2020
DOI: 10.1016/j.jpeds.2020.05.063
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Association of Poor Postnatal Growth with Neurodevelopmental Impairment in Infancy and Childhood: Comparing the Fetus and the Healthy Preterm Infant References

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Cited by 21 publications
(34 citation statements)
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“…The matched timing suggests that preceding clinical practices may impact gut microbiome succession which changes infant HCG trajectories; this relationship is defined as mediation and the interactions between these three factors (clinical variables, the gut microbiome and infant HCG) will thus be examined in further detail. Preterm infant HCG trajectory was assessed as the difference in head circumference z-score from birth to 36 weeks PMA by the Fenton growth curve, 14 , 39 and study groups were stratified by 0.5 interval losses in z-score: AHCGT (≥0.5), mildly SHCGT (<0.5–1), moderately SHCGT (<1-1.5), and severely SHCGT (<1.5). Alterations in α-diversity between study groups were first considered using ANOVA on multivariate regression with PMA as a covariate and patient as a random effect, but no significant differences were found (Table S1).…”
Section: Resultsmentioning
confidence: 99%
“…The matched timing suggests that preceding clinical practices may impact gut microbiome succession which changes infant HCG trajectories; this relationship is defined as mediation and the interactions between these three factors (clinical variables, the gut microbiome and infant HCG) will thus be examined in further detail. Preterm infant HCG trajectory was assessed as the difference in head circumference z-score from birth to 36 weeks PMA by the Fenton growth curve, 14 , 39 and study groups were stratified by 0.5 interval losses in z-score: AHCGT (≥0.5), mildly SHCGT (<0.5–1), moderately SHCGT (<1-1.5), and severely SHCGT (<1.5). Alterations in α-diversity between study groups were first considered using ANOVA on multivariate regression with PMA as a covariate and patient as a random effect, but no significant differences were found (Table S1).…”
Section: Resultsmentioning
confidence: 99%
“…This study not only determined that β-diversity of the gut microbiome signi cantly differentiated infants with SHCGT from AHCGT, but also that the key time point when most faecal microbial taxa exhibited a shift in mean abundance of 30 weeks PMA matched the onset of signi cant SHCGT. Preterm infant HCG trajectory was assessed as the difference in HCZ from birth to 36 weeks PMA by the Fenton growth curve [14,42], and study groups were strati ed by 0.5 interval losses in HCZ: AHCGT (≥0.5), mildly SHCGT (<0.5-1), moderately SHCGT (<1-1.5) and severely SHCGT (<1.5). Alterations in α-diversity between study groups were rst considered using ANOVA on multivariate regression with PMA as a covariate and patient as a random effect, but no signi cant differences were found [see Additional le 9].…”
Section: Resultsmentioning
confidence: 99%
“…There is a vital need to identify modi able environmental factors for reducing the incidence of developmental impairments at a time point early enough for successful intervention. Thus, it was the aim of this study to determine if infant gut microbiome composition was associated with HCG, the earliest marker of neurodevelopment [13,14]. This study is the rst to show that β-diversity of the gut microbiome was signi cantly distinct between infants with AHCGT versus any SHCGT, and that reduced abundances of Bacteroidota and Lachnospiraceae were speci cally associated with SHCGT independent of concurrent morbidities and caloric restriction.…”
Section: Discussionmentioning
confidence: 99%
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“…An IUGR infant may have an appropriate birth weight as per gestation, but may have suffered any in utero growth deceleration as a consequence of a perinatal insult ( 80 ). Notably, poor neonatal growth categorized using Fenton's preterm size-at-birth growth charts have shown stronger associations with long term neurodevelopment than poor growth categorized using the Intergrowth 21st Standards ( 82 ).…”
Section: Discussionmentioning
confidence: 99%