Height Assessment in the Dutch-Origin Pediatric Cystic Fibrosis Population

Janna W. Woestenenk*, Vincent A M Gulmans, Cornelis K. Van Der Ent, Roderick H J Houwen

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

1 Citation (Scopus)

Abstract

Background: Height evaluation is an integral part of cystic fibrosis (CF) care. Height is compared with reference values by converting it to height-for-age (HFA) z scores. However, HFA z scores do not adjust for genetic potential (ie, target height [TH]), which could result in an incorrect estimation of the height. Materials and Methods: To evaluate the magnitude of this potential problem, we assessed the agreement between HFA and HFA-adjusted-for-TH (HFA/TH) z scores in 474 Dutch children with CF. Results: In this study sample, HFA z scores were -0.07 (95% confidence interval, -0.02 to -0.12) lower than HFA/TH z scores. When HFA and HFA/TH z scores were subdivided into 4 categories (≥0, <0 and ≥-1, <-1 and ≥-2, and ≤-2), a moderate agreement was found. HFA z scores were classified lower than HFA/TH z scores in 21% of the measurements and higher in 15% of the measurements. Conclusion: In clinical routine, height evaluation based on HFA may result in underestimation or overestimation of height growth, which may induce inappropriate nutrition interventions.

Original languageEnglish
Pages (from-to)130-132
Number of pages3
JournalNutrition in Clinical Practice
Volume32
Issue number1
DOIs
Publication statusPublished - Feb 2017

Keywords

  • body height
  • cystic fibrosis
  • growth
  • pediatrics
  • target height

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