I don't think so but I do think cortisol is heavily involved in stress and energy production and thus could relate to (over)exertion.Is there evidence that MECFS causes dysregulated cortisol, or that the arrow of causality is reversed? Or if other systems eg immune are involved?
one thing I've been increasingly conscious of, both (I think) in creating PEM and when in PEM, is that there is the orthostatic and there is the just supporting one's own body - and in that the more upright but also if for example you have a supportive chair which supports arms, neck, back. My car seat for example is a pretty good fit, and is a best fit for supporting everything I need it to support if it is pretty upright, and stops doing so once recline and so I'd find I was better off with it being upright evne though orthostatic is sort of a big thing for me too.I talked about it here
We've circled around adrenalin (epinephrine I think is usually the term for exogenous adrenalin) as a possible cause of PEM. I can't remember how much of this has been said before.
Exercise definitely increases adrenalin. Cognitive effort can too, especially if it is demanding or there is time pressure. Hot temperatures do. Being upright and not getting enough blood to the brain increases adrenalin.
And adrenalin activates CD8+ t-cells. It seems to result in an increase of them in the blood, followed by them going into tissues. I think we haven't quite worked out how the CD8+...
Exercise/being upright/heat/ mental exertion >adrenalin > activates t-cells >
activated T cells produce interferon, among other things that might contribute to PEM
There's a study in mice.
I'm happy to have it explained why it can't be a mechanism for PEM.
Yes. I don't think there is any good evidence of cortisol levels that are abnormal (given the average lifestyle of people with ME/CFS - waking later, no morning rush) or that the production of cortisol in response to stressors is abnormal. I see that @arnoble has been directed to our thread on cortisol here already, on another thread, but link it here again for completeness.I don't think so but I do think cortisol is heavily involved in stress and energy production and thus could relate to (over)exertion.
I've done the ACTH stimulation test which came back normal, but I do (often) have insomnia. Also, during the test, my gut swelled up severely, I think because I was told to sit still, and it was very uncomfortable.Years ago a friend with ME did the ACTH stimulation test and it came back normal. She didn't have insomnia either.
I've done the ACTH stimulation test which came back normal, but I do (often) have insomnia. Also, during the test, my gut swelled up severely, I think because I was told to sit still, and it was very uncomfortable.
Why? A symptom being subjective doesn't mean that the cause of the symptom has to be subjective as well. Your feeling pain because a car ran over you does not mean the weight of the car is subjective. Or the sound of the backfire from the passing vehicle that triggered the PTSD symptom.But if it is the basis of a symptom that patients are expected to recognise it has to be subjective.
Calories by itself does not cause enough stress/damage. For healthy people anyway. Just living and breathing consumes about 1 cal/min, which means over 1000 cal/day. But you will surely feel the next day the damage from 1000 cal spent in an hour.We should talk of power (calories per time would be power) or of total energy usage. So far I don't think we have established even which of those is relevant - and they are very different in implications.
There could be several triggers for PEM, with physical exertion being but one. Mental exertion or sensory stimuli could be other. We could take just the physical exertion portion, of it, since that is the simplest to objectify, and then establish the relationship between physical exertion and PEM. There could be other factors like emotion, but we could treat them as noises in the model that lowers correlation.Subjectively it feels that a simple measure like calories per unit of time does not correspond to what ever culminates in triggering PEM. Other things interact like the novelty of the activity, additional sensory stimuli or orthostatic issues.
But you do need recovery from mental exertion (I know how my mental ability degrades after 1 hour of thinking), and there is no reason to preclude such stress/damage as the possible trigger for PEM. And how hard you think, and how tired you are afterward, got to be proportional to the amount of expended for thinking within the given time period.Meaning that if PEM has something to do with the processes which increase utilization of different fuel sources (be that AMPK phosphorylation, increased glucose uptake, fatty acid mobilization, etc), this will look different between tissues.
