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

被引:6
|
作者
de Jong, Paul E. [1 ]
Navis, Gerjan [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Med, Div Nephrol, NL-9713 EZ Groningen, Netherlands
来源
NATURE CLINICAL PRACTICE NEPHROLOGY | 2008年 / 4卷 / 12期
关键词
chronic kidney disease; progression; proteinuria; renoprotective therapy;
D O I
10.1038/ncpneph0963
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
This Practice Point commentary discusses the implementation of an intensive, multifactorial intervention in patients who had proteinuria >3g/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treated in the Remission Clinic had a much slower decline in estimated glomerular filtration rate than a matched historical reference group treated with 1.25-5.00 mg ramipril (diastolic blood pressure goal 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.
引用
收藏
页码:654 / 655
页数:2
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