Long-term outcome in 145 patients with assumed benign immunoglobulin A nephropathy

被引:34
|
作者
Knoop, Thomas [1 ,2 ]
Vikse, Bjorn Egil [1 ,3 ]
Mwakimonga, Angela [4 ]
Leh, Sabine [1 ]
Bjorneklett, Rune [1 ,5 ]
机构
[1] Univ Bergen, Dept Clin Med, Renal Res Grp, Bergen, Norway
[2] Haukeland Hosp, Dept Med, Bergen, Norway
[3] Haugesund Hosp, Dept Med, Haugesund, Norway
[4] Muhimbili Univ Hlth & Allied Sci, Dept Pathol, Dar Es Salaam, Tanzania
[5] Haukeland Hosp, Emergency Care Clin, Bergen, Norway
关键词
epidemiology; ESRD; IgA nephropathy; prognosis; renal biopsy; STAGE RENAL-DISEASE; EARLY IGA NEPHROPATHY; MINIMAL PROTEINURIA; OXFORD CLASSIFICATION; PROGNOSTIC-FACTORS; NATURAL-HISTORY; RISK; GLOMERULONEPHRITIS; PREECLAMPSIA; PROGRESSION;
D O I
10.1093/ndt/gfx242
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Background. Patients with immunoglobulin A nephropathy (IgAN) who present with mild to moderate proteinuria and normal renal function are assumed to have excellent short-term renal prognosis, but the long-termprognosis is uncertain. Methods. Patients were selected from the Norwegian Kidney Biopsy Registry based on the following criteria: diagnostic renal biopsy performed in the period 1988-99, with estimated glomerular filtration rate (eGFR) >= 60mL/min/1.73 m(2) and proteinuria <1 g/24 h at the time of biopsy. Patients were invited for a nephrological examination with a review of medical history and investigation of blood pressure, urinary findings and eGFR. Results. A total of 145 patients attended the examination, performed by the first author, after a median of 22 (interquartile range 19-25) years after diagnosis. At the examination, 27 patients (18.6%) had a >= 50% decrease in GFR, of whom 4 (2.8%) had developed end-stage renal disease (ESRD). The mean duration from renal biopsy to >= 50% decrease in GFR was 17.3 +/- 5.1 years in our cohort. Clinical remission was observed in 42 (29.0%) patients. Renal biopsies were re-examined utilizing the Oxford classification criteria. Mesangial hypercellularity was found in 12.3%, endocapillary proliferation was detected in 10.7% and segmental glomerulosclerosis was observed in 23.8%. All biopsies were scored as T0 (tubular atrophy in < 25% of the cortical area). None of the clinical or histopathological variables recorded at the time of biopsy could identify patients with progressive disease. Cumulative risks of >= 50% decrease in eGFR were 2.1% after 10 years, 4.1% after 15 years, 13.9% after 20 years and 24.7% after 25 years. Conclusions. We have shown that 18.6% of patients with assumed benign IgAN had progressive disease after a median duration of 22 years and that these patients could not be predicted at the time of biopsy. Our study demonstrates that an extended follow-up period is needed when assessing prognosis in this group of patients.
引用
收藏
页码:1841 / 1850
页数:10
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