TY - JOUR
T1 - Prime mover or fellow traveller
T2 - 25-hydroxy vitamin D's seasonal variation, cardiovascular disease and death in the Scottish Heart Health Extended Cohort (SHHEC)
AU - Tunstall-Pedoe, Hugh
AU - Woodward, Mark
AU - Hughes, Maria
AU - Anderson, Annie
AU - Kennedy, Gwen
AU - Belch, Jill
AU - Kuulasmaa, Kari
N1 - Funding Information:
Scottish Heart Health Extended Cohort (SHHEC): Scottish Health Department Chief Scientist Organization; British Heart Foundation; FP Fleming Trust. MORGAM: European Commission Seventh Framework Programme FP7/2007-2013 [HEALTH-F4-2007-2014113, ENGAGE; HEALTH-F3-2010-242244, CHANCES]. MORGAM Biomarker Study (Serum biomarkers in the MORGAM Populations): Medical Research Council London [G0601463, No 80983]. BiomarCaRE (Biomarkers for Cardiovascular Risk Assessment in Europe): European Commission Seventh Framework Programme FP7/2007-2013 [HEALTH-F2-2011-278913]. Funding bodies had no role in the planning of the study, analyses, interpretation, writing, or publication of the manuscript, or recruitment of participants.
Publisher Copyright:
© The Author 2015. Published by Oxford University Press on behalf of the International Epidemiological Association.
PY - 2015/10/1
Y1 - 2015/10/1
N2 - 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.
AB - 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.
KW - Cardiovascular disease
KW - Causality
KW - Cohort study
KW - Mortality
KW - Seasonality
KW - Vitamin D
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U2 - 10.1093/ije/dyv092
DO - 10.1093/ije/dyv092
M3 - Article
C2 - 26095374
AN - SCOPUS:84952933460
SN - 0300-5771
VL - 44
SP - 1602
EP - 1612
JO - International journal of epidemiology
JF - International journal of epidemiology
IS - 5
ER -