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Mycophenolate mofetil or standard therapy for membranous nephropathy and focal segmental glomerulosclerosis: a pilot
Lakshmanan Senthil Nayagam1, Anirban Ganguli, Manish Rathi
1Department of Nephrology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Background:
The current treatment regimes for patients with nephrotic syndrome due to idiopathic membranous nephropathy (MN) and focal segmental glomerulosclerosis (FSGS) are based on steroids and/or cytotoxic agents. Data on the effect of mycophenolate mofetil (MMF) for these conditions are scarce and confounding.
Methods:
We compared the efficacy of an MMF-based therapy with standard therapies in inducing remission in adult nephrotics with MN and FSGS in a randomized pilot study. MMF was given at 2 g/day for 6 months along with prednisolone at 0.5 mg/kg/day for 2-3 months. Conventional therapy was prednisolone 1 mg/kg/day for 3-6 months for FSGS and alternating monthly cycles of steroids and cyclophosphamide for 6 months for MN. The primary end point was change in urinary protein/creatinine ratio.
Results:
A total of 54 patients (21 MN and 33 FSGS) were recruited; 28 were randomized to receive MMF (group A) and 26 were on conventional treatment (group B). There was no difference in the proportion of patients achieving remission in two groups (64 and 80% in MN and 70 and 69% in FSGS). The frequency of relapses and incidence of infections was also similar. FSGS patients in group A achieved remission faster and received a lower cumulative steroid dose.
Conclusions:
A 6-month treatment with MMF is as effective as the conventional treatment for primary treatment of MN and FSGS in the short term. It induces remission faster and reduces steroid exposure in FSGS patients. Studies with more cases and longer follow-up are required to evaluate its impact on preservation of kidney function.
Insights
Mycophenolate mofetil (MMF) shows comparable short-term efficacy to standard treatments for nephrotic syndrome in membranous nephropathy (MN) and focal segmental glomerulosclerosis (FSGS). MMF offers faster remission and reduced steroid use in FSGS patients.
Area of Science:
- Nephrology
- Immunosuppressive therapy
- Glomerular diseases
Background:
- Current treatments for nephrotic syndrome in idiopathic membranous nephropathy (MN) and focal segmental glomerulosclerosis (FSGS) rely on steroids and cytotoxic agents.
- Limited and conflicting data exist regarding the efficacy of mycophenolate mofetil (MMF) for these conditions.
Purpose of the Study:
- To compare the efficacy of MMF-based therapy versus standard treatments in inducing remission for adult nephrotic patients with MN and FSGS.
- To evaluate the impact of MMF on remission rates, relapse frequency, infection incidence, and steroid exposure.
Main Methods:
- A randomized pilot study involving 54 adult nephrotic patients (21 MN, 33 FSGS).
- Patients were randomized to receive MMF (2 g/day for 6 months) plus limited prednisolone or conventional therapy (steroids for FSGS, steroids/cyclophosphamide for MN).
- Primary endpoint: change in urinary protein/creatinine ratio.
Main Results:
- No significant difference in remission rates between MMF and conventional therapy groups for either MN or FSGS.
- Similar frequencies of relapses and infections were observed in both groups.
- Patients with FSGS receiving MMF achieved remission faster and had lower cumulative steroid doses.
Conclusions:
- Six-month MMF treatment is as effective as conventional therapy for the primary treatment of MN and FSGS in the short term.
- MMF accelerates remission and reduces steroid exposure in FSGS patients.
- Further studies with larger cohorts and longer follow-up are needed to assess MMF's long-term impact on kidney function preservation.
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