néphropathie à IgA
Berger's disease
Revu par Dr Adrian Bonsall, MBBSDernière mise à jour par Dr Colin Tidy, MRCGPLast updated 15 Jul 2017
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Dans cette série :GlomérulonéphriteSyndrome néphrotiqueScan DMSABiopsie rénale
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IgA nephropathy is a condition in which a protein causes damage to the kidneys. The protein is called immunoglobulin A or IgA. Nephropathy means an illness that damages the kidney.
At a glance
IgA nephropathy is a rare kidney condition where antibodies called IgA get trapped in the kidneys.
These trapped antibodies can cause scarring and inflammation in the kidney filters.
Symptoms can vary, including blood or protein in the urine, or sometimes no symptoms at all.
Some people may develop high blood pressure or chronic kidney disease as a complication.
Diagnosis usually requires a kidney biopsy.
Treatment focuses on protecting the kidneys, for example, by controlling blood pressure with medication.
The outlook for IgA nephropathy varies greatly between individuals.
Dans cet article:
Video picks for Problèmes rénaux
The main job of the kidneys is to clear waste materials from the body and maintain a normal balance of fluids and chemicals in the body. The kidneys also have other functions such as helping to control blood pressure.
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What is the cause of IgA nephropathy?
Diagramme en coupe du tractus urinaire

