CORRECTION - mt DNA loci
are contained in the DecodeME study. The limitation is that it is all common variants.
So (future) US study could look for rare variants.
Interesting Q&A at the end of this section [Genetic correlations with ME/CFS Results]. Seems mitochondrial [EDIT - rare variants] sequencing isn't being done in DecodeME and there was a consensus that it should be included in ME/CFS genetic studies. Chris Ponting suggested that this should be included in the (suggested) US genetic study.
Also, seems to be complicated since muscle (biopsy?) samples may be required i.e. since there may be more mutations in muscle.
Must (re)listen to the summary at the end of this webinar.
Looks like this is something that needs research i.e. [EDIT - rare variants] mitochondrial sequencing.
Some Notes -
Steve Gardner PrecisionLife [1 hr 54 mins from start] - AMPK function - gene AKAP1
made me recall the 2016 paper by Karl J. Tronstad & Øystein Fluge - "
Metabolic profiling indicates impaired pyruvate dehydrogenase function in myalgic encephalopathy/chronic fatigue syndrome" [
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5161229/] Don't recall this paper being trashed/debunked so that may be why the OMF folks are highlighting need for [EDIT - rare variants] mitochondrial sequencing.
Maureen Hanson [1 hr 56 mins from start] - need mitochondrial [EDIT - rare variants] sequencing
Fereshteh - [1 hr 58 mins from start] more [mitochondrial DNA] [EDIT - rare variants] mutations in some tissues e.g. muscle? Also, "hemoplasma in mitochondrial sequencing" needs to be considered?
Chris Ponting [1 hr 59 mins from start]
Fereshteh - [2 hr 3 mins from start] 2.03 - family studies - some evidence that disease coming from mothers side + epigenetics
2.04 - break.
@Dolphin