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Published on: May 31, 2016
MTHFR C677T polymorphism as a risk factor for vascular calcification in chronic hemodialysis patients
So-Young Lee1, Hoe-Young Kim, Kyung Mi Park
1Department of Internal Medicine, Bundang CHA General Hospital, College of Medicine, CHA University, 59 Yatap-ro, Bundang, Seongnam, Korea.
Insights
The MTHFR C677T gene variant is linked to increased vascular calcification (VC) in chronic hemodialysis patients. This polymorphism may be a risk factor for VC, impacting patient outcomes.
Area of Science:
- Genetics and Molecular Biology
- Nephrology and Urology
- Cardiovascular Diseases
Background:
- 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism is a potential risk factor for atherosclerosis.
- Limited research exists on the association between MTHFR C677T polymorphism and vascular calcification (VC) in patients undergoing chronic hemodialysis.
Purpose of the Study:
- To investigate the relationship between the MTHFR C677T polymorphism and the degree of VC in chronic hemodialysis patients.
- To assess the association of MTHFR C677T genotypes with peripheral vascular disease and cerebrovascular accidents in this patient cohort.
Main Methods:
- Genotyping for the MTHFR C677T polymorphism was performed in 152 chronic hemodialysis patients.
- Vascular calcification (VC) scores were evaluated and compared across different MTHFR genotypes (CC, CT, TT).
- Prevalence of peripheral vascular disease and cerebrovascular accidents were analyzed in relation to MTHFR genotypes.
Main Results:
- Patients with the TT genotype showed significantly higher VC scores compared to CC and CT genotypes (P = 0.002).
- The incidence of peripheral vascular disease was higher with MTHFR C677T mutations across all patients.
- Younger patients (≤ 60 yr) with MTHFR mutations had an increased incidence of cerebrovascular accidents. Adjusted odds ratios for VC were 1.39 for CT and 1.58 for TT genotypes.
Conclusions:
- The MTHFR C677T polymorphism is associated with an increased degree of vascular calcification in chronic hemodialysis patients.
- This genetic variation may serve as a risk factor for VC and related vascular complications in this population.
Abstract:
Polymorphism of 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T is one of the suggested risk factors for atherosclerosis. However, few studies have reported on the relationship between MTHFR C677T polymorphism and vascular calcification (VC) in chronic hemodialysis patients. We investigated the relationship between the MTHFR C677T polymorphism and VC in 152 chronic hemodialysis patients. Patients with a TT genotype exhibited significantly higher VC scores than patients expressing CC and CT (P = 0.002). The prevalence of peripheral vascular disease increased with the incidence of MTHFR C677T mutations for all patients, and the incidence of cerebrovascular accidents also increased with the presence of mutations for young patients (≤ 60 yr) (P < 0.05). Patients with CT and TT genotypes had adjusted odds ratios for VC of 1.39 and 1.58, respectively (P < 0.05). In summary, these data suggest that the MTHFR C677T polymorphism affects the degree of VC in chronic hemodialysis patients.
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Translation
Translation is the process of synthesizing proteins from the genetic information carried by messenger RNA (mRNA). Following transcription, it constitutes the final step in the expression of genes. This process is carried out by ribosomes, complexes of protein and specialized RNA molecules. Ribosomes, transfer RNA (tRNA), and other proteins produce a chain of amino acids—the polypeptide—as the end product of translation.
Translation Produces the Building Blocks of Life

