When evaluating liver health, a blood test often measures specific liver enzymes, known as transaminases. These enzymes act as important biochemical markers, providing insight into the condition of the liver cells. Measuring these levels is a routine part of health screenings to detect potential injury or disease early. The relationship between two of these enzymes, Aspartate Aminotransferase (AST) and Alanine Aminotransferase (ALT), is particularly informative. Analyzing their ratio offers a pattern that can suggest the underlying cause of any observed liver cell damage.
Understanding AST and ALT
Aspartate Aminotransferase (AST) and Alanine Aminotransferase (ALT) are enzymes that catalyze specific chemical reactions necessary for cellular metabolism. When cells are damaged, these enzymes leak into the bloodstream, and their elevated presence signals tissue injury. ALT is primarily concentrated within liver cells, making it a highly specific indicator of liver damage.
AST, in contrast, is found in the liver but also in significant amounts in other tissues, including the heart, skeletal muscle, and kidneys. Due to this wider distribution, an elevated AST level alone might suggest injury outside of the liver, such as from muscle trauma or heart conditions.
Calculating and Interpreting the Ratio
The relationship between these two enzymes is formalized by calculating the AST/ALT ratio, also known as the De Ritis ratio. This value is determined by dividing the measured concentration of AST by the concentration of ALT in the blood.
In a healthy liver, or in many types of non-alcohol-related liver inflammation, the resulting ratio is typically less than 1. This occurs because the concentration of ALT is usually higher or equal to AST in the blood of healthy individuals. A ratio less than 1 suggests that the damage is primarily releasing the highly specific ALT enzyme into circulation.
A shift where the AST value becomes disproportionately higher than the ALT value suggests a change in the pattern of liver injury. This deviation indicates a specific type of damage, providing a quick way to categorize the cellular stress the liver is experiencing.
Alcohol’s Specific Impact on Enzyme Levels
Chronic, heavy alcohol consumption creates a unique pattern of liver injury, causing AST levels to rise disproportionately higher than ALT levels. This shift is rooted in two primary biochemical mechanisms.
First, alcohol metabolism generates toxic byproducts, such as acetaldehyde, that directly damage the mitochondria within liver cells. Aspartate Aminotransferase (AST) is concentrated in two forms, with up to 80% being mitochondrial AST (mAST). Damage to these cellular powerhouses leads to a massive release of mAST into the bloodstream, significantly boosting the overall AST reading.
Second, chronic alcohol use often leads to a deficiency of Pyridoxal 5-phosphate, the active form of Vitamin B6. This vitamin is a necessary co-factor for transaminase function. However, the synthesis and activity of Alanine Aminotransferase (ALT) are significantly more dependent on B6 availability than AST.
The resulting B6 depletion suppresses the production and function of ALT, further lowering its measurable level relative to AST. The combination of increased AST release due to mitochondrial breakdown and suppressed ALT activity reliably pushes the AST/ALT ratio above the normal threshold of 1.
The Ratio as a Diagnostic Indicator
Medical professionals use the calculated AST/ALT ratio as a strong indicator to help differentiate between various causes of liver injury. In common conditions like Non-Alcoholic Fatty Liver Disease (NAFLD) or acute viral hepatitis, the ratio is typically below 1. This is because the injury pattern often causes a greater release of the highly liver-specific ALT enzyme from the cell cytoplasm.
A ratio greater than 1 suggests a different pathology, such as advanced liver scarring (cirrhosis) from any cause. A finding of an AST/ALT ratio of 2:1 or greater is highly suggestive of alcohol-related liver disease (ALD). Ratios reaching 3:1 are classic findings in patients with alcoholic hepatitis.
A helpful distinction in ALD is that the absolute levels of both enzymes are generally only moderately elevated, often remaining below 300 U/L. Levels significantly higher than this range often suggest alternative or additional causes of liver damage. While the ratio provides compelling evidence, it is not used in isolation to make a definitive diagnosis. The result must be interpreted alongside a patient’s medical history, clinical symptoms, and other diagnostic tests, such as Gamma-Glutamyl Transferase (GGT) levels, to achieve an accurate assessment.

