Homocysteine, a sulphur-containing amino acid is an intermediate product in the normal biosynthesis of the amino acids methionine and cysteine.  Homocysteine is predominantly metabolised via two pathways.  The enzyme MTHFR converts homocysteine to methionine.  The MTHFR is strongly dependent on cofactors folate and vitamin B12.

In addition, homocysteine can increase coagulability, cause endothelial dysfunction, induce the production of inflammatory factors and accelerate atherosclerosis in animal models.  High levels are also associated with stroke, cognitive deficit, autism, Alzheimer’s disease, bone fracture, osteoporosis and depression.  The role of homocysteine in these disorders may also be related to its pro-oxidant activity, the induction of pro-inflammatory factors and its negative affects on blood vessels.

Common Conditions:

• Alzheimer’s disease
• Autism
• Cardiovascular disease
• Cognitive deficit
• Depression
• Osteoporosis
• Stroke
• NOTICE TO PATIENTS

WellLab practices in the usual practitioner-referral system for pathology laboratories. Patients are highly recommended to seek the supervision and guidance of a qualified healthcare practitioner for the interpretation of any lab results and associated information. WellLab can offer assistance in locating a suitable practitioner.

Analytes

Homocysteine-Fasting