Pulse wave velocity as endpoint in large-scale intervention trial. The Complior (R) study

Citation
R. Asmar et al., Pulse wave velocity as endpoint in large-scale intervention trial. The Complior (R) study, J HYPERTENS, 19(4), 2001, pp. 813-818
Citations number
26
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
JOURNAL OF HYPERTENSION
ISSN journal
02636352 → ACNP
Volume
19
Issue
4
Year of publication
2001
Pages
813 - 818
Database
ISI
SICI code
0263-6352(200104)19:4<813:PWVAEI>2.0.ZU;2-5
Abstract
Objective To evaluate the ability of an antihypertensive therapy to improve arterial stiffness as assessed by aortic pulse wave velocity (PWV) in a la rge population of hypertensive patients. Setting Sixty-nine healthcare centres, private and institutional (19 countr ies). Patients Subjects aged 18-79 years, with essential hypertension. A total of 2187 patients were enrolled; 1703 (52% male) completed the study: mean age = 50 +/- 12 years; mean baseline systolic/diastolic blood pressure (S/D BP ) = 158 +/- 15/98 +/- 7 mmHg; mean baseline carotid-femoral PWV = 11.6 +/- 2.4 m/s. Interventions Patients were treated for 6 months, starting with perindopril (angiotensin converting enzyme (ACE) inhibitor) 4 mg once daily (OD), incr eased to 8 mg OD, and combined to diuretic (indapamide 2.5 mg OD) if BP was uncontrolled (> 140/90 mmHg), Results It was feasible to measure carotid-femoral PWV using the automatic device Complior (R) at inclusion, 2 and 6 months, along with conventional B P assessments in a population of 1703 patients. Significant decreases (P < 0.001) in BP (systolic: -23.7 <plus/minus> 16.8, diastolic: -14.6 +/- 10 mm Hg), and carotid-femoral PWV (-1.1 +/- 1.4 m/s) were obtained at 2 and 6 mo nths, Conclusions The Complier Study is the first study to show the feasibility o f a large-scale intervention trial using PWV as the endpoint in hypertensiv e patients. Adequate results may be obtained using an automatic device and rigorous criteria for assessment. A long-term controlled intervention study is needed to confirm the results of the present uncontrolled trial. (C) 20 01 Lippincott Williams & Wilkins.