Home▸Хронічний вірусний гепатит B та C▸ALT/AST Flare Trend Simulator

🦠 ALT/AST Flare Trend Simulator

A model that simulates the dynamics of liver enzymes (ALT/AST) during an acute flare of chronic hepatitis, visualizing cytolytic waves and their correlation with viral replication activity.

Хронічний вірусний гепатит B та C2DModerate60 FPS
alt-ast-flare-trend-simulator ↗ Open standalone

Baseline Enzymes During Quiescent Chronic Hepatitis

Liver enzymes rest near normal between flares.

  • <40: Normal ALT (male) (U/L upper limit)
  • <38: Normal AST (male) (U/L upper limit)
  • Low: Quiescent viral load (suppressed replication)
  • Steady: Hepatocyte turnover (minimal cell death)

What ALT and AST measure

Both enzymes leak out when liver cells rupture.

Why quiescence happens

Immune control keeps viral replication mostly suppressed.

Monitoring during quiescence

Clinicians still track enzymes for early flare signs.

Viral Replication Activity Begins To Climb

HBV or HCV copies itself faster inside hepatocytes.

  • Log-scale: HBV DNA rise (copies per mL)
  • Log-scale: HCV RNA rise (IU per mL)
  • ~1-2 wk: Enzyme lag time (before injury shows)
  • Activated: Immune sensing (T-cells detect antigen)

Replication precedes injury

Viral load rises before enzymes visibly react.

Triggers for reactivation

Immunosuppression or drug withdrawal can spark replication.

Early warning value

Viral load trends predict the coming enzyme flare.

Hepatocyte Injury From Immune Clearance

Cytotoxic T-cells kill infected liver cells directly.

  • CD8+: Primary killer cell (cytotoxic T-lymphocyte)
  • Apoptosis: Injury mechanism (and necrosis)
  • Rising: Enzyme release (ALT begins climbing)
  • Increasing: Inflammation grade (histologic activity)

Immune-mediated damage

The immune response, not the virus, injures cells.

Cell death releases enzymes

Ruptured hepatocytes spill ALT and AST into blood.

Injury precedes peak flare

Enzyme rise follows injury onset by days.

Enzyme Flare — ALT and AST Spike Sharply

Enzymes surge, reflecting widespread hepatocyte injury.

  • >5×: Flare-level ALT (upper limit normal)
  • >4×: Flare-level AST (upper limit normal)
  • >1: ALT:AST ratio (typical in viral flare)
  • Possible: Symptom onset (fatigue, jaundice)

Peak enzyme magnitude

ALT often rises higher than AST during flares.

Clinical significance

Flares can signal seroconversion or disease progression.

Risk of severe flare

Rare flares trigger acute liver decompensation.

Flare Resolution — Enzymes Decline

Inflammation subsides and enzyme levels fall back.

  • Weeks: Resolution timeframe (to normalize)
  • Falling: Viral load (if immune control wins)
  • Regenerating: Liver architecture (hepatocyte turnover)
  • Possible: Recurrence risk (wave-like pattern repeats)

Enzymes trend downward

ALT and AST gradually return toward baseline.

Outcome depends on control

Successful immune clearance favors lasting remission.

The cycle can repeat

Chronic infection often produces recurring flare waves.

⚙ Under the hood

A model that simulates the dynamics of liver enzymes (ALT/AST) during an acute flare of chronic hepatitis, visualizing cytolytic waves and their correlation with viral replication activity.

CanvasBiomedicine

2D · HTML5 Canvas 2D · 60 FPS target · runs fully client-side, no install

What did you find?

Add reproduction steps (optional)