Skip to content

Does Bimatoprost Cause Pigmentation? A Detailed Examination

4 min read

Studies show that bimatoprost, a prostaglandin analog, can cause pigmentation changes in a notable percentage of users [1.5.4]. The question for many is, does bimatoprost cause pigmentation that is permanent, and what are the specific risks involved with its use for glaucoma or eyelash growth?

Quick Summary

Bimatoprost can cause hyperpigmentation of the iris, eyelids, and eyelashes. Eyelid and eyelash darkening is often reversible, but increased brown pigmentation of the iris is likely to be permanent [1.4.1, 1.4.2].

Key Points

  • Mechanism of Action: Bimatoprost increases melanin production in existing cells (melanogenesis), rather than increasing the number of cells [1.3.2, 1.3.3].

  • Iris Pigmentation: It can cause increased brown pigmentation in the iris, which is likely to be a permanent change [1.4.2, 1.7.1].

  • Eyelid Pigmentation: Darkening of the eyelid skin (periocular hyperpigmentation) is a common side effect that is usually reversible upon discontinuation [1.2.3, 1.4.1].

  • Eyelash Changes: Bimatoprost promotes longer, thicker, and darker eyelashes; this effect is also reversible after stopping the treatment [1.4.2].

  • Risk Factors: Individuals with mixed-color irises (green, hazel) are more susceptible to permanent eye color changes than those with uniformly blue or brown eyes [1.3.7].

  • Prevention: Careful application and blotting excess solution from the skin can help minimize unwanted eyelid darkening [1.7.1, 1.8.2].

  • Comparison: Bimatoprost may cause a higher incidence of periocular pigmentation compared to another prostaglandin analog, latanoprost [1.5.4].

In This Article

Understanding Bimatoprost and Its Uses

Bimatoprost is a synthetic prostaglandin analog used medically for two primary purposes. As an ophthalmic solution (e.g., Lumigan), it effectively reduces elevated intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension [1.4.2]. Its second major application, under brand names like Latisse, is for treating hypotrichosis, a condition of inadequate eyelashes, by promoting their growth, thickness, and darkness [1.3.5]. While highly effective, one of the most discussed side effects is its potential to cause changes in pigmented tissues [1.6.6].

The Link Between Bimatoprost and Pigmentation

The pigmentary side effects of bimatoprost are well-documented and primarily affect three areas: the iris, the periorbital skin (eyelids), and the eyelashes themselves [1.4.2, 1.6.3]. This phenomenon is not unique to bimatoprost but is considered a class effect of prostaglandin analogs [1.3.1].

How Bimatoprost Causes Pigmentation Changes

The underlying mechanism is not an increase in the number of pigment-producing cells (melanocytes) but rather an increase in the production of melanin within these cells [1.3.2, 1.3.3]. Bimatoprost stimulates melanogenesis, leading to a higher concentration of melanin granules [1.3.3]. This process results in the visible darkening of the affected tissues. For the skin, this is caused by increased melanin production and transfer to keratinocytes [1.2.2]. For the iris, the drug stimulates melanocytes in the iris stroma to produce more melanin, leading to a darker appearance [1.3.4].

Specific Pigmentation Effects

Iris Hyperpigmentation

This is often the most concerning side effect because it is likely to be permanent [1.4.2, 1.7.1]. The change is characterized by an increase in brown pigment, which may not be noticeable for several months or even years of use [1.3.2, 1.6.3]. Typically, the brown coloration starts around the pupil and spreads outwards [1.3.2]. This effect is more common in individuals with mixed-color irises (e.g., green, hazel) than in those with uniformly blue or brown eyes [1.3.7]. While cosmetically significant, studies have not shown this to cause other safety concerns like melanocyte proliferation [1.3.6].

Eyelid Skin Darkening (Periocular Hyperpigmentation)

Darkening of the skin on the eyelids and around the eyes is another common side effect [1.2.3, 1.5.6]. This occurs when the medication comes into frequent contact with the skin [1.2.2]. Unlike iris pigmentation, periocular hyperpigmentation is generally considered reversible upon discontinuation of the medication, though it may take several weeks to months to fade [1.4.2, 1.7.1, 1.8.5]. The incidence of this side effect appears to be higher with bimatoprost compared to some other prostaglandin analogs like latanoprost [1.5.4].

