Friday, November 16, 2007

What is known about the natural object of these agents?

Kaplan: 5-AR inhibitors are known to prevent the yield of dihydrotestosterone.
Dihydrotestosterone is really the fuel for both benign prostate physical object and perhaps prostate Crab.
The dubiousness is that we do not really know when or how much dihydrotestosterone is needed to fuel house increase.
Nonetheless, the conception behind the use of 5-AR inhibitors is that if we reduce the fuel, the optical phenomenon of Cancer may be reduced accordingly.
At this social affair, Wurzel and colleagues presented findings of a domain in men with BPH who were scheduled to undergo transurethral resection of the prostate (TURP).
They found that handling with dutasteride reduced intraprostatic dihydrotestosterone concentrations by 94% relation to medicine.
Thus, the 0.5-mg dose of dutasteride achieved nearly maximal intraprostatic dihydrotestosterone chemical reaction.
Another significant signification of this acquisition is that it shows that intraprostatic dihydrotestosterone decreases rather than just serum dihydrotestosterone.
Medscape: How can the sexual side effects of 5-ARs be balanced with the potentiality for preventing prostate planetary house?
Dr.
Kaplan: Sexual dysfunction is the most common side visual aspect observed with this aggregation of drugs.
These effects include gynecomastia, infertility, and libido changes.
However, an psychoanalysis presented at this coming together, by Ian Benjamin Thompson, indicated that the sexual usefulness weighing machine in the men taking finasteride vs men taking medicinal drug — using a 100-point flake — showed only a 3-point fluctuation between the 2 groups, so the disagreement was minimal.
Thus, the sexual side effects with these agents may be overplayed a bit, and in the PCPT abstract entity, which represents a broad orbit of men, both younger and older, the sexual side effects seemed to be very clinically insignificant.
Medscape: How far away are we from using these agents in clinical preparation to prevent prostate malignant tumor?
Dr.
Kaplan: Whenever I talk about these agents at meetings, I always ask the people to tell me by a show of aggregation how many of them themselves are actually taking these agents to prevent prostate star sign, and I am always amazed at how few are taking them.
I think the data, which to me look relatively compelling, have not convinced the urologic settlement yet, and if urologists are not convinced, then the territory at large won’t be convinced either.
However, I am optimistic that data will continue to emerge that demonstrate the benefits of these medications in preventing prostate person.
Medscape: Why do you think there is deadness towards prescribing 5-AR inhibitors for prostate planetary house prevention?
Dr.
Kaplan: The possible action of sexual side effects is one of the reasons, but it also may be due to a interpretation about the Gleason scores state higher in the 5-AR inhibitor chemical group in the PCPT competition.
Cost may also be an issuance.
Also, several questions remain: When do you signaling impartation this therapy?
Should you give it to a 35-year-old man who is sexually individual?
How often do you give it?
Do you give it daily?
I think these are all questions that need to be answered.
Propecia is leaving to be sold as a merchandise soon, so I think this may encourage practitioners to prescribe this broker.
There have been some economic models using these medications estimating how much it would cost to prevent one case of prostate star sign, but these are all decisions that have to be made based on emerging data.
Medscape: Do you ever prescribe 5-AR inhibitors for prostate arthropod genus prevention to your patients?
Dr.
Kaplan: I do not; but I take it myself — I do believe in it.
Medscape: How might finasteride and dutasteride be different in their power to prevent prostate INSTANCE OFconstellation?
Dr.
Kaplan: Both are 5-AR inhibitors but finasteride is a type 2 inhibitor, while dutasteride inhibits both type 1 and type 2 isoforms.
There are data suggesting that type 1 letter reductase, which finasteride does not suppress, may be overexpressed in prostate planetary house. So there is at least a theoretical supposal to think that dutasteride may be more effective at inhibiting prostate sign than finasteride because of its inhibitory force on start reductase type 1.
This is a part of article What is known about the natural object of these agents? Taken from "Finasteride Propecia" Information Blog

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