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Serum transaminases during salicylate therapy
British Medical Journal
|May 22, 1971
Summary
High salicylate levels in juvenile arthritis patients can cause elevated transaminases, indicating potential liver issues. Lowering salicylate levels promptly reversed these effects, suggesting a direct link.
Area of Science:
- Pediatric Rheumatology
- Clinical Biochemistry
- Hepatology
Background:
- Chronic polyarthritis and dermatomyositis are inflammatory conditions affecting children.
- Elevated liver enzymes (transaminases) can be a sign of liver dysfunction.
- Salicylate therapy is sometimes used for inflammatory conditions.
Purpose of the Study:
- To investigate the relationship between salicylate levels and transaminase levels in pediatric patients.
- To determine if elevated transaminases in these patients are linked to salicylate dosage.
- To assess the reversibility of elevated transaminases upon reduction of salicylate levels.
Main Methods:
- Monitoring serum transaminase and salicylate levels in juvenile patients with chronic polyarthritis and dermatomyositis.
- Observing changes in transaminase levels following reduction of salicylate dosage.
- Assessing other indicators of liver function, including alkaline phosphatase.
Main Results:
- 8 out of 32 juvenile patients with chronic polyarthritis and 1 with dermatomyositis had elevated transaminases.
- In these patients, salicylate levels were consistently above 35 mg/100 ml.
- Reducing salicylate levels led to a rapid decrease in serum transaminases.
- Most children showed no other signs of liver dysfunction, though three had elevated alkaline phosphatase.
- One adult patient with mild cirrhosis also showed elevated transaminases.
Conclusions:
- Elevated serum transaminases in pediatric patients with chronic polyarthritis and dermatomyositis may be associated with high salicylate levels.
- Salicylate-induced hepatotoxicity appears to be reversible upon dose reduction.
- Careful monitoring of liver function is recommended for pediatric patients on salicylate therapy.