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Published on: July 14, 2016
Complement factor H gene polymorphism and risk of cardiovascular disease in end-stage renal disease patients
Monika Buraczynska1, Piotr Ksiazek, Pawel Zukowski
1Laboratory for DNA Analysis and Molecular Diagnostics, Department of Nephrology, Medical University of Lublin, Lublin, Poland. monika.buraczynska@am.lublin.pl
Insights
The CFH Y402H gene variant is linked to cardiovascular disease (CVD) in patients with end-stage renal disease (ESRD). This genetic factor significantly increases the risk of CVD in dialyzed individuals.
Area of Science:
- Nephrology
- Cardiology
- Genetics
Background:
- Cardiovascular disease (CVD) is the primary cause of mortality in end-stage renal disease (ESRD).
- Complement factor H (CFH) is implicated in CVD risk, but its specific role in ESRD patients is unclear.
Purpose of the Study:
- To investigate the association between the CFH Y402H polymorphism and CVD risk in a large cohort of ESRD patients.
- To determine if CFH Y402H acts as an independent risk factor for cardiovascular comorbidity in dialyzed patients.
Main Methods:
- Genotyping of the CFH Y402H (T1277C) polymorphism in 1200 ESRD patients and 818 healthy controls.
- Comparison of genotype frequencies between ESRD patients with and without CVD, and with healthy controls.
- Multivariate logistic regression analysis to assess independent associations.
Main Results:
- Significant differences in genotype frequencies were observed between ESRD patients with CVD and those without, as well as healthy controls (p<0.001).
- Homozygosity for the C allele of CFH Y402H was strongly associated with CVD in ESRD patients (OR=7.28, 95% CI 5.32-9.95).
- No significant differences were found between ESRD patients without CVD and healthy controls.
Conclusions:
- The CFH Y402H polymorphism is associated with an increased susceptibility to cardiovascular disease in patients undergoing dialysis.
- This genetic variant represents an independent risk factor for cardiovascular comorbidity in the ESRD population.
Abstract:
The main cause of increased mortality in end-stage renal disease (ESRD) is cardiovascular disease (CVD). Complement factor H (CFH) may affect risk of CVD. Our study investigates a role of CFH Y402H polymorphism as a potential risk factor of CVD in a large group of patients. A group of 1200 patients with ESRD and 818 healthy controls were genotyped for the Y402H (T1277C) polymorphism. There was a significant difference in genotype frequencies between patients with CVD and those without CVD and healthy controls (p<0.001). Homozygosity for the C allele in CVD patients was associated with an odds ratio of 7.28 (95 % CI 5.32-9.95). No significant difference was found between patients without CVD and controls. Multivariate logistic regression analysis showed that Y402H genotype was independently associated with cardiovascular comorbidity in ESRD patients. This is the first study suggesting an association between CFH gene polymorphism and susceptibility to CVD in dialyzed patients.
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