Literature DB >> 27081158

Growth Deficiency in Cystic Fibrosis Is Observable at Birth and Predictive of Early Pulmonary Function.

Rebecca Darrah1, Rebecca Nelson2, Elizabeth G Damato3, Michael Decker3, Anne Matthews4, Craig A Hodges5.   

Abstract

INTRODUCTION: Cystic fibrosis (CF) is a complex disease that includes both pulmonary and gastrointestinal challenges, resulting in decreased weight. Pulmonary symptoms of CF are extremely variable. Greater body mass at an early age is associated with improved pulmonary function, but it is unknown at what age weight becomes predictive of pulmonary disease severity. The purpose of this study was to investigate the relationship between birth weight and pulmonary function in CF.
METHODS: Birth weight and pulmonary data were obtained. Linear regressions were used to examine the relationship between these two variables. A one-tailed t-test was used to compare birth weights between CF patients and the national average.
RESULTS: Birth weight was significantly lower in babies with CF and correlated with pulmonary disease at ages 6 and 10 years but not with age at which Pseudomonas aeruginosa colonization was observed. DISCUSSION: These data suggest that CF growth deficiency has prenatal origins. Early nutritional intervention for babies with CF and a low birth weight is warranted to maximize pulmonary potential.
© The Author(s) 2016.

Entities:  

Keywords:  birth weight; cystic fibrosis; genetics; pediatrics; respiratory

Mesh:

Year:  2016        PMID: 27081158      PMCID: PMC5942479          DOI: 10.1177/1099800416643585

Source DB:  PubMed          Journal:  Biol Res Nurs        ISSN: 1099-8004            Impact factor:   2.522


  43 in total

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Authors:  Elizabeth H Yen; Hebe Quinton; Drucy Borowitz
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Journal:  BMJ       Date:  1991-09-21

8.  Insulin-like growth factors and their binding proteins in the term and preterm human fetus and neonate with normal and extremes of intrauterine growth.

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Authors:  Irene E Olsen; Sue A Groveman; M Louise Lawson; Reese H Clark; Babette S Zemel
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10.  Measures of body habitus are associated with lung function in adults with cystic fibrosis: a population-based study.

Authors:  Doug L Forrester; Alan J Knox; Alan R Smyth; Andrew W Fogarty
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2.  Predictive effects of low birth weight and small for gestational age status on respiratory and nutritional outcomes in cystic fibrosis.

Authors:  Samar E Atteih; Karen S Raraigh; Scott M Blackman; Garry R Cutting; Joseph M Collaco
Journal:  J Cyst Fibros       Date:  2020-02-12       Impact factor: 5.482

3.  Growth failure and treatment in cystic fibrosis.

Authors:  Trang N Le; Abeer Anabtawi; Melissa S Putman; Vin Tangpricha; Michael S Stalvey
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4.  Academy of Nutrition and Dietetics: 2020 Cystic Fibrosis Evidence Analysis Center Evidence-Based Nutrition Practice Guideline.

Authors:  Catherine M McDonald; Jessica A Alvarez; Julianna Bailey; Ellen K Bowser; Kristen Farnham; Mark Mangus; Laura Padula; Kathleen Porco; Mary Rozga
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5.  Growth deficits in cystic fibrosis mice begin in utero prior to IGF-1 reduction.

Authors:  Rebecca Darrah; Ilya Bederman; Megan Vitko; Dana M Valerio; Mitchell L Drumm; Craig A Hodges
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6.  Impact of cystic fibrosis on birthweight: a population based study of children in Denmark and Wales.

Authors:  Daniela K Schlüter; Rowena Griffiths; Abdulfatah Adam; Ashley Akbari; Martin L Heaven; Shantini Paranjothy; Anne-Marie Nybo Andersen; Siobhán B Carr; Tania Pressler; Peter J Diggle; David Taylor-Robinson
Journal:  Thorax       Date:  2018-07-19       Impact factor: 9.102

7.  Alleviation of depression-like behavior in a cystic fibrosis mouse model by Hdac6 depletion.

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