- Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a chronic illness affecting up to 24 million people globally, for which there is currently no specific treatment or cure.
- Two new studies show a link between the gut microbiome and ME/CFS.
- Researchers believe these study results may aid in new treatments and diagnostic tools for the disease.
In recent years, scientists have come to understand the large role the body’s microbiome plays in our overall health.
Previous research shows that a person’s microbiota directly impacts a variety of
Now two recently published studies in the journal Cell Host & Microbe — one on the
ME/CFS is a chronic illness affecting up to 24 million people around the world.
The main symptom of the disease is a feeling of intense fatigue that does not improve with rest. This feeling of tiredness may worsen after both physical and mental activities.
Other symptoms of ME/CFS include:
- trouble sleeping
- problems with thinking and/or memory
- hair loss
- body temperature irregularities
- weight changes
- flu-like symptoms
- sore throat
- muscle aches, cramps, or spasms
- chest pain.
There is currently no specific treatment or cure for ME/CFS. Different treatments and lifestyle changes are aimed at helping to alleviate and manage symptoms, and these include:
- healthy sleep habits
- relaxation techniques, including
massageand deep breathing
- gentle exercises like yoga
- water therapy
- healthy diet
- nutritional supplements.
Upon analysis, the research team found patients with shorter-term disease had changes in their microbiome with regard to diversity, including a lower number of microbes known to produce
Butyrate plays an
“This points to potential mechanisms by which the microbiome can impact the immune system, as immune irregularities have been observed in ME/CFS,” Dr. Julia Oh, an associate professor at the Jackson Laboratory and senior author of this study, explained to Medical News Today.
“This is an exciting association because each of these cell types has been linked to bacterial or fungal infections, responds to microbial metabolites, and has been linked to the pathogenesis of
autoimmuneor chronic inflammatory diseases. Thus, it is possible that the microbiome primes or sustains an aberrant immune response following disease onset.”
– Dr. Julia Oh
Scientists found a correlation between the severity of a participant’s fatigue symptoms and the levels of specific species of gut bacteria, mainly
“F. prausnitzii is an important, abundant bacteria in the microbiome, with health-promoting properties associated with its role in butyrate production and controlling inflammation,” Dr. Brent L. Williams, an assistant professor of epidemiology, pathology, and cell biology in the Center for Infection and Immunity at Columbia University’s Mailman School of Public Health and senior author of this study explained to MNT.
“Deficiency of F. prausnitzii has been associated with a range of other human diseases and may be considered as a biosensor of human health,” he pointed out.
“It has also been previously associated with fatigue experienced by some individuals with inflammatory bowel disease,” Dr. Williams continued. “Thus, it perhaps should not be a complete surprise that F. prausnitzii is also correlated with fatigue symptoms experienced by individuals with ME/CFS.”
“Of course,” he cautioned, “this is just a correlation and doesn’t show causation. Further research will be needed to establish any causal link.”
MNT also spoke with Dr. Hector Bonilla, medical director of the Stanford ME/CFS Clinic, about these two studies.
He commented these studies help explain when people with ME/CFS change their diet, their symptoms improve.
“What people eat affects the gut flora — the microbiome,” he detailed. “The human gut microbiota is a powerful modulator of host immune responses and metabolism.”
“There is increasing evidence that chronic low-grade inflammation plays a significant role in mortality and the pathogenesis of chronic inflammatory-related diseases such as
“In ME/CFS, analysis of the composition of the gut microbiomes had shown a decreased bacterial diversity (
“Furthermore, those changes in the microbiome population are associated with an increase in pro-inflammatory species and a reduction in anti-inflammatory species.”
For the next steps in this research, Dr. Bonilla said he would like researchers to validate these studies in different populations and “see what symptoms are more associated with changes in the microbiome.”
“And besides bacteria, see what kind of proteins have been linked with these panel changes, because knowledge can help us start to develop some targets for therapeutics,” he added.