DOI: 10.31038/EDMJ.2019325

Abstract

Objective

Our study aimed to investigate the effect of vitamin D supplementation on blood pressure in vitamin D insufficient young volunteers compared to an age matched control group with sufficient levels of vitamin D. Secondarily we aimed to evaluate the effect of vitamin D supplementation on the RAAS and sympathetic nervous system.

Design

Single centre, Randomised controlled Trial.

Methods

Fifteen vitamin D insufficient and 15 vitamin D sufficient youngsters (18–25 years) were recruited for a clinically controlled trial of 6 months vitamin D supplementation (30 µg/day). At baseline, 30 days, 90 days and 180 days, 24h systolic and diastolic blood pressure, and 25-hydroxyvitamin D, angiotensinogen, renin, angiotensin (I+II), aldosterone, and catecholamines were measured.

Results

The difference between baseline visit and 180 days visit for the vitamin D insufficiency group compared to the control group was; systolic BP (daytime) decreased -6.6 (Interquartile Range 2.4) mmHg (p = 0.009), diastolic BP (daytime) decreased -4.5 (2.1) mmHg (p = 0.03), norepinephrine decreased -0.80 (0.21) nmol/L, (p = 0.0002). There was no effect of vitamin D supplementation on night time systolic or diastolic BP, and no effect on angiotensinogen, renin, angiotensin (I+II), aldosterone or epinephrine.

Conclusion

We observed that 180 days of vitamin D supplementation in normal youngsters with insufficient vitamin D significantly lowered systolic and diastolic BP during daytime. Vitamin D supplementation also significantly lowered circulating norepinephrine. Nothing happened in the control group with normal vitamin D. Hence, it is tempting to conclude that vitamin D acts on BP through SNS as no changes were observed in the RAAS.

Keywords

Vitamin D, Blood pressure, Catecholamines, Normal Youngsters, RAAS.

Introduction

Vitamin D and its importance for skeletal development is well known. The research field of Vitamin D has been broadend even to gene regulation on a grand scale [1]. Recently, Vitamin D deficiency has been found associated with hypertension and several other diseases in epidemiological studies [2, 3] and is a risk factor for cardiovascular mortality [4] and cardiovascular incidents [5, 6] Vitamin D deficiency is prevalent in all ages [7], races [8], geographical regions [9], socioeconomic strata and seasons [10]. Hypertension and vitamin D deficiency are both prevalent worldwide [9, 11, 12] and a causative link between these may potentially have wide public health implications. Hypertension and heart disease are an enormous burden for society. The total direct and indirect costs in 2010 were estimated to $ 273 billion and $ 172 billion respectively in the US [13]. Vitamin D supplementation could potentially be a novel pathway to ease the burden of hypertension, given the low cost and mild adverse effects [14, 15]. Intervention studies with vitamin D supplementation for treatment of hypertension have yielded inconsistent results [16–34]. This inconsistency could be attributed to factors with influence on S-25[OH]D or attenuate the outcome blood pressure e.g. seasonal variation [20, 30], non-cardiovascular comorbidity [16–18, 20–24, 26, 27, 30–32, 34] , medication [16–18, 21–28, 30–32, 34] and normal physiological (S-25[OH]D >50 nmol/L) vitamin D levels [16–18, 21, 24, 26–28, 30, 32, 34] before treatment.

Regulation of Blood Pressure (BP) acts mainly through the Renin-Angiotensin-Aldosterone System (RAAS) and the Sympathetic Nervous System (SNS) [35]. Vitamin D supplementation is associated with the cardiac autonomic tone in healthy humans [36], and could indicate a modulating role of vitamin D in the SNS.

