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Steroidogenic isoenzymes may help improve treatments for common hair loss.

Inhibiting 5α-reductase can help reduce prostate cancer risk and improve treatment.

Two types of 5α-reductase are in dog skin, which might make dutasteride better than finasteride for treating dog hair loss.

Blocking DHT production more strongly may help control advanced prostate cancer and improve quality of life.

Creating stronger blockers for skin enzymes might lead to better treatment for conditions like acne and excessive hair growth.

Blocking the enzyme that turns testosterone into DHT can safely and effectively treat enlarged prostate.

Flutamide may slightly improve hair loss in women, but finasteride does not work.

Finasteride helps regrow hair and shrink prostate by reducing DHT, with some sexual side effects.

Finasteride, a drug, can block the seizure-preventing effects of a hormone called progesterone in mice.

A new drug, dutasteride, is at least as effective as the older drug, finasteride, for treating enlarged prostate and may have additional uses.

Dutasteride is becoming a popular hair loss treatment, proving more effective than finasteride with similar side effects.

New research is needed to create better drugs that block the enzyme responsible for conditions like male baldness and prostate enlargement.

New treatments for enlarged prostate are being developed to be more effective and have fewer side effects.

Dutasteride is more effective than finasteride for hair loss treatment.

Finasteride reduces prostate cancer risk but may increase high-grade tumors; new drugs and better diagnosis are in development, but funding and industry commitment are challenges.

Dutasteride may help treat prostate cancer by causing cancer cells to shrink and die.

Minoxidil lowers blood pressure effectively but may cause unwanted hair growth and other side effects.

Higher fluence in hair removal damages hair follicles more, while lower fluence mimics natural hair regression, with long-term IPL treatments effectively reducing hair.

5-alpha reductase inhibitors can cause sexual side effects like erectile dysfunction and reduced sexual desire, sometimes lasting after stopping the drug.

5α-reductase inhibitors and alpha-1 adrenergic antagonists together effectively treat benign prostatic hyperplasia, with long-term benefits.

5α-reductase inhibitors, like finasteride and dutasteride, effectively treat BPH, male baldness, and hirsutism, with potential for acne and prostate cancer prevention.

Gene differences may affect baldness treatment response in Korean men.

Finasteride reduces hair growth in women with hirsutism and works better with electrolysis.

The study created a new method to test drugs that affect hormone processing in skin.

Dutasteride is effective for treating prostate enlargement and reducing related surgery risk, but is not approved for preventing prostate cancer.

Antiandrogens and androgen inhibitors like spironolactone, finasteride, and dutasteride can treat hair loss and skin conditions, but they have risks and side effects, including potential harm to pregnant women and risks of cancer and heart issues. Herbal remedies also have antiandrogenic effects but lack safety validation.

The document concludes that the risk of sexual side effects from 5-alpha-reductase inhibitors is low and often temporary, but more research is needed on potential permanent effects.

Dutasteride effectively treats benign prostatic obstruction, improves urinary flow, reduces prostate size, and may prevent prostate cancer, but can cause sexual side effects.

Testosterone's muscle-building effects do not require its conversion to DHT.

Norgestimate is the most effective birth control progestin for reducing an enzyme linked to acne and excessive hair growth in women.