MSD Manual

Please confirm that you are a health care professional

Loading

Immunoglobulin A Nephropathy

(IgA Nephropathy)

By

Frank O'Brien

, MD, Washington University in St. Louis

Last full review/revision Jan 2020| Content last modified Jan 2020
Click here for Patient Education
Topic Resources

Immunoglobulin A (IgA) nephropathy is deposition of IgA immune complexes in glomeruli, manifesting as slowly progressive hematuria, proteinuria, and, often, renal insufficiency. Diagnosis is based on urinalysis and renal biopsy. Prognosis is generally good. Treatment options include angiotensin-converting enzyme (ACE) inhibitors, angiotensin II receptor blockers (ARBs), corticosteroids, immunosuppressants, and omega-3 polyunsaturated fatty acids (fish oil).

IgA nephropathy is a nephritic syndrome, a form of chronic glomerulonephritis characterized by the deposition of IgA immune complexes in glomeruli. It is the most common form of glomerulonephritis worldwide. It occurs at all ages, with a peak onset in the teens and 20s; affects men 2 to 6 times more frequently than women; and is more common in whites and Asians than in blacks. Prevalence estimates for IgA kidney deposits are 5% in the US, 10 to 20% in southern Europe and Australia, and 30 to 40% in Asia. However, some people with IgA deposits do not develop clinical disease.

Cause is unknown, but evidence suggests that there may be several mechanisms, including

  • Increased IgA1 production

  • Defective IgA1 glycosylation causing increased binding to mesangial cells

  • Decreased IgA1 clearance

  • A defective mucosal immune system

  • Overproduction of cytokines stimulating mesangial cell proliferation

Familial clustering has also been observed, suggesting genetic factors at least in some cases.

Renal function is initially normal, but symptomatic renal disease may develop. A few patients present with acute kidney injury or chronic kidney disease, severe hypertension, or nephrotic syndrome.

Symptoms and Signs

The most common manifestations are persistent or recurrent macroscopic hematuria or asymptomatic microscopic hematuria with mild proteinuria. Flank pain and low-grade fever may accompany acute episodes. Other symptoms are usually not prominent.

Gross hematuria usually begins 1 or 2 days after a febrile mucosal (upper respiratory, sinus, enteral) illness, thus mimicking acute postinfectious glomerulonephritis, except the onset of hematuria is earlier (coinciding with or immediately after the febrile illness). When this occurs with an upper respiratory illness, it is sometimes referred to as synpharyngitic hematuria.

Rapidly progressive glomerulonephritis is the initial manifestation in < 10% of patients.

Diagnosis

  • Urinalysis

  • Renal biopsy

Diagnosis is suggested by any of the following:

  • Gross hematuria, particularly within 2 days of a febrile mucosal illness or with flank pain

  • Incidentally noted findings on urinalysis

  • Occasionally, rapidly progressive glomerulonephritis

When manifestations are moderate or severe, diagnosis is confirmed by biopsy.

Urinalysis demonstrates microscopic hematuria, usually with dysmorphic red blood cells (RBCs) and occasionally RBC casts. Mild proteinuria (< 1 g/day) is typical and may occur without hematuria; nephrotic syndrome develops in 20%. Serum creatinine level is usually normal.

Renal biopsy shows granular deposition of IgA and complement (C3) on immunofluorescent staining in an expanded mesangium with foci of segmental proliferative or necrotizing lesions. Importantly, mesangial IgA deposits are nonspecific and also occur in many other disorders, including immunoglobulin A–associated vasculitis, cirrhosis, inflammatory bowel disease, celiac disease, psoriasis, HIV infection, lung cancer, and several connective tissue disorders.

Glomerular IgA deposition is a primary feature of immunoglobulin A–associated vasculitis, and it may be indistinguishable from IgA nephropathy based on biopsy specimens, leading to speculation that immunoglobulin A–associated vasculitis may be a systemic form of IgA nephropathy. However, immunoglobulin A–associated vasculitis is clinically distinct from IgA nephropathy, usually manifesting as hematuria, purpuric rash, arthralgias, and abdominal pain.

Other serum immunologic tests are usually unnecessary. Complement concentrations are usually normal. Plasma IgA concentration may be elevated, and circulating IgA-fibronectin complexes are present; however, these findings are not helpful diagnostically.

