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Proteinuria lowering needs a multifactorial and individualized approach to halt progression of renal disease

Abstract

This Practice Point commentary discusses the implementation of an intensive, multifactorial intervention in patients who had proteinuria >3 g/day despite treatment with angiotensin-converting-enzyme inhibitors. In their 'Remission Clinic' in Bergamo, Italy, Ruggenenti et al. implemented an individual titration regimen using ramipril 5–10 mg/day, losartan 50–100 mg/day, verapamil 80–120 mg/day and atorvastatin 10–20 mg/day in successive steps, aiming for a low blood pressure target of <120/80 mmHg and a proteinuria target of <0.3 g/day. They found that patients treated in the Remission Clinic had a much slower decline in estimated glomerular filtration rate than a matched historical reference group treated with 1.25–5.00 mg ramipril (diastolic blood pressure goal <90 mmHg). Only 3.6% of Remission Clinic patients reached end-stage renal disease, compared with 30.4% of the historical controls. No information was provided on the individual responses to the different titration steps; therefore, the contributions of the specific components of the regimen towards the therapeutic benefit cannot be established. The data do, however, encourage an individualized and more active approach to preventing end-stage renal disease in individuals with proteinuric chronic kidney disease.

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References

  1. Ruggenenti P et al. (2008) Role of remission clinics in the longitudinal treatment of CKD. J Am Soc Nephrol 19: 1213–1224

    Article  Google Scholar 

  2. The GISEN group (1997) Randomised placebo-controlled trial of effect of ramipril on decline in glomerular filtration rate and risk of terminal renal failure in proteinuric, non-diabetic nephropathy. Lancet 349: 1857–1863

  3. de Jong PE et al. (1999) Renoprotective therapy: titration against urinary protein excretion. Lancet 354: 352–353

    Article  CAS  Google Scholar 

  4. Vogt L et al. (2008) Effects of dietary sodium and hydrochlorothiazide on the antiproteinuric efficacy of losartan in non-diabetic proteinuric patients. J Am Soc Nephrol 19: 999–1007

    Article  CAS  Google Scholar 

  5. Vogt L et al. (2005) Individual titration for maximal blockade of the renin–angiotensin system in proteinuric patients: a feasible strategy? J Am Soc Nephrol 16 (Suppl 1): S53–S57

    Article  CAS  Google Scholar 

  6. Ritz E and Wanner C (2008) Lipid abnormalities and cardiovascular risk in renal disease. J Am Soc Nephrol 19: 1065–1070

    Article  CAS  Google Scholar 

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Correspondence to Paul E de Jong.

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The authors declare no competing financial interests.

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de Jong, P., Navis, G. Proteinuria lowering needs a multifactorial and individualized approach to halt progression of renal disease. Nat Rev Nephrol 4, 654–655 (2008). https://doi.org/10.1038/ncpneph0963

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