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What was finasteride originally used for? The surprising history of a dual-purpose drug

5 min read

In 1992, the Food and Drug Administration (FDA) first approved finasteride, not for hair loss, but as a treatment for benign prostatic hyperplasia (BPH), a condition that causes an enlarged prostate. It was marketed under the brand name Proscar. This initial use established the foundation for its later, more widely known application.

Quick Summary

Finasteride was initially developed and approved to treat benign prostatic hyperplasia (BPH) by inhibiting the 5-alpha reductase enzyme. Its effectiveness in treating hair loss was discovered during development and led to a separate, lower-strength approval.

Key Points

  • Initial Purpose: Finasteride was first approved in 1992 under the brand name Proscar to treat benign prostatic hyperplasia (BPH), or an enlarged prostate.

  • Mechanism of Action: It works by inhibiting the enzyme 5-alpha reductase, which is responsible for converting testosterone into dihydrotestosterone (DHT).

  • Hair Loss Approval: A lower-strength version was later approved in 1997 (Propecia) after its effects on hair growth were observed during clinical trials for BPH.

  • Different Strengths: Finasteride is available in different strengths for each condition.

  • DHT Connection: By lowering DHT levels, finasteride addresses a key hormonal factor for both prostate enlargement and male pattern baldness.

  • Reversible Effects: The benefits of finasteride are maintained only as long as treatment continues; if the medication is stopped, the effects may reverse.

In This Article

Before taking any medication, including finasteride, it is essential to consult with a healthcare professional to understand its uses, potential side effects, and appropriate dosage for your specific condition. This article provides general information about the history and development of finasteride and should not be taken as medical advice.

The Scientific Foundation: The 5-Alpha Reductase Discovery

The development of finasteride is a fascinating story rooted in medical observation. In 1974, Dr. Julianne Imperato-McGinley and her colleagues studied a unique group of male children in a rural village in the Dominican Republic. These boys were born with a rare genetic disorder causing a deficiency in the enzyme 5-alpha reductase. The researchers noted that these individuals had very low levels of dihydrotestosterone (DHT) in their bodies. The most significant observation was that, as they matured, their prostates remained small and they did not develop male pattern hair loss. This critical finding demonstrated a direct link between the 5-alpha reductase enzyme, DHT levels, prostate size, and hair loss.

This groundbreaking research prompted scientists at Merck & Co. to develop a drug that could artificially create the same effect by inhibiting the 5-alpha reductase enzyme. The goal was to create a medication to shrink the prostate and potentially prevent hair loss. The initial focus was on the medical, rather than cosmetic, application of the drug.

The First Indication: Treating Benign Prostatic Hyperplasia (BPH)

Following successful research and clinical trials, finasteride received its first FDA approval in 1992. It was launched under the brand name Proscar to treat benign prostatic hyperplasia (BPH) in men aged 50 and older. BPH is a common condition where the prostate gland enlarges with age, pressing on the urethra and causing bothersome urinary symptoms. By blocking the conversion of testosterone to DHT, Proscar works to shrink the prostate, potentially alleviating issues such as frequent urination, weak stream, and incomplete bladder emptying. The therapeutic effect, however, is not immediate, often taking several months to become fully apparent.

The Second Act: Repurposing for Hair Loss

During the clinical trials for BPH, researchers noticed a secondary effect of the drug: it promoted hair growth in some participants. This observation led Merck to pursue a new indication for finasteride. By 1997, a lower-strength version of the drug was approved by the FDA for the treatment of male pattern hair loss, known as androgenetic alopecia. This new product was marketed under the brand name Propecia.

Male pattern baldness is caused by genetically susceptible hair follicles reacting to DHT, which causes them to shrink and produce progressively smaller, finer hair until they eventually stop producing hair altogether. By inhibiting 5-alpha reductase, Propecia lowers the amount of DHT reaching the hair follicles, potentially preventing further miniaturization and stimulating regrowth. Results for hair loss can take three months or more to become noticeable.

The Role of Dihydrotestosterone (DHT)

The shared mechanism of action for finasteride in treating both BPH and hair loss lies in its ability to reduce levels of dihydrotestosterone (DHT).

