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The dose-response relation between serum homocysteine and cardiovascular disease: implications for treatment and
David S Wald1, Malcolm Law, Joan K Morris
1Wolfson Institute of Preventive Medicine, Charterhouse Square, London EC1 M 6BQ, UK. davidwald@hotmail.com
Insights
Lowering serum homocysteine can reduce cardiovascular disease risk. Treatment should target individuals at high risk, not just those with elevated homocysteine levels.
Area of Science:
- Cardiovascular Disease Research
- Nutritional Epidemiology
- Genetic Epidemiology
Background:
- Elevated serum homocysteine is linked to cardiovascular disease.
- Clinical interest exists in measuring homocysteine to guide folic acid treatment.
- Uncertainty remains whether to target treatment based on homocysteine levels or overall risk.
Purpose of the Study:
- To investigate the association between serum homocysteine and cardiovascular events.
- To evaluate the effectiveness of serum homocysteine as a screening test for cardiovascular disease risk.
- To determine optimal strategies for homocysteine-lowering interventions.
Main Methods:
- Meta-analysis of 12 case-control studies on homocysteine and ischemic heart disease/deep vein thrombosis.
- Meta-analysis of 72 studies on the C677T MTHFR polymorphism and disease risk.
- Analysis of homocysteine distributions in a large prospective study to assess screening performance.
Main Results:
- A linear relationship exists between serum homocysteine and disease events.
- Risk reduction from homocysteine lowering is proportional to the decrease, regardless of baseline level.
- Serum homocysteine demonstrated poor screening performance due to overlapping distributions between affected and unaffected individuals.
Conclusions:
- Homocysteine-lowering interventions should be offered to all high-risk individuals, irrespective of their baseline homocysteine levels.
- Targeting interventions based solely on high homocysteine levels may be suboptimal.
- Personalized risk assessment is crucial for guiding homocysteine-lowering therapies.
Background:
With the recognition that serum homocysteine may cause cardiovascular disease there is clinical interest in homocysteine measurement to guide treatment with folic acid. It is uncertain whether treatment is best directed at those with high homocysteine or those at high risk irrespective of initial homocysteine.
Design And Methods:
Dose-response plots of the associations between serum homocysteine and ischaemic heart disease and deep vein thrombosis were determined from retrospective (case-control) studies (a meta-analysis of 12 age-matched studies) prospective studies and studies of the C677T MTHFR polymorphism (a comparison of risk in three genotypes in a meta-analysis of 72 studies). The value of serum homocysteine as a screening test was assessed from distributions of serum homocysteine in men who did and did not die from ischaemic heart disease in a large prospective study.
Results:
There were straight-line relationships between serum homocysteine and disease events in the three types of study; a given decrease in homocysteine would produce a similar proportional risk reduction from any pre-treatment level. There was substantial overlap between the distributions of serum homocysteine in men who did and did not die of ischaemic heart disease, indicating poor screening performance; there was no serum homocysteine cut-off that concentrated the majority of disease events into a small minority of the population.
Conclusion:
Interventions to lower serum homocysteine, if judged to be worthwhile, should not be limited to people with a high homocysteine but should be offered to everyone at high risk, regardless of pre-treatment homocysteine.
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