pages: 14
                Funding
                Funded by: National Heart, Lung, and Blood Institute, DOI 10.13039/100000050;
                Award ID: 5K24HL113128
                Award ID: 5T32HL076136
                Award ID: HL137562
                Award ID: HL146199
                Funded by: National Institute of Allergy and Infectious Diseases, DOI 10.13039/100000060;
                Award ID: UM1 AI068636
                Award ID: UM1 AI106701
                Award ID: P30 DK 040561
                Award ID: R01 MD013493
                Funded by: Oregon Health and Science University, DOI 10.13039/100006668;
                Award ID: 13FTF16450001
                Funded by: Columbia University, DOI 10.13039/100006474;
                Funded by: National Institutes of Health, DOI 10.13039/100000002;
                Award ID: 5R01-HL109711
                Award ID: R01 MD013493
                Award ID: R01AI123001
                Award ID: R01HL137562
                Award ID: R01HL146267
                Award ID: U01HL123336
                Award ID: U01HL123336
                Award ID: R01HL151283
                Funded by: Kowa Pharmaceuticals America, Gilead Sciences, and ViiV Healthcare;
                Funded by: NIA, DOI 10.13039/100000049;
                Award ID: R01 AG054366
                Funded by: NIAID, DOI 10.13039/100000060;
                Award ID: UM1 AI068634
                Award ID: AI068634
                Award ID: AI123001
                Funded by: Statistical and Data Management Center;
                Funded by: AIDS Clinical Trials Group, DOI 10.13039/100006392;
                Award ID: U01 HL123339
                Funded by: REPRIEVE DCC;
                Funded by: REPRIEVE-EU;
                Funded by: Amgen, Cytodyn, ViiV Healthcare, Merck, Janssen, and Pfizer;
                Funded by: KOWA;
                Funded by: Gilead, ViiV Healthcare, and GSK;
                Funded by: Merck, ViiV Healthcare, and Theratechnologies;
                Funded by: Infectious Disease Society of America;
                Funded by: American College of Cardiology, DOI 10.13039/100005485;
                Funded by: Gilead, Merck, Emergent Biosolutions, Glaxo-Smith-Kline, Janssen, Atea, Frontier Technology, Pfizer, Viiv Healthcare, and Regeneron;
                Funded by: Kowa Pharmaceuticals;
                Funded by: Gilead and ViiV Healthcare;
                Funded by: Gilead, Janssen, Merck Sharp and Dohme;
                Funded by: Amarin, BMS, Esperion, Amgen, Sanofi, Regeneron, and Janssen;
                Funded by: Amarin, Amgen, Astra Zeneca, BI, CSL, Esperion, Janssen, Lilly, Sanofi, Regeneron, NovoNordisk, Novartis, The Medicines Company, New Amsterdam, Cerner, 89Bio, and Pfizer;
                Funded by: KOWA;
                Funded by: KOWA;
                Funded by: ViiV Healthcare and Theratechnologies;
                Funded by: KOWA;
                Funded by: Gilead, and ViiV;
                Categories
                Major Articles and Commentaries
                AcademicSubjects/MED00290

                Infectious disease & Microbiology
                atherosclerotic cardiovascular disease,cardiac prevention,cardiovascular health,cardiovascular risk,lifestyle modifications

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