IgA Nephropathy (IgAN), also known as Berger’s disease, is a rare kidney disease that can cause issues with the kidneys’ ability to filter waste from the bloodstream. IgAN occurs when a compound called immunoglobulin A (IgA) builds up in excess within the kidneys, resulting in inflamed tissue and other complications. Thanks to modern treatment methods, IgAN can be effectively managed and its prognosis significantly improved. However, if left untreated, IgAN can lead to serious health problems, underscoring the importance of timely diagnosis and treatment.
IgAN may progress slowly in some individuals over a span of years or even decades, while in others it can progress more quickly. Symptoms may vary from person to person, and some may experience blood in their urine, while others may have proteinuria (the presence of abnormal amounts of protein in the urine) (1). The disease can also lead to complications such as chronic kidney disease, high blood pressure, and end-stage renal disease (ESRD).
Living with IgA nephropathy can be challenging, both physically and emotionally. However, with proper treatment and support, many people are able to manage their symptoms and live fulfilling lives. While the disease may pose some challenges, it’s important to remember that there are many resources and options available to help patients cope and thrive.
If you think you might have IgAN or experience symptoms of this condition, it’s important to seek medical advice. Ask your doctor about getting tested to determine whether you have IgAN. Additionally, don’t hesitate to ask questions and discuss your concerns with your healthcare team. They can help guide you on the best course of action and provide support and resources as needed.
Currently, there are two medications that may be prescribed for IgAN, Tarpeyo (budesonide) and Filspari (sparsetan). Tarpeyo can help reduce proteinuria and slow the decline in kidney function.
Filspari, on the other hand, works by selectively targeting two critical pathways in the disease progression of IgAN: the complement system and the epithelial-mesenchymal transition (EMT) pathway.
The complement system is a part of the immune system that helps to fight off infections, but it can also contribute to inflammation and damage in the kidneys in people with IgAN. Filspari helps to regulate the complement system, which can help to reduce inflammation and slow down the progression of the disease.
The EMT pathway is a process that occurs when kidney cells transform into a different type of cell, which can contribute to scarring and damage in the kidneys. Filspari can help to inhibit this process, which can help to slow down the progression of the disease and protect kidney function.
Like other treatments for IgAN, both medications can cause side effects and may not be suitable for all patients. Talk to your doctor to see if you are a candidate.
In what ways can corticosteroids improve IgAN symptoms? Corticosteroids are a common anti-inflammatory drug generally prescribed to patients suffering from rheumatologic illnesses like lupus, vasculitis, and rheumatoid arthritis. While more research and data are necessary to continue to develop better treatment methods for IgAN, some studies have shown that corticosteroids are effective at reducing proteinuria and improving the risk of progression to end-stage renal disease (ESRD) in IgAN patients (2).
Are there any downsides to using corticosteroids for IgAN? Some patients who have been prescribed corticosteroids may experience one or more side effects including upset stomach or nausea, weight gain in the face, back of the neck, and torso, high blood pressure, and a buildup of fluids within the body, which can cause the lower legs to swell. Not all patients are candidates for this type of therapy, and the decision to use corticosteroids should be made on a case-by-case basis. Your healthcare provider can provide you with more information and help you make an informed decision about whether corticosteroids are right for you.
What are immunosuppressants and how do they impact IgAN treatment? Immunosuppressants are a class of medications that suppress the immune system, which can be useful in treating some types of autoimmune diseases. In IgAN, immunosuppressive therapy can be effective in reducing proteinuria.
However, immunosuppressive therapy comes with a risk of infection and other side effects. It is typically reserved for patients who have significant proteinuria, deteriorating kidney function, or other factors that suggest a high risk of developing end-stage renal disease (ESRD).
In some cases, it may be necessary for patients to go on dialysis or receive a kidney transplant for IgAN. While dialysis can be a helpful way to support the body’s struggling kidneys, the procedure itself can be expensive and disruptive. A kidney transplant can be a good option for some patients, but not all patients are candidates for this type of therapy.
Doctors may also choose to prescribe ACE (angiotensin-converting enzyme) inhibitors or ARBs (angiotensin receptor blockers) to help patients with IgAN. These medications can help lower blood pressure and reduce proteinuria, and they are generally well-tolerated. It should be noted, however, that ACE inhibitors and ARBs are not intended to be taken together, as the combination of the drugs can lead to dangerously low blood pressure or other serious health complications.
In addition to medication, lifestyle changes can also help manage the symptoms of IgAN. Eating a healthy diet and exercising regularly can help control blood pressure and cholesterol levels. It is also important to avoid smoking and limit alcohol consumption.
If you have been diagnosed with IgAN, it is important to work closely with your healthcare provider to monitor your kidney function and adjust your treatment plan as necessary. Early detection and treatment of IgAN can help prevent further kidney damage and improve long-term health outcomes.
Resources:
https://www.mayoclinic.org/diseases-conditions/iga-nephropathy/symptoms-causes
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You may also want to connect with other Alzheimer’s caregivers through a support group, whether it meets in-person or online. In addition to the encouragement and empathy they provide, support groups can be a helpful source of tips, resources, and recommendations for navigating the world of Alzheimer’s.
If your loved one is in the early stages of Alzheimer’s, putting a support system together might not seem like priority #1. But it’s never too soon to build a network of people that you can turn to in times of need. Cultivate connections today with the people who can be there tomorrow, or whenever you might need a hand.
You may also want to connect with other Alzheimer’s caregivers through a support group, whether it meets in-person or online. In addition to the encouragement and empathy they provide, support groups can be a helpful source of tips, resources, and recommendations for navigating the world of Alzheimer’s.
It isn’t always easy to look into the future with Alzheimer’s—but doing the legwork now will save you from stress later. If your loved one is in the early stages of illness, you can involve them in conversations about legal, financial, and long-term care planning decisions. Despite the difficulty of these topics, you’ll all feel empowered by facing them early, and you can move ahead with greater confidence.
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Learn More(from 13 patients with LC-FAOD)
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15 providers / patient
7.5 years of data / patient
(from 13 patients with LC-FAOD)
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