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Complement receptor 1 gene polymorphism and cardiovascular disease in dialyzed end-stage renal disease patients
Monika Buraczynska1, Piotr Ksiazek, Piotr Wacinski
1Laboratory for DNA Analysis and Molecular Diagnostics, Department of Nephrology, Medical University of Lublin, Lublin, Poland. monika.buraczynska@am.lublin.pl
Insights
Genetic variations in the complement receptor 1 (CR1) gene are linked to cardiovascular disease (CVD) in patients with end-stage renal disease (ESRD). The CR1 C5507G polymorphism, specifically the GG genotype, is an independent risk factor for CVD in this population.
Area of Science:
- Genetics
- Cardiology
- Nephrology
Background:
- Inflammation is a key factor in cardiovascular disease (CVD) development.
- The complement system, part of innate and acquired immunity, is implicated in inflammatory processes.
- End-stage renal disease (ESRD) patients exhibit a higher prevalence of CVD.
Purpose of the Study:
- To investigate the association between complement receptor 1 (CR1) gene polymorphisms and CVD in patients with ESRD.
- To determine if CR1 gene variations act as risk factors for CVD in the ESRD population.
Main Methods:
- Genotyping of CR1 gene polymorphisms (C5507G) in 1200 ESRD patients, 360 type 2 diabetes patients, and 924 healthy controls.
- Statistical analysis including odds ratios (OR), confidence intervals (CI), and multivariate logistic regression.
- Comparison of genotype and allele frequencies between patient groups and controls.
Main Results:
- The GG genotype of the CR1 C5507G polymorphism was significantly more frequent in ESRD patients with CVD compared to those without CVD and controls (ORs 3.44-5.46).
- This GG genotype was present in 62% of ESRD patients with a history of myocardial infarction.
- The G allele of C5507G was also more frequent in ESRD patients with CVD (ORs 1.97-2.24) and identified as an independent risk factor (p < 0.001).
Conclusions:
- The CR1 gene C5507G polymorphism is strongly associated with CVD in ESRD patients.
- The GG genotype and G allele carrier status represent significant risk factors for developing CVD in this patient cohort.
- These findings highlight the role of the complement system in CVD pathogenesis within the context of ESRD.
Abstract:
Inflammation plays an important role in cardiovascular disease (CVD). The complement system is a critical component of innate and acquired immunity. We investigated whether the polymorphisms in the complement receptor 1 (CR1) gene are associated with CVD in end-stage renal disease (ESRD) patients. The study groups of 1200 patients with ESRD, 360 patients with type 2 diabetes and 924 healthy individuals were genotyped. The GG genotype of the C5507G polymorphism was significantly more frequent in ESRD patients with CVD than in patients without CVD and controls (odds ratio [OR] = 3.44, 95% confidence interval [CI] = 2.23-5.3, and OR = 5.46, 95% CI = 3.72-8.0, respectively). The GG genotype was observed in 62% of patients with a history of myocardial infarction. The frequency of the G allele was also higher in patients with CVD (OR = 2.24, 95% CI = 1.93-2.61 vs controls, and OR = 1.97, 95% CI = 1.63-2.36 vs patients without CVD). In the multivariate logistic regression analysis the carrier status of G allele of C5507G polymorphism was an independent risk factor of CVD in ESRD patients (p < 0.001). In conclusion, our results suggest strong association between the CR1 gene polymorphism and CVD in ESRD patients.
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