Early Life Nutrition: The First 1000 Days and Healthy Aging in Cystic Fibrosis
Caitlin N Miles1,2,3,4, Gillian M Nixon3,4, Zoe E Davidson1,4
1Department of Nutrition, Dietetics and Food, Monash University, Melbourne, VIC 3168, Australia.
Optimal nutrition in the first 1000 days is crucial for children with cystic fibrosis (CF) to ensure lifelong health. Early interventions can mitigate complications and improve growth trajectories for cystic fibrosis patients.
Area of Science:
- Pediatric Nutrition
- Cystic Fibrosis Research
- Developmental Health
Background:
- Optimal nutritional status within the first 1000 days is critical for children with cystic fibrosis (CF).
- The 'first 1000 days' framework highlights the lifelong impact of early environmental, sociocultural, and nutritional exposures.
- CF presents unique nutritional challenges during this critical developmental window, impacting growth and overall health.
Purpose of the Study:
- To explore early CF disease manifestations and their effects on early life growth and nutrition.
- To examine early life nutrition in CF through the lens of established frameworks like 'the first 1000 days' and 'developmental origins of health and disease'.
- To inform a nuanced and personalized approach to lifelong nutritional care for people with CF.
Main Methods:
- Literature review focusing on early disease manifestations in CF.
- Analysis of the impact of these manifestations on early growth and nutrition.
- Theoretical consideration of early life nutrition in CF using developmental health frameworks.
Main Results:
- Children with CF experience significant nutritional fragility in the first 1000 days due to disease complications.
- Increasing life expectancy and disease-modifying drugs necessitate personalized lifelong nutritional strategies.
- Early nutrition significantly influences pulmonary and extrapulmonary health trajectories in CF.
Conclusions:
- Early nutritional interventions are paramount for optimizing health outcomes in children with CF.
- A personalized approach to nutrition is essential, considering disease progression and new therapies.
- Understanding the developmental origins of health and disease in CF can guide future nutritional care strategies.
More Related Videos
07:38Design and Development of a Model to Study the Effect of Supplemental Oxygen on the Cystic Fibrosis Airway Microbiome
Published on: August 3, 2021
06:57The WinCF Model - An Inexpensive and Tractable Microcosm of a Mucus Plugged Bronchiole to Study the Microbiology of Lung Infections
Published on: May 8, 2017
Related Concept Videos
Cystic Fibrosis: Management
Sinus disease and chronic...
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
Chronic Kidney Disease III: Interprofessional Care
Inflammatory Bowel Disease III: Diagnostic Studies and Management I-Nutritional Therapy
Diagnostic studies
A colonoscopy is the definitive screening test, distinguishing ulcerative colitis from other colon diseases with similar symptoms. During a colonoscopy test, inflamed mucosa with exudate ulcerations can be observed, and biopsies are taken to determine the histologic characteristics of the...
Lifestyle Factors and Health
Benefits of Physical Activity
Physical activity, whether through structured exercise or casual activities like walking, biking, or dancing, is a cornerstone of a...
The Effect of Aging on Tissues
