

Have you been asked by your doctor to do a Ceruloplasmin test?
Are you experiencing unexplained symptoms like fatigue, yellowing of the skin, or liver problems?The Ceruloplasmin test might be the key to understanding the cause—especially if there's a suspicion of copper metabolism disorders or rare genetic diseases like Wilson’s Disease.In this comprehensive guide from Dalili Medical, we’ll walk you through everything you need to know about the Ceruloplasmin test:
✅ What is it?
✅ Why is it ordered?
✅ How is it performed?
✅ What does a high or low level mean?
✅ And who should get tested?
Ceruloplasmin is a protein produced by the liver that plays a crucial role in transporting copper throughout the body. In fact, about 95% of the copper in your blood is bound to this protein.
Because of this, the Ceruloplasmin test is often used to:
Assess copper levels in the body
Help diagnose liver disorders
Evaluate neurological symptoms related to copper imbalance
Monitor diseases like Wilson’s Disease, where copper builds up in tissues due to a genetic defect
Doctors typically request this test in the following situations:
Suspected Wilson’s Disease: A rare genetic condition that causes copper to accumulate in the liver, brain, and eyes.
Chronic liver diseases: Such as cirrhosis or hepatitis.
Copper imbalance: To evaluate suspected copper deficiency or copper toxicity.
Unexplained anemia: Especially when no other cause is found.
Neurological or motor disorders: Including tremors, seizures, or abnormal movements.
Malabsorption syndromes: Like Crohn’s disease or celiac disease, which affect nutrient absorption.
Sample Type: A venous blood sample.
Fasting Required? ❌ No fasting is typically needed.
Time for Results: Usually between 24 to 72 hours depending on the lab.
Normal reference ranges can vary by age, sex, and laboratory. However, general guidelines include:
Age Group | Normal Ceruloplasmin Range |
---|---|
Adults | 20 – 50 mg/dL |
Children | 15 – 45 mg/dL |
May indicate:
Wilson’s Disease – a key diagnostic marker.
Copper deficiency
Acute or chronic liver disease
Nephrotic syndrome (loss of protein through urine)
Autoimmune disorders like Behçet’s disease or lupus
May indicate:
Acute or chronic infections
Pregnancy (levels naturally increase)
Use of estrogen or oral contraceptives
Inflammatory liver diseases
Certain cancers
Yes. It’s often recommended to combine with:
Serum copper and 24-hour urinary copper tests
Liver function tests (ALT, AST, ALP, Bilirubin)
Urinalysis
Eye examination (to check for Kayser-Fleischer rings in Wilson’s Disease)
Inform your doctor of any medications or supplements you’re taking (especially estrogen or liver-related drugs).
Don’t stop any medication unless advised by your doctor.
Avoid testing during active infections, as inflammation may cause temporary elevation in levels.
1. Does low ceruloplasmin always mean Wilson’s Disease?
✅ Not always, but it's a strong indicator. Your doctor will confirm with other tests like 24-hour urine copper.
2. Is the ceruloplasmin test enough for diagnosis?
❌ No. It’s part of a larger diagnostic workup that includes copper tests and liver function evaluation.
3. Is high ceruloplasmin dangerous?
Not necessarily. It can be caused by temporary factors like stress, infection, or pregnancy. Your doctor will interpret it in context.
The Ceruloplasmin test is a valuable diagnostic tool for identifying liver conditions, copper imbalances, and Wilson’s Disease. If your doctor recommends it, don’t ignore it. Provide your full medical history to help ensure an accurate diagnosis and personalized care.