Sucrose intolerance: Difference between revisions

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{{Short description|Overview of sucrose intolerance}}
{{Short description|Overview of sucrose intolerance}}
== Introduction ==
[[File:Sucrose-inkscape.svg|left|thumb|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.
'''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 ==
== Pathophysiology ==

Latest revision as of 15:48, 12 April 2025

Editor-In-Chief: Prab R Tumpati, MD
Obesity, Sleep & Internal medicine
Founder, WikiMD Wellnesspedia &
W8MD medical weight loss NYC and sleep center NYC

Sucrose intolerance
Synonyms Congenital sucrase-isomaltase deficiency (CSID), sucrase-isomaltase deficiency
Pronounce N/A
Specialty N/A
Symptoms Diarrhea, abdominal pain, bloating, gas
Complications N/A
Onset Childhood
Duration Chronic
Types N/A
Causes Genetic mutation in the sucrase-isomaltase gene
Risks Family history
Diagnosis Breath test, stool acidity test, genetic testing
Differential diagnosis Lactose intolerance, fructose malabsorption, irritable bowel syndrome
Prevention N/A
Treatment Dietary management, enzyme replacement therapy
Medication Sacrosidase
Prognosis N/A
Frequency Rare
Deaths N/A


Overview of sucrose intolerance


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]

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]

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]

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]

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]

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.

See also[edit]