Red blood cells are produced by the bone marrow and have a life span of 120 days.
In healthy people, millions are released into the blood stream each day to replace the old ones. To produce new red blood cells the body needs key ingredients such as iron.
Red blood cells contain a protein called haemoglobin. All tissues need oxygen to survive and haemoglobin delivers oxygen from the lungs to all parts of the body. The haemoglobin levels needed for this to happen are different in adult men and women.
For men, the haemoglobin reference range (that is, the range considered normal) is 130–180 grams per litre (g/L) and for women it’s 120–160 g/L.
Anaemia reduces the amount of oxygen in the body. The most common symptoms of this include:
- feeling faint
- becoming easily breathless.
Less common symptoms include headaches, palpitations, altered taste and ringing in the ears.
Depending on what’s causing your anaemia, you may have other symptoms too.
What causes anaemia?
There are many possible causes of anaemia, however it generally occurs by either:
- increased loss of red cells due to blood loss (bleeding) or destruction of red cells (haemolysis)
- problems with red cell production, including low numbers of red cells or abnormal red cells.
In all cases, your doctor will need to work out what’s causing the underlying problem. Some examples could include:
- Increased blood loss
- bleeding from the stomach or bowel
- heavy periods or childbirth
- Destruction of red cells
- sickle cell anaemia
- artificial heart valves
- Decreased number of red cells
- iron deficiency
- other vitamin deficiency such as B12 or folate
- bone marrow and stem cell problems including blood cancer
- medical conditions such as chronic kidney disease
- Abnormal red cells
- hereditary shperocytosis
Iron deficiency is a common cause of anaemia in Australia, and the reason for a lack of iron needs to be worked out by your doctor.
Finding the cause of anaemia and treating it
Genetic causes of anaemia
Two examples of genetic causes of anaemia are sickle cell anaemia and thalassaemia.
Sickle cell anaemia
Sickle cell anaemia is a genetic blood disorder which causes the body to make abnormal haemoglobin.
This affects the shape of the red blood cells causing them to be crescent or sickle shaped, which makes them inflexible and ‘sticky’. They can get stuck in small blood vessels blocking the flow of blood, depriving the tissues of oxygen and causing pain and organ damage.
The sickle cells also don’t last as long in the circulation as normal red blood cells leading to ‘sickle cell anaemia’. Red cell transfusions increase the supply of oxygen carrying haemoglobin.
Thalassaemia is one of the most common genetic blood disorders in the world. Haemoglobin production is abnormal, resulting in anaemia.
Red cell transfusions give a temporary supply of healthy red blood cells with normal haemoglobin levels, which improves oxygen delivery to the tissues in the body.