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Abnormal urinalysis on day 7 in patients with IgA vasculitis (Henoch-Schönlein purpura)
Nozomu Kawashima1, Jun-Ichi Kawada2, Yuichi Nishikado3
1Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan; Children's Medical Center, Japanese Red Cross Nagoya First Hospital, Nagoya, Japan.
Insights
An abnormal urinalysis on day 7 in children with IgA vasculitis (Henoch-Schönlein purpura) may predict persistent kidney disease. This early marker helps identify children at high risk for ongoing nephritis, guiding further management.
Area of Science:
- Pediatric Nephrology
- Immunology
- Vasculitis Research
Background:
- IgA vasculitis (Henoch-Schönlein purpura, HSP) can lead to rare but serious renal failure in children.
- Identifying early markers for persistent nephritis is crucial for managing HSP.
- The predictive value of an abnormal urinalysis on day 7 (7d-UA) for persistent nephritis is not well-established.
Purpose of the Study:
- To retrospectively analyze risk factors for persistent nephritis in children diagnosed with IgA vasculitis.
- To determine if an abnormal 7d-UA is a significant predictor of persistent nephritis 6 months post-diagnosis.
Main Methods:
- Retrospective cohort study of 138 children with IgA vasculitis.
- Analysis of urinalysis results at diagnosis, day 7, and 6 months post-diagnosis.
- Multivariate analysis to identify independent risk factors for persistent nephritis.
Main Results:
- Children with an abnormal 7d-UA had a significantly higher rate of abnormal urinalysis at 6 months (69%) compared to those with normal 7d-UA (6%).
- Abnormal 7d-UA was the sole independent risk factor for abnormal urinalysis at 6 months (OR 54.3, P < 0.0001).
- Negative predictive values for normal urinalysis and negative proteinuria at 6 months were high (0.94 and 0.98, respectively).
Conclusions:
- An abnormal urinalysis on day 7 appears to be a significant independent risk factor for persistent nephritis in children with IgA vasculitis.
- This early urinalysis finding may serve as a valuable surrogate marker for long-term kidney involvement.
- Prospective studies are needed to confirm these findings and establish clinical utility.
Abstract:
Rare progression to renal failure imposes a burden on children with IgA vasculitis (Henoch-Schönlein purpura, HSP). An abnormal urinalysis on day 7 (7d-UA) may be a surrogate marker for persistent nephritis, but this has not been established. We retrospectively analyzed the risk factors for persistent nephritis in a cohort of 138 children. Of 35 children with abnormal 7d-UA, 24 (69%) had an abnormal urinalysis 6 months after the diagnosis of HSP, which was significantly more than 6 of 103 children (6%) with normal 7d-UA (P < 0.0001). The negative predictive values for normal urinalysis and negative proteinuria 6 months after diagnosis were 0.94 (95% confidence interval [CI], 0.90-0.97) and 0.98 (95% CI, 0.95-0.99), respectively. When children with abnormal urinalysis 6 months after diagnosis were compared with those without, the following factors were significantly associated: age at diagnosis, abnormal urinalysis at diagnosis, abnormal 7d-UA, complement C3, steroid treatment, and presence of abdominal pain. However, multivariate analysis revealed that abnormal 7d-UA was the only significant risk factor for abnormal urinalysis 6 months after diagnosis (odds ratio 54.3, 95% CI 15.3-275, P = 1.89 × 10-6). Abnormal 7d-UA may be an independent risk factor for persistent nephritis, but this should be confirmed in a prospective study.
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