Skip to content

Medical Disclaimer: For reference only; may contain errors. Reconfirm with a qualified physician before clinical use. Report an error

MEDICAL CALCULATOR

FIB-4 Index Calculator — Liver Fibrosis Score (HCV, HBV, NAFLD/MASLD)

Free FIB-4 Index calculator for liver fibrosis staging. Non-invasive score using Age, AST, ALT, and platelet count. Validated for HCV, HBV, NAFLD/MASLD. Instant interpretation with F-stage and biopsy guidance.

Free to useClinical decision supportMobile friendly
By Dr. Diamond, MBBS, AFIH · Hepatology
📊 FIB-4 CalculatorHepa Panel
HCV · HBV · NAFLD/MASLDMETAVIR F0–F4 StagingBiopsy GuidanceAASLD / EASL EndorsedNo Login · Free Forever

Normal: 150–400 ×10⁹/L

Aspartate aminotransferase · Normal: 10–40 U/L

Alanine aminotransferase · Normal: 7–56 U/L

📋 Contents — tap to expand
👨‍⚕️
Dr. Diamond, MBBS, AFIH

Medical Officer, AAC Clinic Punjab

1FIB-4 Score Interpretation

The following cutoffs apply to adults with known or suspected chronic liver disease (HCV, HBV, NAFLD/MASLD). Scores in the indeterminate range (1.30–2.67) require additional investigation.

FIB-4 ScoreRisk CategoryFibrosis StageNPV / PPVClinical Action
< 1.30🟢 Low RiskF0–F1 (Mild)NPV ~90%Biopsy can be deferred. Monitor annually with LFTs + repeat FIB-4.
1.30–2.67🔵 IndeterminateF1–F3 (Variable)—Additional testing needed — FibroScan, NAFLD Fibrosis Score, APRI, or liver biopsy.
> 2.67🔴 High RiskF3–F4 (Advanced)PPV ~65%Refer to hepatologist. Consider biopsy to confirm cirrhosis; HCC surveillance if cirrhosis.

⚠️ Age Caveat (important in Indian practice)

FIB-4 is less reliable in patients aged <35 years (may underestimate fibrosis) and >65 years (may overestimate due to age-related thrombocytopenia). For older patients, some authorities use a modified low-risk cutoff of <2.0 instead of <1.30.

2Formula & Variables

// FIB-4 Index (Sterling et al., 2006)
FIB-4 = ( Age [yr] × AST [U/L] ) ÷ ( Platelets [10⁹/L] × √ALT [U/L] )

// Variables:
  Age → Patient age in years
  AST → Aspartate aminotransferase (U/L)
  ALT → Alanine aminotransferase (U/L)
  Platelets → Platelet count (×10⁹/L; i.e. thousands/µL)

// Cutoffs (validated): Low <1.30 · Indeterminate 1.30–2.67 · High >2.67

All four variables are available from a routine complete blood count (CBC) and liver function test (LFT) panel — no additional tests are required. Enter AST and ALT in U/L (not IU/L — they are equivalent). Platelet count must be in ×10⁹/L (same as 10³/µL or thousands/µL as reported in most Indian lab reports).

3What Is the FIB-4 Index?

The FIB-4 (Fibrosis-4) Index is a validated, non-invasive scoring system that estimates the degree of liver fibrosis without the need for a liver biopsy. Originally developed in 2006 by Sterling et al. for HIV/HCV co-infected patients, it has since been validated extensively for:

  • Chronic Hepatitis C (HCV)
  • Chronic Hepatitis B (HBV)
  • NAFLD / MASLD (Metabolic dysfunction-Associated Steatotic Liver Disease)
  • Alcoholic liver disease
  • Post-treatment response monitoring in HCV after direct-acting antivirals (DAAs)

FIB-4 combines four routinely available parameters — Age, AST, ALT, and Platelet count — into a single number that correlates with hepatic fibrosis stage on liver biopsy (METAVIR scale F0–F4). It is endorsed by the AASLD, EASL, and increasingly by Indian hepatology practice guidelines.

Why FIB-4 Matters in India

India bears a significant burden of chronic liver disease, with HBV affecting an estimated 40 million and HCV affecting 6–12 million individuals. MASLD prevalence is rising with the epidemic of obesity and type 2 diabetes. Liver biopsy — the traditional gold standard for fibrosis staging — is invasive, costly, subject to sampling error, and impractical for population-level screening. FIB-4 provides an accessible, cost-effective first-line fibrosis assessment that can be calculated from a standard CBC and LFT — tests already ordered in most outpatient and inpatient encounters.

