Comparison of the clinical manifestations of cystic fibrosis in black and white patients

A. Hamosh, S. C. FitzSimmons, Jr Macek M., M. R. Knowles, B. J. Rosenstein, G. R. Cutting

Research output: Contribution to journalArticle

Abstract

No large-scale studies of the incidence or disease severity of cystic fibrosis (CF) in black patients have been reported to date. In this study, the CF Foundation National Patient Registry was used to established new incidence figures and to compare the clinical status of U.S. black (n = 601) and white patients (n = 17,755) with CF. Results indicate that the incidence of CF is approximately 1 in 3,200 white and 1 in 15,000 black live births in the United States. Black patients with CF are currently, and were at diagnosis, younger and have poorer nutritional status and pulmonary function than white patients with CF. Fewer have meconium ileus, but more have distal intestinal obstruction syndrome. To control for genotype, each black ΔF508 homozygote (n = 47) was compared with four age- and sex-matched white ΔF508 homozygotes. Only the difference in nutritional status remained. The ΔF508 mutation is associated with higher levels of meconium ileus than other genotypes, independent of race. In conclusion, the clinical manifestations of CF are similar in black and white patients except for poorer nutritional status in black patients, which appears to be independent of age and genotype.

Original languageEnglish (US)
Pages (from-to)255-259
Number of pages5
JournalJournal of Pediatrics
Volume132
Issue number2
DOIs
StatePublished - Jan 1 1998

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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