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Reviews

Selenium status in the body and cardiovascular disease: a systematic review and meta-analysis

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Abstract

Background: Both experimental and observational studies have provided conflicting evidence on the associations of selenium with incidence and mortality of cardiovascular disease (CVD). The aim of this study was to evaluate the association between selenium status in the body and incidence and mortality of CVD by performing a systematic review and meta-analysis of observational studies and randomized controlled trials. Methods: A systematic search for articles in MEDLINE (Ovid), Embase, Web of Science (Thomson Reuters) and Cochrane library (Wiley) was conducted. Thirteen of the 1811 articles obtained from the databases met our inclusion criteria and were considered in the final analysis. The effect sizes were presented as weighted relative risk (RR) and 95% confidence intervals (CIs) using random-effects model. To detect dose-response relationships, we used meta-regression. Results: Overall, there was a reduced risk of CVD incidence (RR = 0.66; 95% CI: 0.40–1.09) and mortality (RR = 0.69; 95% CI: 0.57–0.84) in physiologically high selenium status compared to low selenium status in the body. There was a 15% (RR = 0.85, 95% CI: 0.76–0.94) decreased risk of CVD incidence per 10 µg increment in blood selenium concentration. In addition, a statistically significantly nonlinear dose-response relationship was found between CVD mortality and increased blood selenium concentration with the lowest risk at the 30–35 µg increment in blood selenium. Conclusions: Physiologically high selenium levels in the body are associated with decreased risk for CVD incidence and mortality, however, people should be cautious about the potential harmful effects from excessive intake of selenium.

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Acknowledgment

Our sincere gratitude goes to Gun Brit Knutsson and Carl Gornitzki from the Research Consultation Group of the University Library, Karolinska Institutet, Stockholm, Sweden for their immense help during literature search in the various databases.

Disclosure statement

No conflict of interest was declared.

Author’s contribution

This study was designed by Y.C. and J.A. A.K., H.T. and M.L. did the literature screening, data extraction and study quality assessment; Y.C. and A.K. performed statistical analysis and interpreted results. A.K. and Y.C. drafted the manuscript. All authors contributed to the manuscript writing, made critical revision, read, and approved the final manuscript. All authors had full access to all the data and take responsibility for the integrity of the data and the accuracy of the data analysis.

Abbreviations
CHD=

coronary heart disease

CI=

confidence interval

CVD=

cardiovascular disease

GPx=

glutathione peroxidases

ICD=

ischemic cardiovascular disease

MI=

myocardial infarction

RCT=

randomized controlled trial

ROS=

reactive oxygen species

RR=

relative risk