The two studies I have
posted before; Ruud CW Vermeulen et. Al (http://www.translational-medicine.com/content/8/1/93)
and N Booth et. Al (www.ijcem.com /ISSN:1940-5901/IJCEM1204005);
both agrees there is decreased mitochondrial ATP synthesis. However, there is
disagreement with regard to where does the problem lie. While the first one
argues that the transport capacity of oxygen is limited in CFS patients, the
second study apparently finds fault with oxidative phosphorylation.
Both the studies were done
by independent researchers these are yet to be validated by national health
research agencies. Further, more evidence and clarity is needed with regard to
where the actual problem lies, and how the mitochondria, if at all, is
inhibited. Further, probably mitochondrial DNA/RNA sequencing would be able to
reveal the underlying genetic mutation, if any. Also, are these inherited
mutations, if any, or acquired?
Sadly, the national research agencies so far have turned a blind eye on this. More dangerously, lot of time is wasted and lost on theories on virus and others!??? while patient after patient were succumbing to the highly debilitating health condition.
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