Skip to main content

Advertisement

Log in

HLA-DRB1 alleles in Kuwaiti children with idiopathic nephrotic syndrome

  • Original Article
  • Published:
Pediatric Nephrology Aims and scope Submit manuscript

Abstract 

We have studied the effect of HLA-DRB1 alleles on the clinical presentation of 61 Kuwaiti Arab children with idiopathic nephrotic syndrome. DR7(*0701) was the most prevalent DR allele, found in 41/61 patients (67%) compared with 10/59 healthy controls (17%) (p<0.001). DR3(*0301–0308) allele was the second most common, found in 25% of patients compared with 26% of controls (not significant). There was no significant difference between DRB1*0701(DR7)-positive and DRB1*0701-negative patients in terms of steroid sensitivity, steroid dependency, or steroid resistance. Nevertheless, the former group had a significantly lower mean age of onset (35 months vs 53 months) and a shorter remission period following treatment with cyclophosphamide or chlorambucil (8 months vs 29 months). Our data highlight the role of the DRB1*0701 allele in predisposing Kuwaiti Arab children with idiopathic nephrotic syndrome to a more prolonged course of the disease.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Additional information

Received: 2 July 1999 / Revised: 20 April 2000 / Accepted: 23 April 2000

Rights and permissions

Reprints and permissions

About this article

Cite this article

Al-Eisa, A., Haider, M. & Srivasta, B. HLA-DRB1 alleles in Kuwaiti children with idiopathic nephrotic syndrome. Pediatr Nephrol 15, 79–81 (2000). https://doi.org/10.1007/s004670000416

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s004670000416

Navigation