Quality of life in children with celiac disease: A paediatric cross-sectional study
Chiara Biagetti1, Rosaria Gesuita2, Simona Gatti1
1Department of Pediatrics, Università Politecnica delle Marche, Ancona, Italy.
Insights
Children with celiac disease generally have good quality of life on a gluten-free diet. However, co-morbidities and dietary challenges can negatively impact their well-being.
Area of Science:
- Pediatric gastroenterology
- Child psychology
- Dietary science
Background:
- Limited research exists on factors affecting the quality of life for children with celiac disease adhering to a gluten-free diet.
- Understanding these factors is crucial for improving patient outcomes.
Purpose of the Study:
- To assess the psycho-physical well-being of children with celiac disease on a gluten-free diet.
- To identify specific challenges impacting their quality of life.
Main Methods:
- Cross-sectional study involving 76 celiac and 143 non-celiac children (aged 2-18).
- Utilized the Pediatric Quality of Life Inventory Test and an open-ended questionnaire on social impact.
- Statistical analysis included Wilcoxon rank-sum test and quantile regression.
Main Results:
- No significant overall difference in quality of life scores between celiac and non-celiac children.
- Gluten-free diet positively influenced quality of life in children with "intermediate" scores.
- Lower quality of life scores correlated with higher reported diet difficulties and co-morbidities.
Conclusions:
- Celiac children generally exhibit good quality of life compared to controls.
- Co-morbidities and difficulties managing the gluten-free diet are key factors reducing quality of life in celiac children.
- Targeted interventions addressing these specific challenges can further enhance well-being.
Background:
Few studies investigated factors influencing the quality of life of children with celiac disease on a gluten-free diet.
Aims:
To investigate the impact of the gluten-free diet on the psycho-physical well-being of celiac children.
Methods:
In this cross-sectional study, we interviewed 76 celiac and 143 non-celiac children (2-18 years) by using a non-disease specific questionnaire (Pediatric Quality of Life Inventory Test) and we explored the impact of the diet on social life with an open-ended questionnaire. Scores were compared by Wilcoxon rank-sum test. A quantile regression analysis was used to evaluate the impact of celiac disease on score distribution.
Results:
No significant differences in quality of life were found between the two groups (total score: 84.1 (81.1-87.2) vs 81.5 (79.7-83.4), median (95% CI), patients and controls respectively, p=0.4). Treatment positively affected quality of life in children that showed "intermediate" scores in the Pediatric Quality of Life Inventory Test. Lowest scores were observed in children reporting a higher number of diet difficulties or co-morbidities.
Conclusions:
Although celiac patients showed an overall good quality of life in comparison with a control group, by using appropriate analytical methods we elicited specific factors contributing to a lower quality of life in patients, such as co-morbidities and difficulties with the diet.
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