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Diseases

Evaluation of liver dysfunction

OVERVIEW

  • Summary
  • Urgent Considerations
  • Etiology

DIAGNOSIS

  • Differential Diagnosis
  • Diagnostic Approach

IMAGES

  • Library

REFERENCES

  • Citations
  • Credits

Summary

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Liver blood tests are routinely used in diagnosis and management of hepatobiliary disease. Abnormal liver blood test results are often the first indicator of hepatobiliary disease and a common indication for abdominal imaging with ultrasound, computed tomography, or magnetic resonance imaging.[1]​ Serum liver chemistry tests, commonly called liver tests, or (mistakenly) liver function tests, are ordered for many reasons. Most laboratories offer these tests as a bundle, and this usually includes:
  • Bilirubin (breakdown product of red blood cells after conjugation in the liver and secretion in biliary system excretion)

  • Alanine aminotransferase (ALT)

  • Alkaline phosphatase (ALP)

  • Serum albumin.

The following tests may also be included in this bundle:
  • Aspartate aminotransferase (AST)

  • Gamma glutamyl transferase (gamma-GT)

  • Lactate dehydrogenase.

Individual tests in these panels are not specific for liver disease. Therefore, pattern recognition is critical. Evaluation of patients with abnormal liver tests should be guided by history, risk for liver disease, duration and severity of clinical findings, presence of comorbidities and symptoms, the nature of the liver test abnormality noted, and relevant scans and biopsies.[2]​
Traditionally, liver test abnormalities have been grouped under the following patterns:[3]
  • Hepatocellular (predominantly ALT and AST elevations)

  • Cholestatic (predominantly ALP elevation)

  • Mixed/infiltrative (elevation of both ALT/AST and ALP).

Isolated elevation of liver tests is a less common occurrence in liver diseases, and a nonhepatic source should be considered in such instances. Bilirubin may be elevated in any category of liver disease.[4] Isolated gamma-GT elevations are so common and so often unhelpful that many institutions have chosen to delete this test from their liver test panel.[5] When other liver tests are abnormal, categorization according to pattern is helpful to determine the probable etiology.
Clinical correlation is essential when interpreting liver tests. Liver tests are abnormally elevated in 1% to 9% of the asymptomatic population.[6] Further investigations with diagnostic serology and liver biopsy are normal in 6% of these patients.[7] Importantly, people with chronic liver disease or cirrhosis may have normal liver tests.[8] [9]
Liver tests are markers of liver injury, not liver function.[3] Functional assessment of the liver (evaluation of protein synthesis, metabolism, bile production, storage, and detoxification) can be determined by:
  • Conventional liver tests such as albumin and international normalized ratio

  • Scoring systems such as Model for End-Stage Liver Disease and Child-Turcotte-Pugh score, based on laboratory test results and clinical features.

content by BMJ Group
Last updated

Library

  • Eye demonstrating Kayser-Fleischer ring

    Eye demonstrating Kayser-Fleischer ring

  • Possible diagnosis for underlying cause of different patterns of liver test abnormalities

    Possible diagnosis for underlying cause of different patterns of liver test abnormalities

  • Dupuytren contracture

    Dupuytren contracture

  • Acanthosis nigricans involving the axilla of an obese white woman

    Acanthosis nigricans involving the axilla of an obese white woman

  • Plantar ulcer in a patient with type 1 diabetes

    Plantar ulcer in a patient with type 1 diabetes

  • Characteristic autoantibody patterns in primary biliary cholangitis. White arrow: antimitochondrial

    Characteristic autoantibody patterns in primary biliary cholangitis. White arrow: antimitochondrial staining; red arrow: multiple nuclear dot ANA staining

  • Typical ERCP findings in a patient with primary sclerosing cholangitis: multifocal strictures of the

    Typical ERCP findings in a patient with primary sclerosing cholangitis: multifocal strictures of the intra- and extrahepatic bile ducts

Citations

    Key Articles

    • Kwo PY, Cohen SM, Lim JK. ACG clinical guideline: evaluation of abnormal liver chemistries. Am J Gastroenterol. 2017 Jan;112(1):18-35.[Abstract]

    • Crabb DW, Im GY, Szabo G, et al. Diagnosis and treatment of alcohol-associated liver diseases: 2019 practice guidance from the American Association for the Study of Liver Diseases. Hepatology. 2020 Jan;71(1):306-33.[Full Text]

    • Jophlin LL, Singal AK, Bataller R, et al. ACG clinical guideline: alcohol-associated liver disease. Am J Gastroenterol. 2024 Jan 1;119(1):30-54.[Abstract][Full Text]

    • Fontana RJ, Liou I, Reuben A, et al. AASLD practice guidance on drug, herbal, and dietary supplement-induced liver injury. Hepatology. 2023 Mar 1;77(3):1036-65.[Full Text]

    • Rinella ME, Neuschwander-Tetri BA, Siddiqui MS, et al. AASLD practice guidance on the clinical assessment and management of nonalcoholic fatty liver disease. Hepatology. 2023 May 1;77(5):1797-835.[Full Text]

    Other Online Resources

    • The Center for Quality Assessment and Improvement in Mental Health: AUDIT-C overview
    • FDA: acetylcysteine/interpretation of acetaminophen assays
    • American Association of Poison Control Centers

    Referenced Articles

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