OMF Introduces #OMFScienceWednesday

Introducing #OMFScienceWednesday! Every Wednesday, our Research Liaison Raeka Aiyar from Stanford University will post on Facebook about the science that OMF is supporting: background on key areas, updates on the latest research, explanations of topics relevant to ME/CFS… be sure to like our Facebook page so you don’t miss out!
To start with, what do we mean when we say ME/CFS is a molecular disease, and why is that helpful for research? Molecular biology involves DNA, RNA, metabolites, proteins, cytokines – and there is evidence that so many of these are involved in ME/CFS. Molecular biology presents new opportunities to study ME/CFS: this is the golden era of molecular technologies, like genomics and other ‘omics’ (transcriptomics, metabolomics, proteomics) that allow us to measure the full set of these molecules produced by the body, cheaply and effectively. These studies can help us to understand how the disease works – for example, which viruses may trigger it or whether genetics may increase your risk – and to identify molecular biomarkers that are clearly different in patients compared to healthy people, which may be useful in diagnosing ME/CFS. Finally, molecular biology will hopefully lead to new molecular treatments: knowing which molecules are out of balance could point to ways to treat ME/CFS.

A great example of this is the recent metabolomics study published by Dr. Bob Naviaux (http://www.pnas.org/content/113/37/E5472.long), in which he found several metabolites whose levels are different in ME/CFS patients. This metabolic ‘signature’ could be useful as a biomarker, and could help to understand the energy deficiency issues in the disease. OMF is supporting a metabolomics validation study to confirm and extend Dr. Naviaux’s findings, and a collaboration with Dr. Ron Davis’ group to use genome sequencing to understand how genetics may be influencing metabolism in ME/CFS.
Check our Facebook each Wednesday, search #OMFScienceWednesday, and visit our website.
#OMFScienceWednesday
Facebook
Twitter
WhatsApp
Email

Latest News

a multi-water colored image with the words, Severe ME Artists Project 2024 in white font outlined in black. the meaction action logo in the bottom right hand corner.

Severe ME Artists Project 2024

Quick Overview: Submit one piece of artwork – image, writing, or video Label your artwork with your name as you want it to appear, an underscore, and the number of years with severe ME Example: Lastname_FirstName_14 FirstNameOnly_ No copyrighted material If you are submitting a video, it must be under two minutes. Submission due by

Read More »
Light blue square with rainbows in the top left and bottom right corner. In the middle are the words, -Pride is Valid- No Matter How One Celebrates or Experiences It. #MEAction Board Member, Jennifer England, shares her views on Pride. The #MEAction logo in the top right corner.

Pride Is Valid No Matter How One Celebrates or Experiences It

In honor of Pride Month, #MEAction is sharing a heartfelt message from our board member, Jennifer England, about what Pride means to her and her wife who lives with severe ME. My wife and I have both been queer our whole lives, but in the 70s that was the quiet part you didn’t say out

Read More »

Questions to Ask Prospective MPs About ME/CFS

In the next few weeks, candidates will be knocking on doors seeking votes for the upcoming UK Election. It’s important that candidates from all parties are made aware of the challenges facing people with ME and Long Covid. It can be a little daunting to be unprepared so here are some questions you might want

Read More »
Scroll to Top