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Does ALLHAT change the management of hypertension in chronic kidney disease?
Martin MacKinnon1, Frans H H Leenen, Marcel Ruzicka
1Division of Nephrology and Kidney Research Centre, The Ottawa Hospital-Riverside Campus, Room 5-21, 1967 Riverside Drive, Ottawa, Ontario, Canada, K1H 7W9.
Insights
The Antihypertensive and Lipid-Lowering Treatment Trial to Prevent Heart Attack (ALLHAT) found no significant differences in end-stage renal disease (ESRD) rates among chlorthalidone, amlodipine, or lisinopril. Blood pressure control is key for this patient group.
Area of Science:
- Nephrology
- Cardiology
- Pharmacology
Background:
- The Antihypertensive and Lipid-Lowering Treatment Trial to Prevent Heart Attack (ALLHAT) investigated newer antihypertensive agents against thiazide diuretics.
- Secondary outcomes included end-stage renal disease (ESRD) and estimated glomerular filtration rate (GFR) decline.
Purpose of the Study:
- To compare cardiovascular outcomes of newer antihypertensive drugs versus a thiazide diuretic.
- To assess the impact of different antihypertensive treatments on renal outcomes.
Main Methods:
- Randomized controlled trial comparing chlorthalidone, amlodipine, and lisinopril.
- Follow-up for cardiovascular and renal outcomes over 5-6 years.
Main Results:
- No significant differences in overall ESRD rates were observed between the treatment groups.
- A slower GFR decline was noted with amlodipine in both diabetic and non-diabetic participants.
- The composite endpoint of ESRD or a 50% GFR decline was reduced in non-diabetics on amlodipine.
Conclusions:
- For patients with systolic BP > 130 mm Hg, initiating treatment with a thiazide diuretic, calcium channel blocker, or ACE inhibitor shows no difference in renal outcomes over 5-6 years.
- Blood pressure control itself is the primary objective for managing renal outcomes in this population.
Abstract:
ALLHAT was designed to test the hypothesis that "newer" antihypertensive agents are superior to a thiazide diuretic for cardiovascular outcomes. Pre-specified secondary outcomes included the development of end-stage renal disease (ESRD) (dialysis, renal transplantation, or death from renal cause) and estimated glomerular filtration rate (GFR). ALLHAT showed no differences in the overall rates of ESRD between those randomized to chlorthalidone, amlodipine, or lisinopril. It showed a slower rate of decline of GFR among those randomized to amlodipine in both diabetics and nondiabetics, and in the composite end point (ESRD or > or = 50% decline in GFR) in nondiabetics. The results of ALLHAT are consistent with other studies that, for the patient population studied (presumably largely nonalbuminuric patients with and without diabetes), at systolic BP > 130 mm Hg, there is no difference for renal outcomes between a thiazide diuretic, dihydropyridine calcium channel blocker, and ACEI-initiated treatment for 5 to 6 years of follow-up. These results suggest that BP control per se remains the most important objective for this patient population.
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