Adverse effects of Hydroquinone

Hydroquinone (HQ) is regarded as the gold standard for the treatment of disorders of hyperpigmentation including melasma. It competitively inhibits melanin synthesis through the inhibition of sulfhydryl groups and by acting as a substrate for the enzyme tyrosinase. Semiquinone free radicals are then released, which subsequently damage melanocytes and melanosomes in treated skin.

Efficacy

Although HQ is available in concentrations of 2% and 4%, it is the 2% concentration that is commonly available in over-the-counter cosmeceutical products. Clinical studies have reported good to excellent efficacy of HQ 2% in the treatment of disorders of hyperpigmentation

While effective, multiple potential acute adverse effects have been reported, including allergic or irritant contact dermatitis and post inflammatory hyper- and hypopigmentation. Of these, the most common is irritant contact dermatitis.

Adverse effects

Chronic adverse effects of topical HQ are also recognized and include exogenous ochronosis, pigmented colloid milia, nail pigmentation, cataracts, reduction of skin elasticity, development of offensive fish odor, and impaired wound healing.The most common of the chronic adverse effects is exogenous ochronosis.

Ochronosis typically manifests as asymptomatic hyperpigmented macules or patches on sun-exposed skin, specifically the face, upper back, and upper chest. Less common manifestations of ochronosis include asymptomatic erythema, gray-blue colloid milia, and papulonodules on sun-exposed areas.

Though various formulations of HQ are used widely in the United States, ochronosis is an uncommon adverse effect. Of note, the majority of reported cases of ochronosis are secondary to the use of 2% HQ.

In 2006, the Food and Drug Administration (FDA) propositioned a ban on over-the-counter HQ. These measures were proposed due to the potential for development of ochronosis and carcinogenicity. While some animal studies have demonstrated a heightened rate of cancer development with HQ use,no human studies have demonstrated increased cutaneous or internal carcinogenicity with HQ use.