Androgen Levels and Semen Parameters Among PFS users

https://endo.confex.com/endo/2014endo/webprogram/Paper11432.html
http://archderm.jamanetwork.com/article.aspx?articleid=1904925

Thanks for posting this - anyone have any insights (all I really understand is that more research is needed!).

Wonder if someone could enlighten me, how do these studies get funded?

I mean it’s what we have known for long time - the benchmark hormones are normal in Finasteride users yet sexual side-effects persist.

Surely the researchers would have known this prior to the study, they would have read previous studies that have reached the same conclusion.

So what was the motive? Seems an entirely inefficient use of money and effort.

The Italian ones are good are as they explore the lesser known hormones and have highlighted discrepancies between control subjects.

Frustrates me when I hear of doctors exploring TRT and/or viagra. It’s the obvious answer to sexual dysfunction - so would have been the first treatment people tried 10 years ago.

Hopefully the Foundation are more forward thinking in their approach. We need to know why androgens aren’t as potent as they should be. What are the density of the androgen receptors? Whats the activity at these sites compared to controls? How about the hormones that counteract androgens, such as the estrogen agonist 3B-Diol which is higher in PFS subjects. Why is it higher, and how could it be returned to baseline?

Maybe I’m being naive. But it seems such a ponderous and slow process.

If we had a doctor on our side with access to a lab - I’m sure as a community we could pool resources that would be a hell of a lot more efficient. We could publicise the need for subjects more readily and quickly - and target testing of hormones we know little about.

At this rate I’m struggling to see how anything will happen within the next 10 years.

I respect dr irwig but doing same studies over and over is completely pointless.

I still feel most of the people here are hypogonadal. For example, the 8 penile skin study patients were all hypogonadal. And why couldn’t he specify what symptoms the men actually have? Sexual side effects is a broad term and post-finasteride syndrome even more. His papers are not worth much, because they’re so linear, narrow and lazy. I wouldn’t even call it research. I don’t understand that guy. If he has all the patients at hand, why can’t he come up with something more conclusive?
Anybody have access to the full study?