Maternal dietary selenium intake during pregnancy is associated with higher birth weight and lower risk of small for gestational age births in the norwegian mother, father and child cohort study
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Maternal dietary selenium intake during pregnancy is associated with higher birth weight and lower risk of small for gestational age births in the norwegian mother, father and child cohort study. / Solé-Navais, Pol; Brantsæter, Anne Lise; Caspersen, Ida Henriette; Lundh, Thomas; Muglia, Louis J.; Meltzer, Helle Margrete; Zhang, Ge; Jacobsson, Bo; Sengpiel, Verena; Barman, Malin.
I: Nutrients, Vol. 13, Nr. 1, 23, 2021.Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift
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T1 - Maternal dietary selenium intake during pregnancy is associated with higher birth weight and lower risk of small for gestational age births in the norwegian mother, father and child cohort study
AU - Solé-Navais, Pol
AU - Brantsæter, Anne Lise
AU - Caspersen, Ida Henriette
AU - Lundh, Thomas
AU - Muglia, Louis J.
AU - Meltzer, Helle Margrete
AU - Zhang, Ge
AU - Jacobsson, Bo
AU - Sengpiel, Verena
AU - Barman, Malin
PY - 2021
Y1 - 2021
N2 - Selenium is an essential trace element involved in the body’s redox reactions. Low selenium intake during pregnancy has been associated with low birth weight and an increased risk of children being born small for gestational age (SGA). Based on data from the Norwegian Mother, Father and Child Cohort Study (MoBa) and the Medical Birth Registry of Norway (MBRN), we studied the association of maternal selenium intake from diet and supplements during the first half of pregnancy (n = 71,728 women) and selenium status in mid-pregnancy (n = 2628 women) with birth weight and SGA status, according to population-based, ultrasound-based and customized growth standards. An increase of one standard deviation of maternal dietary selenium intake was associated with increased birth weight z-scores (ß = 0.027, 95% CI: 0.007, 0.041) and lower SGA risk (OR = 0.91, 95% CI 0.86, 0.97) after adjusting for confounders. Maternal organic and inorganic selenium intake from supplements as well as whole blood selenium concentration were not associated with birth weight or SGA. Our results suggest that a maternal diet rich in selenium during pregnancy may be beneficial for foetal growth. However, the effect estimates were small and further studies are needed to elucidate the potential impact of selenium on foetal growth.
AB - Selenium is an essential trace element involved in the body’s redox reactions. Low selenium intake during pregnancy has been associated with low birth weight and an increased risk of children being born small for gestational age (SGA). Based on data from the Norwegian Mother, Father and Child Cohort Study (MoBa) and the Medical Birth Registry of Norway (MBRN), we studied the association of maternal selenium intake from diet and supplements during the first half of pregnancy (n = 71,728 women) and selenium status in mid-pregnancy (n = 2628 women) with birth weight and SGA status, according to population-based, ultrasound-based and customized growth standards. An increase of one standard deviation of maternal dietary selenium intake was associated with increased birth weight z-scores (ß = 0.027, 95% CI: 0.007, 0.041) and lower SGA risk (OR = 0.91, 95% CI 0.86, 0.97) after adjusting for confounders. Maternal organic and inorganic selenium intake from supplements as well as whole blood selenium concentration were not associated with birth weight or SGA. Our results suggest that a maternal diet rich in selenium during pregnancy may be beneficial for foetal growth. However, the effect estimates were small and further studies are needed to elucidate the potential impact of selenium on foetal growth.
KW - Birth weight
KW - Intrauterine growth
KW - MBRN
KW - Medical Birth Registry of Norway
KW - MoBa
KW - Selenium
KW - The Norwegian Mother, Father and Child Cohort study
U2 - 10.3390/nu13010023
DO - 10.3390/nu13010023
M3 - Article
C2 - 33374667
AN - SCOPUS:85098659031
VL - 13
JO - Nutrients
JF - Nutrients
SN - 2072-6643
IS - 1
M1 - 23
ER -