4.6 Article

Neonatal anemia relates to intestinal injury in preterm infants

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PEDIATRIC RESEARCH
卷 91, 期 6, 页码 1452-1458

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SPRINGERNATURE
DOI: 10.1038/s41390-021-01903-x

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  1. Tekke Huizinga Fonds, Groningen, the Netherlands
  2. Junior Scientific Master Class of the University of Groningen

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The study found that urinary I-FABP levels were higher in anemic preterm infants before transfusion compared to non-anemic controls, indicating a link between anemia and intestinal injury. Anemia may result in reduced splanchnic oxygen saturation and intestinal tissue hypoxia, contributing to the development of NEC. Lower hemoglobin levels were associated with higher urinary I-FABP levels in anemic preterm infants, supporting the hypothesis that anemia leads to intestinal cell injury and potentially NEC.
Background Anemia is associated with decreased tissue oxygenation in preterm infants and may contribute to developing necrotizing enterocolitis (NEC). We aimed to investigate whether hemoglobin level is associated with intestinal injury, by comparing anemic infants 10 days prior to red blood cell (RBC) transfusion with non-anemic controls. Methods A nested case-control study in which we matched anemic preterms (gestational age (GA) < 32 weeks) with non-anemic controls (1:1), based on GA, birth weight (BW), and postnatal age. We measured urinary intestinal fatty acid-binding protein, I-FABP, marker for intestinal injury, twice weekly. Simultaneously, we assessed splanchnic oxygen saturation (r(s)SO(2)) and r(s)SO(2) variability. Results Thirty-six cases and 36 controls were included (median GA 27.6 weeks, BW 1020 grams). Median I-FABP level was higher in cases from 6 days to 24-h before transfusion (median ranging: 4749-8064 pg/ml versus 2194-3751 pg/ml). RsSO2 and r(s)SO(2) variability were lower in cases than controls shortly before transfusion. Hemoglobin levels correlated negatively with r(s)SO(2) and r(s)SO(2) variability in cases, and negatively with I-FABP in cases and controls together. Conclusions Urinary I-FABP levels were higher in anemic infants before RBC transfusion than in non-anemic matched controls, suggesting intestinal injury associated with anemia. This may predispose to NEC in some anemic preterm infants. Impact Anemia is a common comorbidity in preterm infants and may lead to impaired splanchnic oxygen saturation and intestinal tissue hypoxia, a proposed mechanism for NEC. Lower hemoglobin level is associated with higher urinary I-FABP levels, a marker for intestinal injury, both in anemic preterm infants and in cases and controls together. Lower splanchnic oxygen saturation and reduction of its variability are associated with higher urinary I-FABP levels in anemic preterm infants before their first RBC transfusion. These results support the hypothesis that anemia in very preterm infants results in intestinal cell injury, which may precede NEC development in some.

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