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Impact of Immune Challenge on Triple Network Connectivity in Humans

Exploring the Impact of Peripheral Immune Challenge on the Triple Network and Dorsal Nexus Functional Connectivity in Humans

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02653235
Enrollment
20
Registered
2016-01-12
Start date
2016-01-31
Completion date
2017-01-31
Last updated
2016-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Major Depression

Brief summary

Acquiring, processing and utilising information is crucial to any mental function -including seemingly simple daily functions. Collectively called 'cognitive functions', these processes are a result of different regions of the brain acting together. Disruption of these cognitive functions increases the risk of development of mental health problem. Recently it has been proposed that inflammatory pathways may contribute to disorders of cognition and behaviour like depression. This is largely due to research showing that those with inflammatory conditions like arthritis are more likely to develop mental health problems like depression. Conversely, those who suffer from mental health problems (even in the absence of inflammatory conditions) have large amounts of inflammatory molecules in the blood. Studies in animals suggest that inflammation outside the brain can reach and affect the brain in a number of ways. So, does inflammation play a role in the development of cognitive and behavioural symptoms? What are the pathways involved? The current project tries to address this question. Specifically, the investigators intend to use modern scanning techniques to examine the effect of inducing a low grade inflammation (using a commonly used typhoid vaccine) to see how the inflammation affects how different regions of the act together to perform cognitive functions.

Interventions

BIOLOGICALSalmonella typhi vaccination
BIOLOGICALPlacebo

Sponsors

University of Glasgow
CollaboratorOTHER
NHS Greater Glasgow and Clyde
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

1. Written informed consent 2. Aged 18 - 50 years old 3. Male

Exclusion criteria

1. Female 2. History/family history of medical or/and Axis I DSM IV condition 3. Received typhoid vaccination within the last 3 years 4. Taken oral antibiotics/antiinflammatory agents within the previous 2 weeks 5. Current Smokers 6. Contraindication for MRI scans 7. Contraindication for Salmonella typhi vaccination 8. Known hypersensitivity to a Vi antigen containing vaccine.

Design outcomes

Primary

MeasureTime frame
Functional connectivity measured using resting state functional MRI BOLD time series cross correlations between the network nodes.6 hours

Secondary

MeasureTime frame
Correlation of functional connectivity measures with circulating serum cytokines and POMS/ BDI scores using multivariate general linear models6 hours

Contacts

Primary ContactRajeev Krishnadas, MBBS, MRCPsych, MD, PhD
rajeev.krishnadas@glasgow.ac.uk

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026