MGUS
MGUS (monoclonal gammopathy of unknown significance) is a non-cancerous condition where the body makes an abnormal protein.
What is MGUS?
MGUS stands for monoclonal gammopathy of unknown significance. It is a non-cancerous condition where the body makes an abnormal protein, called a paraprotein.
Although MGUS is not a cancer, people with it have a slightly higher risk of developing:
- myeloma (a cancer of blood cells called plasma cells)
- lymphoma (a cancer of blood cells called lymphocytes).
MGUS affects plasma cells. These are a type of white blood cell made in the bone marrow. Normal plasma cells make proteins called antibodies to help fight infections. With MGUS, some plasma cells make an abnormal type of antibody called a paraprotein (or M protein). For most people, this does not cause any problems.
Each year, about 1 out of 100 people with MGUS (1%) develop a related cancer, such as myeloma or lymphoma. However, most people with MGUS never develop a related cancer and do not need treatment.
Doctors do not know why some people with MGUS develop a cancer and others do not. Your doctor may do regular blood tests to help check for any changes and predict whether the MGUS is likely to change in the future.
MGUS causes
Doctors do not know what causes MGUS, but different things are known to increase the risk of it developing.
Age
MGUS is more common in older people. It is rare in people under the age of 40.
Ethnicity
MGUS is slightly more common in Black ethnic groups than other groups.
Sex
MGUS is almost twice as common in men than in women.
Family history
People who have a close family member with MGUS or some types of blood cancer may have a slightly increased risk of developing MGUS. Close family members are your parents, brothers or sisters.
Autoimmune disease
Autoimmune diseases cause the body’s immune system to attack healthy cells in the body. Some may slightly increase the risk of developing MGUS.
If you have an autoimmune disease and are worried about MGUS, your GP can give you more information.
Diagnosing MGUS
As MGUS does not usually cause symptoms, it is often found when having tests for other possible health problems. Doctors may test you for MGUS if a paraprotein is found in your blood after a blood test. A paraprotein in the blood can also be a sign of more serious conditions, such as myeloma or lymphoma. Doctors may need to do tests to rule out these other conditions before they can diagnose MGUS.
Your GP may arrange these tests, or you may be referred to a doctor who specialises in blood disorders. They are called a haematologist. Not everybody who has MGUS is referred to a haematologist. It will depend on your symptoms and test results. Your doctor may also need to do a physical examination and ask some questions about your health.
You may have some of the following tests.
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Blood tests
You will have a blood test that measures the amount and type of paraprotein made by the plasma cells. You will also have a test to check the number of different types of blood cells. This is called a full blood count.
Your doctor may arrange blood tests to check how well your liver and kidneys are working. This is to check your general health, but also because myeloma can affect these organs. You may also have your calcium levels checked, as myeloma can cause increased calcium levels.
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Tests on your urine
Some types of paraprotein can be found in the urine (pee). You may be asked to give samples of your urine to check for these. You may need to take a container home and collect your urine for 24 hours. This is because larger samples can provide more information. The nurses will explain more about how to do this test.
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Scans
Your doctor may arrange for you to have body scans, such as an MRI or PET-CT scans. This is to look for any changes in your bones.
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Bone marrow test
Some people may have a sample of bone marrow taken (biopsy).
A doctor or specialist nurse takes a small sample of bone marrow from the back of the hip bone (pelvis). The sample is sent to a laboratory. It is checked under a microscope for abnormal cells. This is done to look for myeloma cells in the bone marrow.
MGUS symptoms
MGUS does not usually cause any symptoms.
If people have symptoms related to MGUS, the condition may be called monoclonal gammopathy of clinical significance (MGCS). This is when the abnormal plasma cells cause problems in the body. Your doctor will tell you if you have MGCS.
People with MGCS may have problems with their balance, or numbness or tingling in their hands and feet. This is called peripheral neuropathy. Symptoms may be because of damage to their nerves caused by paraproteins in the blood.
People with nerve problems may be referred to a neurologist. This is a doctor who specialises in conditions of the nervous system.
