Blood Disorders CBC Test Analyzer What Is the Aldolase Test? By Angela Ryan Lee, MD Angela Ryan Lee, MD Dr. Angela Ryan Lee is board certified in cardiology and internal medicine. Her professional interests include preventive cardiology, medical journalism, and health policy. Learn about our editorial process Published on September 26, 2022 Medically reviewed by Rochelle Collins, DO Medically reviewed by Rochelle Collins, DO LinkedIn Rochelle Collins, DO, is a board-certified family medicine doctor currently practicing in Bloomfield, Connecticut. Learn about our Medical Expert Board Print Table of Contents View All Table of Contents Uses Procedure What to Expect Interpreting Results Causes of High Aldolase Levels Frequently Asked Questions Aldolase is an enzyme responsible for breaking down certain sugars for energy. The liver and skeletal muscle tissue contain high levels of this enzyme. Aldolase testing may be done by a healthcare provider who suspects a muscular problem, such as muscle pain or weakness. Aldolase is released when muscles get damaged, so a person with muscular problems will have higher levels of aldolase. Read on to learn why the aldolase test is performed and what an abnormal level could mean. David Silverman / Staff / Getty Images Aldolase Test Uses Your healthcare provider may order an aldolase test when they suspect certain muscle disorders. The aldolase test can also help determine the causes of muscle weakness (myopathy). If the cause of muscle weakness is neurologic (related to the nervous system) aldolase levels will not be elevated, while if a muscular problem causes the weakness, aldolase levels will be elevated. The aldolase test may be ordered if you are experiencing muscle weakness or pain. However, the test is nonspecific, meaning that it does not indicate an exact diagnosis. For example, based on this test alone, you cannot differentiate between a liver or a muscle problem. However, in combination with other tests, an aldolase test can help guide further testing to determine the cause of muscle symptoms. Aldolase Test Procedure The aldolase test is a blood test and requires venipuncture (drawing blood from a vein). A vein in the arm is typically used, and the overlying skin is cleaned. An elastic band is then wrapped around the upper arm to make the vein plump and easier to puncture. Then a needle is placed into the vein, and blood is collected in a tube, which is then sent for laboratory testing. What to Expect Before you have a blood draw for the aldolase test, you may be asked to fast and avoid exercise for a certain period of time, since exercise can transiently increase aldolase levels. The aldolase test, like any blood draw, may cause mild pain, bleeding, and bruising at the puncture site. Some people experience nausea or feel faint with blood draws. If you feel dizzy, notify the technician, who may ask you to lie down or provide water for you to drink. You should also notify your healthcare provider if you develop signs of infection, like redness, warmth, pain, and swelling at the puncture site. Test results can take anywhere from hours to a few days. Interpreting Results Elevated levels of aldolase in the blood may be caused by various muscle or liver problems. Other diagnostic tests are performed to arrive at a correct diagnosis. The normal range of aldolase in the blood can vary between the specific laboratory, but in general, a normal aldolase level in adults is between 1 and 7.5 units per liter. Levels may be slightly higher in men, and are higher in infants and children. Causes of High Aldolase Levels Any problem with muscles can lead to elevated aldolase levels. Some specific conditions are classically associated with elevated levels, and when these conditions are suspected, aldolase tests are often ordered. Duchenne Muscular Dystrophy Duchenne muscular dystrophy (DMD) is an inherited muscle disorder, typically diagnosed in childhood. Due to the genetics of the condition (X-linked recessive), this condition occurs in males. In this condition, muscles become progressively weak, starting in the shoulder and pelvic regions, and spreading throughout the body. This leads to difficulty walking, standing, and even falls. In later stages, the heart muscle can be affected, leading to cardiomyopathy (heart muscle weakness). If muscular dystrophy is suspected, an aldolase lab test is performed. Levels of aldolase in DMD may be very elevated, due to the widespread muscle damage in this condition. Limb-Girdle Muscular Dystrophy Another type of muscular dystrophy that is less common than DMD is limb-girdle muscular dystrophy (LGMD). This is a group of muscular dystrophies with