Circulating 25-hydroxy-vitamin D and risk of cardiovascular disease

Background—Vitamin D status has been linked to the risk of cardiovascular disease (CVD). However, the optimal 25-hydroxy-vitamin D (25[OH]-vitamin D) levels for potential cardiovascular health benefits remain unclear.Methods and Results—We searched MEDLINE and EMBASE from 1966 through February 2012...

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Hauptverfasser: Wang, Lu (VerfasserIn) , Song, Yiqing (VerfasserIn) , Pilz, Stefan (VerfasserIn) , März, Winfried (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: November 2012
In: Circulation. Cardiovascular quality and outcomes
Year: 2012, Jahrgang: 5, Heft: 6, Pages: 819-829
ISSN:1941-7705
DOI:10.1161/CIRCOUTCOMES.112.967604
Online-Zugang:Verlag, Volltext: https://doi.org/10.1161/CIRCOUTCOMES.112.967604
Verlag, Volltext: https://www.ahajournals.org/doi/10.1161/CIRCOUTCOMES.112.967604
Volltext
Verfasserangaben:Wang Lu, Song Yiqing, Manson JoAnn E., Pilz Stefan, März Winfried, Michaëlsson Karl, Lundqvist Annamari, Jassal Simerjot K., Barrett-Connor Elizabeth, Zhang Cuilin, Eaton Charles B., May Heidi T., Anderson Jeffrey L., Sesso Howard D.

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520 |a Background—Vitamin D status has been linked to the risk of cardiovascular disease (CVD). However, the optimal 25-hydroxy-vitamin D (25[OH]-vitamin D) levels for potential cardiovascular health benefits remain unclear.Methods and Results—We searched MEDLINE and EMBASE from 1966 through February 2012 for prospective studies that assessed the association of 25(OH)-vitamin D concentrations with CVD risk. A total of 24 articles met our inclusion criteria, from which 19 independent studies with 6123 CVD cases in 65 994 participants were included for a meta-analysis. In a comparison of the lowest with the highest 25(OH)-vitamin D categories, the pooled relative risk was 1.52 (95% confidence interval, 1.30-1.77) for total CVD, 1.42 (95% confidence interval, 1.19-1.71) for CVD mortality, 1.38 (95% confidence interval, 1.21-1.57) for coronary heart disease, and 1.64 (95% confidence interval, 1.27-2.10) for stroke. These associations remained strong and significant when analyses were limited to studies that excluded participants with baseline CVD and were better controlled for season and confounding. We used a fractional polynomial spline regression analysis to assess the linearity of dose-response association between continuous 25(OH)-vitamin D and CVD risk. The CVD risk increased monotonically across decreasing 25(OH)-vitamin D below ≈60 nmol/L, with a relative risk of 1.03 (95% confidence interval, 1.00-1.06) per 25-nmol/L decrement in 25(OH)-vitamin D.Conclusions—This meta-analysis demonstrated a generally linear, inverse association between circulating 25(OH)-vitamin D ranging from 20 to 60 nmol/L and risk of CVD. Further research is needed to clarify the association of 25(OH)-vitamin D higher than 60 nmol/L with CVD risk and assess causality of the observed associations. 
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