tommybrand
Established Member
Hello,
I'm looking for some perspective on whether my CPET findings are typical for ME/CFS, or whether they point more strongly toward another type of metabolic or mitochondrial problem. Any inputs would be appreciated. Please delete my post if its breaching a forum rule.
I've had exercise intolerance since age 17 following mononucleosis/EBV. I have a ME/CFS diagnosis with significant PEM, cognitive dysfunction, fatigue, and increased exercise intolerance since 2019 after an infection while traveling in SE Asia. Extensive neurological, rheumatological, and metabolic workups have largely been unrevealing. Muscle biopsy reported as normal.
However, my CPET showed:
My question is:
How unusual are findings such as lactate 24 mmol/L, pH 7.16, and a very early anaerobic threshold in ME/CFS patients? Are values like these still seen within the spectrum of ME/CFS, or could it be considered unusually severe and more suggestive of a primary metabolic/myopathic/mitochondrial disorder despite a normal muscle biopsy?
I've been trying to understand my results, and when I research or ask AI models, they seem to say this is abnormal for an ME/CFS patient, yet the doctors at my hospital say this is expected for ME/CFS.
My main concern is that I don't actually have ME/CFS, but something else that they have potentially missed or didn't check thoroughly enough.
Appreciate any inputs!
I'm looking for some perspective on whether my CPET findings are typical for ME/CFS, or whether they point more strongly toward another type of metabolic or mitochondrial problem. Any inputs would be appreciated. Please delete my post if its breaching a forum rule.
I've had exercise intolerance since age 17 following mononucleosis/EBV. I have a ME/CFS diagnosis with significant PEM, cognitive dysfunction, fatigue, and increased exercise intolerance since 2019 after an infection while traveling in SE Asia. Extensive neurological, rheumatological, and metabolic workups have largely been unrevealing. Muscle biopsy reported as normal.
However, my CPET showed:
- VO₂peak: 3118 mL/min (79% predicted)
- VO₂/kg: 43.9 mL/kg/min (92% predicted)
- Anaerobic threshold at 29% of predicted VO₂max
- Peak lactate: 24 mmol/L
- Peak pH: 7.16
- Normal pulmonary function and oxygenation
- The interpreting physician suggested a possible peripheral limitation and recommended consideration of muscular, metabolic, or mitochondrial pathology.
My question is:
How unusual are findings such as lactate 24 mmol/L, pH 7.16, and a very early anaerobic threshold in ME/CFS patients? Are values like these still seen within the spectrum of ME/CFS, or could it be considered unusually severe and more suggestive of a primary metabolic/myopathic/mitochondrial disorder despite a normal muscle biopsy?
I've been trying to understand my results, and when I research or ask AI models, they seem to say this is abnormal for an ME/CFS patient, yet the doctors at my hospital say this is expected for ME/CFS.
My main concern is that I don't actually have ME/CFS, but something else that they have potentially missed or didn't check thoroughly enough.
Appreciate any inputs!