IgA Nephropathy

What is IgA nephropathy?

IgA nephropathy is a kidney disease that happens when a protein called immunoglobulin A builds up in your kidneys. This protein is part of your immune system and normally helps fight infections. When too much IgA deposits in the tiny filters of your kidneys, it causes inflammation and damage over time.

Your kidneys filter waste from your blood and make urine. When IgA deposits collect in the kidney filters, they can't work as well. This leads to blood and protein leaking into your urine. The condition develops slowly and can take years or even decades to cause noticeable problems.

IgA nephropathy is also called Berger's disease. It affects about 1 in 100,000 people each year in the United States. The disease most often appears in people in their teens to 30s. It affects men about twice as often as women.

Celiac Disease Comprehensive Panel, Infant

Pinpoint gluten sensitivity causing your baby's discomfort
Reveal hidden nutrient deficiencies affecting growth
Clarify digestive issues for better health management

^$214

Celiac Disease Comprehensive Panel

Pinpoint gluten sensitivity causing your discomfort
Reveal nutrient absorption issues affecting your energy
Clarify digestive problems for better gut health

^$374

Symptoms

Blood in the urine, which may look pink, red, or cola-colored
Foamy urine caused by excess protein
Swelling in the hands, feet, or face
High blood pressure
Pain in the side or back near the kidneys
Fatigue and low energy
Decreased urine output

Many people with IgA nephropathy have no symptoms in the early stages. Blood or protein in the urine may only be found during routine testing. Symptoms often appear during or after a respiratory infection or stomach bug.

Causes and risk factors

The exact cause of IgA nephropathy is not fully understood. Researchers believe it happens when the body produces abnormal IgA antibodies. These antibodies then form clumps that get stuck in the kidney filters. The immune system attacks these deposits, causing inflammation and scarring over time. Genetic factors play a role, as the condition tends to run in families.

Certain factors may increase your risk of developing IgA nephropathy. These include being of Asian or Caucasian descent, being male, and having a family history of the disease. Liver disease and celiac disease are also linked to higher risk. Respiratory or gastrointestinal infections can trigger flare-ups in people who already have the condition.

How it's diagnosed

IgA nephropathy is diagnosed through a combination of tests. A urinalysis checks for blood and protein in your urine. Blood tests measure kidney function and can show elevated IgA levels, though high IgA alone does not confirm the diagnosis. A kidney biopsy is the only way to definitively diagnose IgA nephropathy. During this procedure, a small piece of kidney tissue is examined under a microscope for IgA deposits.

Blood tests like IgA can provide clues about this condition, but specialized testing is needed for diagnosis. Talk to your doctor about appropriate testing if you have symptoms or risk factors. Regular monitoring of kidney function is important if you have been diagnosed with IgA nephropathy.

Treatment options

Blood pressure medications, especially ACE inhibitors or ARBs, to protect the kidneys
Corticosteroids or immunosuppressants to reduce inflammation in severe cases
Fish oil supplements with omega-3 fatty acids to reduce kidney inflammation
Low-sodium diet to help control blood pressure and reduce swelling
Limiting protein intake to reduce kidney workload
Staying hydrated and avoiding NSAIDs like ibuprofen
Treating infections promptly, as they can worsen the condition
Dialysis or kidney transplant if kidney function declines significantly

Frequently asked questions

The first sign is often blood in the urine, which may appear during or shortly after a cold or other infection. The urine may look pink, red, or tea-colored. Some people notice foamy urine from protein, while others have no visible symptoms at all. Many cases are discovered through routine urine tests.

There is no cure for IgA nephropathy, but many people live normal lives with proper treatment. About 20 to 40 percent of people develop kidney failure within 20 years of diagnosis. Early detection and treatment can slow disease progression. Some cases remain mild and stable for decades without significant kidney damage.

IgA nephropathy is unique because it's caused by deposits of a specific immune protein called IgA. Other kidney diseases may result from diabetes, high blood pressure, or infections. IgA nephropathy often flares up during infections, unlike most other kidney conditions. It requires a kidney biopsy to diagnose definitively.

Blood tests measure IgA levels and kidney function markers like creatinine and blood urea nitrogen. Elevated IgA in the blood can indicate the condition but does not confirm it. A kidney biopsy showing IgA deposits is needed for definite diagnosis. Regular blood tests help monitor kidney function if you have the disease.

No, high IgA levels alone do not mean you have IgA nephropathy. Many other conditions can raise IgA, including infections, liver disease, and autoimmune disorders. A kidney biopsy is the only way to confirm IgA nephropathy. Your doctor will consider your symptoms, urine tests, and other factors before recommending a biopsy.

Yes, diet plays an important role in managing IgA nephropathy. Reducing sodium helps control blood pressure and swelling. Limiting protein can reduce stress on the kidneys. Fish oil with omega-3 fatty acids may reduce inflammation. Stay hydrated and avoid excessive alcohol. Work with a dietitian for personalized recommendations.

Not everyone with IgA nephropathy needs dialysis. Many people maintain stable kidney function with medication and lifestyle changes. About 20 to 40 percent progress to kidney failure over 20 years. If kidney function drops below 10 to 15 percent, dialysis or transplant becomes necessary. Early treatment reduces the risk of progression.

Yes, IgA nephropathy can recur in a transplanted kidney. Studies show it returns in about 20 to 50 percent of patients within 10 years. However, recurrence is usually mild and progresses slowly. Most transplant recipients do well overall. Regular monitoring helps detect any recurrence early.

Yes, avoid NSAIDs like ibuprofen and naproxen, as they can worsen kidney function. These pain relievers reduce blood flow to the kidneys. Use acetaminophen instead for pain relief. Always tell doctors and pharmacists about your kidney condition before taking new medications. Some antibiotics and other drugs also need dose adjustments.

You should have blood and urine tests every 3 to 6 months to monitor kidney function. Your doctor will check creatinine, protein in urine, and blood pressure. More frequent testing may be needed if your condition worsens or treatment changes. Regular monitoring helps catch problems early. Follow your doctor's recommended testing schedule.