The Role of the Microbiota-gut-brain Axis in Brain Development and Mental Health

NCT ID: NCT03835468

Last Updated: 2021-04-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

120 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-02-01

Study Completion Date

2023-03-31

Brief Summary

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The role of the microbiota-gut-brain axis in brain development and mental health

Detailed Description

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Anxiety disorders are debilitating conditions that carry enormous individual, social and economic costs. For example, it has been estimated that lifelong persistent mental health problems cost the UK taxpayer £8.6 billion annually. Many mental health problems have their onset in the transitional period from adolescence to early adulthood, possibly a result of the complex and concurrent hormonal, genetic, brain maturational and social changes during this period. Research has shown that brain development and maturation extends well into the third decade of life and that brain activation patterns in late adolescence and early adulthood still differ significantly from mature adults. In the recent years, the microbiome has emerged as a new and important factor that may increase the mental health risk for an individual. The intestine and the brain are intimately connected via the gut-brain axis, which involves bidirectional communication via neural, endocrine and immune pathways. Research in both the human and animal models has also highlighted the important role that intestinal microbiota play in regulating the brain, subsequent behaviour, and particularly in anxiety-like behaviour. Most importantly, it has been shown that the period of adolescence may be a critical window during development where microbiota help fine-tune the gut-brain axis related to stress responses and anxiety.

The research proposed here will investigate the role of the microbiota-gut-brain axis in brain development and mental health. Specifically, the researchers will investigate the effect of prebiotic intake on mental health and well-being in late adolescence/early adulthood, with a particular focus on cortical excitability and connectivity in the emotion regulation brain network.

This research will extend previous research into gut-brain interactions into the final years of adolescence. The period of adolescence is not only important with regards to fine-tuning emotion regulation networks, but also, as has been shown in recent work, critical for establishing healthy gut-brain communication patterns. Specifically, here we will investigate how prebiotic intake (Galacto-oligosaccharides) for 4 weeks affects cognitive functioning, psychological well-being and the underlying brain networks in a sample of 120 female undergraduate students (aged 18-25 years). Specifically, the proposed research has two main aims:

1. To investigate how prebiotic intake affects cortical excitability and plasticity, such as inhibitory GABA/ excitatory glutamate levels in key emotion regulation brain networks.
2. To investigate how prebiotic intake affects psychological functioning and well-being, in particular with regards to anxiety and thought control abilities.

120 participants will be divided into two group of 60 participants, groups will be matched for age, handedness and socio-economic status. At each testing time (Time 1, 2 and 3), participants in both groups will undergo comprehensive behavioural and psychological testing to establish baseline measures of cognitive functioning and psychological well-being (such as anxiety levels).

Each participant will also be asked to collect a stool sample at home for 16s rRNA sequencing of the microbiome at both testing times. Group 1 will receive a daily dosage of GOS over 4 weeks, whereas group 2 will receive a placebo over the same period. In addition, participants from either group will also participate in a brain imaging session to assess the effect of prebiotic supplement intake on the functional responsiveness of emotion regulation brain networks.

For this study, The researchers predict that the intervention group will show improvements in behavioural and psychological variables related to emotion regulation and anxiety in comparison to the placebo group (Hypothesis 1). Predictions also expect to observe decreased excitability in core emotion regulation brain regions such as the amygdala and prefrontal cortex, as assessed via 1H-magnet resonance spectroscopy (Hypothesis 2).

Conditions

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Gamma-Aminobutyric Acid Anxiety Glutamate Emotion Regulation Abilities

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Participants will be randomly assigned into two groups. Group 1 will receive a daily dosage of GOS over 4 weeks, whereas group 2 will receive a placebo over the same period.
Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Caregivers Investigators

Study Groups

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Galacto-oligosaccharides (GOS) Group

Participants in this group will receive the daily dosage of galacto-oligosaccharides (GOS) prebiotic for 4 weeks

Group Type EXPERIMENTAL

Galacto-oligosaccharides

Intervention Type DIETARY_SUPPLEMENT

GOS is a form of prebiotic, which enhance the growth of beneficial gut bacteria

Maltodextrin Group

Participants in this group will receive the daily dosage of Maltodextrin placebo for 4 weeks

Group Type PLACEBO_COMPARATOR

Maltodextrin

Intervention Type DIETARY_SUPPLEMENT

sugar based placebo

Interventions

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Galacto-oligosaccharides

GOS is a form of prebiotic, which enhance the growth of beneficial gut bacteria

Intervention Type DIETARY_SUPPLEMENT

Maltodextrin

sugar based placebo

Intervention Type DIETARY_SUPPLEMENT

Other Intervention Names

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GOS

Eligibility Criteria

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Inclusion Criteria

* Females
* Aged between 18-25

Exclusion Criteria

* Clinical levels of anxiety and/ or co-morbid diagnoses (e.g. depression)
* Current or previous neurological disorders
* Current or previous psychiatric disorders
* Current or previous gastrointestinal disorders
* Current or previous endocrine disorders
* Antibiotic use 3 months prior to the study
* Regular use of pre- and probiotics, including 3 months prior to the study
* Vegan diets
Minimum Eligible Age

18 Years

Maximum Eligible Age

25 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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FrieslandCampina

INDUSTRY

Sponsor Role collaborator

University of Surrey

OTHER

Sponsor Role lead

Responsible Party

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Katherin Cohen-Kadosh

Associate Professor in Developmental Cognitive Neuroscience

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Kathrin Cohen Kadosh, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Surrey

Locations

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University of Surrey

Guildford, Surrey, United Kingdom

Site Status RECRUITING

Countries

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United Kingdom

Central Contacts

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Kathrin Cohen Kadosh, PhD

Role: CONTACT

01483 68 3968

Facility Contacts

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Kathrin Cohen-Kadosh, Phd

Role: primary

01483683968

Nicola Johnstone, Phd

Role: backup

Other Identifiers

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PrebioticExtensionStudyGU2

Identifier Type: -

Identifier Source: org_study_id

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