IgA nephropathy is one of a group of conditions called glomérulonéphrite. In the outer part of the kidneys, tiny blood vessels cluster together to form structures called glomeruli. These filter the blood to make urine.
IgA nephropathy is caused by antibodies called IgA being trapped in the kidney and causing damage to the kidney. IgA is short for 'immunoglobulin A'. IgA is a type of antibody our body produces to fight infection. Antibodies are small proteins that circulate in the bloodstream. They are part of the body's defence (immune) system and are sometimes called immunoglobulins. They are made by B lymphocytes - a type of white blood cell.
The IgA gets to the kidneys in the bloodstream and then causes scarring and inflammation in the kidney. The scarring and inflammation are very small and can only be seen with a microscope. The glomeruli are damaged by deposits of IgA. IgA nephropathy does not usually run in families, so you need not worry about passing it on to your children.
The cause of IgA nephropathy is not completely understood. IgA is produced by glands around the throat and bowel to fight off infection. IgA is normally two antibody molecules stuck together.
In IgA nephropathy, these molecules appear to get joined up in longer chains. As these travel around in the blood and pass through the kidney they get stuck in the filters (glomeruli) in the kidney.
The trapped IgA then causes an inflammatory reaction. It is not known why these IgA chains develop.
À quel point est-ce courant ?
Retour au sommaireIgA nephropathy is very uncommon. However, IgA nephropathy is the most common cause of glomérulonéphrite. IgA nephropathy most often starts between 16 and 35 years of age.
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What are the symptoms of IgA nephropathy?
Retour au sommaireThe symptoms caused by IgA nephropathy are very variable from person to person. Many people with IgA nephropathy do not have any symptoms. IgA nephropathy is usually painless but sometimes an acute attack can cause pain over the kidneys and a feeling of sickness (nausea) for a couple of days.
However, the damage to the filters (glomeruli) of the kidneys may cause some blood to appear in the urine. Usually there is only a very small amount of blood in the urine. Therefore any traces of blood in the urine are often invisible and only detected on routine medical check-ups. In other cases there may be a lot more blood which you can see and comes in attacks every so often.
There may also be protein leakage from the kidneys. This may be slight and only detectable on urine tests. Occasionally, high levels of protein leakage cause swollen ankles, with very low levels of protein and high levels of cholesterol in your blood. This is called le syndrome néphrotique.
Sometimes a une maladie semblable à la grippe causes an increase in IgA getting to the kidney. This can cause an increased amount of blood in the urine, which then clears after a few days.
What are the complications of IgA nephropathy?
Retour au sommaireIgA may cause the blood pressure to increase (hypertension). This damages the kidneys and may also put a strain on the heart. It is therefore very important to treat high blood pressure if it develops. Maladie rénale chronique may sometimes occur. Very occasionally and much less often, IgA nephropathy may cause lésion rénale aiguë before any other symptoms have developed.
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Comment est-ce diagnostiqué ?
Retour au sommaireThe first tests include urine tests to check for a urine infection and to measure the protein in your urine. Collecting all of your urine over 24 hours may be needed to see how much protein is leaking from your kidneys. Blood tests will include tests to see how well your kidney is working.
The scarring and inflammation in the kidney can only be seen with a microscope. Therefore, IgA nephropathy is normally only diagnosed after a sample (biopsy test of the kidney) is taken.
What is the treatment for IgA nephropathy?
Retour au sommaireThere is no specific treatment to cure IgA nephropathy. However, there are many treatments that can help to protect the kidneys and so improve the outlook:
It is very important to have regular blood pressure checks and to keep your blood pressure normal.
It is also important to have regular urine checks to see if there is any protein or blood in the urine.
Treatment needs to be started early if blood pressure levels become high. Treating high blood pressure levels helps to reduce any damage to the kidneys.
Treatment with steroids is controversial but steroids may reduce the amount of protein leaking from the kidneys into the urine. Steroids may also reduce the risk of chronic kidney disease and kidney failure (end-stage kidney disease).
The medicines used for blood pressure control with IgA nephropathy are Inhibiteurs de l'enzyme de conversion de l'angiotensine (ECA) or angiotensin receptor blockers (ARBs) - for example, losartan. Even if you don't have high blood pressure, Both ACE inhibitors and ARBs can reduce your risk of developing la maladie rénale chronique. Sometimes ACE inhibitors and ARBs are used together.
Corticostéroïdes can also help to reduce the amount of protein in the urine and reduce your risk of chronic kidney disease.
Medicines called statines may be needed to treat high cholesterol. Your cholesterol may increase because of IgA nephropathy.
Other treatments that may help include other medicines to reduce your defence (immune) system (for example, azathioprine). Medicines that prevent blood clotting in your blood vessels (anticoagulants) have also been used. Removing your tonsils (tonsillectomy) may be used to reduce the amount of IgA in your bloodstream and so reduce any further damage to your kidneys.
If you develop la maladie rénale chronique, this may become severe (end-stage kidney disease). You will then probably need treatment with dialysis and a kidney transplant. Most people with IgA nephropathy do not develop chronic kidney disease. There is a risk of the transplanted kidney becoming affected by IgA nephropathy.
Quelle est la perspective ?
Retour au sommaireThe outlook (prognosis) is very variable from person to person.
IgA nephropathy may get better on its own without any further problems.
IgA nephropathy may continue unchanged for many years. You will then only need regular check-ups with urine and blood tests.
About 1 in 3 people with IgA nephropathy develop la maladie rénale chronique.
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Kidney stones are hard stones that can cause severe pain in your side along with blood in your urine, and nausea and vomiting. You are more likely to develop kidney stones if you eat a Western diet, don't drink enough fluids or are overweight. Once you have had one episode they are likely to recur but there are several kidney stone treatment options available.
par Dr Colin Tidy, MRCGP