  • For BPH, the overabundance of DHT in the prostate is a primary driver of prostate cell multiplication and enlargement. By blocking the conversion of testosterone to DHT, finasteride helps to shrink the gland over time.
  • For hair loss, the same reduction of DHT levels can be beneficial. In genetically predisposed individuals, scalp hair follicles are sensitive to DHT, leading to the gradual miniaturization that causes baldness. Lowering DHT can help to reverse this process.

Key Differences Between Finasteride for BPH and Hair Loss

To clarify the distinction, here is a comparison of finasteride's two primary indications:

Feature Benign Prostatic Hyperplasia (BPH) Male Pattern Baldness
Brand Name Proscar Propecia
Typical Strength Higher strength Lower strength
Target Population Typically men aged 50+ Men with androgenetic alopecia
Primary Goal Shrink enlarged prostate and alleviate urinary symptoms Help stop hair loss and potentially promote new hair growth
Time to See Effects Can take up to 6 months for full effect Usually 3 months, but up to a year for full assessment
Side Effect Incidence May be higher due to the larger strength, including sexual side effects May be lower, but includes a similar risk of sexual side effects

Important Usage Considerations

For both conditions, it is crucial for patients to understand the proper use and potential side effects of finasteride. The following are key considerations:

  • Continuous Use May Be Required: The effects of finasteride, for both the prostate and hair, are often dependent on continuous use. If the medication is discontinued, the benefits may reverse over time, and the underlying condition could resume its natural progression.
  • Patient Education is Vital: Proper counseling by a healthcare provider is essential. This includes discussing potential side effects and the importance of consistent use as directed.
  • Not for Women: Finasteride is strictly for use in men. Pregnant women should not handle crushed or broken tablets due to the potential risk of birth defects in a male fetus.
  • Impact on PSA Levels: Finasteride can decrease serum Prostate-Specific Antigen (PSA) levels. This is important for healthcare providers to know when screening for prostate cancer, as they may need to adjust the interpretation of test results.
  • Potential Side Effects: While generally well-tolerated, side effects such as decreased libido, erectile dysfunction, and breast tenderness can occur. There are also reported cases of depression and a rare possibility of breast cancer. Some patients may experience side effects that persist even after stopping the medication, a condition sometimes termed Post-Finasteride Syndrome.

Conclusion: A Medical Innovation with a Two-Decade History

Finasteride’s history is a prime example of pharmaceutical development driven by clinical observation. It was initially developed as a groundbreaking treatment for benign prostatic hyperplasia (BPH) by mimicking a rare genetic condition. The subsequent discovery of its ability to potentially combat male pattern hair loss led to its repurposing for a second major indication. By effectively blocking the 5-alpha reductase enzyme and reducing DHT levels, finasteride addresses a potential hormonal cause of both conditions. The story of finasteride underscores the complex and often serendipitous process of drug development and its ability to impact multiple aspects of patient health.

Resources

  • Proscar (finasteride) Tablets Prescribing Information: Find detailed FDA-approved information on the BPH medication here.
  • Finasteride for the treatment of male pattern hair loss: Read more about finasteride's use for hair loss here.

Frequently Asked Questions

The FDA first approved finasteride (Proscar) in 1992 for the treatment of benign prostatic hyperplasia (BPH), a condition involving an enlarged prostate.

The development was based on research involving males with a genetic deficiency in the 5-alpha reductase enzyme, who had naturally smaller prostates. Scientists aimed to create a drug that could mimic this effect.

During clinical trials for BPH, researchers noted that some men experienced an increase in hair growth. This led to further studies and the subsequent approval of a lower-strength version (Propecia) for male pattern hair loss in 1997.

No, the strength differs significantly. A higher strength is typically used for BPH (Proscar), while a lower strength is used for male pattern hair loss (Propecia).

It works by inhibiting the enzyme 5-alpha reductase, which reduces levels of the hormone dihydrotestosterone (DHT), a key contributor to both conditions.

No, finasteride is intended for use in men only. It is contraindicated in women who are pregnant or may become pregnant due to the risk of birth defects in a male fetus.

For both indications, the positive effects may not be permanent. If you stop taking the medication, your prostate could begin to grow again, and hair loss may resume within months.

References

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.