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 more common in black people than in white people.

Gender

MGUS is almost twice as common in men than in women.

Family history

People who have a close family member (such as a parent, brother or sister) with MGUS have a slightly increased risk of developing it.

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.

These include:

  • lupus – a condition when the immune system attacks your own tissues and organs
  • pernicious anaemia – low levels of red blood cells caused by not having enough vitamin B12 in the body.

MGUS symptoms

MGUS does not usually cause any symptoms. But a small number of people with MGUS 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.

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.

  • Blood tests
  • Tests on your urine
  • X-rays
  • Scans
  • Bone marrow test

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.

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 a lot. They can explain more about your risk and arrange counselling for you if you feel it might help.

Macmillan is also here to support you. If you would like to talk, you can do the following:

Do you need this information in another language or format?

We are committed to making our website as accessible as possible, to make sure that everyone can use it.

If you need Macmillan cancer information in another language, large print, or braille, we can help you. Just email us in English to tell us what information you need.

We also have information available in different formats including audiobooks, British Sign Language and easy read. 

If you would like to speak to someone in your language, please call 0808 808 0000 and tell us, in English, the language you need.

About our information

  • References

  • Reviewers

The language we use

We want everyone affected by cancer to feel our information is written for them.

We want our information to be as clear as possible. To do this, we try to:

  • use plain English
  • explain medical words
  • use short sentences
  • use illustrations to explain text
  • structure the information clearly
  • make sure important points are clear.

We use gender-inclusive language and talk to our readers as ‘you’ so that everyone feels included. Where clinically necessary we use the terms ‘men’ and ‘women’ or ‘male’ and ‘female’. For example, we do so when talking about parts of the body or mentioning statistics or research about who is affected.

You can read more about how we produce our information here.

Date reviewed

Reviewed: 01 September 2021
|
Next review: 01 September 2024

This content is currently being reviewed. New information will be coming soon.

Trusted Information Creator - Patient Information Forum
Trusted Information Creator - Patient Information Forum

Our cancer information meets the PIF TICK quality mark.

This means it is easy to use, up-to-date and based on the latest evidence. Learn more about how we produce our information.