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IgA nephropathy is a chronic kidney disease. It progresses over 10 to 20 years, and it can lead to end-stage renal disease. It is caused by deposits of the protein immunoglobulin A (IgA) inside the filters (glomeruli) in the kidney. These glomeruli normally filter waste and excess water from the blood and send them to the bladder as urine. However, the IgA protein prevents this filtering process. This may lead to:
This is the most common cause of inflammation in the glomeruli. It is more common in white and Asian people. It is most often found in people in their teens to late 30s.
The IgA protein is a normal part of the body's immune system. The causes of IgA deposits in the glomeruli are not known. In more than 10% of affected families, it's inherited. Some people who inherit the gene may not have any symptoms but could pass the gene on. Males are affected more often than females.
IgA nephropathy is a silent disease that may go unseen for years. It can happen at any age, but symptoms most often start before age 40. The most common symptom is blood in the urine (hematuria). It takes many years to progress to the stage where it causes problems. These include swelling, recurrent upper respiratory infections, or intestinal disease. People with IgA nephropathy may also have flank pain and a low fever. In very rare cases, blood pressure can become dangerously high.
Your doctor will review your health history and do a physical exam. Other tests may include:
Treatment will depend on your symptoms, age, and general health. It will also depend on how severe the condition is.
Treatment may include:
Complications include:
If your symptoms get worse or you have new symptoms, let your doctor know.
Tips to help you get the most from a visit to your doctor: