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Homocysteine levels and MTHFR polymorphisms in young patients with acute myocardial infarction: a case control study
Christos Eftychiou1, Loizos Antoniades, Loukia Makri
1Cardiology Department, Nicosia General Hospital, 215 Old Road Nicosia-Limassol, Strovolos, Nicosia, Cyprus. chiou6christos@yahoo.com
Insights
Higher homocysteine levels are linked to acute myocardial infarction (MI) and multi-vessel coronary artery disease (CAD) in young Cypriot men. MTHFR gene variations were not associated with disease risk, but lower HDL cholesterol correlated with elevated homocysteine.
Area of Science:
- Cardiovascular Genetics
- Clinical Biochemistry
- Epidemiology
Background:
- Elevated homocysteine levels are a known risk factor for coronary artery disease (CAD).
- Methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms are a common cause of genetic hyperhomocysteinemia.
- Premature CAD and acute myocardial infarction (MI) represent a significant health concern, particularly in younger populations.
Purpose of the Study:
- To investigate the association between homocysteine levels, MTHFR polymorphisms (C677T and A1298C), and premature CAD in the Cypriot population.
- To determine the role of these factors in acute myocardial infarction (MI).
- To explore the relationship between homocysteine, MTHFR, and disease severity (single-vessel vs. multi-vessel CAD).
Main Methods:
- A case-control study was conducted with 63 male patients under 50 presenting with MI and 54 age-matched controls without CAD.
- Fasting homocysteine and lipid profiles were measured within 24 hours of admission.
- MTHFR C677T and A1298C polymorphisms were genotyped.
Main Results:
- Mean homocysteine levels were significantly higher in patients (14.5 mol/L) compared to controls (12.3 mol/L).
- No significant association was found between MTHFR C677T or A1298C homozygous genotypes and MI risk.
- Higher homocysteine levels were observed in patients with multi-vessel CAD compared to single-vessel CAD.
- Lower HDL cholesterol was associated with higher homocysteine levels (OR=0.901).
Conclusions:
- Elevated homocysteine levels are associated with acute MI and multi-vessel CAD in Cypriot men under 50.
- MTHFR polymorphisms do not appear to be a significant risk factor for premature CAD or MI in this population.
- Lower HDL cholesterol is a contributing factor to higher homocysteine levels, suggesting a complex interplay in cardiovascular risk.
Introduction:
Increased levels of homocysteine are known to be associated with coronary artery disease (CAD). The most common form of genetic hyperhomocysteinemia results from MTHFR polymorphisms. To examine the role of homocysteine levels and MTHFR polymorphisms in premature CAD and acute myocardial infarction (MI) in the Cypriot population, a case control study was performed in Nicosia General Hospital.
Methods:
Sixty-three male patients less than 50 years old who presented with MI in Nicosia General Hospital were compared with 54 controls without CAD. Fasting homocysteine and lipids were tested within 24 hrs from admission, while MTHFR C677T and A1298C polymorphisms were also tested.
Results:
Mean homocysteine levels were 14.5 mol/L in patients and 12.3 mol/L in controls (p=0.017). Mutant homozygous MTHFR C677T was present in 17.7% of the patients and 19.2% of the controls (p=0.838), while mutant homozygous MTHFR A1298C was found in 16.1% of patients and 13.5% of controls (p=0.690). Mean homocysteine levels were 12.6 mol/L in patients with single-vessel CAD and 15.5 mol/L in patients with multi-vessel CAD (p=0.025). Lower HDL appeared to be associated with higher levels of homocysteine with an odds ratio of 0.901, indicating that for each unit increase in HDL, the expected odds of having high homocysteine levels decreased by approximately 10%.
Conclusions:
Higher levels of homocysteine are associated with acute MI and multi-vessel disease in Cypriot patients under the age of 50. The existence and extent of disease are not associated with MTHFR polymorphisms. Lower HDL is associated with higher levels of homocysteine.
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