Prognosis

IgA nephropathy usually progresses slowly; renal insufficiency and hypertension develop within 10 years in 15 to 20% of patients. Progression to end-stage renal disease occurs in 25% of patients after 20 years. When IgA nephropathy is diagnosed in childhood, prognosis is usually good. However, persistent hematuria invariably leads to hypertension, proteinuria, and renal insufficiency. Risk factors for progressive deterioration in renal function include the following:

  • Proteinuria > 1 g/day

  • Elevated serum creatinine level

  • Uncontrolled hypertension

  • Persistent microscopic hematuria

  • Extensive fibrotic changes in the glomerulus or interstitium

  • Crescents on biopsy

Treatment

  • Often angiotensin-converting enzyme (ACE) inhibitors or angiotensin II receptor blockers (ARBs) for hypertension, serum creatinine > 1.2 mg/dL (106.08 micromol/L), or macroalbuminuria (urinary protein > 300 mg/day) and with a target urinary protein of < 500 mg/day

  • Corticosteroids for progressive disease, including increasing proteinuria especially into the nephrotic range, or increasing serum creatinine level

  • Corticosteroids and cyclophosphamide for proliferative injury or rapidly progressive glomerulonephritis

  • Transplantation in advanced disease

Normotensive patients with intact renal function (serum creatinine < 1.2 mg/dL [106.08 micromol/L]) and only mild proteinuria (< 0.5 g/day) usually are not treated beyond angiotensin inhibition (with an ACE inhibitor or ARB) and omega-3 fatty acids (fish oil). Patients with renal insufficiency or more severe proteinuria and hematuria are usually offered treatment, which ideally should be started before significant renal insufficiency develops.

Angiotensin inhibition in IgA nephropathy

ACE inhibitors or ARBs are used on the premise that they reduce blood pressure, proteinuria, and glomerular fibrosis. Patients with the DD genotype for the ACE gene may be at greater risk of disease progression but may also be more likely to respond to ACE inhibitors or ARBs. For patients with hypertension, ACE inhibitors or ARBs are the antihypertensives of choice even for relatively mild chronic kidney disease.

Corticosteroids and immunosuppressants in IgA nephropathy

Corticosteroids have been used for many years, but benefit is not well documented. One protocol uses methylprednisolone 1 g IV once a day for 3 days at the beginning of months 1, 3, and 5 plus prednisone 0.5 mg/kg orally every other day for 6 months. Another regimen uses prednisone beginning 1 mg/kg orally once a day with dose gradually tapered over 6 months.

Because of the risk of adverse effects, corticosteroids should probably be reserved for patients with any of the following:

  • Worsening or persistent proteinuria (> 1 g/day), especially if in the nephrotic range despite maximal ACE inhibitor or ARB therapy

  • Increasing serum creatinine level

Combinations of IV corticosteroids and cyclophosphamide plus oral prednisone are used for severe disease, such as proliferative or crescentic (rapidly progressive) nephropathy. Evidence for mycophenolate mofetil is conflicting; it should not be used as first-line treatment. None of these drugs, however, prevents recurrence in transplant patients. Immunosuppressive therapy should also be avoided in patients with advanced fibrotic kidney disease, which is not reversible.

Other treatments

Omega-3 polyunsaturated fatty acids (eg, 4 to 12 g/day), available in fish oil supplements, have been used to treat IgA nephropathy, but data on efficacy are contradictory. Mechanism of effect may include alterations in inflammatory cytokines.

Other interventions have been tried to lower IgA overproduction and to inhibit mesangial proliferation. Elimination of gluten, dairy products, eggs, and meat from the diet; tonsillectomy; and immune globulin 1 g/kg IV 2 days a month for 3 months followed by immune globulin 0.35 mL/kg of 16.5% solution IM every 2 weeks for 6 months all theoretically reduce IgA production. Heparin, dipyridamole, and statins are just a few examples of in vitro mesangial cell inhibitors. Data supporting any of these interventions are limited or absent, and none can be recommended for routine treatment.

Kidney transplantation is better than dialysis because of excellent long-term disease-free survival. The condition recurs in 15% of graft recipients.

Key Points

  • IgA nephropathy is the most common cause of glomerulonephritis worldwide and is common among young adults, whites, and Asians.

  • Consider the diagnosis in patients with unexplained signs of glomerulonephritis, particularly when it occurs within 2 days of a febrile mucosal illness or with flank pain.

  • Treat patients who have creatinine > 1.2 mg/dL (106.08 micromol/L) or proteinuria > 300 mg/day with ACE inhibitors or ARBs.

  • Reserve corticosteroids for patients with worsening renal function or proteinuria (> 1 g/day) despite maximal ACE inhibitor or ARB treatment.

  • Treat patients who have proliferative injury or rapidly progressive glomerulonephritis with corticosteroids and cyclophosphamide.

Click here for Patient Education
NOTE: This is the Professional Version. CONSUMERS: Click here for the Consumer Version
Professionals also read

Also of Interest

Videos

View All
Overview of Intrarenal Acute Kidney Injury
Video
Overview of Intrarenal Acute Kidney Injury
3D Models
View All
Male Reproductive System
3D Model
Male Reproductive System

SOCIAL MEDIA

TOP