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Published on: May 2, 2013
Correlation between total homocysteine and cyclosporine concentrations in cardiac transplant recipients
D E Cole1, H J Ross, J Evrovski
1Department of Laboratory Medicine & Pathobiology, University of Toronto, Ontario, Canada. davidec.cole@utoronto.ca
Insights
Cardiac transplant recipients commonly have high total homocysteine (tHcy) levels, a risk factor for atherosclerosis. Folate, kidney function, and cyclosporine levels influence tHcy in these patients.
Area of Science:
- Cardiology
- Nephrology
- Pharmacology
Background:
- Elevated total homocysteine (tHcy) is linked to atherosclerotic disease.
- Accelerated coronary atherosclerosis is a major cause of cardiac allograft failure.
- Limited data exists on tHcy levels in cardiac transplant recipients.
Purpose of the Study:
- To investigate the prevalence of hyperhomocysteinemia in cardiac transplant patients.
- To identify factors associated with elevated tHcy in this population.
Main Methods:
- A cohort of 72 cardiac transplant recipients was studied.
- tHcy concentrations were measured and compared to a reference group.
- Multiple linear regression analysis was used to assess predictors of tHcy.
Main Results:
- All transplant patients exhibited tHcy levels above the upper reference limit.
- Mean tHcy was significantly higher in transplant recipients compared to controls.
- Creatinine and cyclosporine concentrations positively predicted tHcy, while folate and time post-transplant negatively predicted it.
Conclusions:
- Hyperhomocysteinemia is prevalent in cardiac transplant recipients.
- Folate status and renal function are key contributors to tHcy levels.
- Cyclosporine levels may also influence tHcy, impacting treatment response interpretation.
Abstract:
Increased circulating total homocysteine (tHcy) has been implicated as an independent risk factor for atherosclerotic disease. In cardiac transplant patients, accelerated coronary atherosclerosis is an important cause of late allograft failure; however, studies of tHcy in this at-risk group are limited. We sampled a cohort of 72 subjects 3.95+/-3.14 (mean +/- SD) years after transplantation and found that all had tHcy concentrations above our upper reference limit (15.0 micromol/L). The mean tHcy in the transplant group (25.4+/-7.1 micromol/L) was significantly greater than in our reference group (9.0+/-4.3 micromol/L; n = 457; P <0.001). We also examined the effect of age, gender, time since transplant, serum folate and cobalamin, total protein, urate, creatinine, albumin, and trough whole blood cyclosporine concentrations. In a multiple linear regression model, only creatinine (mean 144+/-52 micromol/L; P = 0.021) and trough cyclosporine concentrations (191+/-163 microg/L; P = 0.015) were independent positive predictors of tHcy, whereas serum folate (8.35+/-7.43 nmol/L; P = 0.018) and time since transplant (P = 0.049) were significant negative predictors. We conclude that hyperhomocysteinemia is a common characteristic of cardiac transplant recipients. Our analysis suggests that folate and renal glomerular dysfunction are important contributory factors; however, whole blood cyclosporine concentrations may also predict the degree of hyperhomocysteinemia in this population and therefore influence interpretation of any apparent response to treatment.
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