More Extensive Mitochondrial Testing Proposed
A letter to the editor of the BioMed Central Journal urged more in depth mitochondrial testing than has been done be done in ME/CFS. The letter referred to a study done by an ME/CFS researcher, Maureen Hanson, and funded by the Chronic Fatigue Initiative.
The CFI is very interested in the mitochondria and it is funding more research by Dr. Hanson - so they made an honest effort to find something. They did find something, but the results were not particularly encouraging.
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The two researcher researchers proposed that study into the mitochondria in ME/CFS be deepened. They proposed
Mitochondria Affected - But Not the Problem?
Maureen Hanson is at work on another mitochrondrial study and we should know more soon from Ron Davis and Robert Naviaux when their paper gets published. Their findings, by the way, do not necessarily suggest that the mitochondria are broken. My understanding is that it's more likely that the mitochondria are fine, but that something in the blood is turning them off in ME/CFS patients. (The same may apply with NK cells).
Absent some genetic abnormality it's been hard for me to understand how the mitochondria across the body get damaged unless by something in the blood. The good news is that given the dearth of drug options for mitochondrial problems a problem in the blood seems like a far, far easier problem to deal with than an issue in the mitochondria themselves.
A letter to the editor of the BioMed Central Journal urged more in depth mitochondrial testing than has been done be done in ME/CFS. The letter referred to a study done by an ME/CFS researcher, Maureen Hanson, and funded by the Chronic Fatigue Initiative.
The CFI is very interested in the mitochondria and it is funding more research by Dr. Hanson - so they made an honest effort to find something. They did find something, but the results were not particularly encouraging.
[fright]
Results
No ME/CFS subject exhibited known disease-causing mtDNA mutations. Extent of heteroplasmy was low in all subjects. Although no association between mtDNA SNPs and ME/CFS vs. healthy status was observed, haplogroups J, U and H as well as eight SNPs in ME/CFS cases were significantly associated with individual symptoms, symptom clusters, or symptom severity.
Conclusions
Analysis of mitochondrial genomes in ME/CFS cases indicates that individuals of a certain haplogroup or carrying specific SNPs are more likely to exhibit certain neurological, inflammatory, and/or gastrointestinal symptoms. No increase in susceptibility to ME/CFS of individuals carrying particular mitochondrial genomes or SNPs was observed.
The two researcher researchers proposed that study into the mitochondria in ME/CFS be deepened. They proposed
- that nuclear DNA (nDNA) be studied (as well as mtDNA)
- that parts of the mitochondria other than the respiratory chain such as betaoxidation, hem synthesis, calcium handling, coenzyme-Q metabolism, or the urea cycle be examined
- that analyses be done on other than blood lymphocytes
- that immune-histological and biochemical examinations of muscle biopsies be done. In fact, they said these types of investigations "were essential not to miss dysfunction of the respiratory chain or other mitochondrial pathways.
Mitochondria Affected - But Not the Problem?
Maureen Hanson is at work on another mitochrondrial study and we should know more soon from Ron Davis and Robert Naviaux when their paper gets published. Their findings, by the way, do not necessarily suggest that the mitochondria are broken. My understanding is that it's more likely that the mitochondria are fine, but that something in the blood is turning them off in ME/CFS patients. (The same may apply with NK cells).
Absent some genetic abnormality it's been hard for me to understand how the mitochondria across the body get damaged unless by something in the blood. The good news is that given the dearth of drug options for mitochondrial problems a problem in the blood seems like a far, far easier problem to deal with than an issue in the mitochondria themselves.
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