What is the treatment for Gilbert's syndrome?

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Gilbert's Syndrome Treatment

Gilbert's syndrome does not require any therapeutic intervention as it is a benign condition characterized by mild, chronic unconjugated hyperbilirubinemia. 1

Understanding Gilbert's Syndrome

Gilbert's syndrome is a hereditary condition caused by a mutation in the UDP glucuronosyltransferase enzyme that conjugates bilirubin with glucuronic acid, resulting in reduced enzyme activity (approximately 30% of normal levels). 2, 1 This leads to:

  • Mild unconjugated hyperbilirubinemia
  • Normal liver enzyme values
  • No signs of hemolysis or liver disease

Diagnosis

The diagnosis of Gilbert's syndrome can be established with relative certainty based on:

  • Mild hyperbilirubinemia with a high fraction of unconjugated bilirubin
  • Normal values of liver enzymes
  • No overt signs of hemolysis 3

Diagnostic tests that may be used to confirm Gilbert's syndrome include:

  1. Caloric restriction test: Fasting increases unconjugated bilirubin levels significantly more in patients with Gilbert's syndrome than in normal subjects 3, 2
  2. Rifampicin test: A non-invasive diagnostic tool that helps confirm Gilbert's syndrome 2

Important note: Liver biopsy is not mandatory or recommended for diagnosing Gilbert's syndrome. 3

Management Approach

Since Gilbert's syndrome is a benign condition, the management focuses on:

  1. Patient education and reassurance about the benign nature of the condition
  2. No specific treatment is required for Gilbert's syndrome itself 1
  3. Avoidance of triggering factors that may exacerbate hyperbilirubinemia:
    • Prolonged fasting
    • Dehydration
    • Intercurrent illness
    • Excessive physical exertion

Special Considerations

  • Medication metabolism: Patients with Gilbert's syndrome may have altered metabolism of certain drugs due to the reduced UDP-glucuronosyltransferase activity 4
  • Stress-induced exacerbations: Conditions related to fasting, stress, or comorbidities might reveal the disease in previously asymptomatic individuals 5
  • Protective effects: Recent research suggests that mild hyperbilirubinemia may have protective antioxidant effects against various oxidative stress-mediated diseases 1

Differential Diagnosis

It's important to differentiate Gilbert's syndrome from more serious conditions that cause hyperbilirubinemia:

  • Hemolytic disorders
  • Viral hepatitis
  • Drug-induced liver injury
  • Other hereditary hyperbilirubinemia syndromes (Crigler-Najjar, Dubin-Johnson, Rotor syndrome) 4

The correct diagnosis of Gilbert's syndrome is crucial to avoid unnecessary invasive procedures for suspected more severe hepatobiliary disease.

References

Research

[Gilbert's syndrome--myths and reality].

Casopis lekaru ceskych, 2004

Research

Two easy-to-perform diagnostic tests for Gilbert's syndrome.

Zhonghua yi xue za zhi = Chinese medical journal; Free China ed, 2002

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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