Eyelash Darkening

In addition to making eyelashes longer and thicker, bimatoprost also causes them to darken [1.2.5]. This is due to the same mechanism of increased melanogenesis. This change is also usually reversible when the treatment is stopped [1.4.2].

Comparison with Latanoprost

Bimatoprost and latanoprost are both prostaglandin analogs used for glaucoma, but they exhibit different side effect profiles regarding pigmentation.

Feature Bimatoprost (Lumigan) Latanoprost
Efficacy (IOP Reduction) Often considered more effective in achieving greater IOP reductions [1.5.1]. Effective, but may result in slightly less IOP reduction than bimatoprost [1.5.1].
Periocular Pigmentation Higher incidence; one study noted 6% of patients experienced this within 12 months [1.5.4]. It also causes more marked periocular changes [1.5.3]. Lower incidence; the same study found it in 1% of patients [1.5.4].
Iris Pigmentation A known risk, more prominent in mixed-color eyes [1.3.7]. The incidence was 1.5% in one study for the 0.3 mg/ml solution [1.3.2]. Also a risk, and may be more likely to cause this than bimatoprost in some comparisons [1.5.1].
Eyelash Growth Known for causing significant eyelash growth, leading to its cosmetic use (Latisse) [1.5.1]. Also causes eyelash growth, but the effect may be less pronounced than with bimatoprost [1.3.7].

Minimizing Unwanted Pigmentation

While iris color change cannot be prevented, the risk of eyelid skin darkening can be reduced. Users are advised to:

  • Apply the product carefully: When used for eyelash growth (Latisse), apply it precisely to the base of the upper eyelashes using the provided sterile applicator [1.8.2].
  • Avoid lower lid application: Do not apply the solution to the lower eyelid [1.7.1].
  • Blot excess solution: Immediately wipe away any excess medication that comes into contact with the skin outside the treatment area with a tissue or absorbent material [1.7.1, 1.8.2]. Studies have shown that reducing drop-skin contact can lower the incidence of skin pigmentation [1.8.6].

Conclusion

Bimatoprost does cause pigmentation as a notable side effect. The most significant of these is the potential for permanent darkening of the iris, particularly in individuals with lighter or mixed-color eyes. Other pigmentary changes, such as eyelid skin darkening and increased eyelash pigmentation, are also common but are typically reversible after stopping the medication [1.4.2, 1.7.1]. Patients using bimatoprost for either glaucoma or eyelash enhancement should be thoroughly informed by their physician about these potential cosmetic changes to make an educated decision about their treatment.


For more information from an authoritative source, you can visit the Bimatoprost page on MedlinePlus, a service of the National Library of Medicine.

Frequently Asked Questions

Yes, the increased brown pigmentation in the iris (the colored part of the eye) caused by bimatoprost is considered likely to be permanent, even after you stop using the medication [1.4.2, 1.7.1].

Yes, in most cases, the darkening of the eyelid skin caused by bimatoprost (Latisse) is reversible. The pigmentation is expected to fade over several weeks to months after discontinuing the product [1.4.1, 1.8.5].

Bimatoprost stimulates existing pigment cells called melanocytes to produce more melanin. This increase in melanin content, not an increase in the number of cells, is what causes the darkening of the iris, skin, and eyelashes [1.3.2, 1.3.3].

There are no proven methods to prevent the iris color change associated with bimatoprost, as it is a direct effect of the medication's mechanism [1.4.4]. This risk should be discussed with a doctor before starting treatment.

Studies suggest that periocular skin hyperpigmentation is more common with bimatoprost than with latanoprost. One retrospective study found the incidence to be 6% with bimatoprost versus 1% with latanoprost over a 12-month period [1.5.4].

Periocular hyperpigmentation (eyelid darkening) can appear between 3 to 6 months after starting therapy [1.2.4]. Changes in iris color may not be noticeable for several months or even years [1.3.2].

Lumigan and Latisse both contain bimatoprost as the active ingredient. Lumigan is an eye drop prescribed to treat high eye pressure in glaucoma patients [1.6.2]. Latisse is a solution applied to the base of the upper eyelashes to promote eyelash growth for those with hypotrichosis [1.3.5].

References

  1. 1
  2. 2
  3. 3
  4. 4
  5. 5
  6. 6
  7. 7
  8. 8
  9. 9
  10. 10
  11. 11
  12. 12
  13. 13

Medical Disclaimer

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