Question; Why is anastrozole the drug of choice?

totalburnout

New member
Question -

Why is anastrozole the drug of choice to manage estrogen? I think we have seen a significant number of instances on this forum and similar forums that have shown users to have issues with over dosing and creating low estrogen issues. Why then is it the go to versus a SERM like aromasin for a standard testosterone replacement therapy (TRT) protocol? Aromasin seems to be the estrogen management tool for many running PCT but not during TRT.

discuss please.
 
Aromasin is not a SERM...It's an Aromatase inhibitor (AI), just like anastrozole. I can't speak for others but I do use Aromasin as part of my testosterone replacement therapy (TRT) protocol. Anastrozole lowered my E2 too much, even at a low dose.
 
Take a look at this thread here:
steroidology.com/forum/anabolic-steroid-forum/644282-estrogen-cycle-good-bad-proper-management-both.html

So we see we have 2 categories of compounds that can be of use to us in properly managing Estrogen or its side effects, Serms and AIs. Let''s take a look at our options in categories, their differences and potential interactions with one another, and how they might be used together to accomplish our goal.

First we will look at AIs as in my opinion they are the core of our Estrogen Management program. [We essentially have 2 types of AI''s to choose from. Type 1 AIs like Exemestane and Type 2 AI''s such as letrozole or Anastrozole (arimidex). The difference in these types is as follows. A Type 1 Aromatase inhibitor (AI) like Exemestane binds permanently to the site on the Aromatase Enzyme where it binds to testosterone allowing its conversion to Estrogen. This permanent binding renders the Aromatase totally and permanently inactive. In contrast Type 2 AIs temporarily bind to this site on the Aromatase Enzyme rendering it inactive as long as the Aromatase inhibitor (AI) is being used. Onçe use of type 2 Aromatase inhibitor (AI) stops the aromatase will reactivate. So whats the difference in these Aromatase inhibitor (AI) types for our purposes? Well Due to the '"reactivation" if you will of existing Aromatase with a Type 2 Aromatase inhibitor (AI), when you stop using it a spike in Estrogen (often referred to as rebound) will occur due to the sudden increase availability of Aromatase Enzyme. Another important distinction when it comes to Type 1 and Type 2 AI''s. A Type 1 Aromatase inhibitor (AI) like Exemestane remains unaffected by the introduction of a serm into your Estrogen management program. Type 2 AIs like letrozole and Arimidex suffer a reduced in blood levels and effectiveness with the introduction of some serms. I will touch more on why we may need to introduce a serm a little farther on in this article.

When it comes to the strength of these AI''s letrozole would be the strongest followed by Arimidex and then by Exemestane. Now people might be up in arms saying Exemestane is stronger than Arimidex however when one looks and compare data from studies done on MALES the order of strength is exactly as I stated it, quite often much confusion comes in to play when people recite data on AI's taken from studies on women. The fact is AI's behave differently in males, they are less effective in males, and for our purposes it is only prudent to compare data gathered from studies on males to portray an accurate picture.

The next aspect to be considered when looking at AIs are the effects they indirectly illicit in other areas. We stated the positive effects of Estrogen, we must realize by lowering Estrogen via Aromatase inhibitor (AI) use some of these positive effects may be compromised. It is important to look at the various Aromatase inhibitor (AI) options available and possibly use the data to help pick which Aromatase inhibitor (AI) we use. letrozole is an extremely potent Aromatase inhibitor (AI) and its effects demonstrate this as would be expected. letrozole has an adverse effect on lipid profile and somewhat on IGF levels. On the other hand Arimdex has a small impact in the area of IGF and depending upon which studies you cite a small adverse impact on lipids to no adverse impact on lipids. Exemestane seems to have no clinical impact on either IGF or lipids.

It is important to realize that it may seem like Exemestane shines as a clear cut winner when it comes to choice of Aromatase inhibitor (AI), however I do not necessarily believe this to be the case for everyone. In some cases or maybe better said in some people, an extremely powerful Aromatase inhibitor (AI) like letrozole must be used to manage Estrogen properly. Some may respond better to Arimidex than Exemestane. I believe there is a place for all 3 of these. That being said, if possible my personal first choice of Aromatase inhibitor (AI) is Exemestane due to its lack of interaction with other compounds we may need to introduce such as certain serms, its positive effects on IGF and Lipids over other options, and also its lack of potential "rebound"(although I think that is an overstated issue quite often)
 
Well the first thing we need to clear up is Exemestane is not a SERM.

Noted.

Question still remains the same and is even more pertinent since its comparing one Aromatase inhibitor (AI) to another. Obviously I know little of aromasin because I have never had it prescribed - that just makes me raise the question why not?

The article that was posted echoes what I had previously read that essentially aromasin is milder, with less sides, and isn't a temporary inhibitor.
 
Noted.

Question still remains the same and is even more pertinent since its comparing one Aromatase inhibitor (AI) to another. Obviously I know little of aromasin because I have never had it prescribed - that just makes me raise the question why not?

The article that was posted echoes what I had previously read that essentially aromasin is milder, with less sides, and isn't a temporary inhibitor.

Aromasin is not milder, it is actually stronger than anastrozole. It is also the only steroidal Aromatase inhibitor (AI) on the market.

The only reason it seems that it is milder is because of the dosing, it is a larger amount so titration seems to be easier. There are other negatives to using a steroidal Aromatase inhibitor (AI) though. Wether or not it is temporary inhibitor does not make a difference for those on testosterone replacement therapy (TRT), the only positive to a suicidal is there is no rebound effect when it is discontinued, but I personally have never seen a rebound effect anyway, this is something is merely talked about yet never seen.

Anastrozole, due to cost and efficiency is the easy first choice.

Keep in mind wether one is stronger than another only has to do with the ability to penetrate dense lipid cells, and there are very few reasons why anastrozole would be insufficient, and if those reasons arise Letro is a better alternative anyway.

Please keep in mind I am not speaking of research chems at all, to roll the dice with these does not make any sense to me.
 
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