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Updated: Jun 5, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Extra-skeletal effects of vitamin D deficiency in chronic kidney disease
Michel Chonchol1, Jessica Kendrick, Giovanni Targher
1University of Colorado Denver, Aurora, CO, USA. Michel.Chonchol@ucdenver.edu
Insights
Vitamin D deficiency is linked to increased risks of cardiovascular and infectious diseases in chronic kidney disease (CKD) patients. Addressing this deficiency may offer a modifiable strategy to improve outcomes for CKD individuals.
Area of Science:
- Nephrology
- Endocrinology
- Cardiology
Background:
- Cardiovascular diseases (CVD) and infectious diseases are leading causes of mortality in chronic kidney disease (CKD) patients.
- Traditional CVD risk factors do not fully explain the elevated CVD risk observed in CKD.
- Vitamin D deficiency is recognized as a significant, potentially modifiable, non-traditional risk factor for CVD in CKD.
Purpose of the Study:
- To review the clinical and experimental evidence linking 25-hydroxyvitamin D (25(OH)D) deficiency/insufficiency to adverse cardiovascular and infectious disease outcomes.
- To explore the non-calcemic, autocrine, and paracrine functions of vitamin D.
- To examine the role of vitamin D in both the general population and CKD patients.
Main Methods:
- Review of existing clinical and experimental studies.
- Analysis of the conversion of 25-hydroxyvitamin D (25(OH)D) to its active form, 1,25-dihydroxyvitamin D (1,25(OH)(2)D).
- Investigation of extrarenal 1α-hydroxylase and vitamin D receptor expression and function.
Main Results:
- Strong association found between 25(OH)D deficiency/insufficiency and increased risk of adverse CVD outcomes.
- Evidence supports a link between low vitamin D levels and higher risk of infectious diseases.
- Vitamin D exhibits significant non-calcemic autocrine and paracrine actions in various tissues.
Conclusions:
- Vitamin D deficiency is a critical factor contributing to CVD and infectious disease risks in CKD.
- The non-calcemic actions of vitamin D are crucial for physiological functions beyond calcium homeostasis.
- Further research and clinical attention to vitamin D status in CKD patients are warranted to mitigate risks.
Abstract:
Cardiovascular diseases (CVD) and infectious diseases represent the two most important causes of death in patients with chronic kidney disease (CKD). The traditional risk factors of CVD do not appear to account sufficiently for the increased risk of CVD in patients with CKD, and vitamin D deficiency appears to be an important non-traditional, and potentially modifiable, CVD risk factor in this patient population. 25-Hydroxyvitamin D (25(OH)D) is converted to its biologically active form, 1,25-dihydroxyvitamin D (1,25(OH)(2)D), by the enzyme 1α-hydroxylase in the kidneys. The recent discovery that many extrarenal tissues also possess both the 1α-hydroxylase enzyme and the vitamin D receptors has provided new insights into the important physiologic autocrine and paracrine roles of vitamin D in various tissues and organs that are mainly dependent on the availability of 25(OH)D from the circulating plasma. Accordingly, the present review focuses on the rapidly expanding body of clinical and experimental evidence that supports a strong association between 25(OH)D deficiency/insufficiency and the risk of adverse CVD outcomes and infectious diseases as well as on the non-calcemic autocrine and paracrine actions of vitamin D both in the general population and in patients with CKD.
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