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*There are no specific and sensitive diagnostic laboratory findings associated with IgA nephropathy.
*There are no specific and sensitive diagnostic laboratory findings associated with IgA nephropathy.
*Some patients with IgA nephropathy may have elevated concentration of serum total IgA.
*Some patients with IgA nephropathy may have elevated concentration of serum total IgA.
**There is not enough evidence of serum total IgA concentration for the measurement of the severity or activity of IgA nephropathy.
**There is not enough evidence of [[serum]] total [[Immunoglobulin A|IgA]] concentration for the measurement of the severity or activity of IgA nephropathy.
*Urinary Immunoglobulins are not distinctive in IgA nephropathy.
*The urinary [[Immunoglobulins]] are not distinctive in IgA nephropathy.
===Initial Evaluation===
===Initial Evaluation===
# Assess all patients with biopsy-proven IgA nephropathy for secondary causes to rule out common causes of secondary IgA nephropathy
# Assess all patients with biopsy-proven IgA nephropathy for secondary causes to rule out common causes of secondary IgA nephropathy

Revision as of 13:58, 21 May 2018

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

  • There are no specific and sensitive diagnostic laboratory findings associated with IgA nephropathy.

Laboratory Findings

  • There are no specific and sensitive diagnostic laboratory findings associated with IgA nephropathy.
  • Some patients with IgA nephropathy may have elevated concentration of serum total IgA.
    • There is not enough evidence of serum total IgA concentration for the measurement of the severity or activity of IgA nephropathy.
  • The urinary Immunoglobulins are not distinctive in IgA nephropathy.

Initial Evaluation

  1. Assess all patients with biopsy-proven IgA nephropathy for secondary causes to rule out common causes of secondary IgA nephropathy
    1. Viral serologies: HIV, HBV, HCV
    2. Liver function tests
    3. Electrophoresis of serum immunoglobulins
  2. Assess the risk of progression and prognosis by the following parameters at diagnosis and at follow-up:
    1. Blood pressure measurement
    2. Serum creatinine to estimate glomerular filtration rate (GFR)
    3. Proteinuria
    4. Pathological features

A kidney biopsy is to be considered only if signs of AKI and macroscopic hematuria persist for at least 5 days since the onset of kidney injury.

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