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The HALT Polycystic Kidney Disease Trials
Author(s) -
Arlene B. Chapman,
Vicente E. Torres,
Ronald D. Perrone,
Theodore I. Steinman,
Kyongtae T. Bae,
J. Philip Miller,
Dana C. Miskulin,
Frederic F. Rahbari-Oskoui,
Amirali Masoumi,
Marie C. Hogan,
Franz T. Winklhofer,
William E. Braun,
Paul A. Thompson,
Catherine M. Meyers,
Cass Kelleher,
Robert W. Schrier
Publication year - 2010
Publication title -
clinical journal of the american society of nephrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.755
H-Index - 151
eISSN - 1555-905X
pISSN - 1555-9041
DOI - 10.2215/cjn.04310709
Subject(s) - medicine , autoantibody , rheumatoid arthritis , rheumatoid factor , synovitis , gastroenterology , antibody , immunology
Two HALT PKD trials will investigate interventions that potentially slow kidney disease progression in hypertensive autosomal dominant polycystic kidney disease (ADPKD) patients. Studies were designed in early and later stages of ADPKD to assess the impact of intensive blockade of the renin-angiotensin-aldosterone system and level of BP control on progressive renal disease. Design, settings, participants, and measurements: PKD-HALT trials are multicenter, randomized, double-blind, placebo-controlled trials studying 1018 hypertensive ADPKD patients enrolled over 3 yr with 4 to 8 yr of follow-up. In study A, 548 participants, estimated GFR (eGFR) of >60 ml/min per 1.73 m(2) were randomized to one of four arms in a 2-by-2 design: combination angiotensin converting enzyme inhibitor (ACEi) and angiotensin receptor blocker (ARB) therapy versus ACEi monotherapy at two levels of BP control. In study B, 470 participants, eGFR of 25 to 60 ml/min per 1.73 m2 compared ACEi/ARB therapy versus ACEi monotherapy, with BP control of 120 to 130/70 to 80 mmHg. Primary outcomes of studies A and B are MR-based percent change kidney volume and a composite endpoint of time to 50% reduction of baseline estimated eGFR, ESRD, or death, respectively.

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