Distinct Plasma Metabolomic and Gut Microbiome Profiles after Gestational Diabetes Mellitus Diet Treatment: Implications for Personalized Dietary Interventions.
Kameron Y SuginoTeri L HernandezLinda A BarbourJennifer M KofonowDaniel N FrankJacob E FriedmanPublished in: Microorganisms (2024)
Gestational diabetes mellitus (GDM) triggers alterations in the maternal microbiome. Alongside metabolic shifts, microbial products may impact clinical factors and influence pregnancy outcomes. We investigated maternal microbiome-metabolomic changes, including over 600 metabolites from a subset of the "Choosing Healthy Options in Carbohydrate Energy" (CHOICE) study. Women diagnosed with GDM were randomized to a diet higher in complex carbohydrates (CHOICE, n = 18, 60% complex carbohydrate/25% fat/15% protein) or a conventional GDM diet (CONV, n = 16, 40% carbohydrate/45% fat/15% protein). All meals were provided. Diets were eucaloric, and fiber content was similar. CHOICE was associated with increases in trimethylamine N-oxide, indoxyl sulfate, and several triglycerides, while CONV was associated with hippuric acid, betaine, and indole propionic acid, suggestive of a healthier metabolome. Conversely, the microbiome of CHOICE participants was enriched with carbohydrate metabolizing genes and beneficial taxa such as Bifidobacterium adolescentis , while CONV was associated with inflammatory pathways including antimicrobial resistance and lipopolysaccharide biosynthesis. We also identified latent metabolic groups not associated with diet: a metabolome associated with less of a decrease in fasting glucose, and another associated with relatively higher fasting triglycerides. Our results suggest that GDM diets produce specific microbial and metabolic responses during pregnancy, while host factors also play a role in triglycerides and glucose metabolism.
Keyphrases
- pregnancy outcomes
- weight loss
- pregnant women
- physical activity
- antimicrobial resistance
- blood glucose
- adipose tissue
- microbial community
- insulin resistance
- decision making
- high density
- protein protein
- inflammatory response
- open label
- genome wide
- ms ms
- dna methylation
- fatty acid
- clinical trial
- type diabetes
- randomized controlled trial
- study protocol
- oxidative stress
- small molecule
- birth weight
- phase iii
- transcription factor
- combination therapy
- immune response