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[Clinical and pathological differences between children with various genotypes of hepatitis B virus-associated
Yong-Hong Sun1, Xiao-Yan Lei, Hong Yuan
1Department of Pediatrics, People's Hospital of Gansu Province, First Hospital of Lanzhou University, Lanzhou 730000, China. leixiaoyan601@163.com.
Insights
Hepatitis B virus-associated glomerulonephritis (HBV-GN) in children is predominantly caused by genotypes C and B. Genotype C infections present more severe clinical symptoms than genotype B, though pathological features remain similar.
Area of Science:
- Nephrology
- Virology
- Pediatrics
Context:
- Hepatitis B virus-associated glomerulonephritis (HBV-GN) is a significant cause of kidney disease in children.
- Understanding the impact of different HBV genotypes on disease presentation is crucial for effective management.
Purpose:
- This study aimed to compare the clinical and pathological characteristics of HBV-GN in children across various hepatitis B virus (HBV) genotypes.
- Investigate differences in clinical manifestations, renal and liver pathology, and HBV cccDNA levels based on HBV genotype.
Summary:
- The study analyzed 41 children with HBV-GN, finding genotype C (71%) to be dominant over genotype B (24%).
- Children with genotype C HBV-GN exhibited significantly higher rates of hematuria, albuminuria, decreased complement 3, elevated alanine transaminase, and renal insufficiency compared to genotype B.
- HBV cccDNA positivity was also significantly higher in the genotype C group. No significant differences were noted in pathological renal tissue types or liver inflammation/fibrosis between genotype groups.
Impact:
- Genotype C is associated with more severe clinical manifestations in pediatric HBV-GN.
- Findings highlight the importance of HBV genotyping in assessing disease severity and guiding treatment strategies in children with HBV-GN.
- This research contributes to a better understanding of the genotype-specific clinical spectrum of HBV-GN in pediatric populations.
Objective:
To compare the clinical and pathological features between children with various genotypes of hepatitis B virus-associated glomerulonephritis (HBV-GN).
Methods:
Forty-one children with HBV-GN concurrently undergoing liver and renal biopsy were randomly selected. Serum specimens were collected for genotyping and hepatitis B virus (HBV) cccDNA assay. The clinical, pathological, and HBV cccDNA differences between HBV-GN children of various genotypes were analyzed.
Results:
Among the 41 HBV-GN children, 29 (71%) were genotype C, 10 (24%) were genotype B, and 2 (5%) were genotype B/C. The incidence rates of hematuria, albuminuria, complement 3 decrease, alanine transaminase increase, and renal insufficiency in the genotype C group were significantly higher than those in the genotype B group (P<0.05). Similarly, the HBV cccDNA positive rate was significantly higher in the genotype C group than that in the genotype B group. No difference was observed in the distribution of pathological types of renal tissues betwee the two geonotype groups. There were no significant differences in the degrees of hepatic inflammation and fibrosis between the two groups.
Conclusions:
Mainly genotypes C and B occur in children with HBV-GN and the former genotype is dominant. The clinical symptoms of patients with genotype C are more serious than those with genotype B. However, there is no difference in the pathological features between them.
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