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Winter 2000–2001
CONTENTS

Drugs Found to
Protect the Kidneys

NIDDK Contributions
to Dialysis

What's New in CHID?

New Publications
From NKUDIC

New DKUHD
Programs for 2001

Bladder Research
Progress Review
Group

Research Needs in
Pediatric Kidney
Disease: 2000 and
Beyond

Upcoming Meetings

Recent Meetings

Three Join DKUHD

NIDDK Grantees
Market Hemodialysis
Monitoring Device

Home : About NKUDIC : Research Updates : Winter 2000–2001
 

Research Updates in Kidney and Urologic Health

Drugs Found To Protect the Kidneys

On the advice of an independent data and safety monitoring board, the National Institutes of Health (NIH) called an early halt to one arm of a study after finding that people with kidney disease and protein in their urine were more likely to postpone kidney failure if they took either an ACE (angiotensin-converting enzyme) inhibitor or a beta blocker rather than a calcium channel blocker (CCB).

Compared with the CCB amlodipine (Norvasc), the ACE inhibitor ramipril (Altace) or the beta blocker metoprolol (Toprol) significantly reduced the risk of kidney failure in a group of patients who had at least 1 gram of protein in a 24-hour urine sample when they joined the African American Study of Kidney Disease and Hypertension (AASK). Blood pressures were comparable.

Paradoxically, CCBs are one of two first-line choices for high blood pressure in African Americans1; 62 percent of AASK patients took CCBs before joining the study. The type of CCB used in AASK, a dihydropyridine, was found in this study and in other recent studies to be associated with increases in protein in the urine. Such increases are linked to advancing kidney disease.

ACE inhibitors have been preferred for kidney disease of diabetes since 1994. Subsequent studies of other kidney diseases have found an association between protein in the urine and protection by ACE inhibition. Considered with the results of these other studies, AASK extends the value of ACE inhibitors to kidney disease of hypertension, at least for people with protein in their urine.

"This trial will have a tremendous effect on how we care for people," predicts Dr. Janice Douglas, director of the hypertension division at Case Western Reserve in Cleveland and chair of the study's steering committee. "Most striking to me is the correlation between elevated urine protein and faster disease progression, something we can look for in all people with kidney disease," she explains. Dr. Douglas presented the study at the 33rd annual meeting of the American Society of Nephrology last October in Toronto.

Dr. Lawrence Agodoa, a kidney specialist and AASK director at NIH, cautions patients to keep taking prescribed blood pressure medicine until they have worked out an alternative with their doctor. "Calcium channel blockers are good for controlling high blood pressure, and patients are not in immediate risk," he explains.

AASK will continue to compare the ACE inhibitor and beta blocker and to test whether a lower blood pressure target of 125/75 is more protective of the kidneys than 140/90. A CCB may be used as a secondary treatment if needed to reach blood pressure goals. AASK enrolled 1,094 African Americans at 21 centers and is scheduled to end in the fall of 2001.

African Americans make up 12.6 percent of the U.S. population but 29.8 percent of those treated for kidney failure. Hardest hit are African Americans between the ages of 25 and 44, who are 20 times more vulnerable to hypertension-related kidney failure than whites in the same age group. Better management of high blood pressure has led to fewer strokes and heart disease, but kidney failure is still increasing.

Reference

1. The sixth report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC-VI). Archives of Internal Medicine. 1997;157:2413–2446.

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