4When to Use FIB-4

✅ Appropriate Use
  • Initial fibrosis assessment in newly diagnosed HCV, HBV
  • Screening for advanced fibrosis in NAFLD/MASLD before FibroScan
  • Post-DAA SVR monitoring in HCV
  • Risk stratification in primary care before hepatology referral
  • Avoiding unnecessary liver biopsy in low-risk patients (<1.30)
⛔ Limitations / Not Ideal
  • Age <35 or >65 years (unreliable; use with caution)
  • Acute hepatitis (AST/ALT spuriously high)
  • Immune thrombocytopenia or other causes of low platelets unrelated to portal hypertension
  • Haemolysis (falsely elevated AST)
  • Active myositis / strenuous exercise (elevated AST)
  • Not validated for autoimmune hepatitis, PBC, PSC

5FIB-4 in NAFLD / MASLD

MASLD (formerly NAFLD) has emerged as the most common chronic liver disease globally, affecting ~25–38% of adults in India. Identifying patients with significant fibrosis (F≥2) is critical because advanced fibrosis — not steatosis or NASH activity — is the primary driver of liver-related mortality in MASLD.

The AASLD 2023 and EASL 2024 MASLD guidelines recommend using FIB-4 as the initial non-invasive test in all patients with suspected MASLD:

  • FIB-4 <1.30: Reassure patient; manage metabolic risk factors; repeat FIB-4 in 1–2 years.
  • FIB-4 1.30–2.67: Indeterminate — proceed to vibration-controlled transient elastography (FibroScan) or ELF (Enhanced Liver Fibrosis) test.
  • FIB-4 >2.67: High likelihood of advanced fibrosis — refer to hepatologist for further workup and HCC surveillance consideration.

FIB-4 performs slightly less well in MASLD than in viral hepatitis (AUROCs of 0.76–0.82 for F≥3 detection), partly because metabolic inflammation causes AST/ALT elevation that may inflate the score independently of fibrosis. However, it remains the most practical initial gating tool.

6FIB-4 vs Other Non-Invasive Tests

TestVariablesBest Used ForAvailability in India
FIB-4Age, AST, ALT, PlateletsHCV, HBV, NAFLD — initial screen✅ Free (routine labs)
APRIAST, PlateletsHCV — WHO-endorsed in low-resource settings✅ Free (2 parameters)
NAFLD Fibrosis ScoreAge, BMI, IFG, AST, ALT, Platelets, AlbuminNAFLD/MASLD — more variables, higher accuracy✅ Free (calculated)
FibroScan (LSM)Liver stiffness (kPa)All chronic liver diseases — gold standard non-invasive⚠️ Tertiary centres; ₹3,000–8,000
ELF TestHA, PIIINP, TIMP-1MASLD — regulatory approved❌ Rarely available in India
Liver BiopsyHistologyGold standard — confirms stage⚠️ Available; invasive; ₹5,000–20,000+

7Clinical Workflow: How to Use This Score

  1. Order baseline labs — CBC (for platelet count) + LFT (AST, ALT) if not already available. These are available in any NABL-accredited lab at ₹200–500.
  2. Enter values into this calculator and note the FIB-4 score.
  3. If FIB-4 <1.30: Reassure patient; address underlying cause (antiviral therapy for HCV/HBV, metabolic management for MASLD); repeat FIB-4 in 12 months.
  4. If FIB-4 1.30–2.67: Refer for FibroScan (if available) or hepatology consultation. Consider NAFLD Fibrosis Score as complementary tool.
  5. If FIB-4 >2.67: High priority hepatology referral. Discuss liver biopsy vs. elastography. Begin HCC surveillance (6-monthly USG abdomen ± AFP) if cirrhosis is confirmed or strongly suspected.

For HCV patients post-SVR: FIB-4 improves significantly after sustained virological response (SVR) with DAAs but may remain elevated if cirrhosis was already established. A FIB-4 >2.0 at 12 weeks post-SVR warrants continued HCC surveillance regardless of symptom resolution.

8Frequently Asked Questions

📋
Key takeaway:

The FIB-4 index uses routine age, liver enzymes, and platelet count to non-invasively stratify liver fibrosis risk in HCV, HBV, and NAFLD/MASLD, helping defer unnecessary biopsies in low-risk patients.

Related Calculators

⚠️ Clinical Disclaimer: The FIB-4 Index calculator is intended as a clinical decision-support aid for qualified healthcare professionals and medical students. It does not replace clinical judgment, full history and examination, or specialist evaluation. FIB-4 is a screening tool — it should not be used as the sole basis for patient management decisions. Scores in the indeterminate range require further investigation. Always interpret results within the full clinical context. Not intended for patient self-diagnosis. Validated for adults (18–75 years); exercise caution outside this range.