Urinary albumin excretion: a predictor of glomerular findings in adults with microscopic haematuria

被引:21
作者
Eardley, KS
Ferreira, MAS
Howie, AJ
Gosling, P
Lipkin, GW [1 ]
机构
[1] Univ Hosp Birmingham, Dept Nephrol, Birmingham, W Midlands, England
[2] Univ Hosp Birmingham, Dept Clin Chem, Birmingham, W Midlands, England
[3] Univ Birmingham, Dept Pathol, Birmingham, W Midlands, England
关键词
D O I
10.1093/qjmed/hch049
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Microscopic haematuria without proteinuria is a common clinical finding. When urological causes are excluded, usual findings on renal biopsy are IgA nephropathy (which can progress to end-stage renal failure) or thin basement membrane nephropathy (which has an excellent prognosis). A non-invasive test to discriminate between the two would be useful. Aim: To examine the value of measurement of urinary albumin excretion in discriminating glomerular causes of microscopic haematuria in patients without proteinuria on urine dipstick tests. Design: Single-centre retrospective cross-sectional observational study. Methods: Adult patients who underwent renal biopsy for microscopic haematuria over a 6-year period from January 1994 were identified. Study entry required normal renal function, no proteinuria detected by dipstick, and urinary albumin excretion <300 mg/24 h. Patients with IgA nephropathy had follow-up for a mean of 58 months after biopsy. Results: Of 169 patients fulfilling study criteria, 119 (70%) had normoalbuminuria (<30 mg/24 h); 52 (30%) had microalbuminuria (30-299 mg/24 h). Of those with normoalbuminuria, 106 (89%) had thin basement membrane nephropathy or no glomerular abnormality. Thirteen (11%) had IgA nephropathy, and of 12 of these followed-up for a mean 64 months, none developed overt, dipstick-positive proteinuria. In contrast, 24 (48%) of those with microalbuminuria had IgA nephropathy, and of 22 followed-up for a mean 55 months, five developed overt proteinuria. Discussion: Urinary albumin excretion is an indicator of likely glomerular findings in microscopic haematuria, and may influence whether a renal biopsy is necessary.
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页码:297 / 301
页数:5
相关论文
共 29 条
[1]  
ANTON TMG, 1989, NEW ENGL J MED, V320, P14
[2]  
Auwardt R, 1999, CLIN NEPHROL, V52, P1
[3]  
Badenas C, 2002, J AM SOC NEPHROL, V13, P1248, DOI 10.1681/ASN.V1351248
[4]   ESTABLISHING THE DIAGNOSIS OF BENIGN FAMILIAL HEMATURIA - THE IMPORTANCE OF EXAMINING THE URINE SEDIMENT OF FAMILY MEMBERS [J].
BLUMENTHAL, SS ;
FRITSCHE, C ;
LEMANN, J .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1988, 259 (15) :2263-2266
[5]   COL4A4 mutation in thin basement membrane disease previously described in Alport syndrome [J].
Buzza, M ;
Wang, YY ;
Dagher, H ;
Babon, JJ ;
Cotton, RG ;
Powell, H ;
Dowling, J ;
Savige, J .
KIDNEY INTERNATIONAL, 2001, 60 (02) :480-483
[6]   RENAL SURVIVAL RATE OF IGA NEPHROPATHY [J].
CHIDA, Y ;
TOMURA, S ;
TAKEUCHI, J .
NEPHRON, 1985, 40 (02) :189-194
[7]   Natural history of idiopathic IgA nephropathy: Role of clinical and histological prognostic factors [J].
D'Amico, G .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2000, 36 (02) :227-237
[8]   A comparison of the clinical, histopathologic, and ultrastructural phenotypes in carriers of X-linked and autosomal recessive Alport's syndrome [J].
Dagher, H ;
Buzza, M ;
Colville, D ;
Jones, C ;
Powell, H ;
Fassett, R ;
Wilson, D ;
Agar, J ;
Savige, J .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2001, 38 (06) :1217-1228
[9]  
FLINTER FA, 1998, INHERITED DISORDERS, P192
[10]  
FULANO G, 2000, AM J KIDNEY DIS, V35, P448