Lifestyle
- Reduce alcohol intake
- Maintain healthy weight
- Regular exercise
- Avoid hepatotoxic substances
Alanin-Aminotransferase · ALAT · GPT · SGPT
ALT quantifies the enzyme alanine aminotransferase, which is involved in amino acid metabolism and is indicative of liver cell integrity.
Reference ranges can vary slightly between laboratories. Fasting is not required, but recent exercise may affect results.
ALT (GPT), or Alanine Aminotransferase, is an enzyme primarily found in the liver. It plays a crucial role in the conversion of alanine, an amino acid, into pyruvate, a key intermediate in cellular energy production. ALT is released into the bloodstream when liver cells are damaged, making it a useful marker for liver health. Clinically, elevated ALT levels are indicative of liver injury or inflammation, often associated with conditions such as hepatitis, fatty liver disease, and alcohol-related liver damage. It is also used to monitor the progression of liver diseases and the effectiveness of treatments. For athletes and biohackers, maintaining optimal ALT levels is important as it reflects overall liver health, which is essential for metabolic efficiency and detoxification processes. However, intense physical activity can transiently elevate ALT levels, potentially confounding interpretations. Factors such as time of day, fasting status, and recent exercise can influence ALT measurements, necessitating standardized testing conditions for accurate assessment.
Klinische Bedeutung
Elevated ALT levels suggest liver damage or inflammation, commonly seen in hepatitis, fatty liver disease, and alcohol-related liver injury. Low ALT levels are less common and may not be clinically significant.
Progressively rising ALT levels suggest worsening liver function; re-test in 4 weeks if outside optimal range.
Falling ALT levels may indicate improving liver health or resolution of an acute liver insult.
Re-test Interval
4 weeks if outside optimal range
Note:
Consult a healthcare provider before starting any supplementation, especially if liver disease is suspected.
ALT levels can vary throughout the day; morning tests are recommended for consistency.
Testing Frequency
Annually for healthy adults, more frequently if liver disease is present.
Correlated with
Current research suggests that the reference ranges and optimal targets for ALT (GPT) in various clinical contexts, such as liver disease and alcohol-related organ damage, remain debated, particularly regarding confounding factors like age, sex, and coexisting conditions. Researchers have not yet established standardized guidelines for interpreting ALT levels in specific populations, such as those with sarcoidosis or glycogen storage disease. Unanswered clinical questions include the significance of ALT elevation in asymptomatic patients and its role in monitoring treatment efficacy.
582
Total Citations
30
Human/RCT
2.7
Avg. Influence
2025
Latest
This meta-analysis examined biomarkers associated with the severity of COVID-19. Researchers found that ALAT levels were significantly higher in severe cases compared to non-severe cases. The study indicates that ALAT, among other biomarkers, may help in prognostic risk stratification.
This study reviewed the use of serum enzymes in diagnosing alcohol-related organ damage. Researchers found that elevated ALAT levels can indicate alcohol-induced liver injury, particularly when combined with other enzyme markers. The study emphasizes the need for a combination of tests for accurate diagnosis.
This study focused on dietary management in children with glycogen storage disease type III. Researchers observed that monitoring laboratory parameters, including ALAT, is critical for managing fasting intolerance and preventing complications. The findings suggest that over-treatment with carbohydrates could be harmful.
This study investigated the effects of ursodeoxycholic acid (UDCA) on liver function in patients with hepatic sarcoidosis. Researchers found that serum liver tests improved in patients treated with UDCA compared to those receiving no treatment or corticosteroids. The results support the use of UDCA in symptomatic patients with liver involvement.
In a randomized controlled trial, researchers tested ursodeoxycholic acid (UDCA) for intrahepatic cholestasis of pregnancy, finding a significant reduction in ALAT levels after treatment. The study involved 20 pregnant women and demonstrated that UDCA improved liver function without adverse effects on pregnancy outcomes.
This study examined the frequency of intrahepatic cholestasis in patients with non-alcoholic fatty liver disease (NAFLD) and found that those with cholestasis had significantly higher ALAT levels. Researchers included 163 patients and concluded that cholestasis correlates with more severe liver inflammation and fibrosis.
This study assessed muscle function and laboratory parameters in patients with hypomagnesaemia. Researchers found elevated liver enzymes, including ALAT, in some cases, indicating liver damage. The study highlights the relationship between magnesium levels and muscle performance.
Researchers compared serum biomarkers in patients with systemic sclerosis-associated interstitial lung disease (SSc-ILD) and found that elevated ALAT levels were associated with the disease's presence. The study included 225 patients and highlighted the importance of various biomarkers in assessing SSc-ILD progression.
This study analyzed clinical manifestations of leptospirosis in elderly patients, finding slightly elevated ALAT levels among those with severe forms of the disease. Researchers observed that 80% of the cases were severe, with a high mortality rate, emphasizing the need for prompt treatment.
This study aimed to identify clinical and laboratory predictors of severe COVID-19. Researchers found that elevated ALT levels, among other laboratory features, were associated with worse outcomes in hospitalized patients. The study provides insights into potential early warning signs for severe disease progression.
2
Total Trials
82
Total Enrolled
Pfizer
40
2014
Number of Participants With Dose-limiting Toxicities (DLT) (Part 1)
GlaxoSmithKline
42
2009
Number of Participants With Adverse Events (AE) and Serious Adverse Events (SAE)
Research publications about ALT (GPT) over time
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