Why Paul needed T3-Only Medication - An Update

Just a brief update on the very likely reasons why I could only get well with T3-Only medication.


I have a defective DIO1 and DIO2 gene. I recently did the DIO2 gene test with Regenerus labs. It turns out that I do have the homozygous variant of the gene defect. I also inherited it from both of my parents. The fact that I inherited it from both of my parents makes the effect likely to be stronger, i.e. that I was always likely to convert T4 to T3 very poorly. The D2 Deiodinase enzyme is used by the brain, pituitary, thyroid gland, heart and muscles. D2 is far more efficient in converting T4 to T3 than D1. See the Watts Study for more information on the DIO2 deiodinase gene defect: http://www.metabolism.com/2009/11/07/breakthrough-discovery-thyroid-hormone-therapy-part-2/

I have also completed a 23andMe genetic test. I have the DIO1 gene mutation also. Again, I inherited this from both parents. D1 is used by the liver and kidneys. D1 is less effiient in converting T4 to T3. However, in the liver D1 is very important as it is used to clear rT3, i.e. to deiodinate it to T2, T1 and then T0 before removing it from the body within 24 hours. So, a DIO1 defect can cause higher rT3.

I have both DIO1 and DIO2, and in both cases I have two copies. I was always likely to have conversion problems.

Secondly, Hashimoto's destroyed by thyroid gland. his is another reason that so many with Hashimoto's or thyroidectomy need additional T3. The thyroid is the biggest converter of T4 to T3 in the body (relatively new research) - more than the liver and kidneys and peripheral tissues. The net of this is that the blood flowing through the thyroid gland carries T4 and the thyroid converts some of this flowing T4 to T3. This is more significant than any T3 produced by the thyroid tissue itself. The thyroid is responsible for 25% of our total circulating T3 (through production and T4 to T3 conversion capability). So, when you lose thyroid tissue, you also lose this T3 and the T4 to T3 conversion capability.

Thirdly, I was also driven to T3 because I had extremely low cortisol levels when on T4 based medication. The pituitary uses the D2 deiodinase enzyme to convert 80% of the T4 that passes through its cells. It keeps this converted T3 internally, i.e. the pituitary gland NEEDS high levels of FT3 in order to function. With worsening conversion through the DIO2 gene defect and loss of thyroid conversion, I would have had lower T3 levels in the pituitary. This can induce dysfunction in the pituitary and lower ACTH and TSH. T3-Only is known to stimulate the hypothalamic-pituitary system and the mitochondria far more than T4 or T4/T3. My cortisol levels were terribly poor, so much so that my blood pressure was horribly low and I used to pass out quite often due to it. Only when I managed to rectify my hypocortisolism through the use of T3 and the Circadian T3 Method did I begin to recover. It is possible that I also had less than optimal aldosterone, but this was never tested. Note: Anything that lowers T3 levels, including lower conversion through any mechanism, e.g. DIO1 or DIO2 gene mutations, or any other mechanism or nutrient defect, can affect the pituitary, and the way it is supposed to work.

The three things combined to be a 'perfect storm' for me. One that made using T4 impossible.

I will write more about all of this in due course. But I believe the above points may be relevant to a vast number of thyroid patients. 

I will say one more thing as this has come up recently in a few 'discussions'.

I cannot cope with T4 medication, even in small amounts

T4 in any quantity brings back my hypothyroid symptoms. I am healthy, fit, active and symptom-free whilst on T3 replacement therapy. So, when I hear views like, "everyone needs some T4", I would like to be able to respond, "why would I wish to be ill once again, just to appease your dogmatic and closed-minded viewpoint!” These types of views are stated from time to time, usually by doctors, but also, sometimes by thyroid patients. Unsurprisingly, the patients concerned are on some form of T4 based medication, and they think everyone else should be taking it too. They have sometimes found a not especially compelling piece of research that shows that T4 has some minor effect on some system in the body, and then they extrapolate from there that everyone needs T4. This is not the case. One of the big flaws in that type of argument is that people who are living well on T3 alone have not been studied for the very likely compensatory adjustments that the body makes when using T3 on its own. The other big flaw is that small pieces of research often get found to be inadequate or incomplete when further research comes along: http://recoveringwitht3.com/blog/t4-not-needed-brain-adults-new-research-backs-t3-users-experience

I have used T3 replacement for over twenty years. I know many thyroid patients, who have recovered their health using T3 replacement, and have been using it for a long time. There are also excellent reasons why I could not get well on more conventional T4-based (T4/T3 or NDT) thyroid treatement (see the above points).
T3 replacement therapy can be a very effective, safe, long-term thyroid hormone treatment.
Me, and the many others like me, would not be so well if we actually needed T4 - that is just simple, inarguable logic.

Best wishes,