Vitamin D is a secosteroid hormone although it can be obtained through food intake [37]. The main source of vitamin D is represented by its synthesis in the body itself [38]. Vitamin D in its active form, 1, 25-dihydroxyvitamin D₃ [1, 25(OH)₂D₃], crosses the cell membrane, enters the target cell and binds to a specific nuclear vitamin D receptor. The receptor is found in the kidneys, and in mice a decrease in vitamin D is found to increase renin [39]. Vitamin D supplementation could potentially lower renin, which is the first step in the RAAS-pathway and might have a cascading effect on the RAAS-pathway resulting in lowering angiotensin and aldosterone with a lower systemic BP as a result. In rats, vitamin D depletion leads to increases in norepinephrine [40] and increases in systolic BP [41].

To take into account the factors that could blunt or attenuate the effect of vitamin D on BP regulation an investigative setting; with healthy young adults and a group with constant vitamin D concentration acting as control group would be preferable to deal with the seasonal variation. In such a setting, it would be possible to get a more clear view of the effects of vitamin D on BP regulation. To our knowledge, this has not yet been done.

Our clinical trial aimed to investigate the effect of vitamin D supplementation on the BP in two groups; one with vitamin D insufficiency and one with normal levels of vitamin D. The secondary aim was to investigate the effects of vitamin D supplementation on RAAS and the autonomous nervous system, hopefully elucidating possible underlying mechanisms.

Methods

Study Design and Participants

The study was carried out from October 2012 to August 2014 as a single center, parallel-group, clinical controlled trial conducted at the Department of Clinical Physiology, Nuclear Medicine & PET, Rigshospitalet, Copenhagen, Denmark.

Subjects were recruited from a screening of 99 young adults aged 18–25 years. We found 27 potential controls with sufficient vitamin D levels (S-25[OH]D > 80 nmol/L) and 33 with insufficient vitamin D levels (S-25[OH]D <50 nmol/L) and all were invited to participate by e-mail. Participants were excluded if they suffered from diseases or took medication known to interfere with vitamin D as well as pregnancy, hypertension, heart- or kidney disease, diabetes, epilepsy, bone diseases, use of anabolic or systemic steroids

After 15 controls and 15 vitamin D insufficient volunteers accepted the invitation further enrollment was stopped. After enrolment serum 25[OH]D was remeasured to assure that each participant was within inclusion limits of each group on the first day of the study. Each subject’s respective vitamin D level was a result of their lifestyle and genes as all participants were vitamin D so-called naive as only subjects who did not take supplementation was included in the study.

Ethics

We performed the study in accordance to the Helsinki II declaration considering biomedical research. Informed, written consent was obtained from all participants prior to enrollment. The Ethical Committee of the Capital Region, Denmark (ref. no. H-1–2012–023) approved the project.

Intervention

The vitamin D insufficiency group was supplemented to increase the concentration of S-25[OH]D and the control group were supplemented to be kept at S-25[OH]D normal steady state concentration > 80 nmol/L. All participants were supplemented by 30 µg cholecalciferol and 1.200 mg of calcium per day. The participants were instructed to bring all supplied containers and remaining tablets to next visit for compliance estimation.

Study Program

The program comprised four visits, at baseline, after one month, three months, and six months. All visits took place between 08.00 and 17.00; participants had fasted for two hours prior to all visits.

Participants rested 30 min supine position before blood sampling for the assessment of S-25[OH]D, angiotensinogen, renin activity, angiotensin I, angiotensin II, aldosterone, epinephrine, and norepinephrine. Office BP in sitting position was measured and 24-hour ambulatory BP (24hr-AMBP) recording was performed. Vitamin D supplementation needed until next visit was handed to the participants in containers of 180 tablets to be taken three every day (vitamin D₃ 10 µg and calcium 400 mg per tablet). The second, third, and fourth visit was carried out as the first visit, with the addition of compliance estimation by count of remaining tablets.

Outcome measures

The primary outcome measure was the between-group differences in day and night values from the 24hr-AMBP recording systolic and diastolic BP. The secondary outcome was the between-group comparisons of angiotensinogen, renin activity, angiotensin I, angiotensin II, aldosterone, epinephrine, and norepinephrine.

