Clinical Nephrology – Epidemiology – Clinical Trials

Kidney International (2002) 61, 1098–1114; doi:10.1046/j.1523-1755.2002.00214.x

Mycophenolate mofetil treatment for primary glomerular diseases

Michael J Choi, Joseph A Eustace, Luis F Gimenez, Mohamed G Atta, Paul J Scheel, Renuka Sothinathan and William A Briggs

Nephrology Division, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA

Correspondence: Michael J. Choi, M.D., Division of Nephrology, Suite 416, The Johns Hopkins School of Medicine, 1830 E. Monument Street, Baltimore, Maryland 21205-2196, USA. E-mail mchoi3@jhmi.edu

Received 21 February 2001; Revised 18 October 2001; Accepted 19 October 2001.

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Abstract

Mycophenolate mofetil treatment for primary glomerular diseases.

Background

 

Treatment of primary glomerular diseases may be unsuccessful or have potential toxicities. Therefore, we evaluated the use of mycophenolate mofetil (MMF) for empirical treatment of primary glomerulopathies.

Methods

 

Forty-six patients with biopsy-proven primary glomerulopathies received MMF for greater than or equal to3 months as adjunctive or primary treatment. Median (range) 24-hour urine protein to creatinine ratio (Up/c) and serum creatinine at the start and end of MMF therapy were compared using the Wilcoxon signed-ranks test.

Results

 

Overall, the median Up/c decreased from 4.7 (range <0.1, 20.3) to 1.1 (<0.1, 14.3; P < 0.001) at the end of MMF treatment with no significant change in median serum creatinine 1.3 (0.6 to 6.1) to 1.2 (0.5 to 6.5) mg/dL. Median serum albumin increased from 3.4 (1.4, 4.6) to 4.1 (1.7, 48) g/dL (P < 0.001) and the median serum cholesterol decreased from 270 (148, 795) to 220 (140, 309) mg/dL (P < 0.001) post-treatment. For those with minimal change disease, a complete steroid withdrawal was accomplished in 5/6 steroid dependent patients. Focal segmental glomerulosclerosis (FSGS) patients had a median Up/c that decreased from 2.7 (0.1, 20.3) to 0.8 (<0.1, 8.2; P = 0.001) in 18 patients. In membranous nephropathy (MN) patients, the median Up/c decreased from 7.3 (0.1, 18.5) to 1.5 (<0.1, 14.3) (P = 0.001) in 17 patients. No significant change in median serum creatinine was detected in FSGS or MN patient groups during treatment.

Conclusions

 

Empirical MMF therapy in the majority of patients with primary glomerulopathies was well tolerated and achieved the goals of steroid withdrawal, improvement of nephrotic syndrome, and stabilization of renal function.

Keywords:

mycophenolate mofetil, nephrotic syndrome, focal segmental glomerulosclerosis, minimal change disease, membranous nephropathy, renal insufficiency

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