Cited by 306Cystic Fibrosis Research AdvancesClinical Nutrition and GastroenterologyGenetic and Kidney Cyst Diseases

Better nutritional status in early childhood is associated with improved clinical outcomes and survival in patients with cystic fibrosis

Yen, Elizabeth H., Quinton, Hebe, Borowitz, Drucy·2013·The Journal of Pediatrics

Abstract

Objectives To evaluate the relationship between nutritional status early in life and the timing and velocity of height growth, lung function, complications of cystic fibrosis, and survival. Study design Prospective, observational study using data from the Cystic Fibrosis Foundation Registry (US) for patients born between 1989 and 1992 (n = 3142). Results Weight-for-age percentile (WAP) at 4 years of age was positively associated with height-for-age percentiles throughout childhood. Age 4 years WAP >10% was associated with better lung function from 6-18 years of age. In boys and girls with current WAP >50%, peak pubertal height velocities approximated but remained lower than that of the healthy reference population. By age 18 years, patients with an age 4 years WAP >50% suffered fewer acute pulmonary exacerbations, spent fewer days in the hospital, and had lower rates of impaired glucose tolerance or diabetes. Patients attaining higher age 4 years WAP and height-for-age percentiles had a survival advantage throughout childhood. Conclusion For the population studied, greater weight at age 4 years is associated with greater height, better pulmonary function, fewer complications of cystic fibrosis, and better survival through age 18 years. Furthermore, greater weight-for-age in the peripubertal period is associated on average with improved tempo and timing of pubertal height growth.

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Crossref · 10.1016/j.jpeds.2012.08.040

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Authors
Yen, E. H., Quinton, H., & Borowitz, D.
Affiliations
  • Boston Children's Hospital (US)
  • Dartmouth College (US)
  • Women & Children's Hospital of Buffalo (US)
Corresponding author
Yen, Elizabeth H.
Venue
The Journal of Pediatrics
Publisher
Elsevier BV
Published
2013-03
Volume
162
Issue
3
Pages
530-535.e1
ISSN
0022-3476 (ISSN-L)
OpenAlex
W2114745077
Cited by
306
References
1
Citations by year
2026: 5 · 2025: 8 · 2024: 18 · 2023: 27 · 2022: 21 · 2021: 31 · 2020: 30 · 2019: 32 · 2018: 18 · 2017: 21 · 2016: 32 · 2015: 33 · 2014: 21 · 2013: 8
FWCI
15.96
Type
journal article
Language
en
Open access
closed
Locations
  • The Journal of Pediatrics (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Cystic Fibrosis Research Advances
  • Health Sciences › Nursing › Nutrition and Dietetics › Clinical Nutrition and Gastroenterology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic and Kidney Cyst Diseases
Keywords
cystic fibrosis, height-for-age, lung function, pulmonary exacerbations, diabetes mellitus, impaired glucose tolerance, survival
MeSH terms
Adolescent, Body Height, Body Weight, Child, Child, Preschool, Cystic Fibrosis, Female, Humans, Lung, Male, Nutritional Status, Prospective Studies, Respiratory Function Tests, Survival Analysis, Glucose Intolerance

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