Related Experiment Video
Updated: Aug 8, 2026

Mouse Kidney Transplantation: Models of Allograft Rejection
Published on: October 11, 2014
Methylenetetrahydrofolate-reductase gene C677T variant and kidney-transplant survival
1Department of Internal Medicine, Universitätsklinikum Benjamin Franklin, Berlin, Germany.
Insights
The methylenetetrahydrofolate reductase (MTHFR) C677T gene variant does not significantly impact kidney transplant survival. This study found no link between MTHFR genotype and allograft survival rates in renal transplant patients.
Area of Science:
- Nephrology
- Genetics
- Transplantation Immunology
Background:
- Hyperhomocysteinemia is a known risk factor for atherosclerosis and is prevalent in patients undergoing hemodialysis and renal transplantation.
- Atherosclerotic lesions in hyperhomocysteinemia share similarities with chronic allograft injury.
- The methylenetetrahydrofolate reductase (MTHFR) C677T gene variant is associated with elevated homocysteine levels in renal failure patients.
Purpose of the Study:
- To investigate the hypothesis that the MTHFR C677T gene variant influences renal allograft survival.
- To determine if MTHFR genotype is a significant determinant of long-term kidney transplant success.
Main Methods:
- Prospective DNA collection from 336 renal transplant recipients and their donors.
- Analysis of patient and allograft survival over 36 months via blinded record review.
- Genotyping for MTHFR C677T using PCR-RFLP and survival analysis using Kaplan-Meier and log-rank tests.
Main Results:
- The MTHFR C677T allele frequency was consistent across recipients, donors, and long-term survivors.
- Kaplan-Meier analysis showed similar 36-month allograft survival rates among different MTHFR genotype groups (CC, CT, TT).
- Other potential risk factors were evenly distributed across genotype groups.
Conclusions:
- The findings do not support the hypothesis that the MTHFR C677T gene variant is a significant determinant of renal transplant survival.
- The MTHFR C677T genotype does not appear to be a critical factor in predicting kidney allograft outcomes.
Unlabelled:
BACKGROUND. Hyperhomocysteinaemia, a risk factor for atherosclerosis, is common in haemodialysis and renal-transplant patients. As atherosclerotic lesions in hyperhomocysteinaemia resemble those of chronic allograft injury, we examined the hypothesis that the C677T variant of the methylenetetrahydrofolate reductase (MTHFR) gene, which is linked to elevated plasma homocysteine levels in patients with renal failure, determines renal allograft survival.
Methods:
DNA was prospectively collected from 336 patients undergoing renal transplantation in our clinic between 1988 and 1994 and their corresponding donors. Patient and allograft survival was analysed by blinded review of all case records over a follow-up period of 36 months. Additionally, we recruited 83 patients surviving with a functional kidney allograft for at least 10 years (mean: 156, range 120-240 months). MTHFR-C677T genotype was determined by a PCR-RFLP technique. The influence of genotype on transplant survival was analysed by Kaplan-Meyer life-table analysis and two-tailed global log-rank testing.
Results:
Frequency of the MTHFR-C677T allele in the cohort group was identical in recipients (0.35) and donors (0.34), and comparable to that in the longterm allograft survivors (0.37). Furthermore, life-table analysis revealed a similar allograft survival over 36 months between the genotype groups (CC 74%, CT 69%, TT 75%). Other risk factors including donor and recipient age, hypertension, body-mass index, and number of rejection therapies were evenly distributed between the different genotype groups.
Conclusions:
These findings do not support the hypothesis that the C677T variant of the MTHFR gene is an important determinant of renal-transplant survival.
More Related Videos
Related Concept Videos
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu
Pharmacogenetics of Phase II Enzymes: N-acetyltransferase, Thiopurine S-methyltransferase, UDP-glucuronosyltransferase
Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase
Kidney Transplant I: Introduction
Kidney Transplant II: Surgical Procedure
Kidney Transplant III: Nursing Management

