Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 638-641 |
| Number of pages | 4 |
| Journal | Pediatric Pulmonology |
| Volume | 43 |
| Issue number | 7 |
| DOIs | |
| State | Published - Jul 2008 |
Keywords
- Cystic fibrosis
- Immunoreactive trypsinogen
- Newborn screen
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