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Diagnostic value of sucrose tolerance test in children evaluated by breath hydrogen measurement

Insights

Congenital sucrase-isomaltase deficiency is rare in children with digestive issues. The oral sucrose tolerance test is not recommended for screening secondary disaccharidase deficiencies.

Area of Science:

  • Pediatric Gastroenterology
  • Nutritional Science
  • Clinical Diagnostics

Background:

  • Episodic diarrhea and abdominal pain are common in children.
  • Disaccharide malabsorption, such as lactose intolerance, is a frequent cause.
  • Congenital sucrase-isomaltase deficiency is a rare genetic disorder affecting sucrose digestion.

Purpose of the Study:

  • To evaluate the utility of the oral sucrose tolerance test (OSTT) in diagnosing sucrose malabsorption in children presenting with gastrointestinal symptoms.
  • To compare the diagnostic performance of OSTT with the lactose tolerance test (LTT) in this pediatric population.
  • To determine the incidence of sucrose malabsorption in children with unexplained episodic diarrhea and/or abdominal pain.

Main Methods:

  • 103 children (3 months–15 years) with episodic diarrhea/abdominal pain underwent OSTT.
  • Expired hydrogen levels were measured to assess sucrose malabsorption.
  • Results were compared with a previously established LTT incidence in the same cohort.
  • Blood glucose response during both tests was analyzed.

Main Results:

  • Only 3 children (1%) exhibited sucrose malabsorption, diagnosed as congenital sucrase-isomaltase deficiency.
  • This incidence is significantly lower than lactose malabsorption (33%).
  • OSTT showed a higher mean blood glucose rise and fewer false flat curves compared to LTT, indicating better diagnostic accuracy for sucrase deficiency.

Conclusions:

  • Congenital sucrase-isomaltase deficiency is uncommon in children with these symptoms.
  • The OSTT is not a suitable screening tool for secondary disaccharidase deficiencies in pediatric patients.
  • Lactose malabsorption is a more prevalent issue in this symptomatic pediatric group.

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