NDT Advance Access originally published online on January 14, 2009
Nephrology Dialysis Transplantation 2009 24(5):1663-1671; doi:10.1093/ndt/gfn721
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Aliskiren Trial in Type 2 Diabetes Using Cardio-Renal Endpoints (ALTITUDE): rationale and study design
1 Department of Medical Endocrinology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark 2 Faculty of Health Science, Aarhus University, Aarhus, Denmark 3 Department of Medicine, Brigham and Women's Hospital, and Harvard Medical School, Boston, MA, USA 4 BHF Cardiovascular Research Centre, University of Glasgow, Glasgow, UK 5 Department of Clinical Pharmacology, University Medical Centre Groningen, University of Groningen, The Netherlands 6 Department of Medicine and Clinical Epidemiology, San Antonio, TX, USA 7 Imperial College, London, UK 8 Novartis Pharma AG, Basel, Switzerland
Correspondence and offprint requests to: Hans-Henrik Parving, Department of Medical Endocrinology, Rigshospitalet, Blegdamsvej 9, DK-2100 Copenhagen, Denmark. Tel: +45 22 17 81 60; E-mail: hhparving{at}dadlnet.dk
 |
Abstract |
|---|
Background. Patients with type 2 diabetes are at increased risk of macro- and microvascular disease, and the presence of albuminuria and/or reduced kidney function further enhances macrovascular risk. Angiotensin-converting-enzyme inhibitors reduce both macro- and microvascular events, yet the residual renal and cardiovascular risk still remains high. Aliskiren a novel oral direct renin inhibitor that unlike ACEi and ARBs, lowers plasma renin activity, angiotensin I and angiotensin II levels, may thereby provide greater benefit compared to ACEi or ARB alone.
Methods. The primary objective of the ALTITUDE trial is to determine whether aliskiren 300 mg once daily, reduces cardiovascular and renal morbidity and mortality compared with placebo when added to conventional treatment (including ACEi or ARB). ALTITUDE is an international, randomized, double-blind, placebo-controlled, parallel-group study, which will include three categories of high-risk patients with type 2 diabetes (aged 
35 years): those with either urinary albumin/creatinine ratio (UACR) 200 mg/g; microalbuminuria (UACR) 20 <200 mg/g and eGFR 30 <60 mL/min/1.73 m2; and thirdly, those with a history of cardiovascular disease and eGFR 30 <60 mL/min/1.73 m2 with or without microalbuminuria. ALTITUDE is an event driven trial that aims to randomize 8600 patients with a planned follow-up time of 48 months. The primary outcome measure is time to first event for the composite endpoint of cardiovascular death, resuscitated death, myocardial infarction, stroke, unplanned hospitalization for heart failure, onset of end-stage renal disease or doubling of baseline serum creatinine concentration. Secondary endpoints include a composite CV endpoint and a composite renal endpoint.
Conclusion. ALTITUDE will determine whether dual RAAS blockade with the direct renin inhibitor aliskiren in combination with an ACEi or ARB will reduce major morbidity and mortality in a broad range of high-risk patients with type 2 diabetes.
Keywords: albuminuria; aliskiren; cardiovascular disease; diabetes; kidney disease
Received for publication: 29. 9.08
Accepted in revised form: 1.12.08
CiteULike 
Connotea 
Del.icio.us What's this?
This article has been cited by other articles:
|
|
 |
|
  F. Persson, P. Rossing, H. Reinhard, T. Juhl, C. D.A. Stehouwer, C. Schalkwijk, A.H. J. Danser, F. Boomsma, E. Frandsen, and H.-H. Parving Renal Effects of Aliskiren Compared With and in Combination With Irbesartan in Patients With Type 2 Diabetes, Hypertension, and Albuminuria Diabetes Care, October 1, 2009; 32(10): 1873 - 1879. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 R. Haynes, P. Mason, K. Rahimi, and M. J Landray Dual blockade of the renin-angiotensin system: are two better than one? Nephrol. Dial. Transplant., September 17, 2009; (2009) gfp458v1. [Full Text] [PDF]
|
|
|
|
 |
|
 H.-H. Parving, B. M. Brenner, J. J.V. McMurray, D. de Zeeuw, S. M. Haffner, S. D. Solomon, N. Chaturvedi, and M. A. Pfeffer Dual Renin-Angiotensin system blockade and kidney disease. J. Am. Coll. Cardiol., July 14, 2009; 54(3): 278 - 279. [Full Text] [PDF]
|
|