Key result
Pentoxifylline 1200 mg/day did not significantly reduce microalbuminuria or improve eGFR compared with placebo in type 2 diabetic patients over 6 months (P > 0.05).
Why the study?
The antiproteinuric effect of pentoxifylline in diabetic patients without glomerular diseases was not well established.
Does pentoxifylline reduce microalbuminuria in type 2 diabetic patients with eGFR > 60 mL/min/1.73 m2?
RCT (n=40)
Double-blind
randomized
Does pentoxifylline reduce microalbuminuria in type 2 diabetic patients with eGFR > 60 mL/min/1.73 m2?
p-value: p=>0.05
Pentoxifylline does not provide a significant additive benefit in reducing microalbuminuria when added to standard therapy in type 2 diabetic patients with early-stage kidney disease.
Does not reduce microalbuminuria or improve eGFR in early diabetic kidney disease; confirms lack of efficacy and supports standard care without pentoxifylline.
Background. Pentoxifylline is a nonspecific phosphodiesterase inhibitor with anti-inflammatory properties. Human studies have proved its antiproteinuric effect in patients with glomerular diseases, but this study was designed to assess the effects of add-on pentoxifylline to available treatment on reduction of microalbuminuria in diabetic patients without glomerular diseases. Methods. In a double-blind placebo-controlled, randomized study we evaluated the influence of pentoxifylline on microalbuminuria in type 2 diabetic patients. 40 diabetic patients with estimated glomerular filtration rate (eGFR) of more than 60 mL/min/1.73 m(2) in eight weeks and microalbuminuria were randomized to two groups which will receive pentoxifylline 1200 mg/day or placebo added to regular medications for 6 months. albuminuria; eGFR was evaluated at three- and six-month follow-up period. Results. Baseline characteristics were similar between the two groups. At six months, the mean estimated GFR and albuminuria were not different between two groups at 3- and 6-month follow-up. Trend of albumin to creatinine ratio, systolic and diastolic blood pressure, and eGFR in both groups were decreased, but no significant differences were noted between two groups (P value > 0.05). Conclusion. Pentoxifylline has not a significant additive antimicroalbuminuric effect compared with placebo in patients with type 2 diabetes with early stage of kidney disease; however, further clinical investigations are necessary to be done.
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Shahidi et al. (2015) conducted an RCT in Type 2 diabetes with microalbuminuria (n=40). Pentoxifylline vs. Placebo was evaluated on Microalbuminuria and estimated GFR (p=>0.05). Pentoxifylline 1200 mg/day did not significantly reduce microalbuminuria or improve eGFR compared with placebo in type 2 diabetic patients over 6 months (P > 0.05).
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