Microbiota during pregnancy and early life: role in maternal-neonatal outcomes based on human evidence.
Alessio FasanoBenoit ChassaingDirk HallerEduard Flores VenturaMaria Carmen ColladoNitida PastorOmry KorenRoberto Berni CananiPublished in: Gut microbes (2024)
Here, we explored the vast potential of microbiome-based interventions in preventing and managing non-communicable diseases including obesity, diabetes, allergies, celiac disease, inflammatory bowel diseases, malnutrition, and cardiovascular diseases across different life stages. We discuss the intricate relationship between microbiome and non-communicable diseases, emphasizing on the "window of opportunity" for microbe-host interactions during the first years after birth. Specific biotics and also live biotherapeutics including fecal microbiota transplantation emerge as pivotal tools for precision medicine, acknowledging the "one size doesn't' fit all" aspect. Challenges in implementation underscore the need for advanced technologies, scientific transparency, and public engagement. Future perspectives advocate for understanding maternal-neonatal microbiome, exploring the maternal exposome and delving into human milk's role in the establishment and restoration of the infant microbiome and its influence over health and disease. An integrated scientific approach, employing multi-omics and accounting for inter-individual variance in microbiome composition and function appears central to unleash the full potential of early-life microbiome interventions in revolutionizing healthcare.
Keyphrases
- early life
- healthcare
- human milk
- cardiovascular disease
- type diabetes
- birth weight
- pregnancy outcomes
- celiac disease
- physical activity
- mental health
- metabolic syndrome
- weight gain
- public health
- human health
- risk assessment
- social media
- glycemic control
- insulin resistance
- health information
- pregnant women
- skeletal muscle
- gestational age
- adipose tissue
- mesenchymal stem cells
- single cell
- preterm birth
- quality improvement
- cardiovascular events
- adverse drug
- pluripotent stem cells
- drug induced