Literature DB >> 27916550

BMI fails to identify poor nutritional status in stunted children with CF.

Michael W Konstan1, David J Pasta2, Jeffrey S Wagener3, Donald R VanDevanter4, Wayne J Morgan5.   

Abstract

BACKGROUND: Body mass index (BMI) is currently emphasized for evaluating nutritional status in children with cystic fibrosis (CF). Weight for age (WFA) and height for age (HFA) may get less attention.
METHODS: Data from the Epidemiologic Study of Cystic Fibrosis were used to compare patient WFA, HFA, and BMI percentiles for children age 2 to 18years.
RESULTS: For children with BMI between the 25th and 50th percentiles, 16.8% had WFA <10th percentile and 26.6% had HFA <10th percentile.
CONCLUSIONS: BMI fails to identify a substantial proportion of children with CF who have stunting or potentially poor nutritional status as measured by WFA and/or HFA.
Copyright © 2016 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Body mass index; Cystic fibrosis; Growth; Height for age; Weight for age

Mesh:

Year:  2017        PMID: 27916550     DOI: 10.1016/j.jcf.2016.11.005

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  9 in total

1.  The association between Sodium Urinary Discharge (FENa) and growth parameters in pediatrics with cystic fibrosis.

Authors:  Mohsen Reisi; Majid Keivanfar; Mahboobe Rezaie; Silva Hovsepian
Journal:  Am J Clin Exp Urol       Date:  2022-08-15

2.  Growth failure and treatment in cystic fibrosis.

Authors:  Trang N Le; Abeer Anabtawi; Melissa S Putman; Vin Tangpricha; Michael S Stalvey
Journal:  J Cyst Fibros       Date:  2019-10       Impact factor: 5.482

Review 3.  Epidemiologic Study of Cystic Fibrosis: 25 years of observational research.

Authors:  Michael W Konstan; David J Pasta; Donald R VanDevanter; Jeffrey S Wagener; Wayne J Morgan
Journal:  Pediatr Pulmonol       Date:  2021-01-12

4.  Multivariate joint modeling to identify markers of growth and lung function decline that predict cystic fibrosis pulmonary exacerbation onset.

Authors:  E R Andrinopoulou; J P Clancy; R D Szczesniak
Journal:  BMC Pulm Med       Date:  2020-05-19       Impact factor: 3.317

5.  BODY MASS INDEX AND ALBUMIN LEVELS ARE ASSOCIATED WITH PULMONARY FUNCTION PARAMETERS IN PEDIATRIC SUBJECTS WITH CYSTIC FIBROSIS.

Authors:  Miriam Isabel Souza Dos Santos Simon; Gabriele Carra Forte; Paulo José Cauduro Marostica
Journal:  Rev Paul Pediatr       Date:  2019-05-09

Review 6.  Trends in Growth and Maturation in Children with Cystic Fibrosis Throughout Nine Decades.

Authors:  Kelly A Mason; Alan D Rogol
Journal:  Front Endocrinol (Lausanne)       Date:  2022-07-12       Impact factor: 6.055

7.  Determining the Factors That Influence Stunting during Pandemic in Rural Indonesia: A Mixed Method.

Authors:  Esti Yunitasari; Bih O Lee; Ilya Krisnana; Rayi Lugina; Fitriana Kurniasari Solikhah; Ronal Surya Aditya
Journal:  Children (Basel)       Date:  2022-08-08

8.  Reduced bone length, growth plate thickness, bone content, and IGF-I as a model for poor growth in the CFTR-deficient rat.

Authors:  Michael S Stalvey; Viktoria Havasi; Katherine L Tuggle; Dezhi Wang; Susan Birket; Steve M Rowe; Eric J Sorscher
Journal:  PLoS One       Date:  2017-11-30       Impact factor: 3.240

9.  Most Short Children with Cystic Fibrosis Do Not Catch Up by Adulthood.

Authors:  Margaret P Marks; Sonya L Heltshe; Arthur Baines; Bonnie W Ramsey; Lucas R Hoffman; Michael S Stalvey
Journal:  Nutrients       Date:  2021-12-10       Impact factor: 5.717

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.