MND microbiome study
MND microbiome study
UK Chief Investigator
Professor Chris McDermott
Research summary
Amyotrophic lateral sclerosis (ALS, or motor neuron disease) is the result of a complex interaction between patient genetics and the environment. We know this because although certain genetic changes have been identified which cause motor neuron death, most patients with ALS do not carry any of these changes and have no family history of the disease.
One way in which the environment can affect the body, including the brain, is the bacteria within our gut. Gut bacteria are relatively easy to manipulate, making them an ideal target for design of new ALS treatments. Interestingly, the population of gut bacteria within an individual is influenced by other environmental features which have been linked to ALS such as diet, exercise and antibiotic use. Gut bacteria have been linked to the development of neurodegenerative diseases similar to ALS. Our first aim is to determine whether gut bacteria influence the development and severity of ALS. Our study is carefully designed; gut bacteria in ALS patients will be compared with gut bacteria in controls who are matched for diet, BMI and environment to avoid spurious signals. Our second aim is to integrate measures of gut bacteria with sequencing of patient genomes – capturing both sides of the gene-environment interaction avoids confounding by genetic heterogeneity but also opens the door to personalised medicine in which a specific treatment may be targeted at patients with good genomes and bad gut bacteria or visa versa. We will also begin collecting pilot data to investigate how chemicals produced by gut bacteria may impact disease severity.
Current status
Active – recruiting
Key dates
Actual opening date: 19th April 2024
Planned recruitment end date: 31st March 2025
Recruitment groups
Patients with MND
Family members of patients with MND
Neurologically healthy controls
Recruitment target
200 participants in total, broken down into:
30-100 MND patients
30-100 controls (disease controls, family members and neurologically healthy controls)
Click here to see how many participants have been recruited into this study to date (external link to the NIHR public study search)
Location
Sheffield (Principal Investigator: Chris McDermott)
Stoke (Principal Investigator: Tom Lambert) site opening soon
Liverpool (Principal Investigator: Carolyn Young) site opening soon
Exeter (Principal Investigator: Tim Harrower) site opening soon
Salford (Principal Investigator: John Ealing) site opening soon
South Wales (Principal Investigator: Caroline Bidder) site opening soon
Contact details
Email Sarah Boddy: s.l.boddy@sheffield.ac.uk
Inclusion / exclusion criteria
Inclusion criteria
Age 18 years or over
Participant is willing and able to give informed consent for participation in the study. If the participant is unable to provide written consent due to physical disability, an independent witness will be present at the informed consent discussion and sign the consent form on the participant’s behalf.
Additional inclusion criterion for patients with MND only:
Diagnosis made by an experienced neurologist.
Additional inclusion criterion for family members of patients with MND only:
Known to have an MND gene mutation, or is a genetic relative of an affected MND or FTD patient.
Exclusion criteria
Age under 18 years
Pregnancy or any other condition that, in the opinion of the investigator, could interfere with the interpretation of the study results.
Funder
MND Association & NIHR Sheffield Biomedical Research Centre
Sponsor
University of Sheffield
Study design
Observational