GLUCOCORTICOID-INDUCED POLYCYSTIC KIDNEY-DISEASE - A THRESHOLD TRAIT

被引:27
作者
MCDONALD, ATJ
CROCKER, JFS
DIGOUT, SC
MCCARTHY, SC
BLECHER, SR
COLE, DEC
机构
[1] IWK CHILDRENS HOSP, DEPT PEDIAT, 5850 UNIV AVE, HALIFAX B3J 3GR, NS, CANADA
[2] DALHOUSIE UNIV, DEPT PEDIAT, HALIFAX B3H 4H2, NS, CANADA
[3] UNIV GUELPH, SCH HUMAN BIOL, DEPT PEDIAT, GUELPH N1G 2W1, ONTARIO, CANADA
基金
英国医学研究理事会;
关键词
D O I
10.1038/ki.1990.64
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Administration of hydrocortisone acetate (250 mg/kg) to newborn mice caused polycystic kidney disease (PKD) of varying proportions in each of 18 different inbred strains; none of the injected controls were affected. All kidneys were histologically examined and scored for degree of cyst formation using a semi-continuous (0 to 4+) grading scheme. Results suggested that this condition is a multifactorial threshold trait. For each strain, estimates of the mean and standard deviation of normally distributed liability were determined by maximum likelihood methods. Concomitant analyses showed: 1) a significant environmental effect related to drug source; 2) a variation in thresholds ranging from 0.94 (N = 46) for the B10.M strain to -0.71 (N = 297) for the C57Bl/6J strain; and 3) three groups of strains with different susceptibility to PKD. These results are consistent with a multifactorial basis for susceptibility to PKD. Quantitative analysis of thresholds and liability distributions reveals that genetic, environmental and random elements all contribute to the expression and extent of the cystic trait.
引用
收藏
页码:901 / 908
页数:8
相关论文
共 41 条
[1]  
BAXTER H, 1950, McGill Med J, V19, P245
[2]  
BAXTER TJ, 1960, BRIT J EXP PATHOL, V41, P140
[3]  
BIDDLE FG, 1977, GENETICS, V85, P289
[4]  
BLECHER SR, 1978, NATURE, V275, P748, DOI 10.1038/275748a0
[5]   POLYCYSTIC DISEASE OF KIDNEYS AND LIVER PRESENTING IN CHILDHOOD [J].
BLYTH, H ;
OCKENDEN, BG .
JOURNAL OF MEDICAL GENETICS, 1971, 8 (03) :257-+
[6]  
BRISSENDEN JE, 1988, CLIN INVEST MED, V11, pC499
[7]  
BRUENING MH, 1989, PROGR CLIN BIOL RES, V305, P69
[8]  
CROCKER JFS, 1971, PEDIATR CLIN N AM, V18, P355
[9]  
CROCKER JFS, 1987, CLIN INVEST MED, V10, pB104
[10]  
CROCKER JFS, 1985, ABNORMAL FUNCTIONAL, P281