Dr Charles Shepherd, Hon Medical Adviser, ME Association.
The ME/CFS Biomedical Partnership has launched a new website. Visit the platform for more information about the project and to leave comments and suggestions on recruitment etc.
- Last Monday, the ME/CFS Biomedical Partnership met with the Medical Research Council (MRC) and the National Institute for Health Research (NIHR) to discuss an application for funding a large genome-wide association study (GWAS).
- If the funding application is successful, the GWAS will collect saliva samples from 20,000 people with M.E.
- The research team is planning on using both the Canadian Consensus Criteria and Institute of Medicine criteria. This means that the 20,000 people recruited will need to meet one or both of these criteria, with post-exertional malaise being mandatory.
- A research application will be submitted to MRC and NIHR in January for consideration for funding, following peer review.
- Before the ME/CFS Biomedical Partnership do so, they would like to hear your thoughts on whether this is the correct diagnostic criteria to use, and are asking anyone with an interest in M.E. to complete a short poll. The closing date for the survey is Tuesday, 10th December at 5.00pm.
A workshop, hosted by the Medical Research Council (MRC) and the National Institute for Health Research (NIHR) was held on 25 November 2019 and was attended by 30 people with M.E., carers, scientists/researchers, charity representatives and MRC/NIHR representatives.
The purpose of the workshop was to assist the research team management group (Prof Chris Ponting, Dr Luis Nacul, Andy Devereux-Cooke and Sonya Chowdhury) alongside Biomedical Partnership colleague investigators in developing a fully informed and competitive proposal and make recommendations to improve the research proposal.
Following this workshop, a research application will be submitted to MRC and NIHR in January for consideration for funding, following peer review.
For those Patient and Public Involvement (PPI) Steering Group members present, there was a unified view that the workshop delivered on its purpose and was a positive, inclusive experience with patient and carer involvement at its heart.
What was discussed at the workshop?
The workshop was overseen by an external facilitator from Knowinnovation to help ensure that all participants were able to participate effectively and keep the group to task.
After introductions from the MRC/NIHR and the Management Group to set the context, there were two sessions designed to help explore different aspects of the research methodology.
Session 1: Case definitions and PPI
- What is the most appropriate definition of M.E/.CFS that will be used in this project?
- What are the ideal inclusion/exclusion criteria and how are participants matched to this?
- What is the most appropriate method for recruiting patients into the study?
- What are the risks in recruitment and how should these be mitigated?
- What should PPI look like for the project?
Workshop attendees supported the Management Group’s proposal that people should meet the Canadian Consensus Criteria and/or the Institute of Medicine criteria. You can read more about the different case definitions here.
Have your say by voting in our survey. Let the PPI Steering Group know your thoughts on which criteria should be used. The closing date for the survey is Tuesday, 10th December at 5.00pm.
Session 2: Methodology and Governance
- What should an M.E./CFS platform look like?
- What should the balance be between GWAS and more in-depth biomarker studies?
- What further research opportunities are there for each of these cohorts?
- How should frozen samples be biobanked (single or multiple site)?
- What should the governance for access to the samples and data look like?
The group discussed the above questions alongside how to prioritise the different aspects of the research and the budget.
It was agreed that we need to craft a scientifically robust GWAS application but the more detailed costs now available most likely mean that we cannot also expand the biobank with samples other than saliva.
There was consensus that we need to prioritise the GWAS work. There were lots of other suggestions and recommendations from individual participants which the Biomedical Partnership Management Group will now consider.
At the end of the workshop, the importance of this invited application to not only deliver a high-quality genomics project but to also create a new pathway for future research and research funding in the UK was re-stated.
PPI Steering Group Members:
- Sonya Chowdhury (Co-Investigator; Action for M.E.; UK CFS/ME Research Collaborative (CMRC) founding charity representative)
- Andy Devereux-Cooke (Co-Investigator; CURE-ME Biobank Steering Group patient representative)
- Jim Wilson (UK CFS/ME Research Collaborative (CMRC) Patient Advisory Group representative)
- Countess of Mar (Forward ME representative)
- Dr Charles Shepherd (ME Association; CMRC founding charity representative; CURE-ME Biobank Steering Group Chair)
The ME Association
Ramsay Research Fund
We are a national charity working hard to improve the lives of people devastated by an often-misunderstood neurological disease.
We believe biomedical research offers the best hope to people affected by M.E. If you would like to support our investment then please donate to the Ramsay Research Fund.
Just click the image opposite to visit our JustGiving page for single donations or to establish a regular payment. You can even establish your own fundraising event.
ME Association Registered Charity Number 801279