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Beneficial Effects of Pentoxifylline Plus Losartan Dual Therapy in Type 2 Diabetes with Nephropathy

Authors :
Mohsen Afarideh
Soghra Rabizadeh
Mohammad Saadat
Morsaleh Ganji
Fatemeh Dehghani Firouzabadi
Sina Noshad
Behnam Heidari
Sadaf Esteghamati
Mohammad Najafi
Alireza Ghajar
Alireza Esteghamati
Manouchehr Nakhjavani
Source :
The American journal of the medical sciences. 355(5)
Publication Year :
2017

Abstract

This study was designed to comparatively assess the effects of add-on pentoxifylline to losartan versus increasing the dose of losartan on serum N-terminal pro-brain natriuretic peptide (NT-proBNP), serum highly sensitive C-reactive protein (hsCRP) and the urinary albumin excretion (UAE) rate in patients with type 2 diabetes and nephropathy.In an open-label, single-center, parallel-group, randomized clinical trial (NCT03006952), 30 patients received b.i.d. dose of pentoxifylline 400mg plus daily dose of losartan 50mg (pentoxifylline arm) and 29 patients received b.i.d. dose of losartan 50mg (losartan arm) during a 12-week follow-up period.Serum NT-proBNP, serum hsCRP and UAE levels all significantly decreased from baseline in both trial arms. The pentoxifylline and losartan trial arms were equally effective in reducing serum NT-proBNP levels during the course of trial (multivariable adjusted model P value = 0.864, effect size = 0.2%). There was a greater decrease in UAE and serum hsCRP levels in the pentoxifylline arm (P = 0.034, effect size = 7.8%; P = 0.009, effect size = 11.7%, respectively). Conversely, patients in the losartan arm achieved better systolic and diastolic blood pressure control (P0.001, effect size = 25.4%; P = 0.010, effect size = 11.3%, respectively).Circulating NT-proBNP levels equally and significantly reduced from baseline in the pentoxifylline and losartan treatment arms, in parallel with comparatively superior decreases of UAE and serum hsCRP in the pentoxifylline arm, and larger decreases of systolic and diastolic blood pressures in the losartan arm.

Details

ISSN :
15382990
Volume :
355
Issue :
5
Database :
OpenAIRE
Journal :
The American journal of the medical sciences
Accession number :
edsair.doi.dedup.....564f53d5322d4d93a1ed371dbc501d6c