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Captopril-induced reduction of serum levels of transforming growth Factor-β1 correlates with long-term renoprotection in insulin-dependent diabetic patients

1999; Elsevier BV; Volume: 34; Issue: 5 Linguagem: Inglês

10.1016/s0272-6386(99)70037-5

1523-6838

Kumar Sharma, Babiker O. Eltayeb, Tracy McGowan, Stephen Dunn, Bashar Alzahabi, Richard Rohde, Fuad N. Ziyadeh, Edmund J. Lewis,

Renal Diseases and Glomerulopathies

The renoprotective effect of captopril on progression of diabetic nephropathy was demonstrated by the Collaborative Study Group Captopril Trial and might be independent of blood pressure. Because angiotensin II is known to stimulate the prosclerotic cytokine, transforming growth factor-β (TGF-β), we postulated that the renoprotective effect may be due to inhibition of TGF-β1 production. TGF-β1 levels were measured in serum at baseline and 6 months from patients in the captopril trial. TGF-β1 analyses were performed on all available patient sera. Analysis was performed between the percent change in TGF-β1 levels during the first 6 months versus the percent change in glomerular filtration rate (GFR) in the subsequent 2 years. TGF-β1 levels increased by 11% (P = 0.003) in the placebo group (n = 24), whereas there was a decrease of 14% (P = 0.01) in the captopril group (n = 34). There was an inverse correlation between the percent change in TGF-β1 levels during the first 6 months and the percent change in GFR over the ensuing 2-year period in patients from both the placebo (r = −0.55, P = 0.005) and captopril groups (r = −0.45, P = 0.008). In patients with initial GFR below 75 mL/min, there was an even stronger correlation in percent change in TGF-β1 levels and percent change in GFR in both placebo (n = 9, r = −0.69, P = 0.03) and captopril groups (n = 21, r = −0.73, P = 0.0001). Our data suggest that captopril decreases TGF-β1 levels in diabetic nephropathy and that changes in TGF-β1 levels may predict the course of diabetic nephropathy.