What Is Hemolysis and Why Does It Occur?

What Is Hemolysis and Why Does It Occur
Excessive hemolysis can cause a low amount of RBCs and lead to hemolytic anemia

Hemolysis refers to the natural destruction of old or damaged red blood cells (RBCs). Typically, RBCs have a lifespan of about 120 days, after which they are broken down by the body and replaced with new RBCs. 

In normal conditions, the rate of RBC destruction is matched by the rate of formation of new RBCs. However, excessive hemolysis can cause a low amount of RBCs and lead to hemolytic anemia.

What causes hemolytic anemia?

Genetic causes

  • Sickle cell disease (a condition in which a defective hemoglobin, called hemoglobin S, causes RBCs to acquire an abnormal shape)
  • Glucose-6-phosphate dehydrogenase (G-6-PD) deficiency (deficiency of the enzyme G-6-PD that ensures that the RBCs function properly and protects them from harmful substances in the blood)
  • Red cell membrane disorders such as hereditary spherocytosis, hereditary elliptocytosis, and hereditary poikilocytosis 
  • Thalassemia (a condition in which the body does not produce enough hemoglobin [the oxygen-carrying pigment in RBCs])

Acquired causes

Even in people with hereditary cases of hemolytic anemia, certain environmental conditions may act as a trigger for hemolysis. For example, anemia due to G-6-PD deficiency may be triggered by certain medications or infections. Certain foods, particularly fava beans, can trigger hemolysis in susceptible people with the Mediterranean variant of G-6-PD deficiency.

What are symptoms of hemolytic anemia?

Symptoms of hemolytic anemia vary depending on the underlying cause and severity of the condition. They may not always be apparent but can be triggered by a stressful event, medication, or infection (called a hemolytic crisis). 

Symptoms of excess hemolysis in the body include:

Blood tests, urinalysis, and bone marrow aspiration or biopsy may be ordered to confirm a diagnosis.

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What Is Hemolysis and Why Does It Occur?

What Is Hemolysis and Why Does It Occur
Excessive hemolysis can cause a low amount of RBCs and lead to hemolytic anemia

Hemolysis refers to the natural destruction of old or damaged red blood cells (RBCs). Typically, RBCs have a lifespan of about 120 days, after which they are broken down by the body and replaced with new RBCs. 

In normal conditions, the rate of RBC destruction is matched by the rate of formation of new RBCs. However, excessive hemolysis can cause a low amount of RBCs and lead to hemolytic anemia.

What causes hemolytic anemia?

Genetic causes

  • Sickle cell disease (a condition in which a defective hemoglobin, called hemoglobin S, causes RBCs to acquire an abnormal shape)
  • Glucose-6-phosphate dehydrogenase (G-6-PD) deficiency (deficiency of the enzyme G-6-PD that ensures that the RBCs function properly and protects them from harmful substances in the blood)
  • Red cell membrane disorders such as hereditary spherocytosis, hereditary elliptocytosis, and hereditary poikilocytosis 
  • Thalassemia (a condition in which the body does not produce enough hemoglobin [the oxygen-carrying pigment in RBCs])

Acquired causes

Even in people with hereditary cases of hemolytic anemia, certain environmental conditions may act as a trigger for hemolysis. For example, anemia due to G-6-PD deficiency may be triggered by certain medications or infections. Certain foods, particularly fava beans, can trigger hemolysis in susceptible people with the Mediterranean variant of G-6-PD deficiency.

What are symptoms of hemolytic anemia?

Symptoms of hemolytic anemia vary depending on the underlying cause and severity of the condition. They may not always be apparent but can be triggered by a stressful event, medication, or infection (called a hemolytic crisis). 

Symptoms of excess hemolysis in the body include:

Blood tests, urinalysis, and bone marrow aspiration or biopsy may be ordered to confirm a diagnosis.

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