Chemical Pathology

Notes

Caeruloplasmin is the major protein bound form of copper in the circulation.

Caeruloplasmin levels may be low in Wilson's disease, or in rare acquired copper deficiency states (e.g. excessive zinc intake, persistent infantile diarrhoea, severe malabsorption or nephrotic syndrome).

For investigation of possible Wilson's disease, the GHNHST Gastroenterology protocol for abnormal LFT's only recommends caeruloplasmin measurement in patients under 45 years of age who have persistently raised ALT.

Caeruloplasmin is an acute phase protein and is therefore often elevated in infection and inflammation, samples may therefore not be processed if there is evidence of inflammation (indicated by a raised CRP result). Pregnancy, OCP and oestradiol containing medications may also increase caeruloplasmin levels. 24 hour urine copper measurement is an alternative screening test for Wilson's Disease.

Sample requirements

For adults, blood taken into a 5mL gold top tube (or rust top for the Acute Unit)

5ml gold tube


For children, blood taken into a 3.5mL rust top tube

3.5ml rust top tube



Storage/transport

Do not store. Send at ambient temperature to the laboratory the same day.

Required information

Relevant clinical details and a recent CRP level.

Turnaround times

The samples are sent for analysis to King's College Hospital, London with results expected within 10 days.

Reference ranges

Males: 0.15 – 0.30 g/L

Females: 0.16 – 0.45 g/L

Further information

To learn more about caeruloplasmin visit Lab Tests Online: Caeruloplasmin


Page last updated: 22/11/2023