alexa Vitamin D Deficiency and Cardiovascular Risk: weare still in the Dark | Open Access Journals
ISSN: 2155-9600
Journal of Nutrition & Food Sciences
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Vitamin D Deficiency and Cardiovascular Risk: weare still in the Dark

Michelle C. Mann*

Cumming School of Medicine, University of Calgary, Canada

*Corresponding Author:
Michelle C. Mann
Cumming School of Medicine
University of Calgary, Canada
Tel: 14032205110
E-mail: [email protected]

Received date: September 22, 2015; Accepted date: October 09, 2015; Published date: October 19, 2015

Citation: Mann MC (2015) Vitamin D Deficiency and Cardiovascular Risk: we’re still in the Dark. J Nutr Food Sci 5:418. doi: 10.4172/2155-9600.1000418

Copyright: © 2015 Mann MC. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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For decades, observational studies has provided evidence of the association between reduced levels of 25-hydroxy vitamin D and increased risk of cardiovascular disease. It is generally accepted that vitamin D deficiency is in some way related to adverse cardiovascular outcomes [1,2]. It has been postulated that this association may be a result of reverse causality in which unhealthy and less mobile individuals are less likely to be exposed to sunlight [3], or perhaps due to a physiological chain of events in which low vitamin D concentrations promote downstream vascular remodeling and hemodynamic instability [4,5].

And yet, after thousands of studies have been published on the topic, the global medical community remains very much in the dark regarding whether a true relationship exists between vitamin D deficiency and increased cardiovascular risk. A small number of clinical trials which have aimed to assess the possibility of a direct, causal relationship between low vitamin D concentrations and poor cardiovascular outcomes in select patient populations do exist. Unfortunately, metaanalyses of these trials demonstrate widespread inconsistency in trial duration, sample size, type of vitamin D intervention and route of administration, and primary outcomes [6-8]. As a result, the medical landscape is barren of vitamin D trials with consistent, pragmatic designs formulated a priori to assess cardiovascular outcomes and thus the depth of knowledge of vitamin D has remained stagnant [6].

One large patient population may be able to shine a much-needed spotlight on this topic. Individuals with chronic kidney disease (CKD), specifically those with end-stage kidney disease requiring dialysis, experience dramatically increased risk of cardiovascular disease compared to that of the general population [9]. In addition, the progressive loss of kidney function also results in disruption of regular vitamin D metabolism, thus the prevalence of severe vitamin D deficiency in this patient population is extremely high [10]. The concomitant nature of high cardiovascular risk and severe vitamin D deficiency persistent in CKD provides a unique opportunity to analyze this seemingly complex physiological relationship.

In general, approximately 25% of all deaths in CKD are attributed to Sudden Cardiac Arrhythmic death (SCD) [9,11], which results primarily from miscommunication between the sympathetic and parasympathetic branches of the cardiac Autonomic Nervous System (ANS) and the atrio-ventricular and sino-atrial nodes of the heart [12,13]. Changes in sinus rhythm controlled by the electrical signals passed from the ANS to the heart can be quantified by measuring Heart Rate Variability (HRV) with a typical ambulatory heart monitor [14]. Measures of HRV in CKD patients often demonstrate a dramatic shift in ANS activity, in which the heart is predominantly regulated by excitatory sympathetic signaling couple by extreme withdrawal in inhibitory, cardio-protective parasympathetic control [15,16]. This characteristic imbalance in HRV has been associated with the increased risk of SCD in this patient population [15,16]. Interestingly, observational studies have shown evidence of a link between vitamin D deficiency and abnormal HRV in humans both with and without CKD [17,18], as well as an improvement in HRV responses to a vascular stressor following 4 weeks of intensive oral vitamin D supplementation [19]. These findings suggest that vitamin D may play a role in regulating the activity of the cardiac ANS, and therefore may directly impact cardiovascular and SCD-specific risk to some degree in humans.

Looking further into the CKD population, it becomes apparent that the concentration of serum 25-hydroxy vitamin D may not hold all of the answers. Thoughtful and concise studies by Wolf and colleagues [20,21] have demonstrated that higher levels of activated 1,25-dihydroxy vitamin D, rather than 25-hydroxy vitamin D, are very strongly associated with decreased risk of cardiovascular mortality in the CKD population. Because 1,25-dihydroxy vitamin D is produced mainly in the proximal tubules of the functional kidneys and it therefore chronically low in patients with CKD [20], this data would suggest that activated vitamin D concentrations may drive the observed relationship between vitamin D deficiency and increased cardiovascular risk via the disruption of cardiac ANS regulatory function. Lending to this thought, the aforementioned observational studies also showed that cardio-protective parasympathetic activity was dramatically restored only in subjects who achieved the highest quartile of 1,25-dihydroxy vitamin D levels after 4 weeks of oral supplementation [19].

Clinical trials to assess the plausible causal relationship between low 1,25-dihydroxy vitamin D and cardiac ANS activity as a surrogate marker of cardiovascular risk are far and few between. Results of one completed study, the VITAH Trial, have not yet been published [22]. Basic science investigations have also played a role in helping to expose the nature of the relationship between vitamin D, the cardiac ANS, and cardiovascular risk. While 25-hydroxy vitamin D is viewed as the barometer of vitamin D status, activated 1,25-dihydroxyvitamin D holds a much greater affinity for the vitamin D receptor and is therefore much more effective at eliciting its desired target responses [23]. Interestingly, activated vitamin D is capable of crossing the blood-brain barrier in order to interact with neurons and cells within the nervous system [24,25]. Vitamin D receptors have been located in high concentrations within the mid-brain and brainstem structures that house the preganglionic nerves of the ANS [24]. Neuronal cells with exposure to high concentrations of 1,25-dihydroxy vitamin D have been shown to better regulate the transcription, production, and release of neurotransmitters which act to regulate signal transduction between the ANS and the heart, among other organs [24,25]. From a biological standpoint, there is a clear indication that activated vitamin D could directly interact with the ANS to elicit changes in sympathetic and parasympathetic signaling. Whether exposure of 1,25-dihydroxy vitamin D to the cardiac-specific ANS branches translates into clinical outcomes and reduced cardiovascular risk is not yet clear, but it remains an exciting possibility and potential revelation in the long saga that is vitamin D research.

Ultimately, research up to this point has not been executed in a manner that provides definitive evidence of a causal relationship between vitamin D metabolism and cardiovascular risk. Recent insights from the CKD population and the emergence of alternative surrogate markers of cardiovascular risk are opening up further opportunities for long-overdue clarification on this matter. In order to continue to propel the knowledge of this area further, researchers must be cognisant of the large knowledge gap that persists in the literature. As a global scientific community, we must remain diligent in designing and conducting adequate clinical trials that will truly allow us to step into the light and further our understanding of vitamin D and cardiovascular health.

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