Toxic metals are not so rare but are often neglected causes of alopecia areata in men and women. Thallium, arsenic, selenium, and mercury are the most common cause of metals-related alopecia, which is what Vicky Yu and colleagues’ found. Other than the presence of thallium, arsenic, mercury, and selenium, cadmium, bismuth, lithium, and copper should also be taken into account when dermatologists are considering toxic metals as a potential cause of alopecia areata in humans.

To the Editor,

It was a pleasure to read the review article by Vicky Yu and colleagues [1] on the diagnosis of acquired alopecia associated with exposure to toxic metals in humans [1]. In their excellent review of the roles of chemical substances in the pathogenesis of alopecia, the investigators found that some toxic metals – thallium (Tl), arsenic (As), and mercury (Hg), including the trace element selenium (Se) – can cause alopecia in humans [1]. However, we think that clinicians should also consider other 4 metallic elements in patients with alopecia following acute and/or chronic exposure: cadmium (Cd), bismuth (Bi), copper (Cu), and lithium (Li) [2-4].

In 19 years of surveillance for metals-related diseases in Milan, Italy, a cluster of cases of alopecia areata has been identified in our cohort (25 of 1,376 patients) [5]. We would like to share our experience, for instance, in a cohort of patients with adverse events to dental toxic metals [5, 6].

We retrospectively studied 25 consecutive patients with alopecia areata who were seen at a single dental unit (17 of 25, 68%). The remaining patients (8 of 25, 32%) with confirmed disease were from our Department of Dermatology between 2000 and 2019 (unpublished data). Seven physician-researchers took part. Twenty-four patients (90%) had alopecia areata. Of the 25 patients, only one had cicatricial (scarring) alopecia (Table 1).

Table 1.

Sex-specific prevalence of alopecia areata and any alopecia related to toxic metal exposure

Sex-specific prevalence of alopecia areata and any alopecia related to toxic metal exposure
Sex-specific prevalence of alopecia areata and any alopecia related to toxic metal exposure

As estimated from previous studies [7-9], the prevalence of alopecia areata worldwide is between 0.57 and 3.8% [9]. Here, we report the prevalence rate for alopecia areata – in our cohort of patients with adverse health effects to dental toxic metals – which is 1.74% (24 of 1,376) (Table 1). Our prevalence results are similar to that reported in the worldwide literature [9], which has shown that the rates for alopecia areata cases vary widely from 0.57 to 3.8% [8, 9].

Our metal-exposed patients were then confirmed with the use of highly specific laboratory tests (toxicological assessment) [5, 6]. This observation has been established by a recent immunotoxicology textbook [5].

We noted an association between low serum zinc levels and alopecia areata induced by toxic metals [5]. This finding supports the suggestion that such zinc homeostasis imbalance is the underlying pathophysiologic mechanism for the development of alopecia areata. In our view, zinc depletion has an important role in the development of alopecia areata [10-15]. Therefore, alopecia areata can be attributed to an underlying, long-undiagnosed, zinc deficiency state [16, 17]. Zinc deficiency in humans was first described by US researchers in the 1970s under the name “conditioned deficiency of zinc” [17]. Dermatologically, the level of zinc was low in plasma/serum and some tissues in newborn infants as well as in children with zinc deficiency who had partial or total hair loss, and dermatitis [12, 14, 16, 17].

Although specific markers of zinc deficiency have not been reported [15-17], we summarized the literature in Table 2. In our experience, biomarkers from blood samples – particularly when lowered initially – may be useful for clinical prediction of outcomes (Table 2). There is a risk of primary or secondary malabsorption states, both treatable with zinc repletion (mainly zinc sulfate, ZnSO4), that should be considered [15-17].

Table 2.

Indications for biochemical studies that should be tailored to the individual patient, according to the degree of zinc deficiency (below the reference range; zinc plasma/serum <80 μg per dL)

Indications for biochemical studies that should be tailored to the individual patient, according to the degree of zinc deficiency (below the reference range; zinc plasma/serum <80 μg per dL)
Indications for biochemical studies that should be tailored to the individual patient, according to the degree of zinc deficiency (below the reference range; zinc plasma/serum <80 μg per dL)

About mercury, it is important to remember that all forms of mercury compounds (elemental, inorganic, and organic) are able to induce alopecia areata [5, 18, 19]. This may explain why, in the past, there have been cases of alopecia in patients who have been taking intravenous immune globulin injections, containing thimerosal [20].

Our recent reports suggest that mechanisms underlying these hair falls involve acute and/or chronic exposure to toxic metals [5], especially mercury, which could have a varied and widespread influence on the growth of hair (scalp hair), throughout the skin apparatus.

Toxic metals inactivate proteins and may block sulfhydryl cross-linking in keratin (disulfide-linked keratin, Table 3), causing hair loss. Essentially, zinc is replaced by toxic metals through molecular mimicry, substitution, and competition for metabolism in the biological system [5, 17, 21].

Table 3.

Acute and/or chronic exposure to potentially toxic metals as the cause of alopecia areata

Acute and/or chronic exposure to potentially toxic metals as the cause of alopecia areata
Acute and/or chronic exposure to potentially toxic metals as the cause of alopecia areata

Dermatologists should be aware that patients with alopecia should be carefully monitored for acute and/or chronic exposure to potentially toxic metals.

The authors have no conflicts of interest to declare.

The authors did not receive any funding.

P.D.P. designed the work, performed critical revision of the article, and provided final approval of the version to be published; S.M.F. and L.B. carried out data collection; and G.G. performed the statistic interaction and wrote the manuscript with support from P.D.P.

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