Measurements

Lifestyle

Through a questionnaire, the participants habit of exercise, smoking and alcohol consumption status was obtained. Smoking: “How many cigarettes have you smoked in the last seven days?” grouped into smoking yes/no. Alcohol: “How many units (12 g) of alcohol have you beendrinking in the last seven days?” grouped into alcohol yes/no. Exercise habits: “How many hours have you spent on exercise in the last seven days?” grouped into three groups; “0–2”, “2–7”, and “7 or more”.

Medical history was obtained through a personal interview to ensure that the subjects were clinically healthy and did not fulfil any of the exclusion criteria. Height was measured using a vertical mounted cm ruler. Weight was measured using an electronic weight (OBH Nordic 6295). Calculation of compliance as the difference in prescribed intake and actual intake divided by prescribed intake of vitamin D supplementation.

Blood pressure measurement

Twentyfour hour ambulatory blood pressure data was recorded with the SpaceLabs 90207 oscillometric unit (Spacelabs, Redmond CA). The default daytime interval was set from 07.00 to 23.00 hr and night time interval was set from 23.00 to 07.00 hr. If participants reported other sleep habits, default values were not used, instead the actual day and night time were used. In the day time BP was measured for every 20 min and every 30 min at night time to fullfil the European guidelines for AMBP measuring at least 14-day time and seven-night time measurements.

Biochemical Analyses

Sympathetic nervous system activity

Sympathetic nervous system activity (SNS) was assessed by measurement of plasma epinephrine and norepinephrine after 30 min. at rest in supine position. Blood samples were obtained in pre-chilled EDTA-tubes and centrifuged at 5 °C for 10 min. at 3, 000 rpm and afterwards stored at -80 until analyzed. Plasma norepinephrine and epinephrine was analysed with a commercial RIA-kit (2-Cat RIA from Labor Diagnostika Nord, Nordhon Germany). Catecholamine was calculated as the sum of epinephrine and norepinephrine.

Renin-angiotensin-aldosterone system

Renin-angiotensin-aldosterone system activity was assessed after 30 min of rest in supine position applying both in-house and commercial available biochemical methods. Blood samples for angiotensinogen were obtained in lithium heparin tubes and measured with the antibody trapping method. Blood sample for renin was obtained in pre-chilled EDTA tubes and measured with RIA based on renin activity. Blood samples 10 mL each for angiotensin I+II was obtained in tubes prepared with inhibitor and measured with an in-house RIA-based method. Blood samples for aldosterone were obtained in tubes with a serum clot activator and analysed with Siemens RIA Coat-a-count.

Serum-25-Hydroxyvitamin D

Serum-25[OH]D was analyzed with the chemiluminescent immunoassay (Liaison® 25-OH Vitamin D Total Assay; Diasorin Inc., Saluggia (Vercelli), Italy).

Statistical Analyses

Sample size calculation for the primary outcome was based on the least relevant effect size of 6 mmHg with an SD = 5 mmHg, α = 0.05, and β = 0.80, we calculated a sample size of 15 subjects for each group to be enrolled.

The continuous data was reported as means and Standard Deviations (SD) when data followed a normal distribution or medians and Interquartile Range (IQR) when they did not. Visual inspection of the continuous data was used to determinate the distribution. For categorical data, percentages were used.

Skewed variables were log (e) transformed before use in parametric statistical analysis.

Group analysis at baseline was performed with student’s t-test or χ²-test. The main analysis of the outcome was by originally assigned groups. We attempted to follow-up on subjects who withdraw by phone, texting, and e-mail. Missing data was assumed missing at random.

A mixed model was applied to take advantage of repeated measurements and deal with missing data. Comparison of simple effects was performed at each visit without separating data in one analysis, to test for the effect of supplementation on visits. For all statistics, (SAS® Version 9.3, Cary, NC, USA) was used. We considered a p-value of <0.05 statistical significant.

