Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Steroid resistant nephrotic syndrome.

Sushmita Banerjee1

  • 1Department of Pediatrics, Calcutta Medical Research Institute, Kolkata, India. asban@vsnl.com

Indian Journal of Pediatrics
|February 1, 2003
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

From mechanisms to clinical practice: a review of diuretic therapy in pediatric nephrology.

Pediatric nephrology (Berlin, Germany)·2026
Same author

Single (375 mg/m<sup>2</sup>) vs. double dose of rituximab along with mycophenolate mofetil for children with steroid-dependent/frequently relapsing nephrotic syndrome: a multicentre open-label randomized controlled trial.

Pediatric nephrology (Berlin, Germany)·2024
Same author

Pollution status of microplastics in the sediments of warm monomictic Dal lake, India: Abundance, composition, and risk assessment.

Environmental pollution (Barking, Essex : 1987)·2024
Same author

Vitamin D and the Free Hormone Hypothesis.

Indian pediatrics·2024
Same author

An international, multi-center study evaluated rituximab therapy in childhood steroid-resistant nephrotic syndrome.

Kidney international·2024
Same author

Human exposure to uranium through drinking water and its detrimental impact on the human body organs.

Environmental geochemistry and health·2024

Steroid Resistant-Nephrotic Syndrome (NS) is a chronic kidney disease in children. Aggressive therapies improve remission rates, but further studies are needed for optimal treatment strategies.

Area of Science:

  • Pediatric Nephrology
  • Chronic Kidney Disease
  • Steroid Resistant-Nephrotic Syndrome

Background:

  • Steroid Resistant-Nephrotic Syndrome (NS) affects up to 10% of children with NS, causing significant morbidity and mortality.
  • Historically, progression to renal failure was considered inevitable in survivors of childhood NS.
  • Recent advances have identified key genes and proteins involved in NS pathogenesis.

Purpose of the Study:

  • To review current understanding and treatment of Steroid Resistant-Nephrotic Syndrome in children.
  • To highlight the impact of recent genetic and protein insights on disease pathogenesis.
  • To evaluate the efficacy of current therapeutic strategies and identify areas for future research.

Main Methods:

  • Review of recent literature on Steroid Resistant-Nephrotic Syndrome.

Related Experiment Videos

  • Analysis of studies investigating genetic and protein markers.
  • Evaluation of treatment outcomes from aggressive combination therapies and supportive agents.
  • Main Results:

    • Aggressive long-term therapies combining steroids, alkylating agents, and cyclosporine achieve complete or partial remission in 20-80% of pediatric patients.
    • Nonspecific renal protective agents, including ACE inhibitors, ARBs, and lipid-lowering drugs, help slow disease progression.
    • Significant improvements in patient outcomes are evident, though not universally achieved.

    Conclusions:

    • Current aggressive treatment regimens offer substantial benefits for children with Steroid Resistant-Nephrotic Syndrome.
    • Supportive therapies play a crucial role in retarding disease progression and managing complications.
    • Further multicenter controlled studies are essential to establish optimal drug choices and treatment protocols for improved long-term outcomes.