Can Lupus Cause ITP?

Medically reviewed by Zeba Faroqui, M.D. — Written by Emily Wagner, M.S.
Posted on February 14, 2023

  • Having lupus is associated with an increased risk of developing immune thrombocytopenia, or ITP.
  • Lupus and ITP are autoimmune disorders, and each can involve autoantibodies that attack the platelets in the blood.
  • Both lupus and ITP can be treated with corticosteroids and other medications that target the immune system.

Immune thrombocytopenia and lupus are both autoimmune conditions, or conditions in which the immune system attacks the body’s own tissues and organs. When someone with lupus develops ITP, it’s called secondary ITP. Secondary ITP is ITP that is the result of another health condition.

It’s unclear whether lupus can directly cause ITP, but people with lupus have an increased risk of developing ITP. Between 7 percent and 30 percent of people with systemic lupus erythematosus (the most common type of lupus) develop secondary ITP.

Lupus and ITP are both complex autoimmune disorders. Doctors and researchers are still working to understand what causes them and why someone may develop both conditions. This article will discuss the connection between lupus and ITP, including their symptoms, how they’re diagnosed, and how they’re treated.

Lupus, ITP, and the Immune System

Antibodies are normally made by our immune systems to help our bodies fight infections from bacteria and viruses. In autoimmune diseases, the immune system makes antibodies that target your body’s own cells and tissues as invaders that need to be destroyed. The antibodies that attack the body itself are known as autoantibodies.

ITP occurs when autoantibodies tag and destroy your platelets. Platelets are cells that help your blood clot. When platelet counts are low, you’re at an increased risk of excessive bleeding.

Platelets are made by specialized cells in your bone marrow (the spongy tissue inside your bones) known as megakaryocytes. When platelets are destroyed faster than they can be replaced, the platelet count decreases. Some people with ITP also have autoantibodies that tag megakaryocytes for destruction.

In lupus, autoantibodies attack tissue and cells in different parts of the body, like the joints, skin, heart, brain, and kidneys. Sometimes, the autoantibodies target the nucleus, the central part of cells.

While doctors and researchers are still learning about why lupus is associated with an increased risk of ITP, they believe it’s due to a combination of genetic factors and the presence of certain autoantibodies. For example, people with lupus typically have autoantibodies that target platelets — however, these antibodies are not always the same ones seen in ITP.

Symptoms of Lupus and ITP

Symptoms of lupus can vary from person to person. They may depend on what organs and areas of the body are targeted by autoantibodies. Researchers have suggested that, in some cases, ITP can be an early sign of lupus.

Common symptoms of lupus include:

  • Loss of appetite leading to weight loss
  • Extreme fatigue
  • Fever
  • Rash, especially across the nose and cheeks, known as a “butterfly rash”
  • Headaches
  • Hair loss
  • A general feeling of illness or discomfort

Since these symptoms are nonspecific and can be signs of other medical conditions, diagnosing lupus can be difficult.

Symptoms of ITP are typically the same for people with or without lupus. Often, people won’t have any ITP symptoms, and low platelet counts won’t be discovered until there is a blood test for another condition or someone has a bleeding event.

Noticeable symptoms of ITP may include:

  • Frequent nosebleeds or bleeding from the gums
  • Long or heavy menstrual periods
  • Skin that bruises easily, sometimes without any cause
  • Small red dots on the skin (petechiae) from burst blood vessels
  • Blood-filled blisters inside the mouth

Whether or not you have lupus, tell your doctor if you experience any of these symptoms. Giving your doctor an accurate picture of all of your symptoms will help them determine what blood tests and exams to perform for the most accurate diagnosis.

Diagnosing Lupus and ITP

Lupus can be difficult to diagnose because it looks similar to other autoimmune diseases. It can’t be diagnosed with a single blood test or biopsy. Instead, doctors use different tests to help rule out other conditions and make a final diagnosis. These include:

  • A complete blood count (CBC) to check levels of red blood cells, white blood cells, and platelets
  • Blood tests to examine the functioning of your kidneys and liver
  • Blood tests to examine the erythrocyte sedimentation rate, which can help diagnose a systemic disease like lupus
  • A urine test to see if lupus is affecting your kidneys
  • Imaging tests to see if lupus is affecting your heart or lungs

A CBC test is also used to determine whether you have ITP. Doctors will use this test to check if your platelet count is low. If your white blood cell or red blood cell counts are higher than normal, this may point to an infection or a different condition.

