Caeruloplasmin, Plasma

 

Specimen requirement

Adult patient:

 

  Heparin gel tube

 

Minimum blood volume: 5 mL

Paediatric patient:

 

Paediatric heparin gel tube

 

Number of vials: 1

 

Minimum blood volume: 1.3 mL

Authorisation code required

No

24 Hr available service

No

Method

Immunoassay

Reference interval

0.14 - 0.37 g/L

 

(Source: from local population study in 2006)

Clinical indication

Suspected Wilson's disease and Menkes’ disease. (Urinary and hepatic copper are more reliable tests for Wilson’s disease.)

Result interpretation

Low levels are found in Wilson's disease but a normal level does not exclude this diagnosis. The molar copper / caeruloplasmin ratio is increased in Wilson’s disease due to increased albumin-bound copper. 

 

Decreased ceruloplasmin levels occur in liver failure, Menkes’ disease (where the copper / ceruloplasmin ratio is decreased) and also in nephrotic syndrome, kwashiorkor, sprue, and scleroderma of the small bowel.

 

Idiopathic hypoceruloplasminaemia occurs as a non-pathogenic genetic variant but aceruloplasminemia causes massive iron overload.

 

Increased levels may occur in pregnancy and in patients on estrogen therapy. Levels are increased by estrogens, in an acute phase response and in liver disease and this may mask a deficiency state.

Measurement of uncertainty

See table.

Frequency of measurement

Weekly