/SiteAssets/Images/FMOLHSBlankBanner.png

Health Information

Membranoproliferative GN
Bookmarks

Membranoproliferative GN

Print-Friendly  

Membranoproliferative GN I; Membranoproliferative GN II; Mesangiocapillary glomerulonephritis; Membranoproliferative glomerulonephritis; Lobular GN; Glomerulonephritis - membranoproliferative; MPGN type I; MPGN type II

Membranoproliferative glomerulonephritis is a kidney disorder that involves inflammation and changes to kidney cells. It may lead to kidney problems.

I Would Like to Learn About:

  • Causes

    Glomerulonephritis is inflammation of the glomeruli. These structures of the kidney help filter wastes and fluids from the blood to form urine.

    Membranoproliferative GN is a form of glomerulonephritis caused by an abnormal immune response. Deposits of antibodies build up in a part of the kidneys called the glomerular basement membrane. This membrane helps filter wastes and extra fluid from the blood.

    Damage to this membrane affects the kidney's ability to create urine normally. It may allow blood and protein to leak into the urine. If enough protein leaks into the urine, fluid may leak out of the blood vessels into body tissues, leading to swelling (edema). Nitrogen waste products may also build up in the blood (azotemia).

    There are two forms of membranoproliferative GN:

    • Membranoproliferative GN I
    • Membranoproliferative GN II

    Most people with the disease have type I. Membranoproliferative GN II is much less common. It also tends to get worse faster than membranoproliferative GN I.

    Many cases of membranoproliferative GN are due to causes such as:

    • Autoimmune diseases (systemic lupus erythematosus, scleroderma, Sjogren syndrome, sarcoidosis)
    • Cancer (leukemia, lymphoma)
    • Infections (hepatitis B, hepatitis C, endocarditis, malaria)

    The conditions mostly affect people ages 8 to 16.

  • Symptoms

    • Blood in the urine
    • Changes in mental status such as decreased alertness or decreased concentration
    • Cloudy urine
    • Dark urine (smoke, cola, or tea colored)
    • Decrease in urine volume
    • Foamy urine
    • Swelling of any part of the body
  • Exams and Tests

    Your doctor or nurse will examine you. You may have swelling (usually in the legs), along with other signs of fluid overload, such as abnormal sounds when listening to the heart and lungs with a stethoscope.

    Blood pressure is often high.

    Membranoproliferative GN may be seen as:

    • Abnormal urinalysis without symptoms
    • Acute nephritic syndrome
    • Nephrotic syndrome

    The following tests help confirm the diagnosis:

    • BUN and creatinine blood test
    • Blood complement C3 level
    • Blood complement levels
    • Urinalysis
    • Urine protein

    A kidney biopsy confirms the diagnosis of membranoproliferative GN I or II.

  • Treatment

    Treatment depends on the symptoms. The goals of treatment are to reduce symptoms, prevent complications, and slow the progression of the disorder.

    You may need a change in diet. This may include limiting salt, fluids, or protein to help control high blood pressure, swelling, and the buildup of waste products in the blood.

    Medicines that may be prescribed include:

    • Blood pressure medications
    • Dipyridamole, with or without aspirin
    • Diuretics
    • Medications to suppress the immune system, such as cyclophosphamide
    • Steroids

    Treatment is more effective in children than in adults. Dialysis or kidney transplant may eventually be needed to manage kidney failure.

  • Outlook (Prognosis)

    The disorder often slowly gets worse and eventually results in chronic kidney failure.

    Half of patients with this condition develop chronic kidney failure within 10 years. This is more likely in those who have higher levels of protein in their urine.

  • Possible Complications

    • Acute nephritic syndrome
    • Acute renal failure
    • Chronic kidney disease
    • End-stage kidney disease
    • Nephrotic syndrome
  • When to Contact a Medical Professional

    Call for an appointment with your health care provider if:

    • You have symptoms of this condition
    • Your symptoms get worse or do not go away
    • You develop new symptoms, including decreased urine output
  • Prevention

    Prevention is often not possible.

Related Information

  Glomerulonephritis...Immune responseAntibodyAcute nephritic sy...Nephrotic syndrome...UrinalysisSwellingHigh blood pressur...Renin blood test...BUN - blood test...     High blood pressur...

References

Appel GB, Radhakrishnan J. Glomerular disorders and nephrotic syndromes. In: Goldman L, Schafer AI, eds. Cecil Medicine. 24th ed.Philadelphia, PA: Saunders Elsevier; 2011:chap 123.

Nachman PH, Jennette JC, Falk RJ. Primary glomerular disease. In: Taal MW, Chertow GM, Marsden PA, Skorecki K, Yu ASL, Brenner BM,eds. Brenner & Rector's The Kidney. 9th ed. Philadelphia, PA: Saunders Elsevier; 2011:chap 31.

BACK TO TOP 

Review Date: 9/8/2013  

Reviewed By: Charles Silberberg, DO, Private Practice specializing in Nephrology, Affiliated with New York Medical College, Division of Nephrology, Valhalla, NY. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Bethanne Black, and the A.D.A.M. Editorial team.

The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed medical professional should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only -- they do not constitute endorsements of those other sites. © 1997- A.D.A.M., Inc. Any duplication or distribution of the information contained herein is strictly prohibited.

adam.com

 
A.D.A.M. content is best viewed in IE9 or above, Fire Fox and Google Chrome browser.