Gestational Diabetes Is Uniquely Associated With Altered Early Seeding of the Infant Gut Microbiota
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Updated: Nov 25, 2025

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Published on: May 17, 2024
Taylor K Soderborg1, Charles M Carpenter2, Rachel C Janssen1
1Department of Pediatrics, Section of Neonatology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Insights
Gestational diabetes mellitus (GDM) alters infant gut microbes, potentially increasing risks for childhood obesity and inflammatory diseases. Maternal GDM impacts early gut bacteria colonization, influencing long-term health outcomes.
Area of Science:
- Microbiology
- Neonatal Health
- Public Health
Background:
- Gestational diabetes mellitus (GDM) is a global health issue linked to offspring obesity and inflammation.
- Infant gut microbiota development is crucial for immune and metabolic health, but GDM's impact is unclear.
- Maternal obesity may interact with GDM to affect infant gut colonization.
Purpose of the Study:
- To investigate how GDM, alone and with maternal overweight/obesity, alters neonatal gut microbiota composition, diversity, and short-chain fatty acid (SCFA) levels.
- To identify specific microbial taxa affected by GDM and maternal BMI.
- To explore correlations between microbial changes and SCFA levels in neonates.
Main Methods:
- Analysis of gut microbiota in 46 full-term neonates from mothers with/without GDM and varying BMI.
- Microbial composition and diversity assessment at 2 weeks of age.
- Consideration of confounders like delivery mode, breastfeeding, and antibiotic exposure.
Main Results:
- Neonates born to mothers with GDM showed altered abundance in 26 microbial taxa, with 14 remaining significant after BMI adjustment.
- Key beneficial taxa like *Lactobacillus* and *Flavonifractor* were reduced in GDM-exposed infants.
- An increase in *Phascolarctobacterium*, linked to immune suppression, was observed in neonates from mothers with GDM.
Conclusions:
- GDM significantly influences the seeding of specific infant gut microbes, independent of maternal BMI.
- These microbial alterations may predispose offspring to future inflammatory and metabolic diseases.
- The study highlights GDM's unique role in shaping the early-life microbiome and associated health risks.
Abstract:
Gestational diabetes mellitus (GDM) is a worldwide public health problem affecting up to 27% of pregnancies with high predictive values for childhood obesity and inflammatory diseases. Compromised seeding of the infant gut microbiota is a risk factor for immunologic and metabolic diseases in the offspring; however, how GDM along with maternal obesity interact to alter colonization remains unknown. We hypothesized that GDM individually and in combination with maternal overweight/obesity would alter gut microbial composition, diversity, and short-chain fatty acid (SCFA) levels in neonates. We investigated 46 full-term neonates born to normal-weight or overweight/obese mothers with and without GDM, accounting for confounders including cesarean delivery, lack of breastfeeding, and exposure to antibiotics. Gut microbiota in 2-week-old neonates born to mothers with GDM exhibited differences in abundance of 26 microbial taxa; 14 of which showed persistent differential abundance after adjusting for pre-pregnancy BMI. Key pioneering gut taxa, including potentially important taxa for establishing neonatal immunity, were reduced. Lactobacillus, Flavonifractor, Erysipelotrichaceae, and unspecified families in Gammaproteobacteria were significantly reduced in neonates from mothers with GDM. GDM was associated with an increase in microbes involved in suppressing early immune cell function (Phascolarctobacterium). No differences in infant stool SCFA levels by maternal phenotype were noted; however, significant correlations were found between microbial abundances and SCFA levels in neonates. Our results suggest that GDM alone and together with maternal overweight/obesity uniquely influences seeding of specific infant microbiota in patterns that set the stage for future risk of inflammatory and metabolic disease.
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