Long-term Prognosis of thin Glomerular Basement Membrane Nephropathy in Children: A Retrospective Single Center Study.
10.3339/jkspn.2017.21.2.41
- Author:
Myung Hee LIM
1
;
Hee Jung BAE
;
Kyung Mi JANG
;
Yong Hoon PARK
Author Information
1. Department of Pediatrics, Yeungnam University Hospital, Yeungnam University College of Medicine, Daegu, Korea. yhpark@ynu.ac.kr
- Publication Type:Original Article
- Keywords:
Hematuria;
Children;
Thin basement membrane nephropathy;
Alport syndrome;
School urinalysis screening
- MeSH:
Age of Onset;
Biopsy;
Child*;
Female;
Follow-Up Studies;
Glomerular Basement Membrane*;
Glomerulonephritis, IGA;
Hematuria;
Humans;
Nephritis, Hereditary;
Prognosis*;
Renal Insufficiency;
Renal Insufficiency, Chronic;
Retrospective Studies*
- From:Childhood Kidney Diseases
2017;21(2):41-46
- CountryRepublic of Korea
- Language:English
-
Abstract:
PURPOSE: Thin glomerular basement membrane nephropathy (TBMN) is, along with the IgA nephropathy, the most common cause of asymptomatic hematuria in Korean children. TBMN is usually a benign renal disease not requiring treatment and is associated with a good prognosis, but some cases hematuria is indicative of a state of progressive renal insufficiency. We aimed to retrospectively evaluate clinical manifestations and renal prognosis of patients with TBMN. METHODS: Among the 428 renal biopsies performed on children at Yeungnam University Hospital between January 2000 and February 2017, 167 patients were diagnosed as having TBMN. We retrospectively investigated 167 pediatric patients and identified 59 children with follow-up duration >3 years. RESULTS: Among 59 patients, there were 33 boys and 26 girls. Mean age of onset of hematuria was 7.18±2.64 years, and mean time from onset of disease until a renal biopsy was performed was 2.48±2.10 years. There were no clinical features or laboratory findings among studied children to indicate decreased renal function during follow-up; however, one case progressed to chronic kidney disease (CKD) due to an unknown cause. There were seven patients among these related a positive family history of hematuria or renal insufficiency. CONCLUSION: Although almost all patients had normal renal functions during follow-up, there were one patient who progressed to CKD and seven patients with family history of hematuria or renal insufficiency. Moreover, four among the 428 patients over 17 years underwent repeat renal biopsies, which showed results different from their earlier biopsies.Thus, large-scales studies may be required to determine long-term prognosis of TBMN in children, and further evaluation for Alport syndrome in TBMN cases is essential.