Some people may also have problems with the kidneys.
People with MGCS may need treatment to help any problems they have. Your doctor will tell you if you need any treatment.
Treatment and follow-up for MGUS
MGUS does not usually need treatment as it rarely causes any symptoms. In most people, MGUS remains stable and never causes any problems.
There is a small risk of MGUS developing into a cancer, such as myeloma or lymphoma. If this happens, it is usually a slow-growing lymphoma. This can cause certain symptoms. Always contact your doctor if you have any of these symptoms:
- new or constant bone pain (such as in the back, ribs, hip or pelvis)
- different infections, one after another, that need antibiotics to treat them
- feeling short of breath
- extreme tiredness (fatigue)
- unexplained weight loss
- night sweats
- new lumps or swellings.
Your doctor may also recommend you have regular blood tests. These will be like the ones you had at diagnosis.
In the first year, you may have blood tests every few months. If your blood tests are normal after this time and you have no new symptoms, you have blood tests less often.
If you have new symptoms or blood tests show changes, such as a rising paraprotein level, your doctor may arrange for you to have more frequent tests.
Not everyone with MGUS needs regular follow-up appointments and blood tests. For some people, the chance of it causing problems in their lifetime is so small, no checks are needed. But it is still important to tell your doctor if you get any of the symptoms mentioned above.
Symptoms to be aware of
There is a small risk of MGUS developing into a cancer, such as myeloma or lymphoma. If this happens, it is usually a slow-growing lymphoma. This can cause certain symptoms. Always contact your doctor if you have any of these symptoms:
- new or constant pain in 1 area (such as in the back, ribs, or pelvis)
- different infections, one after another, that need antibiotics to treat them
- feeling short of breath
- extreme tiredness (fatigue)
- unexplained weight loss
- night sweats
- new lumps or swellings.
Other conditions
Having MGUS can increase your risk of developing other health conditions. These include:
- bone problems
- blood clots
- infection
Speak to your doctor if you are worried about other health conditions. They can give you more information.
Follow-up tests
Your doctor may also recommend you have regular blood tests. These will be like the ones you had at diagnosis.
In the first year, you may have blood tests every few months. If your blood tests are normal after this time and you have no new symptoms, you may have blood tests less often.
If you have new symptoms or blood tests show changes, such as a rising paraprotein level, your doctor may arrange for you to have more frequent tests.
Not everyone with MGUS needs regular follow-up appointments and blood tests. For some people, the chance of it causing problems in their lifetime is so small, no checks are needed. But it is still important to tell your doctor if you get any of the symptoms mentioned above.
Your feelings about MGUS
If you are told you have MGUS and need further tests, it is normal to feel worried. But most people with MGUS do not go on to develop cancer. Talk to your doctor if you feel anxious. They can explain more about your risk and arrange counselling for you if you feel it might help.
You can also get support from Macmillan by:
- calling the Macmillan Support Line for free on 0808 808 0000
- chatting to us online
- visiting our Online Community.
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About our information
This information has been written, revised and edited by Macmillan Cancer Support’s Cancer Information Development team. It has been reviewed by expert medical and health professionals and people living with cancer.
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References
Below is a sample of the sources used in our myeloma information. If you would like more information about the sources we use, please contact us at informationproductionteam@macmillan.org.uk
Hughes D, Yong K, Ramasamy K, et al. Diagnosis and management of smouldering myeloma: A British Society for Haematology Good Practice Paper. Br J Haematol. 2024;204(4):1193-1206. Available from: www.doi.org/10.1111/bjh.19333
Sive J, Cuthill K, Hunter H, et al. Guidelines on the diagnosis, investigation and initial treatment of myeloma: a British Society for Haematology/UK Myeloma Forum Guideline. Br J Haematol.2021;193(2):245-268. Available from: www.doi.org/10.1111/bjh.17410
Reviewer
Senior Clinical Research Fellow and Honorary Consultant in Molecular Diagnostics and Leukaemia
Date reviewed

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