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      SPARTE Study: Normalization of Arterial Stiffness and Cardiovascular Events in Patients With Hypertension at Medium to Very High Risk

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          Abstract

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          Abstract

          The SPARTE study (Strategy for Preventing cardiovascular and renal events based on ARTErial stiffness; URL: https://www.clinicaltrials.gov; Unique identifier: NCT02617238) is a multicenter open-label randomized controlled trial with blinded end point evaluation, undertaken at 25 French research centers in university hospitals. Patients with primary hypertension were randomly assigned (1:1) to a therapeutic strategy targeting the normalization of carotid-femoral pulse wave velocity (PWV) measured every 6 months (PWV group, n=264) versus a classical therapeutic strategy only implementing the European Guidelines for Hypertension Treatment (conventional group, n=272). In the PWV group, the therapeutic strategy used preferably a combination of ACE (angiotensin-converting enzyme) inhibitor or angiotensin receptor blocker and calcium channel blockers, as well as maximal recommended doses of ACE inhibitors and angiotensin receptor blockers. The primary outcome was a combined end point including particularly stroke and coronary events. Secondary outcomes included the time-course changes in brachial office blood pressure (BP), ambulatory BP, PWV, and treatments. After a median follow-up of 48.3 months, there was no significant between-group difference in primary outcome (hazard ratio, 0.74 [95% CI, 0.40–1.38], P=0.35). In the PWV group, combinations of renin-angiotensin-system blockers and calcium channel blockers were prescribed at higher dosage ( P=0.028), office and ambulatory systolic blood pressure and diastolic blood pressure decreased more ( P<0.001 and P<0.01, respectively), and PWV increased less ( P=0.0003) than in the conventional group. The SPARTE study lacked sufficient statistical power to demonstrate its primary outcome. However, it demonstrated that a PWV-driven treatment for hypertension enables to further reduce office and ambulatory systolic blood pressure and diastolic blood pressure and prevent vascular aging in patients with hypertension at medium-to-very-high risk, compared with strict application of guidelines.

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          2018 ESC/ESH Guidelines for the management of arterial hypertension

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            General cardiovascular risk profile for use in primary care: the Framingham Heart Study.

            Separate multivariable risk algorithms are commonly used to assess risk of specific atherosclerotic cardiovascular disease (CVD) events, ie, coronary heart disease, cerebrovascular disease, peripheral vascular disease, and heart failure. The present report presents a single multivariable risk function that predicts risk of developing all CVD and of its constituents. We used Cox proportional-hazards regression to evaluate the risk of developing a first CVD event in 8491 Framingham study participants (mean age, 49 years; 4522 women) who attended a routine examination between 30 and 74 years of age and were free of CVD. Sex-specific multivariable risk functions ("general CVD" algorithms) were derived that incorporated age, total and high-density lipoprotein cholesterol, systolic blood pressure, treatment for hypertension, smoking, and diabetes status. We assessed the performance of the general CVD algorithms for predicting individual CVD events (coronary heart disease, stroke, peripheral artery disease, or heart failure). Over 12 years of follow-up, 1174 participants (456 women) developed a first CVD event. All traditional risk factors evaluated predicted CVD risk (multivariable-adjusted P<0.0001). The general CVD algorithm demonstrated good discrimination (C statistic, 0.763 [men] and 0.793 [women]) and calibration. Simple adjustments to the general CVD risk algorithms allowed estimation of the risks of each CVD component. Two simple risk scores are presented, 1 based on all traditional risk factors and the other based on non-laboratory-based predictors. A sex-specific multivariable risk factor algorithm can be conveniently used to assess general CVD risk and risk of individual CVD events (coronary, cerebrovascular, and peripheral arterial disease and heart failure). The estimated absolute CVD event rates can be used to quantify risk and to guide preventive care.
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              A Randomized Trial of Intensive versus Standard Blood-Pressure Control

              New England Journal of Medicine, 373(22), 2103-2116
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                Author and article information

