Homocysteine

Note: this site is for informational purposes only. To view test results or book a test, use the NHS app in England or contact your GP.

The homocysteine test measures the level of homocysteine, a sulphur-containing amino acid, in the blood using a blood sample taken from a vein in the arm. It is used to help assess the risk of cardiovascular disease and to investigate conditions such as vitamin B12 or folate deficiency and disorders affecting blood clotting.

Also known as 
Plasma Total Homocysteine; Urine Homocysteine 

Why get tested?

To find out if you have a rare inborn error of metabolism (homcystinuria); also used to determine if you are folate-deficient or vitamin B12-deficient as blood homocysteine concentration can be raised in both conditions.

When to get tested?

If you have symptoms consistent with homocystinuria, for example dislocation of the lens of the eye or some blood clots, and all newborn babies are tested via heel prick in the newborn screening program. Rarely when vitamin B12 concentrations are borderline and suspicion is high that B12 deficiency is present homocysteine (or methylmalonic acid) can help prove tissue deficiency in the face of a normal blood concentration.

Sample required?

A blood sample taken by needle from a vein in the arm.

Test preparation needed?

You may be instructed to fast for 10 to 12 hours prior to this test.

Common questions