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10.1016/j.redox.2020.101709

http://scihub22266oqcxt.onion/10.1016/j.redox.2020.101709
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32905881!7462470!32905881
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suck abstract from ncbi

pmid32905881      Redox+Biol 2020 ; 37 (?): 101709
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  • Selenium deficiency is linearly associated with hypoglycemia in healthy adults #MMPMID32905881
  • Wang Y; Rijntjes E; Wu Q; Lv H; Gao C; Shi B; Schomburg L
  • Redox Biol 2020[Oct]; 37 (?): 101709 PMID32905881show ga
  • OBJECTIVE: The trace element selenium (Se) is needed for regular biosynthesis of selenoproteins, which contribute to antioxidative defense systems and affect redox-regulated signaling. Elevated Se intake and selenoprotein expression levels have been associated with impaired hydrogen peroxide-dependent signaling by insulin, leading to hyperglycemia and insulin resistance. The relation of low Se intake with glucose status and carbohydrate metabolism is poorly known. RESEARCH DESIGN AND METHODS: A cross sectional analysis among healthy subjects residing in two Chinese counties with different habitual Se intakes was conducted. Fasted glucose levels were related to Se concentrations of 5686 adults by linear regression analysis with Se, body mass index, age, thyroid status, insulin and sex as independent variables. RESULTS: Serum Se correlated strongly and positively with glucose in the Se-deficient population. There was no strong relationship of Se and glucose in the non-deficient population. Overt hypoglycemia (serum glucose < 2.8 mM) was observed in 19.2% of this random sample of subjects in the Se-deficient and in 1.4% of the moderately supplied population, respectively. CONCLUSIONS: An adequate Se supply constitutes an important factor for glucose homeostasis in human subjects. The interaction between Se status and glucose control is not limited to hyperglycemia, but apparently extends to hypoglycemia risk in Se deficiency. This newly identified relationship may be of relevance for the course of severe disease including major trauma, sepsis and COVID-19, where Se deficiency has been associated with mortality risk.
  • |Adult[MESH]
  • |Blood Glucose/analysis/*metabolism[MESH]
  • |COVID-19/complications[MESH]
  • |Cross-Sectional Studies[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Hypoglycemia/blood/complications/*metabolism[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]


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