Results

Two participants with vitamin D insufficiency and one vitamin D sufficient were excluded on the basis of S-25[OH]D, as they were no longer within the inclusion criteria. Two men and one woman in the control group and two men and one woman in the insufficient group did not complete all four visits, Table 1.

Table 1. Baseline characteristics of participants

Baseline characteristics of the youngsters with sufficient levels of S-25[OH]-vitamin D (controls) and with insufficient levels of S-25[OH]-vitamin D

The first baseline visit was performed in October 2012 and the last follow-up visit was performed in August 2014.The analysis comprised in total 11 males aged 20.4 ± 1.7 yrs and 16 females aged 21.0 ± 2.2 yrs. The baseline characteristics of the participants are given in Table 1. At baseline, no significant differences were found regarding age, height, weight, systolic BP, sex, tobacco, and alcohol consumption between the two groups. At baseline, the group with insufficient vitamin D had higher diastolic BP compared to controls.

The period of supplementation (median [Interquartile Range (IQR)]) for vitamin D was 184 [180–200] days for the insufficiency group and 183 [179–200] days for the control group.

The effect of vitamin D supplementation on S-25[OH]D is shown in Figure 1A. Serum-25[OH]D in the insufficiency group increased from 32.0 (IQR 16.5) nmol/L at visit one to 64.5 (IQR 8.6) nmol/L at visit four. In the control group the change was from 99.9 (IQR 24.1) nmol/L at first visit to 96.1 (IQR 27.1) nmol/L at visit four. The estimated treatment effect of vitamin D supplementation on S-25[OH]D (95% Cl) was an impressive mean increase of 38.1 (Range 25.1 to 51.1) nmol/L for the insufficiency group compared to the controls (p<0.0001).

Figure 1. Treatment effect of Vitamin D supplementation compared to baseline values

Overall treatment effect over four visits of vitamin D supplementation (ergocholecalcipherol 30 µg/day) in healthy young adults. All BPs are 24hr-AMBP. (A) Treatment effect on S-25[OH]-vitamin D (nmol/L) is significant at visit two (p = 0.0001), three (p<.0001) and four (p<.0001); (B) Treatment effect on catecholamines (nmol/L) is significant at visit four (p = 0.0009); (C) Treatment effect on systolic-BP (mmHg) in daytime (0700–2300 hour) is significant at visit four (p = 0.009); (D) Treatment effect on diastolic-BP (mmHg) in daytime (0700–2300 hour) is significant at visit four (p = 0.03).

The effect of vitamin D supplementation on systolic-BP (24 hr-AMBP, daytime) is shown in Figure 1C.
Systolic BP (24 hr-AMBP, daytime) in the insufficiency group decreased from 124.5 (IQR 12.3) mmHg at visit one to 120.4 (IQR 9.5) mmHg at visit four. In the control group systolic-BP (24 hr-AMBP, daytime) remained unchanged from 115.8 (IQR 8.2) mmHg at first visit to 115.6 (IQR 7.3) mmHg at visit four. The estimated treatment effect of vitamin D supplementation on systolic-BP (24 hr-AMBP, daytime) was a significant decrease of -6.6 (IQR 2.4) mmHg, (p = 0.009) for the insufficiency group compared to the control group.

The effect of vitamin D supplementation on diastolic-BP (24 hr-AMBP, daytime) is shown in Figure 1D. Diastolic-BP (24hr-AMBP, daytime) in the insufficiency group decreased from 73.1 (IQR 10.9) mmHg at visit one to 71.1 (IQR 9.3) mmHg at visit four. In the control group diastolic-BP (24 hr-AMBP, daytime) remained unchanged from 68.1 (IQR 5.4) mmHg at first visit to 69.3 (IQR 4.5) mmHg at visit four. The estimated treatment effect of vitamin D supplementation on diastolic-BP (24hr-AMBP, daytime) was a significant decrease of -4.5 (IQR 2.1) mmHg, (p = 0.03) for the insufficiency group compared to the control group.

