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The development of intestinal dysbiosis in anemic preterm infants
Thao T B Ho1,2, Ambuj Kumar3, Adetola F Louis-Jacques3,4
1College of Medicine, University of South Florida, Tampa, FL, 33606, USA. tho1@usf.edu.
Insights
Anemia in premature infants is linked to gut bacteria imbalances. Lower hematocrit levels correlate with increased Proteobacteria and decreased Firmicutes, suggesting anemia may drive intestinal dysbiosis.
Area of Science:
- Neonatal research
- Microbiome studies
- Gastroenterology
Background:
- Anemia and Proteobacteria-dominant intestinal dysbiosis are associated with necrotizing enterocolitis in very low birth weight (VLBW) infants.
- The relationship between anemia of prematurity and intestinal dysbiosis requires further investigation.
Purpose of the Study:
- To investigate the hypothesis that anemia of prematurity is related to the development of intestinal dysbiosis in VLBW infants.
Main Methods:
- Prospective collection of 342 weekly stool samples from 80 VLBW infants.
- Analysis of bacterial microbiomes using 16S rRNA sequencing.
- Application of a linear mixed-effects model to assess relationships between anemia onset and intestinal dysbiosis.
Main Results:
- Hematocrit levels showed a significant association with intestinal microbiomes.
- Lower hematocrit correlated with increased Proteobacteria and decreased Firmicutes.
- Infants with hematocrit <30% exhibited a shift towards Proteobacteria dominance and reduced microbial diversity after the first postnatal month, with changes related to anemia severity.
Conclusions:
- Findings support a potential microbiological explanation for anemia as a risk factor for intestinal dysbiosis in preterm infants.
- Anemia may play a causal role in the development of gut dysbiosis in VLBW infants.
Objective:
Anemia and Proteobacteria-dominant intestinal dysbiosis in very low birth weight (VLBW) infants have been linked to necrotizing enterocolitis, a severe gut inflammatory disease. We hypothesize that anemia of prematurity is related to the development of intestinal dysbiosis.
Study Design:
Three hundred and forty-two weekly stool samples collected prospectively from 80 VLBW infants were analyzed for bacterial microbiomes (with 16S rRNA). Linear mixed-effects model was used to determine the relationships between the onsets of anemia and intestinal dysbiosis.
Results:
Hematocrit was associated with intestinal microbiomes, with lower Hct occurring with increased Proteobacteria and decreased Firmicutes. Infants with a hematocrit <30% had intestinal microbiomes that diverged toward Proteobacteria dominance and low diversity after the first postnatal month. The microbiome changes were also related to the severity of anemia.
Conclusions:
This finding supports a potential microbiological explanation for anemia as a risk factor for intestinal dysbiosis in preterm infants.
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