Why? A symptom being subjective doesn't mean that the cause of the symptom has to be subjective as well. Your feeling pain because a car ran over you does not mean the weight of the car is subjective. Or the sound of the backfire from the passing vehicle that triggered the PTSD symptom.
But you will surely feel the next day the damage from 1000 cal spent in an hour.
My theory is that the accumulated stress, or working against it, is what causes damage and subsequent PEM.
I wouldn't be surprised if the tolerance/sensitivity is highly variable in some cases. Some people report oscillation between remission and relapse after all. That's an ultimate case of tolerance variability. Your guess is as good as mine as to why. I'm mainly interested in a steady state response to physical exertion though, mainly because that is the easiest to establish, and that will probably help the most since PEM from physical exertion is universal in ME/CFS.Does @poetinsf have something with the idea of tolerance?
To me, none of it seems like inputs and outputs. It's a substantial, often variable, and sometimes devastating reduction in tolerance to almost everything—perhaps caused by some kind of biological brake being applied.
This is what I meant by "the idea of subjective exertion can be positively dismissed by the typical delay of 12-48 hours". I'm not aware of any psychological process that a perceptual "apparent trigger" can actually worsen the symptoms, subjectively or otherwise, after 12-48 hours.Those examples are not equivalent. PEM is defined as a worsening following exertion. Whether or not it is caused by exertion is a different issue. It is elicited as a temporal symptom profile in which the apparent trigger is a subjective sense of having done a lot or 'exerted'
So, are you questioning PEM being a delayed response to exertion? Or even a response to an actual exertion at all? That would be easy to settle, I think. Do a CPET test, and measure VAS every hour. The symptom response may be subjective, but the exertion there will be objectively objective and there would be no question what particular exertion proceeded.and the time relation is nearly always subjective in that when PEM is elicited by a physician in clinic or in a questionnaire nobody really knows whether any particular exertion was what the worsening followed.
Well, I did. It's something like integral over time of the difference between the arrival and clearance in exponential form. I don't have the notebook with me here in NYC, but it was borrowed from queuing model.Maybe but from what members say, the length of time at that rate is also relevant. So we seem to need a complex measure of a high work rate for a certain length of time. I agree that total work done is not going to cut it but nor is just work rate. So we are likely to need some new measure that so far nobody has calculated.
I don't know why you are so allergic to abstract terms. Can we call it a concept, build a model for it and test?What would 'stress' be here? It is another lay term that may not help I suspect.
We can always build a model and test.I continue to think that what may trigger PEM is some cumulative tissue response to microtrauma - like the response to using your hands that leads to calluses on your palm. It is partly the intensity of force involved and partly the duration, but not a simple multiplication of the two.
I don’t think what you’re quoting from me is in opposition to what you’re saying here, it could well be that a failure to upregulate one of those mechanisms may substantially lower the time or activity it takes to get to whatever biological state needs to be recovered fromBut you do need recovery from mental exertion (I know how my mental ability degrades after 1 hour of thinking), and there is no reason to preclude such stress/damage as the possible trigger for PEM. And how hard you think, and how tired you are afterward, got to be proportional to the amount of expended for thinking within the given time period.
Maybe thinking too much outside of the box but would there any non-exertion things that should also trigger PEM if that's the case?I continue to think that what may trigger PEM is some cumulative tissue response to microtrauma - like the response to using your hands that leads to calluses on your palm. It is partly the intensity of force involved and partly the duration, but not a simple multiplication of the two.
Maybe thinking too much outside of the box but would there any non-exertion things that should also trigger PEM if that's the case?
I was more so thinking about non-muscle microtrauma.Passive movement would be the obvious thing, but that isn't easy. If it is necessary for internal forces to be generated in muscle you might need electrical stimulation and that is pretty nasty over an extended period.
A 'non-exertion' thing that gives me serious fatigue is maintaining posture when in a moving vehicle or on a boat. But that involves muscle work, despite one not being aware of it.
People with ME/CFS talk of PEM being precipitated by having to travel in an ambulance, even if lying down. Goodness knows what calories are involved there.
I think the whole thing is wide open.