Literature DB >> 30887107

Nutritional Status in Childhood as a Prognostic Factor in Patients with Cystic Fibrosis.

Moshe Ashkenazi1,2, N Nathan3, I Sarouk4,3, B E Bar Aluma4,3, A Dagan4,3, Y Bezalel4,3, S Keler4,3, D Vilozni4,3, O Efrati4,3.   

Abstract

INTRODUCTION: There is a strong association between cystic fibrosis and malnutrition, mainly because of the higher energy needs combined with lower intake. There is also a well-established correlation between good nutritional status and better lung function. To date, however, there are no studies examining nutritional status in childhood and adult lung function. To respond to this need, this innovative study explored the long-term correlations between nutritional status in childhood and lung function in adulthood for the same patient population.
METHODS: A retrospective patient file study was conducted to identify putative correlations between nutritional status in childhood and lung function in adulthood. The medical archives at Sheba Medical Center were examined for a period of 31 years between 1986 and 2017 for age, gender, mutations, pancreatic sufficiency or insufficiency (PI/PS), sputum cultures, cystic fibrosis related diabetes, body mass index (BMI) at the age of 10, and FEV1 at 20 and 30 in patients who underwent or did not undergo lung transplantation.
RESULTS: The database was composed of the records of sixty-five patients, thirteen of whom underwent lung transplantation. The correlations (R²) between BMI at age of 10 years and FEV1 at the age of 20 and 30 years were 0.35 and 0.28, respectively, p < 0.001. A BMI of lower than - 0.75 at the age of 10 emerged as a risk factor for lung transplantation (OR 3.42 p = 0.023) and had a negative predictive value of 90%. Kaplan-Meier survival curve showed significant lower lung transplantation rate in the group of BMI z score higher than - 0.75 at the age of 10 years. Logistic regression found nutritional at the age of 10 years as a dominant risk factor for lung transplantation.
CONCLUSIONS: This study reports a clear, significant and important correlation for the first time between nutritional status in childhood and lung function for the same patients at adulthood. Hence, nutritional status sets a clear trajectory and should be treated aggressively. The findings emphasize the importance of new-born screening and early implementation of nutritional guidelines for cystic fibrosis patients.

Entities:  

Keywords:  Body mass index; Cystic fibrosis; Lung function; Lung transplantation; Nutrition

Mesh:

Year:  2019        PMID: 30887107     DOI: 10.1007/s00408-019-00218-3

Source DB:  PubMed          Journal:  Lung        ISSN: 0341-2040            Impact factor:   2.584


  8 in total

1.  Nutritional status and lung function in children with pancreatic-sufficient cystic fibrosis.

Authors:  Ankitha Madde; William Okoniewski; Don B Sanders; Clement L Ren; Daniel J Weiner; Erick Forno
Journal:  J Cyst Fibros       Date:  2021-12-28       Impact factor: 5.527

2.  Nutritional status and lung transplantation: an intriguing problem.

Authors:  Mario Nosotti; Michele Ferrari
Journal:  Ann Transl Med       Date:  2020-02

3.  Gastrointestinal Factors Associated With Hospitalization in Infants With Cystic Fibrosis: Results From the Baby Observational and Nutrition Study.

Authors:  Meghana Sathe; Rong Huang; Sonya Heltshe; Alexander Eng; Elhanan Borenstein; Samuel I Miller; Lucas Hoffman; Daniel Gelfond; Daniel H Leung; Drucy Borowitz; Bonnie Ramsey; A Jay Freeman
Journal:  J Pediatr Gastroenterol Nutr       Date:  2021-09-01       Impact factor: 3.288

4.  Outcomes of Children With Cystic Fibrosis Admitted to PICUs.

Authors:  Michael A Smith; Meghan E McGarry; Ngoc P Ly; Matt S Zinter
Journal:  Pediatr Crit Care Med       Date:  2020-10       Impact factor: 3.971

5.  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

Review 6.  Nutrition in Cystic Fibrosis-Some Notes on the Fat Recommendations.

Authors:  Birgitta Strandvik
Journal:  Nutrients       Date:  2022-02-18       Impact factor: 5.717

7.  Decreased Wait Time and Increased Satisfaction With Bedside Pancreatic Enzyme Dosing for the Inpatient Adolescent With Cystic Fibrosis: A Quality Improvement Project Comparing Enzyme Self-Administration to Nurse Administration.

Authors:  Brandi Middour-Oxler; Margaret Gettis; Betsy Dye
Journal:  J Patient Exp       Date:  2021-01-12

Review 8.  What Do We Know about the Microbiome in Cystic Fibrosis? Is There a Role for Probiotics and Prebiotics?

Authors:  Josie M van Dorst; Rachel Y Tam; Chee Y Ooi
Journal:  Nutrients       Date:  2022-01-22       Impact factor: 5.717

  8 in total

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