Granulomatosis with polyangiitis (GPA) is a form of vasculitis—a family of rare disorders characterized by inflammation of the blood vessels, which can restrict blood flow and damage vital organs and tissues. Formerly called Wegener’s granulomatosis, GPA typically affects the sinuses, lungs, and kidneys but can also involve other tissues and organs. GPA can worsen rapidly, so early diagnosis and treatment are essential to prevent organ damage or failure.
In early stages, GPA symptoms resemble a common cold with persistent runny nose and nasal congestion, but may include nosebleeds, shortness of breath, coughing up blood, sinus pain, hoarseness or middle ear symptoms. Besides potential damage to the kidneys and respiratory tract, other serious complications may include vision or hearing loss, heart disease, and stroke.
GPA is a potentially serious but treatable disease. Corticosteroids such as prednisone are used in combination with medications that suppress the immune system, to control inflammation. Even with effective treatment, relapse can occur, so ongoing medical follow-up is usually necessary.
The cause of GPA is not yet fully understood by researchers. Vasculitis is classified as an autoimmune disorder, a disease which occurs when the body’s natural defense system mistakenly attacks healthy tissues. Abnormal function of white blood cells (neutrophils) is thought to be involved in the disease.
Researchers believe an infection may contribute to the onset of GPA, but it is unlikely that an infection alone can explain this complex disorder. Environmental and genetic factors may play a role as well. Research is ongoing, but so far, no specific infectious, genetic, or environmental factor has been conclusively associated with GPA.
GPA affects an estimated 3 out of every 100,000 people. Although the disorder can occur at any age, onset is usually between 40 and 65 years of age, affecting males and females in equal numbers. The disease is rare in children but does occur. GPA can affect people of any race or ethnic background but appears to mostly affect Caucasians. Because GPA often goes unrecognized, researchers believe it is underdiagnosed, making it difficult to accurately determine its frequency.
The symptoms of GPA can vary greatly from person to person. For some, the disease is mild, while for others it may be severe or even potentially life-threatening. GPA symptoms may come on slowly over a period of months, or develop rapidly in a matter of days. Early symptoms can include:
- Runny nose/nasal congestion
- Sinus pain
- Ear pain/hearing loss
- Shortness of breath
- Coughing up blood
Other symptoms include:
- Joint pain
- Loss of appetite/weight loss
- Eye problems
- Skin sores
- Night sweats
- Numbness in the fingers, toes, or limbs
- Kidney problems (Note: Kidney disease can be present without symptoms; therefore, patients with vasculitis should have regular urine tests.)
Serious complications may occur, including inflammation, bleeding and scarring of the lungs, kidney damage or failure, heart disease, hearing loss, skin scarring, deep vein thrombosis (blood clot), or damage to the bridge of the nose from weakened cartilage.
See your doctor if you have cold symptoms that don’t get better with over-the-counter cold medications, especially if you have nosebleeds, are coughing up blood or have other warning signs.
There is no single test for diagnosing GPA, so your doctor will consider a number of factors, including symptoms, medical history, physical exam findings, laboratory tests, and imaging studies. A biopsy of the affected tissue is sometimes required to confirm the diagnosis.
- Urine tests: A urinalysis can detect red blood cells or excess protein in the urine, which can indicate whether the kidneys are being affected.
- Blood tests: The most common blood test for GPA checks for an antibody called ANCA, or anti-neutrophil cytoplasmic antibody. The ANCA test is positive in most individuals with GPA, so it may help support a suspected diagnosis of GPA. However, a positive test alone does not confirm diagnosis.
- Imaging studies: Chest X-rays can show changes in the lungs. Computed tomography (CT) scans and magnetic resonance imaging (MRI) provide more detailed images of the internal organs and can reveal abnormalities in the sinuses, chest, brain, blood vessels or abdominal organs.
- Tissue biopsy: This surgical procedure removes a small tissue sample from an affected organ, such as the lung, kidney, skin or sinuses, which is examined under a microscope for signs of inflammation or tissue damage.
The course of treatment for GPA depends on the organs affected and disease severity. Patients with milder disease are commonly prescribed corticosteroids such as prednisone, in combination with an immunosuppressant drug called methotrexate, to control inflammation.
Patients with severe disease may be prescribed the biologic drug rituximab, used in conjunction with corticosteroids. Rituximab was approved in 2011 by the U.S. Food and Drug Administration for the treatment of GPA and another form of vasculitis, microscopic polyangiitis. Biologic medications are complex proteins derived from living organisms. Biologics target certain parts of the immune system to control inflammation.
Another option for those with severe disease is cyclophosphamide—a chemotherapy-type drug that blocks abnormal growth of certain cells in the body. It is used in combination with prednisone. Cyclophosphamide is usually limited to a three- to six-month period, then replaced with less toxic drugs such as methotrexate, mycophenolate mofetil, or azathioprine.
Once the disease is in remission, patients will need to continue taking maintenance medications, such as azathioprine, methotrexate or rituximab, to keep the disease under control. The dose of steroids is usually tapered during remission.
Some individuals may experience kidney failure, a serious complication that requires dialysis and/or a kidney transplant. Finally, an option for those with very serious GPA affecting the kidneys or lungs is “plasmapheresis.” Plasmapheresis is a dialysis-like procedure that clears proteins from the plasma of the blood and replaces it with plasma from a donor, or with a plasma substitute.
