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Measuring Oral Fatty Acid Thresholds, Fat Perception, Fatty Food Liking, and Papillae Density in Humans
Published on: June 4, 2014
Oral fructose absorption in obese children with non-alcoholic fatty liver disease
1Section of Pediatric Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Digestive Health Institute, Children's Hospital Colorado, University of Colorado School of Medicine, Aurora, CO, USA.
Insights
Children with non-alcoholic fatty liver disease (NAFLD) show enhanced fructose absorption and metabolism compared to lean individuals. This is linked to a worsened metabolic profile after fructose consumption.
Area of Science:
- Pediatric Gastroenterology and Hepatology
- Metabolic Disorders
- Nutritional Science
Background:
- Fructose consumption is a known risk factor for developing non-alcoholic fatty liver disease (NAFLD).
- Understanding fructose metabolism is crucial for managing pediatric NAFLD.
- This study investigates differences in fructose handling in children with and without NAFLD.
Purpose of the Study:
- To quantify and compare the absorption and metabolic processing of fructose in children diagnosed with NAFLD.
- To evaluate these parameters against those in both obese and lean control groups.
- To identify potential metabolic alterations related to fructose in pediatric NAFLD.
Main Methods:
- A cohort of children with confirmed NAFLD, along with obese and lean controls, ingested a standardized oral fructose dose.
- Serum and urine samples were collected at intervals up to 360 minutes post-ingestion to measure glucose, insulin, uric acid, and fructose levels.
- Breath hydrogen levels were also monitored as an indicator of carbohydrate absorption.
Main Results:
- Children with NAFLD exhibited higher serum glucose, insulin, and uric acid levels compared to lean controls post-fructose intake.
- NAFLD patients showed significantly lower urinary fructose excretion and breath hydrogen production compared to lean controls.
- When compared to obese controls, NAFLD patients had elevated serum uric acid and reduced urinary fructose excretion, with similar glucose, insulin, and breath hydrogen responses.
Conclusions:
- Children diagnosed with NAFLD demonstrate a more efficient absorption and metabolism of fructose compared to their lean counterparts.
- This enhanced fructose processing in pediatric NAFLD is associated with a more pronounced adverse metabolic response following fructose ingestion.
- Findings suggest altered fructose metabolism contributes to the pathophysiology of NAFLD in children.
Background:
Fructose intake is associated with non-alcoholic fatty liver disease (NAFLD) development.
Objective:
The objective of this study was to measure fructose absorption/metabolism in paediatric NAFLD compared with obese and lean controls.
Methods:
Children with histologically proven NAFLD, and obese and lean controls received oral fructose (1 g kg(-1) ideal body weight). Serum glucose, insulin, uric acid, and fructose, urine uric acid, urine fructose, and breath hydrogen levels were measured at baseline and multiple points until 360 min after fructose ingestion.
Results:
Nine NAFLD (89% Hispanic, mean age 14.3 years, mean body mass index [BMI] 35.3 kg m(-2)), six obese controls (67% Hispanic, mean age 12.7 years, mean BMI 31.0 kg m(-2)) and nine lean controls (44% Hispanic, mean age 14.3 years, mean BMI 19.4 kg m(-2)) were enrolled. Following fructose ingestion, NAFLD vs. lean controls had elevated serum glucose, insulin and uric acid (P < 0.05), higher urine uric acid (P = 0.001), but lower fructose excretion (P = 0.002) and lower breath hydrogen 180-min AUC (P = 0.04). NAFLD vs. obese controls had similar post-fructose serum glucose, insulin, urine uric acid and breath hydrogen, but elevated serum uric acid (P < 0.05) and lower urine fructose excretion (P = 0.02).
Conclusions:
Children with NAFLD absorb and metabolize fructose more effectively than lean subjects, associated with an exacerbated metabolic profile following fructose ingestion.
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