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Published on: October 12, 2017
Clinical usefulness of plasma homocysteine in vascular disease
Graeme J Hankey1, John W Eikelboom, Wai Khoon Ho
1Department of Neurology, Royal Perth Hospital, Wellington Street, Perth, Western Australia, 6001. gjhankey@cyllene.uwa.edu.au
Insights
High homocysteine (tHcy) levels are linked to vascular disease risk. Folic acid therapy did not significantly reduce stroke risk in a recent trial, suggesting current evidence is insufficient for routine screening and treatment.
Area of Science:
- Cardiovascular Medicine
- Nutritional Science
- Clinical Trials
Background:
- Elevated plasma homocysteine (tHcy) is associated with atherogenesis and thrombosis.
- This association is independent of other vascular risk factors but causality remains unproven.
- Causes include genetic mutations, vitamin deficiencies, diseases, drugs, and aging.
Purpose of the Study:
- To evaluate the efficacy of folic acid-based multivitamin therapy in lowering tHcy.
- To assess the impact of tHcy reduction on atherothrombotic vascular disease risk.
Main Methods:
- A randomized controlled trial involving 3680 patients with recent ischemic stroke.
- Intervention group received folic-acid-based multivitamin therapy.
- Comparison group received placebo or standard care.
Main Results:
- No significant benefit was observed from lowering tHcy concentration with folic acid therapy.
- A potential modest reduction in stroke risk (up to 20%) could not be reliably excluded.
- Small tHcy differences between groups may be due to widespread folate fortification and vitamin use.
Conclusions:
- Insufficient evidence currently supports routine screening and treatment of high tHcy.
- Folic acid and other vitamins are not recommended for preventing atherothrombotic vascular disease based on current data.
Abstract:
Raised plasma homocysteine (tHcy) concentrations are caused by genetic mutations, vitamin deficiencies, renal and other diseases, numerous drugs, and increasing age. Raised tHcy concentrations are associated with laboratory evidence of atherogenesis (eg, endothelial dysfunction) and thrombosis, and epidemiological evidence of an increased risk of atherothrombotic vascular disease. An association between raised tHcy concentration and an increased risk of atherothrombosis is independent of other vascular risk factors, strong, dose-related and biologically plausible, but has not been proven to be causal in randomised controlled trials. A recent trial identified no significant benefit from lowering tHcy concentration by folic-acid-based multivitamin therapy among 3680 patients with recent ischaemic stroke, but did not reliably exclude a modest but important reduction in the relative risk of stroke of up to 20%; a difference of only 2 mmol/L in tHcy concentration between the two treatment groups was probably due to widespread vitamin use and fortification of grains and staple foods with folate in North America. There is currently insufficient evidence to recommend routine screening and treatment of high tHcy concentrations with folic acid and other vitamins to prevent atherothrombotic vascular disease.
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