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Hyperhomocysteinemia is a risk factor of recurrent coronary event in young patients irrespective to the MTHFR C677T
J R Gonzalez-Porras1, F Martin-Herrero, R Garcia-Sanz
1Department of Hematology, University Hospital of Salamanca, Paseo de San Vicente, 58-182, Salamanca, 37007, Spain. gonzapor@hotmail.com
Insights
Elevated homocysteine levels in young adults after a first acute coronary syndrome increase the risk of recurrent coronary events. This finding highlights homocysteine as a key predictor, independent of MTHFR C677T gene variants.
Area of Science:
- Cardiovascular Medicine
- Clinical Biochemistry
- Genetics
Background:
- Hyperhomocysteinemia is a known risk factor for cardiovascular disease.
- Limited data exists on its impact on recurrent coronary events (RCE) in younger populations.
- Acute coronary syndrome (ACS) in patients under 55 necessitates understanding long-term risks.
Purpose of the Study:
- To investigate the association between admission total homocysteine (tHcy) levels and RCE incidence in young ACS patients.
- To evaluate the role of MTHFR C677T polymorphism as a risk factor for RCE.
- To identify independent predictors of RCE in this demographic.
Main Methods:
- Prospective follow-up of 140 patients (<55 years) post-first ACS for approximately 49 months.
- Plasma tHcy levels measured at admission and categorized into quartiles.
- Analysis included MTHFR C677T polymorphism screening and multivariate risk factor assessment.
Main Results:
- 35% of patients experienced RCE during follow-up.
- Higher tHcy levels (particularly quartile 4, >12.37 mumol/L) were significantly associated with increased RCE risk (HR=2.5).
- Independent predictors of RCE included older age (>45 years), higher BMI (>25), and elevated tHcy levels.
Conclusions:
- Elevated plasma tHcy at admission is an independent risk factor for RCE in young ACS patients.
- MTHFR C677T polymorphism did not show an association with increased RCE incidence.
- Homocysteine levels are crucial for risk stratification in young individuals post-ACS.
Abstract:
Despite the well-known pro-coagulant effect of hyperhomocysteinemia, data is limited regarding the result on recurrent coronary event (RCE) in young people. One hundred and forty patients <55 years old with a first acute coronary syndrome (ACS) were prospectively followed for a mean (+/-S.D.) follow-up of 49+/-14 months in order to investigate the relationship between homocysteine levels (tHcy) at admission and the incidence of RCE. The tHcy values were divided into quartiles to examine their relationship with end points. Furthermore, we determined the effect of C677T methylene tetrahydrofolate reductase (MTHFR) polymorphism, as well as other risk factors for developing a RCE. The median plasma homocysteine concentration was 9.6 mumol/L (interquartile range, 3.7). In the screening of MTHFR C677T polymorphism in patients with ACS, the T allele frequency was 0.4 and the genotype frequency distributions were in Hardy-Weinberg equilibrium. At time of final evaluation, 49 (35%) of the 140 valuable patients had developed a RCE. Increasing numbers of RCE were observed for increasing quartiles of tHcy according to Kaplan-Meier survival (Log-rank test=0.0092). The MTHFR C677T polymorphism was not associated with an increased incidence of RCE. In multivariate analysis, the variables independently associated with a higher risk of RCE were age older than 45 years [HR=2.7; (95% CI, 1.3-6.1); p=0.030], body mass index more than 25 [HR=2.6; (95% CI, 1.1-5.9); p=0.034] and tHcy levels into quartile 4 (tHcy>12.37 mumol/L) [HR=2.5; (95% CI, 1.1-4.7); p=0.04]. Elevated plasma homocysteine level at admission is an independent risk factor for RCE after the first episode of ACS in young patients irrespective of the status of MTHFR C677T.
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