Your doctor may also take a sample for a blood smear. In this test, a drop of blood is smeared on a piece of glass and stained with chemicals to mark different blood cells. A specialist then looks at the smear under a microscope to check if you have fewer platelets than normal or if they’re bigger or smaller than they should be.

Since you can have lupus and ITP at the same time, when diagnosing ITP, your doctor may also test you for comorbid lupus. Tests for lupus in someone with ITP include testing for the antinuclear antibody (ANA), as well as several others. Presence of certain antibodies shows disease activity in the immune system and can lead to a lupus diagnosis.

Treating Lupus and ITP

Since lupus and ITP both affect the immune system, most of their treatments work in the same way — aiming to reduce immune system activity and calm inflammation. Treatment plans will depend on your specific symptoms. For example, if you have ITP with no symptoms, you may only need follow-up monitoring and blood tests from your doctor.

For people with lupus and ITP who do have symptoms, there are several treatment options. In cases where platelet counts are extremely low, the first-line treatment is corticosteroids. These medications help decrease inflammation and prevent the immune system from attacking platelets. Two corticosteroids commonly prescribed for ITP are prednisone and dexamethasone. Corticosteroids are usually only prescribed for short periods, because they have side effects when used long term.

Another treatment for incidences of extremely low platelet counts in people with ITP and lupus is intravenous immunoglobulin (IVIG). This treatment uses concentrated antibodies from donors to stop the immune system from targeting platelets. It helps to raise platelet counts within a few days, and it has been effective in treating ITP in people with lupus.

The biologic drug rituximab (Rituxan) is also used to treat refractory cases of lupus and ITP — cases that have not been helped by the initial treatment. Rituximab blocks B cells, which are responsible for making autoantibodies. In some case studies, rituximab has been shown to help treat both conditions in children and adults.

Other treatment options for people who have both lupus and ITP may include:

  • Immunosuppressants — These reduce the activity of the immune system. Examples include azathioprine (Imuran), cyclosporine (Sandimmune), and mycophenolate mofetil (CellCept).
  • Thrombopoietin receptor agonists (TPO-RAs) — These medications stimulate the production of platelets. Examples include eltrombopag (Promacta) and romiplostim (Nplate).
  • Splenectomy — This is surgery to remove your spleen, which traps platelets in ITP. This is an option for cases of persistent or severe thrombocytopenia.

If you have lupus and ITP, work with your doctor to determine the best treatment plan for you. You may want to seek specialist care from experts in both hematology (study of blood and blood disorders) and rheumatology (study of diseases in the bones, muscles, and joints). While there’s not yet a cure for ITP or lupus, treatments can help relieve pain and other symptoms and improve your quality of life.

Talk With Others Who Understand

On myITPcenter, the site for people with immune thrombocytopenia and their loved ones, people come together to gain a new understanding of ITP and share their stories with others who understand life with ITP.

Are you living with both lupus and ITP? What helps you manage both conditions? Share your experience in the comments below.

    Posted on February 14, 2023


    I feel for you, I struggled from late 2018/19, could barely walk and move myself around, I lost so much weight I was covered in bruises no energy, constant nose bleeds, couldn't even lift my arm up to brush my hair.
    After 7 months going to my doctor, the usual naproxen and painkillers and I wasn't getting better. If anything I was finding it harder to walk stand or move around. I got to see a rheumatologist, I was misdiagnosed given a steroid injection. Another 6 months alter, I was referred to another specialist who then diagnosed the lupus. I was so relieved that eventually someone had an answer, only to get a phone call 5 hours later from another department telling me to go to the hospital immediately as my bloods had shown another problem.
    I was put on a high dose of steroids for 48 hours and diagnosed with ITP. I have been on many medications some have worked some haven't now I am on a medication that keeps me steady and often need a low dose of steroids to help me. Although Lupus doesn't normally leave permanent damage to joints, I have been left with a lot of deformities in small joints.
    I was very fortunate as my diagnoses came just before covid hit and I have had the best support from my rheumatologist and haematologist who work together. I am on combination meds just now one of which is used for rheumatoid arthritis, but with the use of mycophenolate alongside it, I find I get a few more good days, which is a bonus

