EVALUATION OF ULTRASONOGRAPHIC DIAGNOSTIC-CRITERIA FOR AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY DISEASE-1

被引:445
作者
RAVINE, D
GIBSON, RN
WALKER, RG
SHEFFIELD, LJ
KINCAIDSMITH, P
DANKS, DM
机构
[1] ROYAL CHILDRENS HOSP,MURDOCH INST,PARKVILLE,VIC 3052,AUSTRALIA
[2] ROYAL MELBOURNE HOSP,DEPT RADIOL,PARKVILLE,VIC 3050,AUSTRALIA
[3] ROYAL MELBOURNE HOSP,DEPT NEPHROL,PARKVILLE,VIC 3050,AUSTRALIA
关键词
D O I
10.1016/S0140-6736(94)92026-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although ultrasound is commonly used for screening subjects at risk of polycystic kidney disease 1 (PKD1), there has been no evaluation of ultrasonographic diagnostic criteria. We used DNA linkage among subjects from 128 sibships within 18 PKD1 families as the basis for an assessment of ultrasound sensitivity. Positive and negative predictive values were calculated to allow assessment of different diagnostic cut-off points in previously undiagnosed cases. Currently used criteria (bilateral cysts with at least two in one kidney) provided good sensitivity (88.5% at age 15-29 years and 100% at 30 years and above) but performance could be improved by less stringent criteria in subjects aged 15-29 years and more stringent criteria in older family members, in whom simple renal cysts are frequent. The presence of at least two renal cysts (unilateral or bilateral) in individuals at risk and younger than 30 years may be regarded as sufficient to establish a diagnosis; among those aged 30-59 years, the presence of at least two cysts in each kidney may be required, and among those aged 60 years and above, at least four cysts in each kidney should be required.
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收藏
页码:824 / 827
页数:4
相关论文
共 30 条
[1]   AGE AT CLINICAL ONSET AND AT ULTRASONOGRAPHIC DETECTION OF ADULT POLYCYSTIC KIDNEY-DISEASE - DATA FOR GENETIC-COUNSELING [J].
BEAR, JC ;
MCMANAMON, P ;
MORGAN, J ;
PAYNE, RH ;
LEWIS, H ;
GAULT, MH ;
CHURCHILL, DN .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1984, 18 (01) :45-53
[2]   AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY-DISEASE - NEW INFORMATION FOR GENETIC-COUNSELING [J].
BEAR, JC ;
PARFREY, PS ;
MORGAN, JM ;
MARTIN, CJ ;
CRAMER, BC .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 43 (03) :548-553
[3]  
BENNETT WM, 1990, SEMIN NEPHROL, V10, P552
[4]   A TAQI POLYMORPHISM IDENTIFIED BY 26-6 (D16S125) PROXIMAL TO THE LOCUS AFFECTING ADULT POLYCYSTIC KIDNEY-DISEASE (PKD1) ON CHROMOSOME-16 [J].
BREUNING, MH ;
SNIJDEWINT, FGM ;
SMITS, JR ;
DAUWERSE, JG ;
SARIS, JJ ;
VANOMMEN, GJB .
NUCLEIC ACIDS RESEARCH, 1990, 18 (10) :3106-3106
[5]  
BREUNING MH, 1987, LANCET, V2, P1359
[6]   GENETIC AND CLINICAL-STUDIES IN AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY-DISEASE TYPE-1 (ADPKD1) [J].
COTO, E ;
AGUADO, S ;
ALVAREZ, J ;
DIAZ, MJM ;
LOPEZLARREA, C .
JOURNAL OF MEDICAL GENETICS, 1992, 29 (04) :243-246
[7]  
DISNEY APS, 1990, ANZDATA13TH QUEEN EL, P22
[8]  
FICK GM, 1993, J AM SOC NEPHROL, V3, P1863
[9]  
GERMINO GG, 1990, AM J HUM GENET, V46, P925
[10]  
HOGEWIND BL, 1980, CLIN GENET, V18, P168