Sucrose intolerance

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Overview of sucrose intolerance


Classification
External resources


Overview[edit | edit source]

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Chemical structure of sucrose

Sucrose intolerance, also known as congenital sucrase-isomaltase deficiency (CSID), is a condition where an individual lacks the enzyme needed to digest sucrose, a common sugar found in many foods. This enzyme deficiency leads to gastrointestinal symptoms when sucrose is consumed.

Pathophysiology[edit | edit source]

Sucrose intolerance is caused by a deficiency in the enzyme sucrase-isomaltase, which is responsible for breaking down sucrose into glucose and fructose. This enzyme is located on the brush border of the small intestine. When sucrase-isomaltase is deficient or absent, sucrose cannot be properly digested, leading to symptoms such as diarrhea, abdominal pain, and bloating.

Symptoms[edit | edit source]

The symptoms of sucrose intolerance can vary in severity and may include:

  • Chronic diarrhea
  • Abdominal pain and cramping
  • Bloating and gas
  • Nausea
  • Vomiting

These symptoms typically occur after the ingestion of foods containing sucrose.

Diagnosis[edit | edit source]

Diagnosis of sucrose intolerance can be challenging and often involves a combination of dietary history, symptom assessment, and diagnostic tests. Common diagnostic methods include:

  • Breath hydrogen test: Measures hydrogen in the breath after ingestion of sucrose.
  • Sucrose tolerance test: Monitors blood glucose levels after sucrose ingestion.
  • Genetic testing: Identifies mutations in the sucrase-isomaltase gene.

Management[edit | edit source]

Management of sucrose intolerance primarily involves dietary modification to limit or avoid sucrose intake. Patients may benefit from:

  • Sucrose-free diet: Avoiding foods high in sucrose such as sweets, certain fruits, and processed foods.
  • Enzyme replacement therapy: Use of enzyme supplements to aid in the digestion of sucrose.

Prognosis[edit | edit source]

With appropriate dietary management and enzyme supplementation, individuals with sucrose intolerance can lead normal, healthy lives. Early diagnosis and intervention are crucial to prevent complications and improve quality of life.

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