Welcome to BRMEC10

Day 1 of the Colloquium.
BRMEC10 is the tenth Biomedical Research into ME Colloquium organised by the charity.

All delegates to BRMEC10 will have received instructions on joining the meeting via email beforehand including information about the topics under discussion.
Each day will begin promptly at the published times.


Status Review

The Colloquium begins with an overview of the current status of research and has presentations from different areas.
Speakers are to be announced.

Epidemiology of ME (and Covid)

Speakers:




This section will look at the epidemiological evidence related to ME as well as reviewing the recent accruement of knowledge from COVID-19 research.

Hypotheses discussed include historical evidence for infectious agents including environmental and endogenous viruses and bacteria being associated with the onset and “outbreaks” of ME/CFS
and
in relation to COVID-19, genetically susceptible individuals are at increased risk of developing ME/CFS after SARS-CoV-2 infection resulting in an increase of symptoms fulfilling the diagnostic criteria of ME/CFS amongst infected individuals.

Speakers will represent these hypotheses which will then be discussed by delegates.

ANS and Autoimmunity

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Hypothesis: Autonomic dysfunction and autoantibodies

Mitochondrial Dysfunction

Speakers:




Hypothesis: Mitochondrial dysfunction in ME is metabolic memory of post-inflammatory danger exposure

SUMMARY - DAY 1

Speakers:

To be confirmed

Welcome to BRMEC10

Day 2 of the Colloquium.

OVERVIEW of DAY 2

To be confirmed

To be confirmed

IMMUNOGENETICS

Speakers:





Hypothesis: Immune and Immune genetic factors drive the development and progression of ME/CFS

HOST-MICROBE INTERACTIONS

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Hypothesis: To be confirmed

THERAPEUTICS (CURRENT/FUTURE)

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Hypothesis: Therapeutic strategies should target the triggering and subsequent signalling events that cause the hallmark clinical symptoms of ME.

SUMMARY BRMEC10

Speakers:

  1. tbc

To be confirmed

Research tools for ME/CFS-related data and biospecimens

Speakers:


Two new research tools developed by RTI International, the Data Management and Coordinating Center for the NIH-funded ME/CFS Collaborative Research Centers (CRCs) Network, are now available to help advance ME/CFS research by allowing researchers to access and share data and biospecimens. mapMECFS is an online data sharing platform that allows researchers to discover, share, and access data from multi-omic studies. The platform was initially developed to support the ME/CFS Network CRCs that employ a variety of research methods (e.g., microbiome screens, RNA sequencing, mitochondrial assays, metabolomic assays) to identify potential biomarkers and study the underlying cause(s) of ME/CFS. mapMECFS allows researchers to search the contents of data sets across multiple studies, quickly compare results for specific molecules or markers of interest, and download relevant data to be used for exploration or validation studies. Additionally, mapMECFS encourages and facilitates sharing of new data by capturing key study metadata to make results easier to find. searchMECFS is an online, interactive search tool that allows researchers to query and request available biospecimens (e.g., DNA, RNA, urine, plasma, and peripheral blood mononuclear cells) based on specific demographic and clinical characteristics. The initial cohort, the Chronic Fatigue Initiative, was a research study supported by the Hutchins Family Foundation. Biospecimens and associated data were collected from 201 individuals with ME/CFS and 200 matched controls. The biospecimens are housed at BioSEND, NINDS’ biomarker repository at Indiana University, and the data are hosted by RTI International. Investigators may also request access to just the clinical data for analysis. Additional cohorts’ biospecimens and datasets will be available in the future. Researchers who access biospecimens through searchMECFS will be able to upload the completed assay results into mapMECFS to make the information widely available to other investigators. The development of these tools was supported by U24-NS105535 to RTI International.



Last Update March 2021