Nutritional Benefits of Neonatal Screening for Cystic Fibrosis
Philip M. Farrell, M.D., Ph.D., Michael R. Kosorok, Ph.D., Anita Laxova, B.S., Guanghong Shen, M.S., Rebecca E. Koscik, M.S., W. Theodore Bruns, M.D., Mark Splaingard, M.D., Elaine H. Mischler, M.D., for The Wisconsin Cystic Fibrosis Neonatal Screening Study Group
Background Many patients with cystic fibrosis are malnourishedat the time of diagnosis. Whether newborn screening and earlytreatment may prevent the development of a nutritional deficiencyis not known.
Methods We compared the nutritional status of patients withcystic fibrosis identified by neonatal screening or by standarddiagnostic methods. A total of 650,341 newborn infants werescreened by measuring immunoreactive trypsinogen on dried bloodspots (from April 1985 through June 1991) or by combining thetrypsinogen test with DNA analysis (from July 1991 through June1994). Of 325,171 infants assigned to an early-diagnosis group,cystic fibrosis was diagnosed in 74 infants, including 5 withnegative screening tests. Excluding infants with meconium ileus,we evaluated nutritional status for up to 10 years by anthropometricand biochemical methods in 56 of the infants who received anearly diagnosis and in 40 of the infants in whom the diagnosiswas made by standard methods (the control group). Pancreaticinsufficiency was managed with nutritional interventions thatincluded high-calorie diets, pancreatic-enzyme therapy, andfat-soluble vitamin supplements.
Results The diagnosis of cystic fibrosis was confirmed by apositive sweat test at a younger age in the early-diagnosisgroup than in the control group (mean age, 12 vs. 72 weeks).At the time of diagnosis, the early-diagnosis group had significantlyhigher height and weight percentiles and a higher head-circumferencepercentile (52nd, vs. 32nd in the control group; P = 0.003).The early-diagnosis group also had significantly higher anthropometricindexes during the follow-up period, especially the childrenwith pancreatic insufficiency and those who were homozygousfor the F508 mutation.
Conclusions Neonatal screening provides the opportunity to preventmalnutrition in infants with cystic fibrosis.
Source Information
From the Department of Pediatrics and Biostatistics, University of Wisconsin, Madison (P.M.F., M.R.K., A.L., G.S., R.E.K.), and the Department of Pediatrics, Medical College of Wisconsin, Milwaukee (W.T.B., M.S., E.H.M.).
Address reprint requests to Dr. Farrell at the University of Wisconsin Medical School, 1300 University Ave., Madison, WI 53706.
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