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利用肌酸激酶水平的判别分析改进杜氏肌营养不良症杂合子的检测。

Improved detection of Duchenne muscular dystrophy heterozygotes using discriminant analysis of creatine kinase levels.

作者信息

Muir W A, Knoke J, Martin A, Vignos P, McErlean A

出版信息

Am J Med Genet. 1983 Jan;14(1):125-34. doi: 10.1002/ajmg.1320140117.

Abstract

We have assessed the sensitivity and specificity of tests to detect carriers of Duchenne muscular dystrophy by use of three serum enzymes (creatine kinase, pyruvate kinase, and aldolase) and discriminant analysis in 21 obligate heterozygotes and 28 normal controls. We found no significant age effects on enzyme levels. Each enzyme level considered separately was significantly higher in heterozygotes. Use of logs improved discrimination, and log CK was sufficient by itself as a discriminant (that is, addition of other enzymes did not significantly improve discrimination). We present procedures to generate posteriori probabilities for genetic counselling that incorporate prior probabilities and enzyme levels. Our results show both improved sensitivity (90%) and specificity (86%).

摘要

我们通过使用三种血清酶(肌酸激酶、丙酮酸激酶和醛缩酶)以及判别分析,对21名确诊的杂合子和28名正常对照进行检测,以评估检测杜氏肌营养不良症携带者的测试的敏感性和特异性。我们发现年龄对酶水平没有显著影响。单独考虑每种酶水平时,杂合子中的酶水平显著更高。使用对数提高了判别能力,并且对数肌酸激酶本身作为判别指标就足够了(也就是说,添加其他酶并没有显著提高判别能力)。我们提出了一些程序,用于生成结合先验概率和酶水平的遗传咨询后验概率。我们的结果显示敏感性(90%)和特异性(86%)均有所提高。

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