What does a median liver stiffness of 6.02 kPa indicate?

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Last updated: October 22, 2025View editorial policy

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Interpretation of Liver Stiffness Measurement of 6.02 kPa

A median liver stiffness of 6.02 kPa indicates normal or minimal fibrosis and is below the threshold for significant liver disease or advanced fibrosis in most clinical contexts. 1

Understanding Liver Stiffness Measurements

  • Liver stiffness measurement (LSM) using transient elastography (FibroScan®) is a non-invasive method to assess liver fibrosis and is considered an excellent surrogate marker for advanced fibrosis and cirrhosis 1
  • Values below 6 kPa are generally considered normal and typically exclude ongoing significant liver disease 1
  • At 6.02 kPa, this measurement falls just slightly above the normal range but well below clinically significant thresholds for advanced fibrosis or cirrhosis 1

Clinical Significance by Disease Etiology

Hepatitis C

  • For patients with hepatitis C, the American Gastroenterological Association (AGA) recommends a cutoff of 12.5 kPa for diagnosing cirrhosis 2
  • A value of 6.02 kPa is significantly below this threshold, suggesting absence of cirrhosis in HCV patients 2

Hepatitis B

  • In chronic hepatitis B, the AGA suggests a cutoff of 11.0 kPa to detect cirrhosis 2
  • A measurement of 6.02 kPa is well below this threshold, indicating absence of cirrhosis in HBV patients 2

Alcoholic Liver Disease

  • For alcoholic liver disease, a cutoff of 12.5 kPa is used to diagnose cirrhosis 2
  • At 6.02 kPa, this value suggests minimal to no fibrosis in patients with alcoholic liver disease 2

Autoimmune Hepatitis

  • In autoimmune hepatitis patients achieving biochemical remission, an average liver stiffness of 6.4 ± 3.2 kPa has been observed 2
  • A value of 6.02 kPa is consistent with well-controlled disease in autoimmune hepatitis patients 2

Reliability Considerations

  • For accurate interpretation, the reliability of the measurement should be assessed 3
  • Reliable liver stiffness evaluations typically require:
    • ≥10 valid measurements
    • ≥60% success rate
    • Interquartile range/median ratio (IQR/M) ≤0.30 3
  • A measurement with IQR/M ≤0.10 would be considered "very reliable" 3

Factors That May Influence Liver Stiffness Values

  • Gender: Men typically have higher baseline liver stiffness values than women (5.81±1.54 vs 5.23±1.59 kPa in healthy subjects) 4
  • BMI: Subjects with BMI>30 kg/m² tend to have higher liver stiffness values (6.26±1.89 vs 5.37±1.51 kPa) 4
  • Metabolic syndrome: Can independently increase liver stiffness values (6.51±1.64 vs 5.33±1.51 kPa) 4
  • Acute inflammation, congestion, or cholestasis can falsely elevate liver stiffness measurements 1

Prognostic Implications

  • Patients with liver stiffness <10 kPa have a very low risk of liver-related complications 5
  • A value of 6.02 kPa suggests excellent prognosis regarding risk of decompensation or mortality 5
  • For patients with compensated cirrhosis, higher values (≥22 kPa) would indicate increased risk of decompensation 6

Clinical Recommendations

  • A liver stiffness of 6.02 kPa does not require specific hepatology follow-up for fibrosis concerns if other clinical parameters are normal 1
  • If the measurement was obtained during monitoring of known liver disease, this value suggests stable or improved liver health 5
  • Any underlying risk factors for liver disease (alcohol use, metabolic syndrome, viral hepatitis) should still be addressed despite the reassuring liver stiffness value 4

Common Pitfalls to Avoid

  • Do not interpret liver stiffness in isolation; always consider clinical context, laboratory values, and imaging findings 2
  • Acute hepatitis, alcohol consumption within 24 hours, or right heart failure can falsely elevate liver stiffness measurements 1
  • Technical limitations may affect accuracy, particularly in obese patients where failure rates increase significantly with BMI >40 kg/m² 4

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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