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. 2015 Oct;44(5):1602-12.
doi: 10.1093/ije/dyv092. Epub 2015 Jun 21.

Prime Mover or Fellow Traveller: 25-hydroxy Vitamin D's Seasonal Variation, Cardiovascular Disease and Death in the Scottish Heart Health Extended Cohort (SHHEC)

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Free PMC article

Prime Mover or Fellow Traveller: 25-hydroxy Vitamin D's Seasonal Variation, Cardiovascular Disease and Death in the Scottish Heart Health Extended Cohort (SHHEC)

Hugh Tunstall-Pedoe et al. Int J Epidemiol. .
Free PMC article

Abstract

Background: Theoretical links between seasonal lack of sunlight, hypovitaminosis D and excess cardiovascular disease and death prompted our adding novel to conventional cohort analyses.

Methods: We tested three postulates on 13,224 Scottish Heart Health Extended Cohort participants, assayed for 25-hydroxyvitamin D (25OHD) and followed for 22 years. (i) Endpoints enumerated by month of occurrence mirror annual seasonal oscillation in 25OHD. (ii) Endpoint seasonality is increased in people with below median 25OHD. (iii) Low 25OHD predicts endpoints independently of major risk factors.

Results: Baseline median 25OHD level was 36.4 (other quartiles 26.7, 51.7) nmol/l. The March trough was half the August peak, both well after seasonal solstices. (i) There was no demonstrable monthly variation in First Cardiovascular Event (n = 3307). Peaks and troughs for All Death and Cardiovascular Death (n = 2987, 1350) were near the solstices, earlier than extremes of 25OHD. (ii) Endpoint variability showed no difference between those above and below median 25OHD. (iii) Cox model hazard ratios (HR), by decreasing 25OHD, increased modestly and nonspecifically for all endpoints examined, with no threshold, the gradients diminishing by ∼ : 60% following multiple adjustment. For Cardiovascular Disease, HR, by 20 (∼ SD) nmol/l decrease, =1.224 (1.175, 1.275) adjusted for age and sex; additionally adjusted for family history, deprivation index, smoking, systolic blood pressure, total and HDL cholesterol, =1.093 (1.048, 1.139); All Deaths = 1.238 (1.048, 1.139) and 1.098 (1.050, 1.149). 25OHD made no independent contribution to cardiovascular discrimination and reclassification.

Conclusions: Our analyses challenge vitamin D's alleged role as major prime mover in cardiovascular disease and mortality.

Keywords: Vitamin D; cardiovascular disease; causality; cohort study; mortality; seasonality.

Figures

Figure 1.
Figure 1.
Childhood rickets from hypovitaminosis D, especially prevalent in Scotland in the early 1900s. (Wellcome Library, London).
Figure 2.
Figure 2.
Radar plots from the SHHEC population of monthly variation in: A, recruitment 25-hydroxyvitamin D (25OHDraw); B, First Cardiovascular Event; C, All Death; and D, Cardiovascular Death, testing Seasonality Postulate 1. Sexes combined, n = 11 597, 22-year follow-up. Mean for all months (100%) shown in black. (Plotted from Supplementary Table W1, available as Supplementary data at IJE online).*Outside coefficient of variation, **Highest and lowest monthly values (see text).

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References

    1. Brøndum-Jacobsen P, Benn M, Jensen GB, Nordestgaard BG. 25-Hydroxyvitamin D levels and risk of ischemic heart disease, myocardial infarction, and early death: population-based study and meta-analyses of 18 and 17 studies. Arterioscler Thromb Vasc Biol 2012;32:2794–802. - PubMed
    1. Tomson JT, Emberson J, Hill M, et al. Vitamin D and risk of death from vascular and non-vascular causes in the Whitehall study and meta-analyses of 12,000 deaths. Eur Heart J 2013;34:1365–74. - PubMed
    1. Chowdhury R, Kunutsor S, Vitezova A, et al. Vitamin D and risk of cause specific death: systematic review and meta-analysis of observational cohort and randomised intervention studies. BMJ 2014:348:g1903. - PMC - PubMed
    1. Theodoratou E, Tzoulaki I, Zgaga L, Ioannidis JP. Vitamin D and multiple health outcomes: umbrella review of systematic reviews and meta-analyses of observational studies and randomised trials. BMJ 2014;348:g2035. - PMC - PubMed
    1. Manson JE, Bassuk SS, Lee IM, et al. The VITamin D and OmegA-3 Trial (VITAL): rationale and design of a large randomized controlled trial of vitamin D and marine omega-3 fatty acid supplements for the primary prevention of cancer and cardiovascular disease. Contemp Clin Trials 2012;33:159–71. - PMC - PubMed

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