    posted March 20


    Around 1979 or so I was diagnosed with ITP. But I stood for idiopathic, because I guess the cause was unknown. Now I was two at the time and I underwent a splenectomy. I am now 45 and have suffered all my life with skin disorders, psoriasis,excema,dermatitis, seborrheic dermatitis, etc. Back in 2017 I went through a quite stressful period that brought on a terrible scalp flare up this bc wasn't my first experience. I lost hair, had red blustery patches. It was nearly unbearable. I had the area biopsied and it was a subcutaneous Lupus. I didn't have SLE, just some systemic symptoms, joint pain and such!

    posted March 20


    Currently dealing with exactly this.. And I asked my rheum. She said the I in ITP stands for idiopathic meaning no known cause. And she said when you got lupus and symptoms, she says it's no longer idiopathic at that point, it's lupus.

    I've got anti-cardiolipin antibodies. Never had a clotting event. Have had miscarriages but since they were early never officially given APS dx. I think the weirdest part of all this is being both at risk of bleeding out from low platelets and still having a high clot risk. 😒

    posted March 20


    I have both ITP and APS along with SLE and frequently shake my head at the anomaly of having both sticky and runny blood.

    posted March 20


    I was diagnosed with SLE lupus in Aug 2013

    posted March 20


    I was diagnosed with SLE lupus in Aug 2013. Prompt aggressive treatment put me in stable remission which I have been in for 10 years.

    Knowing what I know now when I was a 10 year old child in 1963 I had ITP. It spontaneously disappeared but reappeared in my late 20s. A year of unpleasant medication followed by a splenectomy in 1978 seemed to cure that. I’ve had good health since until lupus in 2013. I firmly believe ITP and Lupus are connected

    posted March 20


    I was diagnosed with SLE Lupus in 1991 by University of Miami. I have struggled with it for years. I also have FIBROMYALGIA, Sjogron's disease, Hypothyroidism, Hypertension, 2 Brain aneurysms, Degenative Disc Disease, now as of last year I was diagnosed with ITP, I actually almost died from it. By the time I saw the Oncologist My platelets were at around 3! I immediately had within a half hour got IV of Gamagoblin, 6 and a half hours of IV. The following week I started Retuxemb Chemotherapy for another 4 weeks. It was pretty bad,, and I was pretty ill from it all. Now I have my platelets somewhat stable in the 100's. But I a, possibly going to need treatments all my life. The treatments only last 1.5 years to 2 years. This all started after I had my First 2 vaccines with Phizer. My Oncologist told me not to take any boosters or any other vaccines for that matter. I am holding my own for now!

    posted March 23


    You poor thing! What were you experiencing before your last diagnosis?

    posted April 17


    I was experiencing vision problems, spots if I'm go out when very sunny. I also had Cataract Surgery in my right eye. They will probably do the left eye also. I was doing real well until Placqueniltisity showed up.

    posted April 17


    I was diagnosed years ago with lupus and was being treated and monitored by my rhiatmatoligist with good success. I had vasculititus on the brain and also wasn't making any new blood cells. I've had lost part of my lung do to massive abscess on lung and now have a cavity due to a secondary infection. I moved to another district and changed my hospital snd have never had any treatment since as my doctor thinks it was a false positive on my blood tests and hasn't even seen my files from my last consultant. I'm left to just get on with it now. I'm scared I will die

    posted April 17
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    Zeba Faroqui, M.D. earned her medical degree from the SUNY Downstate College of Medicine. Learn more about her here.
    Emily Wagner, M.S. holds a Master of Science in biomedical sciences with a focus in pharmacology. She is passionate about immunology, cancer biology, and molecular biology. Learn more about her here.

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