The effect of vitamin D supplementation on systolic-BP (24 hr-AMBP, nighttime) is given in Table 2. Systolic-BP (24 hr-AMBP, night time) in the insufficiency group decreased from 106.8 (IQR 11.2) mmHg at visit one to 103.2 (IQR 12.7) mmHg at visit four. Within the control group systolic-BP (24 hr-AMBP, night time) decreased from 105.3 (IQR 7.1) mmHg at first visit to 102.8 (IQR 6.7) mmHg at visit four. The estimated treatment effect of vitamin D supplementation on systolic-BP (24 hr-AMBP, nighttime) was an insignificant increase of in average 0.7 (IQR 3.4) mmHg, (p = 0.8) for the insufficiency group compared to the controls.

Table 2. Effect of vitamin D supplementation on blood pressure and S-25[OH]-vitamin D

Controls have normal S-25[OH]-vitamin D at baseline whereas all vitamin D insufficient participants had S-25[OH]-vitamin D below 50 nmol/L at baseline. All BP are 24hr-AMBP. Estimated treatment effect (individual change from baseline compared to groups). Statistically significant (p<0.05) treatment effects are marked with bold. Data presented as median (Interquatile Range)

The effect of vitamin D supplementation on diastolic-BP (24 hr-AMBP, nighttime) is presented in Table 2. Diastolic-BP (24 hr-AMBP, night time) in the insufficiency group remained unchanged from 55.3 (IQR 7.1) mmHg at visit one to 54.7 (IQR 10.8) mmHg at visit four. In the control group diastolic-BP (24 hr-AMBP, night time) remained unchanged from 56.8 (IQR 6.2) mmHg at the first visit to 57.5 (IQR 3.9) mmHg at visit four. The estimated treatment effect of vitamin D supplementation on diastolic-BP (24hr-AMBP, night time) shows a decreasing trend of -1.3 (IQR 2.8) mmHg, (p = 0.6) for the insufficiency group compared to the controls.

For the secondary outcome, we observed an effect of vitamin D supplementation from visit one to visit four on catecholamines. The effect of vitamin D supplementation on catecholamine is shown in Figure 1B. Catecholamines in the insufficiency group decreased from 1.79 (IQR 0.49) nmol/L at visit one to 1.26 (IQR 0.37) nmol/L at visit four, estimated treatment effect in the group was a significant decrease of -0.47 (IQR 0.20) nmol/L, (p = 0.02). Catecholamines in the control group showed a trend of increased from 1.04 (IQR 0.26) nmol/L at visit one to 1.40 (IQR 0.51) nmol/L at visit four, estimated change in the group was 0.33 (IQR 0.21) nmol/L, (p = 0.11). The estimated effect of vitamin D supplementation on catecholamines was a significant decrease of -0.77 (IQR 0.22) nmol/L for the insufficiency group compared to the controls (p = 0.0009).

Norepinephrine in the insufficiency group decreased from 1.61 (IQR 0.48) nmol/L at visit one to 1.19 (IQR 0.37) nmol/L at visit four, estimated effect in the group was a significant decrease in norepinephrine of -0.46 (IQR 0.19) nmol/L, (p = 0.02). Norepiniphrine in the control group increased from 0.94 (IQR 0.25) nmol/L at first visit to 1.40 (IQR 0.51) nmol/L at visit four, estimated effect was an insignificant decrease of 0.36 (IQR 0.19) nmol/L, (p = 0.06). The estimated effect of vitamin D supplementation on norepinephrine was a significant decrease of -0.80 (IQR 0.21) nmol/L, for the insufficiency group compared to the controls (p = 0.0002).

Vitamin D supplementation showed no effect within groups nor overall for angiotensinogen, renin activity, angiotensin I, angiotensin II, aldosterone or epinephrine. No adverse events were recorded through the study.

