Literature DB >> 20926519

Body composition assessed by the 4-component model and association with lung function in 6-12-y-old children with cystic fibrosis.

Jane E Williams1, Jonathan Ck Wells, Christian Benden, Adam Jaffe, Ranjan Suri, Catherine M Wilson, Mary S Fewtrell.   

Abstract

BACKGROUND: Malnutrition is an indicator of a poor prognosis in patients with cystic fibrosis (CF). Previous body-composition (BC) studies in children with CF used 2-component models (2CMs) to assess fat mass (FM) and fat-free mass (FFM), but to our knowledge no study has used the gold-standard 4-component model (4CM), which allows for a more accurate evaluation of the nature of both elements.
OBJECTIVE: We measured BC by using the 4CM in 6-12-y-old children with CF to 1) compare findings with those of healthy, matched control children and reference data; 2) relate BC to lung spirometry [forced expired volume in 1 s (FEV₁)]; and 3) compare findings with those from more commonly used 2CM techniques.
DESIGN: One hundred clinically stable children with CF (57% girls) aged 6-12 y were measured by using the 4CM. Children with CF underwent spirometry (FEV₁).
RESULTS: Girls with CF had significantly less FM than did healthy girls, even after adjustment for height and pubertal status; boys with CF had higher body mass index SD scores than did healthy boys. FM in girls was positively associated with the FEV₁ percentage predicted. The 2CM FM was significantly different from the 4CM FM, with differences dependent on sex and condition, although most techniques identified a relation between FM and FEV₁ in girls.
CONCLUSIONS: Although shorter than healthy children, boys with CF were heavier and had a BC within the normal range; however, girls with CF had lower FM than did healthy girls, and this was associated with poorer lung function. Given the worse prognosis in girls, this finding merits more attention. The reliability of 2CM techniques varied with sex and health status.

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Year:  2010        PMID: 20926519     DOI: 10.3945/ajcn.2010.29847

Source DB:  PubMed          Journal:  Am J Clin Nutr        ISSN: 0002-9165            Impact factor:   7.045


  7 in total

1.  Body composition and lung function in children with cystic fibrosis and meconium ileus.

Authors:  Artemis Doulgeraki; Argyri Petrocheilou; Glykeria Petrocheilou; George Chrousos; Stavros-Eleftherios Doudounakis; Athanasios G Kaditis
Journal:  Eur J Pediatr       Date:  2017-04-13       Impact factor: 3.183

2.  Body composition and lung function in cystic fibrosis and their association with adiposity and normal-weight obesity.

Authors:  Jessica A Alvarez; Thomas R Ziegler; Erin C Millson; Arlene A Stecenko
Journal:  Nutrition       Date:  2015-10-30       Impact factor: 4.008

3.  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
Journal:  J Acad Nutr Diet       Date:  2020-06-19       Impact factor: 5.234

4.  Body composition and pulmonary function in cystic fibrosis.

Authors:  Saba Sheikh; Babette S Zemel; Virginia A Stallings; Ronald C Rubenstein; Andrea Kelly
Journal:  Front Pediatr       Date:  2014-04-15       Impact factor: 3.418

5.  Body composition in young female eating-disorder patients with severe weight loss and controls: evidence from the four-component model and evaluation of DXA.

Authors:  J C K Wells; D Haroun; J E Williams; D Nicholls; T Darch; S Eaton; M S Fewtrell
Journal:  Eur J Clin Nutr       Date:  2015-07-15       Impact factor: 4.016

6.  Childhood Body Composition Trajectories and Adolescent Lung Function. Findings from the ALSPAC study.

Authors:  Gabriela P Peralta; Elaine Fuertes; Raquel Granell; Osama Mahmoud; Célina Roda; Ignasi Serra; Deborah Jarvis; John Henderson; Judith Garcia-Aymerich
Journal:  Am J Respir Crit Care Med       Date:  2019-07-01       Impact factor: 21.405

7.  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
Journal:  J Cyst Fibros       Date:  2012-09-05       Impact factor: 5.482

  7 in total

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