Literature DB >> 19547848

Association between nutritional status measurements and pulmonary function in children and adolescents with cystic fibrosis.

Célia Regina Moutinho de Miranda Chaves1, José Augusto Alves de Britto, Cristiano Queiroz de Oliveira, Miriam Martins Gomes, Ana Lúcia Pereira da Cunha.   

Abstract

OBJECTIVE: To evaluate the association between nutritional status measurements and pulmonary function in children and adolescents with cystic fibrosis.
METHODS: We evaluated the nutritional status of 48 children and adolescents (aged 6-18 years) with cystic fibrosis based on body mass index (BMI) and body composition measurements-mid-arm muscle circumference (MAMC) and triceps skinfold thickness (TST)-at a referral center in the city of Rio de Janeiro, Brazil. Pulmonary function was assessed by means of spirometry, using FEV1 to classify the severity of airway obstruction. We used Student's t-tests for comparisons between proportions and linear regression analysis for associations between continuous variables. The level of significance was set at p < 0.05.
RESULTS: The evaluation of nutritional status based on BMI identified a smaller number of malnourished patients than did that based on MAMC (14 vs. 25 patients, respectively). Most of the patients presented mild pulmonary disease. Mean FEV1 was 82.5% of predicted. Pulmonary function was found to correlate significantly with BMI, MAMC and TST (p = 0.001, p = 0.001 and p = 0.03, respectively). All subjects with moderate or severe pulmonary involvement were considered malnourished based on BMI and body composition parameters. Of the 25 patients considered malnourished based on body composition (MAMC), 19 were considered well-nourished based on their BMI.
CONCLUSIONS: In the present study, all nutritional status measurements correlated directly with the pulmonary function of children and adolescents with cystic fibrosis. However, body composition measurements allowed earlier detection of nutritional deficiencies.

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Year:  2009        PMID: 19547848     DOI: 10.1590/s1806-37132009000500004

Source DB:  PubMed          Journal:  J Bras Pneumol        ISSN: 1806-3713            Impact factor:   2.624


  7 in total

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Journal:  Clinics (Sao Paulo)       Date:  2010-04       Impact factor: 2.365

2.  Persistence of Candida dubliniensis and lung function in patients with cystic fibrosis.

Authors:  Atqah AbdulWahab; Husam Salah; Prem Chandra; Saad J Taj-Aldeen
Journal:  BMC Res Notes       Date:  2017-07-26

3.  Rural-urban disparity in lung function parameters of Nigerian children: effects of socio-economic, nutritional and housing factors.

Authors:  Bankole Peter Kuti; Oluwatoyin Ibukun Oladimeji; Demilade Kehinde Kuti; Adewuyi Temidayo Adeniyi; Emmanuel Oluwatosin Adeniji; Yetunde Justinah Osundare
Journal:  Pan Afr Med J       Date:  2017-11-15

Review 4.  Review: Quality of Life in Children with Non-cystic Fibrosis Bronchiectasis.

Authors:  Anna Marie Nathan; Jessie Anne de Bruyne; Kah Peng Eg; Surendran Thavagnanam
Journal:  Front Pediatr       Date:  2017-04-24       Impact factor: 3.418

5.  THE USE OF ULTRASONOGRAPHY TO EVALUATE MUSCLE THICKNESS AND SUBCUTANEOUS FAT IN CHILDREN AND ADOLESCENTS WITH CYSTIC FIBROSIS.

Authors:  Rodrigo Pereira de Souza; Márcio Vinícius Fagundes Donadio; João Paulo Heinzmann-Filho; Rafael Reimann Baptista; Leonardo Araújo Pinto; Matias Epifanio; Paulo José Cauduro Marostica
Journal:  Rev Paul Pediatr       Date:  2018 Oct-Dec

6.  Triage for Malnutrition Risk among Pediatric and Adolescent Outpatients with Cystic Fibrosis, Using a Disease-Specific Tool.

Authors:  Dimitrios Poulimeneas; Maria G Grammatikopoulou; Argyri Petrocheilou; Athanasios G Kaditis; Tonia Vassilakou
Journal:  Children (Basel)       Date:  2020-12-04

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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