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Syndrome néphrotique
Nephrotic syndrome is a condition where the 'filters' in the kidney become 'leaky' and large amounts of protein leak from the blood into the urine. The main symptom is fluid retention (oedema) which is mainly due to the low protein level in the blood. Various diseases can cause nephrotic syndrome, some more serious than others. Treatment and outcome (prognosis) vary, depending on the cause. The most common cause in children, minimal change disease, usually responds very well to treatment.
par Dr Surangi Mendis, MRCGP
Questions fréquemment posées
Can IgA nephropathy be passed down in families?
IgA nephropathy does not typically run in families, so you usually don't need to be concerned about passing it on to your children.
If I have IgA nephropathy, will I always have noticeable symptoms?
Not necessarily. Many people with IgA nephropathy don't experience any symptoms. Sometimes, the only signs are small amounts of blood or protein in the urine, which are often only found during routine medical tests. Occasionally, you might see more noticeable blood in your urine, which can come and go in attacks.
How does IgA nephropathy affect blood pressure?
IgA nephropathy can cause your blood pressure to increase, which is known as hypertension. High blood pressure can further damage the kidneys and put a strain on your heart. Therefore, it's very important to treat high blood pressure if it develops.
What is nephrotic syndrome and how is it related to IgA nephropathy?
Nephrotic syndrome is a condition that can occur with IgA nephropathy if there is a significant leakage of protein from the kidneys. This high level of protein leakage can lead to symptoms like swollen ankles, very low protein levels, and high cholesterol levels in your blood.
Is there a cure for IgA nephropathy?
Currently, there is no specific treatment that can cure IgA nephropathy. However, there are many treatments available that can help protect your kidneys and improve your long-term outlook.
Why would tonsil removal be considered as a treatment?
Removing your tonsils (tonsillectomy) is an unconventional treatment that may be used to try and reduce the amount of IgA in your bloodstream. The aim is to lessen any further damage to your kidneys caused by these IgA deposits.
What are ACE inhibitors and ARBs, and why are they used in IgA nephropathy?
ACE inhibitors (angiotensin-converting enzyme inhibitors) and ARBs (angiotensin receptor blockers) are types of medicines used to control blood pressure. Even if you don't have high blood pressure, these medications can be prescribed to help reduce your risk of developing chronic kidney disease in people with IgA nephropathy. Examples include losartan.
Lectures complémentaires et références
- Reid S, Cawthon PM, Craig JC, et al; Non-immunosuppressive treatment for IgA nephropathy. Cochrane Database Syst Rev. 2011 Mar 16;(3):CD003962. doi: 10.1002/14651858.CD003962.pub2.
- Kamei K, Nakanishi K, Ito S, et al; Long-term results of a randomized controlled trial in childhood IgA nephropathy. Clin J Am Soc Nephrol. 2011 Jun;6(6):1301-7. doi: 10.2215/CJN.08630910. Epub 2011 Apr 14.
- Cheng J, Zhang X, Tian J, et al; Combination therapy an ACE inhibitor and an angiotensin receptor blocker for IgA nephropathy: a meta-analysis. Int J Clin Pract. 2012 Oct;66(10):917-23. doi: 10.1111/j.1742-1241.2012.02970.x.
- Lv J, Xu D, Perkovic V, et al; Corticosteroid therapy in IgA nephropathy. J Am Soc Nephrol. 2012 Jun;23(6):1108-16. doi: 10.1681/ASN.2011111112. Epub 2012 Apr 26.
- Vecchio M, Bonerba B, Palmer SC, et al; Immunosuppressive agents for treating IgA nephropathy. Cochrane Database Syst Rev. 2015 Aug 3;(8):CD003965. doi: 10.1002/14651858.CD003965.pub2.
- Lai KN, Leung JC, Tang SC; Recent advances in the understanding and management of IgA nephropathy. F1000Res. 2016 Feb 11;5. pii: F1000 Faculty Rev-161. doi: 10.12688/f1000research.7352.1. eCollection 2016.
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About the authorView full bio

Dr Colin Tidy, MRCGP
Médecin généraliste, Auteur médical
MBBS, MRCGP, MRCP (Paediatrics), DCH
Dr Colin Tidy is an NHS Doctor, based in Oxfordshire.
About the reviewerView full bio

Dr Adrian Bonsall, MBBS
Medical Author
MA (Chemistry), MBBS (Hons), DCH
Since 2000 Adrian has been employed in emergency and critical care paediatrics based in Sydney, with particular interests in toxicology, trauma and resuscitation.
Historique de l'article
Les informations sur cette page sont rédigées et examinées par des cliniciens qualifiés.
15 Jul 2017 | Dernière version

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