Sucrose intolerance: Difference between revisions
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{{Short description|Overview of sucrose intolerance}} | {{Short description|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. | '''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.