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Vitamin D receptor activation and prevention of arterial ageing
M Cozzolino1, A Stucchi, M A Rizzo
1Renal Division, DMCO, University of Milan, San Paolo Hospital, Via A. di Rudinì 8, Milan, Italy. mario.cozzolino@unimi.it
Insights
Vitamin D deficiency increases cardiovascular risk in chronic kidney disease (CKD) patients. Selective vitamin D receptor activators like paricalcitol may offer cardiovascular benefits in CKD by mitigating risks associated with traditional activators.
Area of Science:
- Nephrology
- Cardiology
- Endocrinology
Background:
- Patients with chronic kidney disease (CKD) exhibit significantly higher cardiovascular (CV) morbidity and mortality.
- Common comorbidities in CKD, including hypertension, diabetes, and mineral bone disease, contribute to elevated CV risk.
- Vitamin D deficiency is increasingly recognized as a critical factor exacerbating CV risk in the CKD population.
Purpose of the Study:
- To investigate the role of vitamin D deficiency in cardiovascular risk among chronic kidney disease patients.
- To evaluate the potential cardiovascular benefits of selective vitamin D receptor activators (VDRAs), such as paricalcitol, in CKD.
- To explore the impact of paricalcitol on specific CV risk factors including diabetic nephropathy, hypertension, and vascular calcification.
Main Methods:
- Review of recent data and studies focusing on vitamin D receptor (VDR) activation in CKD.
- Analysis of the effects of non-selective VDRA (calcitriol) versus selective VDRA (paricalcitol) on serum calcium and phosphate levels.
- Examination of clinical evidence regarding paricalcitol's influence on diabetic nephropathy, cardiac disease, hypertension, and vascular calcification in CKD.
Main Results:
- Non-selective VDRA, calcitriol, is associated with increased serum calcium and phosphate, potentially worsening CV risk in CKD.
- Emerging data suggest that selective VDRA, paricalcitol, may possess ameliorative cardiovascular effects in CKD patients.
- Paricalcitol shows potential for positive impact on diabetic nephropathy, cardiac disease, hypertension, and vascular calcification.
Conclusions:
- Vitamin D deficiency is a significant contributor to cardiovascular disease in chronic kidney disease.
- Selective VDRAs like paricalcitol represent a promising therapeutic strategy to mitigate cardiovascular risk in CKD patients.
- Further research into paricalcitol's role may offer new avenues for managing cardiovascular complications in CKD.
Abstract:
In chronic kidney disease (CKD) patients, cardiovascular (CV) morbidity and mortality rate is higher than in the general population, because of frequently concomitant hypertension, peripheral vascular disease, heart failure, vascular calcification (VC), diabetes and mineral bone disease. Recently, another important factor associated to CV risk in CKD has been deeply investigated: vitamin D deficiency. Vitamin D Receptors (VDRs) are present in several systems and tissues and VDR activation is associated to positive effects, resulting in better blood pressure control and prevention of diabetic nephropathy. Unfortunately, the natural, non-selective vitamin D receptor activator (VDRA), calcitriol, is associated to higher serum calcium and phosphate levels, thus worsening CV risk in CKD. Recent data showed that the selective VDRA paricalcitol might have ameliorative CV effects. The potential positive impact of the use of paricalcitol on diabetic nephropathy, cardiac disease, hypertension, and VC may open new paths in the fight against CV disease in CKD patients.
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