TPOAbTgAb rT3TSHFT4FT3
Thanks
TPOAbTgAb rT3TSHFT4FT3
Thanks
Here
bluehorizonbloodtests.co.uk...
Requires private blood draw so that adds to the cost
bluehorizonbloodtests.co.uk...
Thank you TM. Sorry to ask for more but are you aware of one that also includes an iron panel
You don't need rT3. It's very expensive, irrelevant and doesn't give you any useful information that you can't get from testing just FT4 and FT3.
Thank you gg but Paul Robinson has specifically requested it as a one-off and although I’ve read lots that suggests it isn’t useful, I’ve also read that it can be useful. Who does one believe🤷♀️
Obviously I prefer not to have the expense but if there’s a small chance that I can get to the bottom of a few questions then I’ll be happy
Thank you for your view on it
Can you tell me in what way it can be useful? I'd be interested to know.
Forty years is a very long time!
Maybe some more recent research (this article is based on much more up to date information):
thyroidpatients.ca/2019/11/...
Or a search of that site for all rT3 references:
It isn't that rT3 testing doesn't ever tell us anything at all. But it might add nothing, or very little, and what it does add might be in a different area than the very obvious T4 and T3 pathways.
Out of curiosity - do you know the reason why Paul Robinson requests it as a one of?
Apparently it can block T3 and reduce certain enzymes that will have a negative effect on T4 to T3 conversion
I cannot pretend to have a deep understanding, I’m merely paraphrasing what I’ve read but while there’s a chance that the test will be relevant, I’ll get it done
Apparently it can block T3 and reduce certain enzymes that will have a negative effect on T4 to T3 conversion
This is the old thinking about rT3. Research has moved on.
According to our late-lamented diogenes, it doesn't block T3 receptors, it has it's own receptors. It is totally inert and doesn't do anything, and only stays in the system for a couple of hours before being converted to T2.
Pretty certain it doesn't have any effect on any enzymes. And doesn't affect T4 to T3 conversion. It is the result of poor conversion, not the cause.
And to know how well you convert, you don't need to test rT3, just FT4 and FT3 and compare them. What is your FT4 level? It it's up near the top of the range then your rT3 is going to be high. That's just the way it is. But it doesn't mean anything. It's just a safety device the body has to stop you 'going hyper' - i.e. syphoning off some of the t4 and converting it to rT3 rather than FT3.
But what does he propose to do if your rT3 is high? Does he know that there are many, many causes of high rT3, and only one of them has anything to do with thyroid. So, he could be leading you up the garden path on that one.
I’m still trying to get a feel for him really
Late Diogenes? I had no idea
As for knowing how well I convert? Impossible, I’m on Metavive
So you don't even know how much T3 or T4 you're getting. In which case, how can Paul Robbinson help you? RT3 won't be of much help.
It's interesting Greygoose. When I was put on Amiodarone post op for a month.....taken me 15months so far to sort out the mess that drug did to my ability to tolerate thyroid hormones. Nearly back to where I was. One of the features is the body converts into a lot of rt3. Amiodarone works also by blocking receptors and inhibiting conversion..I assumed the reason for the high rt3 was a way of getting rid of the t4 building up in the body? I never did a rt3 test itself but read about it in research docs about effects of Amiodarone.
So if your body can't convert aa well or absorb via the receptors is this how it reduces the levels? In which case you wouldnt be aware of this in a blood test for TSH ft4 & ft3. None of the Endos I saw during this period recommended testing for rt3. Though they knew about the drugs impact. They guesstimated about how long it eould do this for at about 6 months. Managed by lowering dose of thyroid hormones. Infact it's been 15months. The half life being 142 days. I wonder now if the rt3 might have been useful after all. Though the effects dtill would've been reduced treatment of thyroid hormones.
So if you have a problem with tolerating thyroid hormones given does an rt3 test help in knowing your body is resistant......
Like mine was albeit due to a drug inhibiting tolerance.
Sometimes I wonder how much science knows..... about this area...
An rT3 test will give you no clue as to why it's high, it will just tell you if it is high. And there are many, many possible reasons for it being high. And just being ill will raise it, without the accompanying drugs.
OK but it's known that rt3 goes up to clear the thyroid hormones due to Amiodarones effects. I wasn't ill. Post op recovery but not ill with other conditions. I'm just suggesting it maybe helpful and form a part of a whole picture. Made no difference to my actual treatment. Which has to be massively lowered. It would've been interesting to have tracked the rt3 to see if it lowered as I managed to increase. Sadly put a ton of weight on as a consequence of under treatment for so long. Lol...
Post op recovery counts as 'ill' in this context. But, whatever, I still can't see that testing rT3 would have been helpful because it could have been high due to other factors as well.
No this has lasted 15months well after any operation recovery which was keyhole. Ive had other ops without this affect on my thyroid hormones.....they went through the roof. Starved at cellular level....felt very ill.
I can imagine you must have! And all because of Amioderones? Hope you're feeling better now.
Thanks Greygoose. Yes taken 15months but nearly there....probably need one more dose increase in a while. Most endos seem ignorant of the secondary effect at cellular level....theyre all taught Amiodarone only affects the thyroid gland. Not the whole picture! Nor are they aware of its true longevity.... Sigh....
They're not really aware of much at all, are they. So that doesn't surprise me.
So true Greygoose. Well.paid & Ignorant! So 3 told me.....ahh Amiodarone it's gone out the system by 6 months!! Not true of course given its half life length. One was more open and listened but was surprised but went with it. I would've doubted myself if I hadn't already got 20yrs of experience of managing my own hypothyroidism....& then heard of others with pre existing hypothyroidism having exactly the same problem themselves & taking a good 15months to recover. It's all poorly researched and what's there isn't usually read. Lol.
It does leave me feeling that it really is safer to self treat.....because it's largely my actions that's got me back to where I am. Very little advice if any forth coming. They thought I was unusual. Nope I wasn't. Probably why NICE guidelines state that its contrary indicated for those with pre existing hypothyroidism. Do not prescribe.
Bet that's not been read either. Sigh...lol
It's criminal, really. That's our lives they're playing around with!
The Doctors Laboratory
They do reverse T3 - and a massive range of other tests. But, as with many of these services, location might be important for phlebotomy. And cost.
They also say:
No appointment is required for routine tests (a doctor or clinic’s request form or referral letter is required)
I read only recently that a proper understanding of the effects of hypothyroidism only began in the ‘70’s. So a 40 year article would represent the understanding at that time. Early Days. We’ve gone to obtain T3 through a private prescription via Roseway Labs.
After 8 weeks on 2.5mcg Helen’s Ferritin, Cholesterol & bit D are are all up and her Cortisol jumped nearly 200 units, her t4 remained the same and ft3 went from 3.8 to 5.5. Also her CPR went from 2 to 1 suggesting that even a ‘normal’ high CPR may indicate you may have inflammation in your thyroid (could be something else but it went down on treatment which to me is no coincidence) and it took her TSH to a low normal. Prescriber said increasing to 5mcg not a good idea.
NHS Endo put Helen on 20 mcg day and reduced her Levi to 75 from 100 with predictable outcome. As someone previously said starting like that is like putting high octane fuel in a clapped out motor with predictable outcome results. Helen blew up - almost as if she was being set up to fail.
This is the clinic I used and they were excellent.
Randox Health
I believe they may also have some clinics in the US too.