Abstract

Objective To assess the efficacy and safety of losartan combined with prostaglandin E1 therapy for diabetic nephropathy at early phase. Methods 117 patients with diabetic nephropathy at stage 3 were randomly treated with losartan (ARB), prostaglandin E1 (PGE1) or losartan plus prostaglandin E1 (ARB+ PGE1). Patients were followed up for 6 months, the urinary albumin excretion rate(UAER), serum creatinine(CR), creatinine clearance rate (CCr), serum potassium(K) were observed at 14th day and 6th month after the initiation of therapy. Results 117 patients (ARB, n=38; PGE1, n=39; ARB+ PGE1, n=40) finished the follow-up.There were significant differences in UAER on the 14th day and 6th month[(88.2±42.8)μg/min, (61.0±22.0)μg/min, (50.3±15.2)μg/min; (58.0±22.8)μg/min, (50.6±18.1)μg/min, (31.7±7.3)μg/min], respectively (t=8.517, 7.056, 7.989, t=7.442, 8.947, 7.992, all P 0.05), but significant differences on the 6th month examination (t=9.283, 9.978, 9.876, t=-2.398, -2.838, -3.088, all P 0.05). Conclusion The results suggest that both short-term and long-term treatment with ARB and PGE1 is effective and safe for early-phase diabetic nephropathy. Key words: Diabetic nephropathy; Early phase; Losartan; Prostaglandin E1

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.