Giusti Robert
Department of Pediatrics, Long Island College Hospital, Brooklyn, New York, USA.
Pediatr Pulmonol. 2008 Jul;43(7):638-41. doi: 10.1002/ppul.20824.
During the first 4 years of newborn screening (NBS) for Cystic Fibrosis (CF) in New York there was a statistically significant, twofold greater relative risk of an Immunoreactive Trypsinogen (IRT) level greater than 95% in African-American infants. The reason for this previously reported increase in IRT level in African-American infants is unclear. The positive predictive value of a screen positive result in this population was only 0.3%. The bulk of screen-positive African-American infants were in the top 0.2% (IRT) group, with no CF mutations isolated. Repeat IRT testing at 2-3 weeks of age may represent a suitable approach to decrease the false-positive rate in this population.
在纽约针对囊性纤维化(CF)进行新生儿筛查(NBS)的头4年里,非裔美国婴儿免疫反应性胰蛋白酶原(IRT)水平高于95%的相对风险在统计学上显著高出两倍。此前报道的非裔美国婴儿IRT水平升高的原因尚不清楚。该人群筛查阳性结果的阳性预测值仅为0.3%。大部分筛查呈阳性的非裔美国婴儿属于最高的0.2%(IRT)组,未检测到CF突变。在2至3周龄时重复进行IRT检测可能是降低该人群假阳性率的合适方法。