                Contributors
                Journal
                Hypertension
                Hypertension
                HYP
                Hypertension (Dallas, Tex. : 1979)
                Lippincott Williams & Wilkins (Hagerstown, MD )
                0194-911X
                1524-4563
                30 August 2021
                October 2021
                : 78
                : 4
                : 983-995
                Affiliations
                [1 ]From the Université de Paris, France (S.L., G. Chatellier, M.A., N.D., R.-M.B., P.B.)
                [2 ]Assistance-Publique Hopitaux de Paris, Georges Pompidou European Hospital, Paris, France (S.L., G. Chatellier, M.A., N.D., H.K., R.-M.B., P.B.)
                [3 ]Clinical Research Unit, INSERM U970, Paris (G. Chatellier, H.P.)
                [4 ]Hypertension Department and DMU CARTE, Paris, France (M.A.)
                [5 ]INSERM, CIC1418, Paris, France (M.A.)
                [6 ]Neurology department, GHU Paris Psychiatrie Neurosciences, Sainte-Anne Hospital (D.C.)
                [7 ]INSERM UMR 1266, FHU NeuroVasc, Paris, France (D.C.)
                [8 ]Nephrology Dialysis Transplantation Department, CHU Amiens, France (G. Choukroun)
                [9 ]MP3CV Research Unit, University Picardie Jules Verne, France (G. Choukroun)
                [10 ]Cardiology Department, Georges Pompidou Hospital, Paris, France (N.D.)
                [11 ]CHU Lille, Institut Cœur Poumon, Lille, France (P.D.)
                [12 ]ICAN, Sorbonne University, Assistance-Publique Hopitaux de Paris, Paris, France (X.G.)
                [13 ]Cardiology Department, Saint Andre Hospital, CHU Bordeaux, France (P.G.)
                [14 ]INSERM U970, Cardiovascular Research Center - PARCC, Paris, France (H.K., R.-M.B., P.B.)
                [15 ]Department of Nephrology, Manhes Hospital, Fleury Merogis, France(G.L.)
                [16 ]Paris Saint-Joseph Hospital, Paris, France (J.-J.M.)
                [17 ]Department of Internal Medicine, Manhes Hospital, Fleury Merogis, France (B.P.)
                [18 ]University of Strasbourg, France (D.S.)
                [19 ]UMR 1260, INSERM-University of Strasbourg, France (D.S.)
                [20 ]Unit of Endocrinology-Diabetology-Nutrition, Assistance-Publique Hopitaux de Paris, Jean Verdier Hospital, University Sorbonne Paris Cite, Bondy, France (P.V.)
                [21 ]Center for the Research and Treatment of Arterial Hypertension and Cardiovascular Risk, Internal Medicine Department, Guimaraes, Portugal (P.C.)
                [22 ]Life and Health Research Institute (ICVS/3B’s), Minho University, Portugal (P.C.)
                [23 ]Department of Hypertension and Diabetology, Faculty of Medicine, Medical University of Gdansk, Debinki, Gdansk, Poland (K.N.).
                Author notes
                Correspondenece to: Stephane Laurent, Department of Pharmacology, Université de Paris, Hôpital Européen Georges Pompidou, 56 Rue Leblanc, 75015 Paris. Email stef.laurent53@ 123456gmail.com
                Article
                00010
                10.1161/HYPERTENSIONAHA.121.17579
                8415523
                34455813
                c296b4fc-610d-40b5-89d0-b1d82282abea
                © 2021 The Authors.

                Hypertension is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial-NoDerivs License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited, the use is noncommercial, and no modifications or adaptations are made.

                This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.

                History
                : 20 April 2021
                : 29 June 2021
                Categories
                10111
                Original Articles
                Arterial Stiffness
                Custom metadata
                TRUE
                T

                blood pressure,clinical trial,hypertension,renin-angiotensin system,surrogate end point,vascular stiffness

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