2020
DOI: 10.1007/s00404-020-05571-w
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Prenatal effects of maternal nutritional stress and mental health on the fetal movement profile

Abstract: Purpose Prenatal sub-optimal nutrition and exposure to maternal stress, anxiety and depression in pregnancy have been linked to increased postnatal morbidity and mortality. Fetal growth is most vulnerable to maternal dietary deficiencies, such as those evident in hyperemesis gravidarum (HG), early in pregnancy. The purpose of this pilot study was to examine the effects of HG on fetal movement profiles as a measure of fetal healthy development in the 3rd trimester of pregnancy, and to assess whether nutritional… Show more

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Cited by 9 publications
(6 citation statements)
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References 45 publications
(64 reference statements)
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“…Stable carbon and nitrogen isotope analyses can also inform infant feeding patterns (Tsutaya & Yoneda, 2015). Nitrogen isotope values from hair among pregnant people have been shown to decrease slightly (0.5‰–1‰; Fuller et al, 2004) when compared to pre‐pregnancy values, although conversely, can increase due to muscle catabolism stemming from nutritional stress or severe morning sickness, resulting in 15 N‐enrichment (Fuller et al, 2005; Reissland et al, 2020). Prior to breastfeeding, fetal bone collagen isotope values are thought to be relatively indistinguishable from that of maternal bone collagen (Katzenberg et al, 1996), although neonatal δ 13 C and δ 15 N values derived from rapidly‐forming tissues such as hair and nails can vary slightly from that of the mother (de Luca et al, 2012; Fuller et al, 2006), likely due to short‐term changes in diet (Beaumont et al, 2015).…”
Section: Reconstructing Diet Using Stable Isotopesmentioning
confidence: 99%
“…Stable carbon and nitrogen isotope analyses can also inform infant feeding patterns (Tsutaya & Yoneda, 2015). Nitrogen isotope values from hair among pregnant people have been shown to decrease slightly (0.5‰–1‰; Fuller et al, 2004) when compared to pre‐pregnancy values, although conversely, can increase due to muscle catabolism stemming from nutritional stress or severe morning sickness, resulting in 15 N‐enrichment (Fuller et al, 2005; Reissland et al, 2020). Prior to breastfeeding, fetal bone collagen isotope values are thought to be relatively indistinguishable from that of maternal bone collagen (Katzenberg et al, 1996), although neonatal δ 13 C and δ 15 N values derived from rapidly‐forming tissues such as hair and nails can vary slightly from that of the mother (de Luca et al, 2012; Fuller et al, 2006), likely due to short‐term changes in diet (Beaumont et al, 2015).…”
Section: Reconstructing Diet Using Stable Isotopesmentioning
confidence: 99%
“…We chose a target sample size of 100 before recruitment to obtain 85% power ( f = .25) for the main comparison, that is, fetal FMs depending on the flavor exposure. Given that a recent study (Reissland et al, 2020) reported a large and significant effect size in fetal movements at 32 weeks, medium and even large effect sizes are not unusual in this type of research. We opted to stop collecting data in the study when we reached a predetermined number of participants.…”
Section: Methodsmentioning
confidence: 70%
“…Other bioarchaeology studies have found high fetal/perinate ẟ 15 N values (relative to adult females) [ 100 , 111 ] and research on modern mother-infant dyads suggests a non-dietary cause related to fetal amino acid metabolism, placental fractionation, and/or maternal nutritional stress [ 58 , 112 114 ] [also see 115 ]. The latter seems slight or uncommon in this sample because nutritional stress causes maternal fat stores, depleted in 13 C relative to proteins and carbohydrates, to be used by the fetus causing lower fetal ẟ 13 C values [ 76 , 116 ] which is absent here (the fetal ẟ 13 C mean is 0.3‰ higher than the reproductively-aged Fs which is similar to the 0.4‰ difference in modern paired fetal-maternal samples observed by [ 112 ]).…”
Section: Discussionmentioning
confidence: 99%