ssnimcj2026v11i2s6


Original
Role of Montelukast in Reducing the Rate of Relapse of Childhood Idiopathic Nephrotic Syndrome
*Akter S,1 Hoque M,2   Chowdhury MZ,3    Ahmed A,4 Mollah MS,5   Rahman N6

  1. *Dr. Salma Akter, MD(Paediatrics), Resident, Department of Paediatrics, Sylhet MAG Osmani Medical College, Sylhet, Bangladesh. salmatania0123@gmail.com. ORCID: https://orcid.org/0009-0007-0848-1880
  2. Professor Dr. Mujibul Hoque, Department of Paediatrics, Sylhet MAG Osmani Medical College, Sylhet.
  3. Professor Dr. Md Ziaur Rahman Chowdhury, Principal and Head, Department of Paediatrics, Sylhet MAG Osmani Medical College.
  4. Proessor Dr. Akhlaq Ahmed, Professor of Paediatrics, Sylhet MAG Osmani Medical College, Sylhet.
  5. Dr. Muhammad Solaiman Mollah, DCH, FCPS(Paediatrics), Associate Professor, Department of Paediatrics, Sylhet MAG Osmani Medical college, Sylhet. ORCID: https://orcid.org/0009-0007-9007-3965
  6. Dr. Naima Rahman, MD (Paediatrics), Department of Paediatrics, Sylhet MAG Osmani Medical college, Sylhet. ORCID: https://orcid.org/0009-0003-4524-0542

*For correspondence

Abstract
Background: Relapse of idiopathic nephrotic syndrome is caused by overexpression of IL-13. Montelukast a leukotriene receptor antagonist that may reduce relapse by inhibiting IL-13.
Objective: To assess the effect of montelukast in reducing the rate of relapse of childhood idiopathic nephrotic syndrome.
Methods: A randomized controlled trial was conducted in the Department of Paediatrics, Sylhet MAG Osmani Medical College Hospital, Sylhet from January 2023 to October 2024. A total of 104 children with 1st attack of nephrotic syndrome aged 2 to 10 years were included. Every case was allocated to either Group-A or group-B by block randomization. Thus, each group consisted of 52 children. Prednisolone was started in both groups in a dose of 60mg/m2 daily for 6 weeks. Then, prednisolone was given in a dose of 40 mg/m2 every alternate day for another 6 weeks.  Group A (cases) also received montelukast (4mg for children up to5 years of age and 5 mg for children aged 6 years and above) for 12 months. In group B (control) montelukast was not given. Patients in both groups were followed up 3 monthly for one year to monitor the number of relapse and adverse effect of montelukast. Thirteen patients were excluded from final analysis due to lost to follow up (n = 6; 3 in group A and 3 in group B) or steroid resistance (n = 7; 4 in group -A and 3 in group -B).
Results: Out of 91 children (45 in group –A and 46 in group –B), 49(53.8%) patients had relapse. Relapse rate was significantly higher in group -B than group A (71.7% vs 35.6%). In group A, majority 7 (43.8%) had relapse at 9 months whereas in group B, 16 (48.5%) had relapse at 6 months, that was significant between two groups. In group A, 13 (81.3%) patients had IFRNS (Infrequent relapse nephrotic syndrome) whereas in group B, 15 (45.5%) had FRNS (Frequent relapse nephrotic syndrome), the difference between two groups were statistically significant (p=.001). Few adverse effects of montelukast were found.
Conclusion: The result of this study showed that montelukast is effective in reducing the rate of relapse of childhood idiopathic nephrotic syndrome.

[Shaheed Syed Nazrul Islam Med Col J 2026, July; 11 (2):138-143]
DOI: https://www.doi.org/10.69699/ssnimcj.2026.11.2.6

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