The medications used to treat GPA have potentially serious side effects, such as lowering your body’s ability to fight infection, and potential bone loss (osteoporosis), among others. Therefore, it’s important to see your doctor for regular checkups. Medications may be prescribed to offset side effects. Infection prevention is also very important. Talk to your doctor about getting a flu shot, pneumonia vaccination, and/or shingles vaccination, which can reduce your risk of infection.
GPA is a chronic disease with periods of relapse and remission. If your initial symptoms return or you develop new ones, report them to your doctor as soon as possible. Regular doctor visits and ongoing monitoring of lab and imaging tests are important in detecting relapses early.
Effective treatment of GPA may require the coordinated efforts and ongoing care of a team of medical providers and specialists. In addition to a primary care provider, you may need to see the following specialists: rheumatologist (joints, muscles, and immune system); pulmonologist (lung); otolaryngologist (ear, nose and throat); nephrologist (kidneys); dermatologist (skin); cardiologist (heart); neurologist (brain/and nervous system); or others as needed.
The best way to manage your disease is to actively partner with your health care providers. Get to know the members of your health care team. It may be helpful to use a health care journal to keep track of medications, symptoms, test results and notes from doctor appointments. To get the most out of your doctor visits, make a list of questions beforehand and bring along a supportive friend or family member to provide a second set of ears and take notes.
Remember, it’s up to you to be your own advocate. If you have concerns with your treatment plan, speak up. Your doctor may be able to adjust your dosage, or offer different treatment options. It is always your right to seek a second opinion.
Living with a chronic disease such as GPA can be challenging at times. Fatigue, pain, emotional stress, and medication side effects can take a toll on your sense of well-being, affecting relationships, work and other aspects of your daily life. Sharing your experience with family and friends, connecting with others through a support group, or talking with a mental health professional can help.
There is no cure for GPA at this time, but early diagnosis and effective treatment can bring the disease into remission, and many patients can lead full, productive lives. Left untreated, GPA can lead to potentially life-threatening organ damage or failure. Even with treatment, many patients will experience periods of relapse, so ongoing medical care is important.
California Runner Finds Helpful Support Through VF and Brandon HudginsArt Diaz, a 49-year-old married father of two, embodies the southern California lifestyle of health and vitality. A native resident of Garden Grove in Orange County, Art works as a retail manager at Skechers, the lifestyle apparel brand headquartered in nearby Manhattan Beach. An avid runner, Art has spent many hours logging countless miles on […]
Creating Vasculitis Awareness in a Remote Corner of OntarioA personal and professional mission for Dr. Michael Fernando and his wife, Patti Kemp. Michael Fernando, MD, is a family practice and emergency physician who lives and practices medicine in rural southwestern Ontario, Canada. Following medical school in the UK (Bart’s and the London School of Medicine), Dr. Fernando trained in family medicine near Fort […]
Brian Kilgarif: A Success Story in Using MobileCause to Raise Funds for VasculitisIf you ever need a shot of motivation, just talk to Brian Kilgarif. Brian is raising money for the VF on behalf of his wife, Steph, who was diagnosed with granulomatosis with polyangiitis (GPA) in 2002, when she was 16. His goals are to raise vasculitis awareness, and to honor the strength of his wife […]
Ronnie Saunders – Student Athlete Inspired to Excel by the Vasculitis Foundation’s Victory Over Vasculitis CampaignFor our final Vasculitis Foundation Patient Profile of 2018, I had the pleasure of sitting down with Ronnie Saunders, a senior at Wheeling Park High School in Wheeling, West Virginia. Like many of the other young vasculitis patients I’ve met over the past two years working with the Vasculitis Foundation, Ronnie’s path to diagnosis included […]
Abby – Triathlete with GPA, Coached by U.S. Olympics Hopeful Brandon Hudgins,On Sunday, July 22, Abby woke up in Lake Placid, New York, a village in the Adirondack Mountains known for its picturesque natural environs—trees, trails and lakes—and for being the site of the 1932 and 1980 Winter Olympic Games. It was an important day for Abby, a psychologist from Alexandria, Virginia, who has dedicated her […]
Declares Victory Over Vasculitis
Brandon Hudgins – Victory Over Vasculitis Update: Brandon Battles BackOn a hot, muggy evening in July, Brandon Hudgins competed in the Liberty Mile in Pittsburgh, Pennsylvania, and finished third, ahead of one longtime rival, but behind two others. “My times weren’t very fast due to the sweltering conditions,” Brandon recalled, “but the effort was there. I fought off many demons and negative thoughts during […]
Ximena Romo Quintana – Raising Awareness and Impacting the Health Care System in Chile through Fundación Vasculitis ChileXimena Romo Quintana is leading the Fundación Vasculitis Chile’s campaign to improve early diagnosis of vasculitis in Chile. My name is Ximena Romo Quintana. I was born in Concepción, which is 500 kilometers south of Santiago, the capital of Chile, and where I have lived since 1988. I studied at the University of Concepción, Chile […]
Gabby O’Donnell – GPA/Wegener’s Patient Blog Connects Her with Young Adults Throughout the WorldAs part of the recently celebrated National Rare Disease Day, I Skyped with Gabriella (Gabby) O’Donnell, a 16-year-old from the Netherlands who was diagnosed with GPA/Wegener’s over two years ago. She recently started a blog to talk about her experiences dealing with vasculitis, which you can read here: http://bit.ly/2FQh1up Hearing her story, I was amazed […]