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Effect of renal transplantation on endothelial function in haemodialysis patients
Huseyin Kocak1, Kaan Ceken, Asuman Yavuz
1Department of Nephrology, Akdeniz University School of Medicine, Kampus 07070, Antalya, Turkey. hkocak@akdeniz.edu.tr
Insights
Renal transplantation (RTx) significantly improves endothelial function in haemodialysis (HD) patients by enhancing flow-mediated dilatation (FMD). This suggests that eliminating uraemic toxins through successful RTx may reduce cardiovascular risk in HD patients.
Area of Science:
- Cardiovascular Medicine
- Nephrology
- Vascular Biology
Background:
- Haemodialysis patients exhibit high rates of atherosclerotic cardiovascular disease, not fully explained by traditional risk factors.
- Uraemic toxins are implicated in endothelial dysfunction, a key factor in atherosclerosis development in this population.
- Endothelial dysfunction may play a pivotal role in the progression of atherosclerosis in haemodialysis patients.
Purpose of the Study:
- To investigate the impact of renal transplantation (RTx) on endothelial function in haemodialysis (HD) patients.
- To assess if the elimination of uraemic toxins post-RTx improves endothelial function, measured by brachial artery flow-mediated dilatation (FMD).
Main Methods:
- Assessed endothelial function using FMD and glyceryltrinitrate-induced dilatation (NMD) in 30 chronic HD patients before and after RTx.
- Studied 20 age- and gender-matched healthy controls.
- Patients selected had no known atherosclerotic disease or traditional cardiovascular risk factors.
Main Results:
- Flow-mediated dilatation (FMD) significantly improved after RTx in HD patients (6.69% to 10.50%, P<0.001).
- FMD remained lower in HD patients post-RTx compared to healthy controls (10.50% vs 14.02%, P<0.01).
- Nitroglycerin-mediated dilatation (NMD) showed no significant change after RTx and was similar to controls.
Conclusions:
- Successful renal transplantation improves endothelial function, specifically FMD, in haemodialysis patients.
- The elimination of uraemic toxins following RTx is likely responsible for the observed improvement in endothelial function.
- Further research into managing vascular risk in HD patients is warranted.
Background:
Haemodialysis patients (HD) have been characterized by a high incidence and prevalence of atherosclerotic cardiovascular disease. Based on the traditional cardiovascular risk factors in this population, we cannot explain this high incidence and prevalence. One of the mechanisms contributing to cardiovascular risk in HD patients may be to uraemic toxins. Cardiovascular risk factors and uraemic toxins themselves may cause endothelial dysfunction, which may play a pivotal role in the development and progression of atherosclerosis in this population. We hypothesized that elimination of uraemic toxins in response to renal transplantation (RTx) can improve endothelial function as assessed by flow-mediated dilatation of brachial artery in haemodialysis (HD) patients.
Methods:
Endothelial function measured by flow-mediated dilatation of the brachial artery (FMD) and glyceryltrinitrate-induced dilatation of the brachial artery (NMD) were assessed twice, during haemodialysis treatment and after RTx in 30 chronic haemodialysis patients. All patients were characterized by absence of known atherosclerotic disease and traditional cardiovascular risk factors. We also studied age- and gender-matched 20 normotensive healthy controls.
Results:
FMD values significantly improved after RTx (6.69+/-3.1% vs 10.50+/-3.0%, P<0.001) in HD patients. FMD of patients both during haemodialysis and after RTx was lower than in healthy controls (6.69+/-3.1%, 10.50+/-3.0% vs 14.02+/-2.3%, P<0.001 and P<0.01, respectively). There was no change in NMD values after RTx in HD patients (16.27+/-1.9% vs 16.30+/-1.8%, P>0.05). Also, NMD values in all patients were similar to healthy control values.
Conclusions:
There is an improvement of endothelial function as assessed by FMD of the brachial artery after RTx in HD patients. This may be attributed to the elimination of uraemic toxins by successful RTx.
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