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Published on: October 2, 2020
Vitamin D receptor alleles and C-reactive protein in hemodialysis patients
Stefania Pacini1, Tiziana Punzi, Massimo Gulisano
1Department of Anatomy, Histology and Forensic Medicine, University of Firenze, Italy. stefania.pacini@unifi.it
Insights
Certain Vitamin D Receptor gene variations (alleles b, a, T) are linked to higher C-reactive protein levels in hemodialysis patients. These variations may indicate increased cardiovascular disease risk due to inflammation and atherosclerosis.
Area of Science:
- Nephrology
- Cardiology
- Genetics
Background:
- Cardiovascular disease (CVD) is a primary cause of death in uremic patients.
- Inflammation, indicated by C-reactive protein (CRP), is crucial in atherosclerosis development and predicts CVD risk.
- Vitamin D Receptor (VDR) gene polymorphisms influence Vitamin D's effects and disease susceptibility.
Purpose of the Study:
- To investigate the association between specific VDR gene polymorphisms (BsmI, ApaI, TaqI, FokI) and serum CRP levels.
- To identify potential genetic risk factors for inflammation-related CVD in hemodialysis patients.
Main Methods:
- Genotyping for four VDR polymorphisms (BsmI, ApaI, TaqI, FokI) in 88 hemodialysis patients.
- Measurement of serum C-reactive protein levels.
- Statistical analysis to compare allele frequencies between patients with normal and elevated CRP levels.
Main Results:
- Alleles b (BsmI), a (ApaI), and T (TaqI) of the VDR gene were significantly more frequent in patients with elevated CRP levels (p < 0.05).
- These VDR alleles were associated with higher inflammation markers in the context of hemodialysis.
Conclusions:
- VDR alleles b, a, and T may serve as novel risk factors for atherosclerosis-dependent CVD in uremic patients.
- These findings highlight the role of VDR genetics in modulating inflammation and cardiovascular risk in chronic kidney disease.
Abstract:
Cardiovascular disease due to atherosclerosis is the major determinant of morbidity and mortality in uremic patients. Inflammation is essential in the development of atherosclerosis and markers of inflammation, in particular C-reactive protein, predict the cardiovascular risk. Vitamin D exerts its effects through the Vitamin D Receptor, coded for by a gene showing several polymorphisms associated with a variety of diseases and differential responses to Vitamin D. We evaluated the association between four Vitamin D Receptor polymorphisms (i.e. those identified by the restriction enzymes BsmI, ApaI, TaqI and FokI) and serum level of C-reactive protein in 88 hemodialysis patients routinely treated with active Vitamin D (calcitriol). Absence or presence of the BsmI, ApaI, TaqI, and FokI restriction sites were denominated B and b, A and a, T and t, F and f respectively. Our results show that the b, a, T, alleles were more frequent in patients with elevated serum level of C-reactive protein compared with patients with normal C-reactive protein level. The differences were statistically significant (p < 0.05). These results suggest that the Vitamin D Receptor alleles b, a, T could be considered novel risk factors in the pathogenesis of inflammation-related, atherosclerosis-dependent cardiovascular disease risk in uremic patients.
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