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Relationship between clinical parameters and linear growth in children with cystic fibrosis

Bibliographic Data

ID19458760
AuthorsPamela J Byard (Rainbow Babies & Children's Hospital, corresponding author)
Year1989
Volume1
Issue6
Pages719-725
Publication date1989-01-01
Open AccessYes
TypeARTICLE
VenueAmerican Journal of Human Biology (JOURNAL)
Journal identifiersISSN: 1042-0533 • E-ISSN: 1520-6300
PublisherWiley (PUBLISHER • GB)
DOI10.1002/ajhb.1310010609
PMID28597530
OpenAlexW1987347023
LanguageEN
Citations received3
References cited20

Mixed longitudinal height data from 1,170 cystic fibrosis patients seen at Rainbow Babies and Childrens Hospital in Cleveland form the basis for this analysis. As a group, the patients experience growth retardation throughout the growth cycle, with median height values below the 25th percentile of NCHS standards until late adolescence. Median height increments are also below normal standards until age 16 years in boys and 14 years in girls. Based on these results, it appears that some CF patients have very delayed adolescent growth spurts, and continue to grow into early adulthood. Pancreataic‐enzyme‐sufficient patients have greater height‐for‐age percentiles than enzyme‐deficient patients after 9 years of age. The overall difference between enzyme‐sufficient and enzyme‐deficient patients is not statistically significant ( P =0.058), perhaps because of small sample size for the enzyme‐sufficient group (n=19). The correlation between pulmonary status assessed from lung X‐rays and height increment peaks at age 10 years in girls and age 15 years in boys, with significant negative correlation occurring after age 16 years in both sexes. Although both pancreatic enzyme deficiency and lung disease appear to have some effect on linear growth in CF, especially during adolescence, these two factors explain a relatively small portion of the variation in growth percentiles

Correlation · Cystic fibrosis · Linear growth · Lung · Percentile · Child Nutrition and Feeding Issues · Child Nutrition and Water Access · Cystic Fibrosis Research Advances · Demography · Medicine · Internal Medicine · Pediatrics

  • The adolescent growth spurt in children with cystic fibrosis

    Open Access•Pamela J Byard•Annals of Human Biology•1994

  • Early childhood growth in patients with cystic fibrosis

    Open Access•Pamela J Byard•Annals of Human Biology•1990

  • Differentially delayed development in the hand–wrist skeletons of children with cystic fibrosis

    Open Access•Michael C Mahaney•American Journal of Human Biology•1991

  • Physical growth

    Open Access•P V Hamill, P V V Hamill et al.•American Journal of Clinical…•1979

Citations per year0.08
Citation span1990 - 1994 (5)
Highly citedNo

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