Discussion

This randomised, controlled trial with vitamin D supplementation in normotensive youngsters over a period of 6 months included 15 controls with sufficient levels of vitamin D and 15 cases with insufficient levels of vitamin D. We observed a significant decrease of both systolic and diastolic blood pressure in the group with insufficient vitamin D levels. Vitamin D supplementation also lowered catecholamines, more specifically a significant decrease in norepinephrine. Conversely, we did not detect any change of the parameters in the RAAS. This points to vitamin D affecting BP through the SNS and not RAAS, contrasting other randomized controlled trials which found lower levels of renin and aldosterone [23, 42, 43].

Most studies investigating vitamin D supplementation on BP show a lack of effect. Looking at meta-analyses with pooled data from 64 randomized controlled trials show that only 8 report of beneficial effects with most studies having been conducted on normotensive participants and a duration of under a year [29, 44–51]. Two large scale trials with vitamin D supplements and a follow-up times of 3 and 7 years show no change in blood pressure [52, 53]. These limitations also apply to our study which investigate normotensive participants over 6 months. Lasting effects beyond the 6 months are unknown, but it is worth noting that during daytime the treatment effect between the control and case groups increased at all visits, indicating that an even greater effect could potentially be seen at further time points.

Vitamin D insufficiency in itself did not activate the RAAS system in our population as the baseline values for the RAAS did not differ between the groups. Rejnmark et al [54] demonstrated in postmenopausal women, that only the concentrations of S-25[OH]D below 80 nmol/L increased 1, –25(OH)₂D₃ and that Parathyroid Hormone (PTH) are better related to 1, –25(OH)₂D₃ than 25[OH]D. A similar effect could well be in play here too, as the 25[OH]D concentration in our subjects was not low enough to alter 1, –25(OH)₂D₃ and stimulate the RAAS-system. The lack of changes in the RAAS system under vitamin D supplementation is a strong argument for the RAAS system not to be modulated by S-25[OH]D in healthy young adults. However, the unchanged RAAS system does not exclude an impact of vitamin D insufficiency on the RAAS activation in already hypertensive and elderly patients.

As expected vitamin D supplementation increased the concentration of S-25[OH]D in the insufficient group whereas the control group remained at a steady state level as intended. This study design handled the seasonal variation well as none from the control group decreased significantly.

Besides the short observation period the study has few limitations. The two groups investigated differed only in physical activity at baseline; the control group had a higher mean physical activity, compared to the insufficient group. This might affect BP and explain the initial difference in total plasma catecholamines. The change over time in total catecholamines is only attributable to changes in S-25[OH]D as this was the only parameter that differed between the two groups between visits. Catecholamines in plasma are a useful measure of the activity of the SNS, despite known limitations. It acts as a systemic index, thus providing no pattern of regional activity of the SNS, i.e. in the heart or in the BP modifying arteries. Another factor to consider, is whether calcium supplementation plays a role in itself. Meta analyses have shown a small effect on BP, especially in patients with insufficient dietary intake [55]. Both groups received calcium supplements, but we cannot rule out the possibility that the patients with insuffient vitamin D could have a greater benefit than the controls.

In conclusion, increase in S-25[OH]D by supplementation might have a clinical relevant effect on lowering the blood pressure in healthy young adults, and might be associated with a modulation of the activity of the SNS but not RAAS. The increase of S-25[OH]D by vitamin D supplementation decreases catecholamines at rest. Further investigations of S-25[OH]D modulation of the SNS is needed to elucidate the importance of S-25[OH]D on BP regulation.

Table 3. Effect of vitamin D supplementation on the Renin-Angiotensin-Aldosterone-System

Estimated treatment effect (individual change from baseline compared to groups). Statistically significant (p<0.05) treatment effects are marked with bold. Data presented as median (Interquartile Range)

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