Kidney Function During and After Withdrawal of Long-Term Irbesartan Treatment in Patients With Type 2 Diabetes and Microalbuminuria
- Steen Andersen, MD1,
- Jens Bröchner-Mortensen, MD, DMSC2,
- Hans-Henrik Parving, MD, DMSC13 and
- Irbesartan in Patients With Type 2 Diabetes and Microalbuminuria Study Group
- 1Steno Diabetes Center, Gentofte, Denmark
- 2Department of Clinical Physiology, Aalborg Sygehus, Aalborg, Denmark
- 3University of Aarhus, Faculty of Health Science, Aarhus, Denmark
- Address correspondence and reprint requests to Steen Andersen, MD, Steno Diabetes Center, Niels Steensens Vej 2, DK-2820 Gentofte, Denmark. E-mail: stan{at}dadlnet.dk
Abstract
OBJECTIVE—Irbesartan is renoprotective in patients with type 2 diabetes and microalbuminuria. Whether the observed reduction in microalbuminuria is reversible (hemodynamic) or persistent (glomerular structural/biochemical normalization) after prolonged antihypertensive treatment is unknown. Therefore, the present substudy of the Irbesartan in Patients with Type 2 Diabetes and Microalbuminuria Study (IRMA-2) investigated the reversibility of kidney function changes after withdrawal of 2 years’ antihypertensive treatment.
RESEARCH DESIGN AND METHODS—The substudy included 133 hypertensive type 2 diabetic patients with persistent microalbuminuria in IRMA-2, randomized to double-masked treatment with either placebo, irbesartan 150 mg, or irbesartan 300 mg o.d. for 2 years. Arterial blood pressure, overnight urinary albumin excretion rate, and glomerular filtration rate (GFR) were determined repeatedly.
RESULTS—Baseline characteristics were similar in the placebo, irbesartan 150-mg, and irbesartan 300-mg groups. At the end of the study, mean arterial blood pressure (MABP) was similarly lowered to 105 ± 2 (mean ± SE), 103 ± 2, and 102 ± 2 mmHg, respectively (P < 0.05 versus baseline), and urinary albumin excretion rate reduced by 8% (−16 to 27) (NS), 34% (95% CI 8–53), and 60% (46–70) (P < 0.05). Rates of decline in GFR were 1.3 ± 0.7, 1.2 ± 0.7, and 1.0 ± 0.8 ml · min−1 · 1.73 m−2 per month, respectively, during the initial 3 months of the study and 0.3 ± 0.1, 0.3 ± 0.1, and 0.4 ± 0.1 ml · min−1 · 1.73 m−2 per month in the remaining study period. One month after withdrawal of all antihypertensive medication, MABP remained unchanged in the placebo group, 105 ± 2 mmHg, but increased significantly in the irbesartan groups, to 109 ± 2 and 108 ± 2 mmHg, respectively. Compared with baseline, urinary albumin excretion rate was increased by 14% (−17 to 54) in the placebo group and by 11% (−26 to 65) in the irbesartan 150-mg group but was persistently reduced by 47% (24–73) in the irbesartan 300-mg group (P < 0.05). GFR levels increased to baseline values in the placebo group and approached initial levels in irbesartan groups.
CONCLUSIONS—Persistent reduction of microalbuminuria after withdrawal of all antihypertensive treatment suggests that high-dose irbesartan treatment confers long-term renoprotective effects.
- ARB, angiotensin II receptor blocker
- GFR, glomerular filtration rate
- IRMA-2, Irbesartan in Patients with Type 2 Diabetes and Microalbuminuria Study
- MABP, mean arterial blood pressure
- RAAS, renin-angiotensin-aldosterone system
- TGF-β, transforming growth factor-β
Footnotes
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S.A. receives funds from Merck for research to conduct studies on new treatments in diabetic nephropathy. J.B.-M. has received consulting fees from Merck and Sanofi-Synthelabo. H.-H.P. holds stock in Novo Nordisk, has received honoraria for speaking engagements and consultant fees from Merck and Sanofi-Synthelabo, and receives funds from Merck, Astra Corporation, and Sanofi-Synthelabo for research to conduct studies on new treatments in diabetic nephropathy.
A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances.
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- Accepted August 25, 2003.
- Received June 27, 2003.
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