FOLLOW-UP OF RENAL-FUNCTION AND URINARY PROTEIN EXCRETION IN CHILDHOOD IGA NEPHROPATHY

被引:9
作者
BERG, UB
WIDSTAMATTORPS, UC
机构
[1] Departments of Paediatrics and Renal Medicine, Karolinska Institute, Huddinge University Hospital, Huddinge
关键词
IGA NEPHROPATHY; GLOMERULAR FILTRATION RATE; EFFECTIVE RENAL PLASMA FLOW; ALBUMINURIA; SEGMENTAL SCLEROSIS; END-STAGE RENAL FAILURE;
D O I
10.1007/BF00864371
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Renal haemodynamics and urinary protein excretion (UPE) were investigated in 36 patients with IgA nephropathy more than 3 years after renal biopsy (mean interval 6.3 +/- 0.5 years). At follow-up, 39% of patients had a reduced glomerular filtration rate (GFR) and 11% end-stage renal failure. Twenty-five percent had albuminuria, and a further 25% microalbuminuria. All albuminuric patients had GFRs below the mean, and 78% of the albuminurics had a reduced GFR. However, non-albuminurics also had decreased GFRs and GFR tended to fall with the duration of the disease in this group of patients. On comparing the histological changes in the biopsies with haemodynamic and UPE studies performed 6 years later, we found significant correlations between the extent of segmental glomerular sclerosis and GFR, effective renal plasma flow, urinary albumin and IgG excretion, respectively. Histological grading correlated with the same variables. Of the 4 uraemic patients, 2 were nephrotic at presentation, while the other 2 had a nephritic onset of disease and later developed heavy proteinuria. Three of their biopsies showed greater-than-or-equal-to 10% segmental glomerulosclerosis. Juvenile IgA nephropathy is not a harmless disease. Our results indicate that these children should be carefully monitored with adequate GFR measurements and urine protein analyses.
引用
收藏
页码:123 / 129
页数:7
相关论文
共 41 条
[1]  
Clarkson A.R., Seymour A.E., Thompson A.J., Haynes W.D.G., Chan Y-L, Jackson B., IgA nephropathy: a syndrome of uniform morphology, diverse clinical features and uncertain prognosis, Clin Nephrol, 8, pp. 459-471, (1977)
[2]  
Kobayashi Y., Tateno S., Hiki Y., Shigematsu H., IgA nephropathy: prognostic significance of proteinuria and histological alterations, Nephron, 34, pp. 146-153, (1983)
[3]  
Rambausek M., Seelig H.P., Andrassy K., Waldherr R., Kehry I., Lenhard V., Ritz E., Measangiale IgA Glomerulonephritis. Neue Aspekte zur Diagnose, Klinik and Prognose, Dtsch Med Wochenschr, 108, pp. 125-130, (1983)
[4]  
D'Amico G., The commonest glomerulonephritis in the world: IgA nephropathy, Q J Med, 64, pp. 709-727, (1987)
[5]  
Hogg R.J., A multicenter study of IgA nephropathy in children. A report of the Southwest Pediatric Nephrology Study Group, Kidney Int, 22, pp. 643-652, (1982)
[6]  
Hood S.A., Velosa J.A., Holley K.E., Donadio J.V., IgA-IgG nephropathy: predictive indices of progressive disease, Clin Nephrol, 16, pp. 55-62, (1981)
[7]  
Rekola S., Bergstrand A., Bucht H., IgA nephropathy: a retrospective evaluation of prognostic indices in 176 patients, Scand J Urol Nephrol, 23, pp. 37-50, (1989)
[8]  
Woo K.T., Edmondson R.P.S., Wu A.Y.T., Chiang G.S.C., Pwee H.S., Lim C.H., The natural history of IgA nephritis in Singapore, Clin Nephrol, 25, pp. 15-21, (1986)
[9]  
Levy M., Gonzalez-Burchard G., Brover M., Dommergues J.P., Foulard M., Sorez J.P., Habib R., Berger's disease in children. Natural history and outcome, Medicine (Baltimore), 64, pp. 157-180, (1985)
[10]  
Linne T., Aperia A., Broberger O., Bergstrand A., Bohman S-O, Rekola S., Course of renal function in IgA glomerulonephritis in children and adolescents, Acta Paediatrica, 71, pp. 735-743, (1982)