varying symptoms, severity, and age of onset caused by genetic mutations. LGMD is marked by muscle weakness in the shoulders, upper arms, hips, and legs. Aldolase levels in LGMD are elevated. Dermatomyositis Dermatomyositis is an inflammatory condition that causes skin rash and muscle weakness. Although the symptoms of dermatomyositis vary, it causes soreness and weakness that will affect the muscles in the upper arms, legs, shoulders, and hips. A rash can appear on the face, hands, arms, and skin overlying joints. Symptoms often come and go. Inflammation of the muscles results in the elevation of aldolase levels. And the elevation of aldolase is one of the criteria for diagnosing dermatomyositis. Polymyositis Similar to dermatomyositis, polymyositis is an inflammatory condition affecting the muscles, causing them to become weaker. It does not typically cause a skin rash. Aldolase and other muscle enzymes are elevated in polymyositis, which is the criteria for diagnosing this condition. Muscle biopsy is often required for a definitive diagnosis. Summary Aldolase is an enzyme found in high levels in muscle and liver tissue that is elevated in certain conditions. A healthcare provider may order this test, along with other testing, when a muscle condition is suspected. The aldolase test is performed with a blood draw. Because it is nonspecific, meaning it is not tied to just one condition, other lab tests, imaging studies, and muscle biopsy may be performed to arrive at a diagnosis. A Word From Verywell Having muscle pain and weakness is not only unpleasant but can be confusing and frustrating when you are trying to figure out what is wrong. Many conditions can cause these symptoms. Getting lab tests, including an aldolase test, is one of the first steps in figuring out the cause. Frequently Asked Questions When should an aldolase test be performed? Aldolase tests may be ordered by a healthcare provider who suspects a muscular problem, such as in a person with muscle pain or weakness. Since aldolase is released when muscles are damaged, aldolase levels will be elevated in muscular problems. Aldolase can help differentiate muscular from neurologic conditions that cause weakness. What is a normal aldolase level? The normal range of aldolase in the blood can vary by the specific laboratory. Generally, an adult's average aldolase level is between 1.0 and 7.5 units per liter. Levels may be slightly higher in men, infants, and children. Why is aldolase important? Aldolase is an enzyme found in high levels in muscles and the liver. It is responsible for breaking down certain sugars. A deficiency of aldolase can cause a congenital condition called hereditary fructose intolerance. Learn More: Aldolase Deficiency- Hereditary Fructose Intolerance 12 Sources Verywell Health uses only high-quality sources, including peer-reviewed studies, to support the facts within our articles. Read our editorial process to learn more about how we fact-check and keep our content accurate, reliable, and trustworthy. MedlinePlus. Aldolase blood test. The Myositis Association. Blood tests. Medline Plus. Venipuncture. Kanda K, Sugama K, Sakuma J, Kawakami Y, Suzuki K. Evaluation of serum leaking enzymes and investigation into new biomarkers for exercise-induced muscle damage. Exerc Immunol Rev. 2014;20:39-54. Mayo Clinic. Serum aldolase. Casciola-Rosen L, Hall JC, Mammen AL, Christopher-Stine L, Rosen A. Isolated elevation of aldolase in the serum of myositis patients: a potential biomarker of damaged early regenerating muscle cells. Clin Exp Rheumatol. 2012;30(4):548-553. PMID:22703875 National Organization for Rare Disorders. Duchenne muscular dystrophy. National Organization for Rare Disorders. Limb-girdle muscular dystrophy. National Organization for Rare Disorders. Dermatomyositis. The Myositis Association. Diagnostic criteria for dermatomyositis. The Myositis Association. Polymyositis. National Organization for Rare Disorders. Hereditary fructose intolerance. By Angela Ryan Lee, MD Angela Ryan Lee, MD, is board-certified in cardiovascular diseases and internal medicine. She is a fellow of the American College of Cardiology and holds board certifications from the American Society of Nuclear Cardiology and the National Board of Echocardiography. She completed undergraduate studies at the University of Virginia with a B.S. in Biology, medical school at Jefferson Medical College, and internal medicine residency and cardiovascular diseases fellowship at the George Washington University Hospital. Her professional interests include preventive cardiology, medical journalism, and health policy. 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