High Angiotensin 2 and low ACE2

neophyte32

Established Member (Voting Rights)
Hello, Are there any of you with MECFS who had COVID (I don't know if it was COVID that triggered MECFS, Lyme disease, or something else...) who have very high levels of angiotensin II (but low blood pressure) and very low levels of ACE2? I had a blood test for protein markers at Amatica (I know they're criticized here, but that's okay) and my results are very high compared to other patients (50 for control and 60 for MECFS/long COVID). Is anyone else in the same situation? I've read studies from 2021 and 2022 that explain that it's related to COVID-19 depleting ACE2 in the long term. This could explain the severity of my MECFS (bedridden for 9 months) and my comorbidities (dysautonomia, POTS...).
Thank you.

P.S.: I'm not asking for interpretation of results; I know that's not allowed here. But I'm posting my blood test results with the percentiles anyway.
 

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I have no tests and I am not able to interpret yours.

But I can say I have been encountering symptoms lately since a suspected covid variant infection double whammy of Stratus and then Nimbus (on top of ME CFIDS which has caused recurring viruses of various species over 40 years) which I have been trying to interpret using the model you describe in the thread title.

It is sad yet in a way a relief to know someone else is encountering similar problems though I know they are horrid and I am sorry for you and me both. At least we are not alone. It does suggest some people in some situations can encounter ACE2 depletion and RAS related consequences due to longcovid (though RAS theory would predict higher blood pressure, so not that simple). I feel like this really needs to be recognised more openly than it is.

I have done my best to talk about it here... hope it is of interest...


here...


and here...

 
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