Aldolase

What sample is needed for Aldolase?

1. It is done in the Serum of the patient.
2. Patients should fast for 8 hours before giving the sample.
   1. Take 3 to 5 ml of blood in the disposable syringe. Keep the syringe for 15 to 30 minutes, and then centrifuge for 2 to 4 minutes. Can get a clear serum.
3. Avoid hemolysis and separate serum immediately.
4. It is stable for:
   1. 8 hours at room temperature.
   2. 4 °C for 5 days.
   3. -15 °C for 15 days.

What are the precautions for Aldolase?

1. The previous muscular injection may have increased the aldolase level.
2. Hemolysis and exposure to chlorinated insecticide may increase the level.
3. Hepatotoxic drugs may increase the level.
4. The phenothiazine may decrease the aldolase level.

What are the indications for Aldolase?

1. This test is indicated when inflammatory diseases of the muscles (myopathy) are suspected.
2. To assess the severity of myopathy.
3. Other tests, such as Lactate dehydrogenase, Creatinine Phosphatase, and Aspartate transferase, are advised and helpful for diagnosis, so this test is no longer recommended.

How will you define aldolase enzyme?

1. Aldolase is a glycolytic enzyme that splits fructose-1,6-phosphatase into two triose phosphate molecules in glucose metabolism.
2. Aldolase is present in all tissues, like the brain and kidneys, and is prominent in skeletal and heart muscles.
3. Aldolase enzyme is present in the cell and the nucleus.

What is the chemical reaction of the Aldolase?

1. It converts sugar to energy.
2. Aldolase is described in different forms:
   1. Aldolase – A occurs in most of the tissues.
   2. Aldolase-B is seen in the liver and kidneys.
3. This is a glycolytic enzyme, and it cleaves fructose – 1,6-bisphosphate into dihydroxyacetone phosphate and glyceraldehyde –  3-phosphate.
4. Fructose-1-phosphate is split into D-glyceraldehyde and dihydroxyacetone phosphate by aldolase B, an enzyme found in the liver.
5. Aldolase also takes part in glycolysis by attacking the fructose-1-6-PO4.

What is the clinical significance of Aldolase?

1. For diagnosing muscular dystrophy, these tests are advised: CPK, AST, and Aldolase.
2. The major use of aldolase is for the diagnosis of rhabdomyolysis.
   1. CPK is also raised, which is more sensitive and specific, so aldolase is not recommended.
3. This is greatly increased in Duchenne-type pseudo hypertrophic muscle dystrophy compared to other muscular diseases.
4. It is high in the early stage.
5. But it falls as the disease progresses.
   1. There is a 10 to 15 times increase over the normal level.
6. This is raised in dermatomyositis and limb-girdle dystrophy.
   1. Normal values are seen in poliomyelitis, myasthenia gravis, and multiple sclerosis, where the origin of the muscle disease is neurogenic.
7. It is usually normal in cirrhosis and obstructive jaundice.
8. The aldolase pattern is like ALT, and it comes to normal in 10 to 15 days.
9. This has the main interest in the primary disease of skeletal muscles.
10. If the muscle disease is due to neurological causes, aldolase will be normal.

What are the normal Aldolase levels?

• Adult = 1.0 to 7.5 U /L
• Newborn = 4 x adult level
  • Values are double in early childhood and then slowly fall to a normal level by 18 to 20 years of age.
• Children  10 to 24 months = 3.4  to  11.8 U/L
  • child 25 months to 16 years = 1.2 to  8.8 U/L

Another source

• Adult = 22 to 59 mU/L at 37  °C (SI unit)
• Child = Approximately 2 times the adult value.
• Newborn = Approximately 4 times the adult value.

Another souArce

• Adult/elderly = 3.0 to 8.2 U/dL (22 to 59 mU at 37 °C).
  • Levels are slightly higher in men than women due to increased muscle mass.
• Newborn = 2 to 4 times the adult level.
• Child = Approximately twice the adult result.

Another source

• Maternal serum = 9.5 (7.0) U/L
• Fetal serum = 23.2 (9.4) U/L

What are the causes of increased Aldolase levels?

1. Cell destruction like Acute myocardial infarction (5 to 8 times the normal).
2. Burns.
3. Acute Hepatitis (Viral or toxic). It is raised in the early stage of viral or toxic hepatitis.
4. Inflammatory diseases of muscles (Myopathy).
5. Raised in skeletal muscle disease or injury.
6. Raised in Muscular Dystrophy. It is raised in pseudo hypertrophic muscular dystrophy (as the CPK is also raised).
   1. Duchenne’s muscular dystrophy.
   2. Trauma involving the muscles.
7. Carcinoma of the prostate (about 6 times the normal).
8. Cancer involving the lung, breast, liver, GIT, or genitourinary system.
9. Myelocytic leukemia (about 6 times the normal).
10. Megaloblastic and hemolytic anemia (about 10 to 13 times the normal).
11. In neoplastic diseases like carcinomatous metastasis to the liver, lung, breast, genitourinary system, melanoma, and CNS tumors.
12. This may be raised in eosinophilia-myalgia syndrome.
13. Trichinosis.
14. Hemolytic anemia.
15. Gangrene.
16. Melanoma.

What are the causes of decreased Aldolase levels?

1. Hereditary fructose intolerance.
2. This may indicate late muscular dystrophy.

What are the causes of normal Aldolase levels?

1. Neurogenic muscle atrophy.
2. Cirrhosis (or maybe slightly increased).
3. Obstructive jaundice (or maybe slightly increased).

• This test is nonspecific and is not commonly requested except for follow-ups on muscle diseases.
• This is also not recommended because the CPK level is raised in all these conditions where aldolase is raised.

What is the importance of the treatment at the aldolase level?

• The increase in the level reflects the intensity of the disease, and one can measure it serially to determine the effect of corticosteroid treatment.
• CK is considered the test for muscular diseases.

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