注册 | 登录 | FAQ      [?] 
CiteULike is a free online bibliography manager. Register and you can start organising your references online.
Recent | Unread | Search | Authors | Tags | Export

Reduction of proteinuria by rosiglitazone in non-diabetic renal disease

by: Priscilla K Smith, Kenneth F Fairley, Stephen Farish, James D Best, Joseph Proietto
Nephrology, Vol. 0, No. 0. (0), pp. ???-???.


View FullText article


X Reviews [Write a review of this article]

There are no reviews of this article

X Find related articles from these CiteULike users

X Find related articles with these CiteULike tags

X 摘要

SUMMARY: Aim: To investigate the effect of a thiazolidinedione on proteinuria in patients with non-diabetic renal disease. Methods: In an open-label randomized cross-over study, 40 adults with chronic non-diabetic renal disease completed the study. In a random fashion, one group was treated for 4 months with 4 mg of rosiglitazone first followed by a 4-month period of standard treatment. The opposite order was used for the second group. Results: Baseline urinary protein excretion rate was 1.45 g/24 h. On rosiglitazone, there was a drop of urinary protein level of 0.24 g/24 h (P = 0.045). In contrast, there was a trend for proteinuria to increase during the control period (0.12 g/24 h, P = 0.18). The urine protein level on rosiglitazone was lower than on usual treatment (0.36 g/24 h, P = 0.002, 95% CI 0.15-0.58). There was a similar beneficial effect on systolic blood pressure which was reduced by rosiglitazone by 7.8 mmHg (P = 0.006, 95% CI 2.6-13.1). Although average fasting glucose was only 5.8 mmol/L, there was a significant Spearman correlation between fasting glucose and a reduction in urinary protein levels (r = 0.34, P = 0.045). Conclusion: It is concluded that thiazolidinediones may have a role in the management of non-diabetic proteinuria of various aetiologies. In this study the average body mass index was 28.9 kg/m2. It will be important to repeat these studies in non-overweight subjects with non-diabetic proteinuria and in addition to trial maximal therapeutic doses of the thiazolidenedione.


X BibTeX record

X RIS record



RIS BibTeX