About this trial
The gut-brain axis plays a crucial role in the regulation and development of psychological and physical processes. The first year of life is a critical period for the development of the gut microbiome, which parallels important milestones in establishing sleep rhythm and neurodevelopment. Growing evidence suggests that the gut microbiome influences sleep, cognition, and early neurodevelopment. For term and preterm-born infants, difficulties in sleep regulation can have major consequences on infants' health, attachment between infants and their caregivers, and can even lead to life-threatening consequences such as shaken-baby syndrome. Preterm born infants are at even higher risk for sleep and neurodevelopmental problems. Although neonatal care has improved over recent decades, preterm birth rates continue to rise and lead to a wide range of neurodevelopmental disabilities that are unaddressed with current therapies. Given the importance of sleep and the gut microbiome for brain maturation, neurodevelopment, and behavior, identifying effective interventions within the gut-brain axis at the beginning of life is likely to have long-term implications for health and development of at-risk infants.
The aims of this project are to I) demonstrate the association between the gut microbiome, sleep patterns and health outcomes in children up to two years of age; and II) to leverage gut microbiome-brain-sleep interactions to develop new intervention strategies for at-risk infants. The investigators hypothesize that the establishment of a healthy gut microbiome during early life is crucial for both short- and long-term child health outcomes, as dysbiosis can harm sleep regulation, brain maturation, and neurobehavioral development. The investigators predict that the administration of synbiotics improves microbiota establishment, sleep rhythm, and neurodevelopmental outcomes.
This project integrates a randomized controlled trial (RCT), ex vivo, and in silico experiments with I) key technology platforms for computational modeling to capture the ontogenic norms of gut microbiota; II) neuronal and actimetry-based quantification of multidimensional aspects of infant sleep; III) breath metabolomics (exhalomics) of host and microbiome metabolism; and IV) high-throughput ex vivo models for investigating host-microbiome interactions. Outcomes include I) an understanding of age-normative microbiome composition, its variation (circadian, inter-individual), and the factors that influence the microbiome's plasticity throughout infancy; II) actionable knowledge of microbial species and metabolism that can be targeted to modify sleep regulation and improve neurodevelopmental outcomes, especially in at-risk infants (e.g., preterm-born); III) microbial and metabolic biomarkers with diagnostic potential for later regulatory and behavioral problems; and IV) an open-source analytical "toolbox" for microbial multi-omics that can be immediately applied in other areas of microbiome-host research. To achieve these goals, our strategy combines multiple disciplines focusing on factors that exert the greatest influence on health during infancy: the gut microbiome, sleep regulation, and neurodevelopment.
The impact of this project is substantial and globally relevant, as it advances possible treatment options for supporting neurodevelopmental health in preterm- and term-born infants, explores novel translational approaches for addressing regulatory difficulties, and provides key information for tailored prophylactic synbiotics and possible development of "post-biotics". Further, the study supports the investigation of biomarkers for neurodevelopment and advances early prevention of developmental and mental illnesses.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
neonates born between a gestational age of 34 0/7 to 36 6/7 weeks
partially breast-fed at the time of inclusion
neonates born at a gestational age of ≥ 37 0/7 weeks Infants need to be
partially breast-fed at the time of inclusion
Disqualifiers
receive probiotics outside the trial design
have a birth weight < 1500 g
were prenatally drug-exposed (cannabis, cocaine, heroin, opiates, and alcohol)
have suspected or confirmed immunodeficiency
Trial design
Factorial
Treatments tested in this trial
Synbiotic
Dietary supplementThe capsule contains Lactobacillus helveticus R0052, Bifidobacterium infantis R0033, and Bifidobacterium bifidum R0071 (3 billion bacteria per capsule), as well as zinc oxide, potato starch fructooligosaccharides, coating agent, methyl hydroxypropyl cellulose, anti-caking agent and magnesium stearat
Placebo
Dietary supplementThe capsule contains zinc oxide, coating agent, methyl hydroxypropyl cellulose, anti-caking agent and magnesium stearat
Treatment groups
Trial outcomes
Primary outcomes
Sleep-wake behavior
Brief Infant Sleep Questionnaire BISQ, actinometry and sleep-wake diary
Neuronal connectivity
High-density EEG during sleep
Neurobehavioral development
Bayley Scales of Infant Development
Behavior
Infant Behavior Questionnaire
Secondary outcomes
Eczema
SCORing Atopic Dermatitis scoring system (SCORAD)
Food allergy
Skin prick test
Rates of infection
Number of episodes
Breast milk microbiota
Composition investigated trough shotgun metagenomic sequencing
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Petra Zimmermann
Lead sponsor
University of Fribourg
Sponsor institution
University of Luzern
Collaborator
Swiss Federal Institute of Technology in Zurich (ETHZ)
Collaborator
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