Sources of Elevated SGOT/AST, PT, and ALP
Understanding the Enzyme Sources
ALT (SGOT) is the most liver-specific enzyme, while AST, PT, and ALP have multiple extrahepatic sources that must be considered when evaluating abnormal liver function tests. 1
ALT/SGOT Sources and Specificity
- ALT is highly specific for liver injury because it is primarily concentrated in liver tissue with minimal presence in other organs 1, 2
- ALT has low concentrations in skeletal muscle and kidney, making elevations strongly indicative of hepatocellular damage 1
- Normal ALT ranges are sex-specific: 29-33 IU/L for men and 19-25 IU/L for women 1, 2
AST Sources (Less Liver-Specific)
- AST is significantly less liver-specific than ALT because it is present in multiple tissues 2
- AST is found in cardiac muscle, skeletal muscle, kidneys, brain, and red blood cells 1, 2
- Extrahepatic causes of AST elevation include:
PT (Prothrombin Time) Sources
- PT reflects hepatic synthetic function rather than hepatocellular injury 1
- PT is prolonged when liver synthetic capacity is impaired, indicating advanced liver disease 1
- Non-hepatic causes of prolonged PT include:
ALP (Alkaline Phosphatase) Sources
- ALP is primarily elevated in cholestatic disorders but has significant extrahepatic sources 1
- Hepatic sources: Biliary obstruction, cholestasis, infiltrative liver disease 1
- Extrahepatic sources of ALP elevation include:
Clinical Context: Psoriasis and Seborrheic Dermatitis
Medication-Induced Liver Injury
In patients with scalp psoriasis or seborrheic dermatitis, methotrexate is the most common cause of abnormal liver function tests. 1, 3
- Methotrexate causes hepatotoxicity, fibrosis, and cirrhosis with prolonged use 3
- Acute liver enzyme elevations (ALT/AST) are frequently seen and usually transient 3
- Persistent abnormalities in liver function tests may precede fibrosis or cirrhosis in the rheumatoid arthritis population 3
- 12 of 44 patients (27%) treated with oral methotrexate dropped out due to abnormal liver function tests in one study 1
Systemic Therapy Considerations
- Acitretin causes transaminase elevations in up to 16% of patients and triglyceride elevations in 25-50% 1
- Cyclosporine can cause hepatotoxicity, particularly when combined with other hepatotoxic agents 1
- Alcohol consumption significantly increases hepatotoxicity risk with methotrexate and acitretin 1, 3
Metabolic Syndrome and NAFLD
- Patients with psoriasis have increased prevalence of metabolic syndrome components (obesity, diabetes, hypertension, dyslipidemia) 1
- Non-alcoholic fatty liver disease (NAFLD) is common in this population and presents with AST:ALT ratio <1 2
- Metabolic syndrome increases risk for steatohepatitis, which can elevate liver enzymes independently of psoriasis treatment 1
Diagnostic Algorithm for Abnormal LFTs
Initial Evaluation
- Obtain complete liver panel: ALT, AST, ALP, GGT, total and direct bilirubin, albumin, PT/INR 1, 2
- Check creatine kinase (CK) to exclude muscle injury as source of transaminase elevation 1, 2
- Review all medications against LiverTox® database for hepatotoxic potential 2
- Assess alcohol consumption history (>40g/day for women, >50-60g/day for men) 2
Pattern Recognition
- Hepatocellular pattern: ALT/AST elevation predominates, suggests hepatocyte injury 1
- Cholestatic pattern: ALP elevation predominates, suggests biliary obstruction or cholestasis 1
- Mixed pattern: Both hepatocellular and cholestatic enzymes elevated 1
Common Pitfalls
- Do not assume isolated ALP elevation is hepatic without checking GGT or bone-specific markers 1
- Intensive exercise can cause acute AST/ALT elevations that may be mistaken for liver injury 2
- AST/ALT ratio >2 is highly suggestive of alcoholic liver disease and should prompt detailed alcohol history 2
- Women have lower normal ALT ranges than men, making elevations more significant in female patients 2