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胎粪研究。一种用于检测囊性纤维化的筛查试验方法。

Studies in meconium. An approach to screening tests to detect cystic fibrosis.

作者信息

Shwachman H, Antonowicz I, Mahmoodian A, Ishida S

出版信息

Am J Dis Child. 1978 Nov;132(11):1112-4. doi: 10.1001/archpedi.1978.02120360068012.

Abstract

Screening for cystic fibrosis (CF) in newborns is desirable, and efforts should continue in establishing a system of easily available, reliable, simple, and inexpensive tests. In addition to the Boehringer-Mannheim (BM) test for the detection of albumin, we propose the assay for lactase and beta-D-fucosidase in meconium. These latter two enzymes are present in the meconium of babies with CF and absent in meconium of most healthy babies. In a mass screening program for CF involving 20,182 specimens of meconium using only the BM strip, we found 46 positive results. Twenty-nine specimens came from infants with CF, six of whom had meconium ileus. Seventeen specimens yielded false-positive results by the BM test. Eleven of these would have been excluded by the addition of the lactase and beta-D-fucoside assay, thus reducing the false-positive test results by nearly 61%. In a comparative study of the three methods, the lactase and beta-D-fucosidase yielded 1.2% false-positives when examined independently. Performance of these two assays may allow greater specificity in diagnosis when used in addition to the BM test.

摘要

对新生儿进行囊性纤维化(CF)筛查是很有必要的,应继续努力建立一个易于获得、可靠、简单且廉价的检测系统。除了用于检测白蛋白的勃林格殷格翰(BM)检测外,我们还提议检测胎粪中的乳糖酶和β-D-岩藻糖苷酶。后两种酶存在于患有CF的婴儿的胎粪中,而大多数健康婴儿的胎粪中则不存在。在一项仅使用BM试纸条对20182份胎粪样本进行CF大规模筛查的项目中,我们发现了46个阳性结果。29份样本来自患有CF的婴儿,其中6例有胎粪性肠梗阻。17份样本通过BM检测得出假阳性结果。如果增加乳糖酶和β-D-岩藻糖苷检测,其中11份样本将被排除,从而使假阳性检测结果减少近61%。在对这三种方法的比较研究中,单独检测时,乳糖酶和β-D-岩藻糖苷酶产生1.2%的假阳性。当与BM检测一起使用时,这两种检测方法在诊断中可能具有更高的特异性。

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