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Is POTS a central nervous system disorder? (Blitshteyn, 2021)

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Is postural orthostatic tachycardia syndrome (POTS) a central nervous system disorder? (Blitshteyn, 2021)

Same thread on Dinet forum

Abstract
Postural orthostatic tachycardia syndrome (POTS), a disorder of the autonomic nervous system characterized by a rise in heart rate of at least 30 bpm from supine to standing position, has been traditionally viewed as a dysfunction of the peripheral nervous system. However, recent studies and evidence from overlapping conditions suggest that in addition to being considered a disorder of the peripheral nervous system, POTS should be viewed also as a central nervous system (CNS) disorder given (1) significant CNS symptom burden in patients with POTS; (2) structural and functional differences found on neuroimaging in patients with POTS and other forms of orthostatic intolerance; (3) evidence of cerebral hypoperfusion and possible alteration in cerebrospinal fluid volume, and (4) positive response to medications targeting the CNS and non-pharmacologic CNS therapies. This review outlines existing evidence of POTS as a CNS disorder and proposes a hypothetical model combining key mechanisms in the pathophysiology of POTS. Redefining POTS as a CNS disorder can lead to new possibilities in pharmacotherapy and non-pharmacologic therapeutic interventions in patents affected by this disabling syndrome.
 
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ljimbo423

Senior Member
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Unless those drugs are having an unknown effect outside the CNS then I'd take their usefulness to be a strong indication that POTS is a CNS disorder.

Makes sense.

Since the brain controls everything in the body. I think CNS dysfunction from neuroinflammation causing POTS, isn't a big leap.

To me it also just makes more sense on a gut level. That probably won't make a random controlled study though.:);)
 

ljimbo423

Senior Member
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But that's the caveat.

Yeah, there are usually caveats.

I do think that neuroinflammation is causing soooooo many symptoms in ME/CFS. So for me, it causing POTS makes sense. Studying low grade neuroinflammation is very difficult though. We just don't have really good technology, to do it with great accuracy and detail.
 
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Pyrrhus

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Has nobody considered this before?

If we're going to try to separate out peripheral and central mechanisms, (and I'm not sure we can) then we would have to break POTS down into two components:

Postural Orthostatic Tachycardia Syndrome (POTS) is:
  1. Orthostatic Intolerance, which is generally seen as a failure of peripheral nerves that control blood vessels. This results in regional low blood pressure.
  2. Tachycardia, which is a response of the central nervous system (brainstem) to the regional low blood pressure. By forcing the heart to beat faster, the brainstem is trying to raise the regional low blood pressure.

A lot of people with ME have the first, orthostatic intolerance.
But not as many people also get the second, tachycardia.

People who don't get tachycardia can be diagnosed with Orthostatic Hypotension if their blood pressure drops by a certain amount upon standing.

Of course, the presence of POTS can come with other neurological problems, like ME, so it's not at all surprising to find evidence of brain dysfunction with POTS.

Hope this helps.

EDIT: Emphasized that peripheral and central mechanisms work together, and can't always be fully separated.
 
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Rufous McKinney

Senior Member
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13,354
A lot of people with ME have the first, orthostatic intolerance.
But not as many people also get the second, tachycardia.

I've experienced really intense tachycardia during prolonged crashes and when I was Quite Bad off ME wise- (out of the country). I don' t notice it when I'm not real run down.

I think I was in a state of continuous PEM crash for three months while visiting my new grandchild.

I'm considering- going back down to see them again. But all that stuff: can't be happening. Must be banished.
 

pattismith

Senior Member
Messages
3,937
If we're going to try to separate out peripheral and central mechanisms, then we have to break POTS down into its two components:

Postural Orthostatic Tachycardia Syndrome (POTS) is:
  1. Orthostatic Intolerance, which is a failure of peripheral nerves that control blood vessels. This results in regional low blood pressure.
  2. Tachycardia, which is a response of the central nervous system to the regional low blood pressure. By forcing the heart to beat faster, the brain is trying to raise the regional low blood pressure.

Dont you think that blood vessels are under the control of the brain as well?


Normal autonomic neurophysiology of postural orthostatic tachycardia and recommended physiological assessments in postural orthostatic tachycardia syndrome (nih.gov)

Orthostatic hypotension with brainstem tumors - PubMed (nih.gov)
 
Messages
30
Location
Qld, Australia
Dont you think that blood vessels are under the control of the brain as well?

I don't know which comes first...
I had abnormal ECG results while in orthostatic distress. However, the following Echocardiogram tests (another day) while in supine position didn't show significant abnormality. I think standing ECG (heart) and EEG (brain) are the possible OI diagnostic tool for those patients who don't show significant abnormality with heart rate and blood pressure change.

I also had abnormal lung x-ray while standing, but not in supine position. (Possible asthma... Had misdiagnosed with COPD. IMHO, with COPD, lungs inflate while supine and it's opposite to OI.)

We need to think beyond heart rate and blood pressure to investigate OI in pwME.
 

Pyrrhus

Senior Member
Messages
4,172
Location
U.S., Earth
Dont you think that blood vessels are under the control of the brain as well?

Yes, absolutely! Thank you for pointing that out.

The brainstem can control both heart rate and blood pressure by influencing peripheral nerves.

I had abnormal ECG results while in orthostatic distress.

Very interesting. If you don't mind me asking, what abnormal results did they see?
 

Pyrrhus

Senior Member
Messages
4,172
Location
U.S., Earth
If we're going to try to separate out peripheral and central mechanisms, (and I'm not sure we can) then we would have to break POTS down into two components:

Postural Orthostatic Tachycardia Syndrome (POTS) is:
  1. Orthostatic Intolerance, which is generally seen as a failure of peripheral nerves that control blood vessels. This results in regional low blood pressure.
  2. Tachycardia, which is a response of the central nervous system (brainstem) to the regional low blood pressure. By forcing the heart to beat faster, the brainstem is trying to raise the regional low blood pressure.

A lot of people with ME have the first, orthostatic intolerance.
But not as many people also get the second, tachycardia.

As @pattismith pointed out, it can be difficult or even impossible to try to fully separate activity of the peripheral nervous system from activity of the central nervous system.

Case in point:
In number 2 in the above quote, I say that the tachycardia is a response of the central nervous system, when it is really a combination of both the peripheral and central nervous systems. In fact, it is a well-researched reflex called the baroreflex:

Wikipedia said:
Decreased blood pressure decreases baroreflex activation and causes heart rate to increase and to restore blood pressure levels.[1] The baroreflex can begin to act in less than the duration of a cardiac cycle (fractions of a second) and thus baroreflex adjustments are key factors in dealing with postural hypotension, the tendency for blood pressure to decrease on standing due to gravity.

The system relies on specialized neurons, known as baroreceptors chiefly in the [major arteries] to monitor changes in blood pressure and relay them to the [brainstem]. Baroreceptors are stretch receptors and respond to the pressure induced stretching of the blood vessel in which they are found. Baroreflex induced changes in blood pressure are mediated by [...] the autonomic nervous system.
Source: https://en.wikipedia.org/wiki/Baroreflex