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Published on: July 3, 2013
Childhood AIDS nephropathy: a 10-year experience
D Rajpoot1, C J Kaupke, N D Vaziri
1Department of Pediatrics, University of California, Irvine, USA.
Insights
Pediatric AIDS nephropathy, often caused by perinatal HIV transmission, is linked to poor survival and lower CD4+ counts. This contrasts with adult cases, highlighting HIV
Area of Science:
- Pediatric Nephrology
- Infectious Diseases
- Immunology
Background:
- Acquired immunodeficiency syndrome (AIDS) can lead to kidney complications, known as AIDS nephropathy.
- Understanding AIDS nephropathy in children is crucial, especially given different transmission routes compared to adults.
Purpose of the Study:
- To characterize pediatric AIDS patients with nephropathy.
- To compare these characteristics with adult data on AIDS nephropathy.
- To investigate the role of HIV infection in pediatric nephropathy.
Main Methods:
- Analysis of demographic, immunologic, and clinical data from 62 pediatric AIDS patients treated between 1983-1993.
- Comparison of outcomes between pediatric patients with and without nephropathy.
- Histological examination of renal lesions.
Main Results:
- All 16 pediatric patients with AIDS nephropathy died, with a mean survival of 55.3 months.
- 70% of pediatric AIDS patients without nephropathy survived.
- Nephropathy patients had significantly lower CD4+ lymphocyte counts.
Conclusions:
- Focal segmental glomerulosclerosis is the primary renal lesion in pediatric AIDS patients with perinatal HIV infection.
- AIDS nephropathy in children has a dismal prognosis, similar to adults.
- Vertical HIV transmission is strongly implicated in the pathogenesis of pediatric AIDS nephropathy.
Abstract:
The objective of this study was to define the demographic, immunologic, and clinical characteristics of children with acquired immunodeficiency syndrome (AIDS) and AIDS nephropathy, and contrast this with the existing adult data. Data from 62 pediatric patients with AIDS who were treated at SUNY Health Science Center, Brooklyn, New York, between 1983 and 1993 were analyzed. Human immunodeficiency virus (HIV) infection was acquired during the neonatal period by vertical transmission (n = 60) or blood transfusion (n = 2). All children with AIDS who exhibited clinical nephropathy died (n = 16), with mean survival of 55.3 months. In contrast, 32 of 56 AIDS patients (70%) who did not manifest nephropathy were alive at the end of the study period. Patients with nephropathy were noted to have significantly lower CD4+ lymphocyte counts than those without nephropathy. These observations suggest that the predominant renal lesion in pediatric patients who acquired HIV infection during the perinatal period is focal segmental glomerulosclerosis, although a variety of other histological lesions were present. As in adults, the survival in children is dismal following the onset of clinical renal disease. In contrast to the adult population in whom multiple risk factors can potentially contribute to AIDS-associated nephropathy, occurrence of nephropathy in children with vertical HIV transmission provides convincing evidence for the pathogenetic role of HIV infection.
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