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The Relationship Between Body Composition, Dietary Intake, Physical Activity, and Pulmonary Status in Adolescents and Adults with Cystic Fibrosis

Overview
Journal Nutrients
Date 2022 Jan 21
PMID 35057491
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Abstract

Measures of body fat and lean mass may better predict important clinical outcomes in patients with cystic fibrosis (CF) than body mass index (BMI). Little is known about how diet quality and exercise may impact body composition in these patients. Dual X-ray absorptiometry (DXA) body composition, 24-h dietary recall, and physical activity were assessed in a cross-sectional analysis of 38 adolescents and adults with CF and 19 age-, race-, and gender-matched healthy volunteers. Compared with the healthy volunteers, participants with CF had a lower appendicular lean mass index (ALMI), despite no observed difference in BMI, and their diets consisted of higher glycemic index foods with a greater proportion of calories from fat and a lower proportion of calories from protein. In participants with CF, pulmonary function positively correlated with measures of lean mass, particularly ALMI, and negatively correlated with multiple measures of body fat after controlling for age, gender, and BMI. Higher physical activity levels were associated with greater ALMI and lower body fat. In conclusion, body composition measures, particularly ALMI, may better predict key clinical outcomes in individuals with CF than BMI. Future longitudinal studies analyzing the effect of dietary intake and exercise on body composition and CF-specific clinical outcomes are needed.

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References
1.
Fielding J, Brantley L, Seigler N, McKie K, Davison G, Harris R . Oxygen uptake kinetics and exercise capacity in children with cystic fibrosis. Pediatr Pulmonol. 2015; 50(7):647-54. DOI: 10.1002/ppul.23189. View

2.
Matel J . Nutritional management of cystic fibrosis. JPEN J Parenter Enteral Nutr. 2012; 36(1 Suppl):60S-7S. DOI: 10.1177/0148607111420156. View

3.
Alicandro G, Bisogno A, Battezzati A, Bianchi M, Corti F, Colombo C . Recurrent pulmonary exacerbations are associated with low fat free mass and low bone mineral density in young adults with cystic fibrosis. J Cyst Fibros. 2013; 13(3):328-34. DOI: 10.1016/j.jcf.2013.11.001. View

4.
Moran A, Brunzell C, Cohen R, Katz M, Marshall B, Onady G . Clinical care guidelines for cystic fibrosis-related diabetes: a position statement of the American Diabetes Association and a clinical practice guideline of the Cystic Fibrosis Foundation, endorsed by the Pediatric Endocrine Society. Diabetes Care. 2010; 33(12):2697-708. PMC: 2992215. DOI: 10.2337/dc10-1768. View

5.
Madeira F, Silva A, Veloso H, Goldani M, Kac G, Cardoso V . Normal weight obesity is associated with metabolic syndrome and insulin resistance in young adults from a middle-income country. PLoS One. 2013; 8(3):e60673. PMC: 3610876. DOI: 10.1371/journal.pone.0060673. View