Bloodletting was a "traditional" treatment for a lot of maladies. That doesn't make it preferable to better-informed modern alternatives.
* Standard practice for virtually all hormones—not starting with > physiological production
Do you actually dispute this? If so then ask your favorite AI about it and don't waste my time on it.
* U-shaped mortality curves related to testosterone levels
• Afib risk also U-shaped with levels
Even you should know off the top of your head that when optimum outcomes correlate with TT around 400-500 (which by the way is a peak AM measurement), then taking 10 mg T per day is going to put the average guy at around twice these levels. Do you deny this or are you intentionally wasting bandwidth?
• Dose-related side effects from high estradiol, high prolactin
Not claiming particular frequencies, but these are commonly reported side effects seen even with upper-physiological dosing. Hard to dispute that they are dose related. At one time averaging 6.5 mg T/day put my E2 levels in the lower 50s pg/mL, a full standard deviation above the top of the normal range. You can be sure I felt this. Unsurprisingly the symptoms go away at lower levels. Search for high E2 symptoms in the forum if you like. There is research showing that E2 is a driver of prolactin, so they can rise and fall together.
• Increased blood viscosity with HCT increasing long-term myocardial infarction risk
You act as if you didn't review the study I linked to above. It is concerning, given that it tracked men who were young and healthy at the start and found a linear correlation of MI risk with HCT. These guys would have had HCT in range, yet it's routinely advised here that it's fine to have HCT sit in the low 50s (%). I think this signal is eventually going to show up in long-term TRT users.
I assume you're not denying that elevated HCT is a common dose-dependent side effect of TRT. This study suggests that any increase in HCT is heightening your risk. Many on TRT do not see this rise, but many do, which is why a low-and-slow approach to TRT is more rational than what you advocate.
I listed 20, which are just some of the ones since I started looking. That's more than a handful, and infinitely more than the zero you've offered to demonstrate that physiological dosing causes harm. You'll note that most of them ended up well below 100 mg TC/week, even after trying a range of doses.
The best that can be said about your approach is that many men can tolerate it, but there's no proof of better results compared to what's physiological, and the risk of side effects is undeniably greater.
Another fun side effect of mildly supra levels:
"I experienced this 'dead wood' penis insensitivity on and off for a long time while on dosages around 100 mgs per week of T. When I lowered the dose down to 60-70 mgs, sexual sensitivity improved considerably. Erectile function is also more responsive and reliable.
...Too much testosterone is not a good thing, especially for your penis."
• No documented harm in starting with mid-physiological levels
But it is when you were the one claiming harm in starting physiological. Nice to see that you're abandoning the position.
• No documented benefit to overall health with > physiological levels
Ok, cite one study citing the superiority of supraphysiological testosterone levels for overall health. It doesn't exist, so your denial is pathetic.
This is a false dichotomy. Guys do not have to accept hypergonadism to avoid hypogonadism. If you can only support your claims with fallacious arguments then it's game over.
• Excess dosing tied only to TC injections, not other modalities
Apparently you never looked at a dose-response chart for topicals.
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My evidence stands firm against your empty denials. Meanwhile you continue to offer nothing to support the superiority of supraphysiological starting doses.