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      Characteristics of Mercury Intoxication Induced by Skin-lightening Products

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          Abstract

          Mercury is usually added to skin-lightening products due to its whitening effect. The Food and Drug Administration (FDA) limits the amount of mercury in cosmetics to trace amounts under 1 ppm. Nevertheless, many cosmetics contain mercury above 1000 ppm to increase the whitening effect. In a group of special patients in the study, pain, renal damage, and neuropsychiatric symptoms were the cardinal symptoms observed. The present study included 16 female patients diagnosed with chronic mercury intoxication at the First Affiliated Hospital of Zhengzhou University from 2009 to 2017. The age of these patients ranged from 19 to 50 years. All the 16 patients had a flexuose treatment experience, slow onset, and a hidden history that contributed the delayed diagnosis. There was no history of exposure to mercury in their work, but all of them had a history of using skin-lightening products, which had immediate and dramatic whitening effects. The chief complaint was miserable pain, and limb, head, abdomen, or lumbosacral pain was poorly responsible for nonsteroidal anti-inflammatory drugs, anti-epileptic drugs, and serotonin-norepinephrine reuptake inhibitors. According to the World Health Organization visual analog scale ranking, 0 referred to no pain and 10 referred to baryodynia. The pain of these 16 patients was rated between 4 and 7. Renal damage was another characteristic, in which six of all the patients presented with proteinuria. In addition, all patients had varying degrees of irritability, insomnia, dreams, depression, anxiety, and memory loss. Furthermore, five patients presented with eyelid, tongue, or limb tremors, while three patients presented with gingivitis. The 24-h urine mercury content of these patients was within 0.037–0.170 mg/L (normal value, <0.010 mg/L). In one skin-lightening product sample, the mercury concentration was found to be 19,742 ± 379 ppm, which is 19,000 times higher than the FDA limit. The electromyography examination was normal in 11 patients, while it was abnormal in five patients; and slow sensory nerve conduction velocity and reduced amplitude were mainly observed. Moreover, the brain magnetic resonance imaging and lumbar puncture of seven patients with headache were normal. Hamilton Depression Scale-17 (HAMD-17, normal value <7 points) scores were within 9–20 points [Supplementary Table 1]. All patients received intravenous sodium dimercaptopropane sulfonate at 0.125 g/d and other symptomatic treatments. Supplementary Table 1 Signs, symptoms, and other findings of these patients Case Age (years) Latency from using the product to symptom onset (weeks) Avenue of purchase Main symptoms Accompanied symptoms and signs VAS ranking Urine mercury EMG HAMD score 1 36 4 Online Headache, back pain Hypomnesia, insomnia, irritability, often cries 6 0.160 mg/L Conduction velocity of the bilateral endings of the median sensory nerve was slower, and the amplitude decreased 25 2 33 6 Online Pain in the four limbs, abdominal pain Eyelid tremor, finger tremor, irritability, distraction, renal damage 6 0.140 mg/L Normal 18 3 30 9 Online Pain in the four limbs Both hand tremor, distracted, insomnia, renal damage 7 0.170 mg/L The amplitude of the bilateral common peroneal nerve decreased 16 4 37 13 Beauty shop Headache and pain in the four limbs Insomnia, gingivitis 5 0.110 mg/L Normal 13 5 40 5 Beauty shop Foot pain Difficulty in falling asleep, distracted 5 0.090 mg/L Normal 10 6 19 7 Online Lumbosacral pain, abdominal pain Eyelid tremor, lingual tremor, hand tremor, insomnia, gingivitis, renal damage 6 0.150 mg/L Conduction velocity of the bilateral tibial and peroneal sensory nerve was slower, and the amplitude decreased 26 7 39 10 Online Pain in the four limbs Difficulty in falling asleep 4 0.037 mg/L Normal 17 8 35 6 Store Headache and pain in the four limbs Renal damage, insomnia 6 0.120 mg/L Normal 10 9 29 8 Store Pain in the four limbs Insomnia, distracted 4 0.080 mg/L Normal 12 10 36 5 Store Pain in both lower extremities, lumbosacral pain Insomnia, distracted, hypomnesia, irritability 6 0.130 mg/L Conduction velocity of the bilateral tibial and sensory nerve was slower, and the amplitude decreased 22 11 32 7 Online Pain in both lower extremities and lumbosacral pain Renal damage 4 0.106 mg/L Normal 19 12 27 5 WeChat shop Pain in both lower extremities and abdominal pain Lingual tremor, hand tremor, insomnia, gingivitis, irritability 6 0.120 mg/L Normal 21 13 42 8 Beauty Shop Headache and pain in the four limbs Limb tremor, hypomnesia, insomnia, irritability, renal damage 6 0.110 mg/L Normal 24 14 41 12 Online Pain in the four limbs Difficulty in falling asleep, irritability 4 0.076 mg/L Normal 16 15 50 11 Store Headache, pain in the four limbs Hypomnesia, insomnia, irritability 5 0.130 mg/L Normal 15 16 33 12 Online Pain in both lower extremities and abdominal pain Irritability, insomnia, renal damage, hypomnesia 6 0.110 mg/L Conduction velocity of the bilateral tibial and sensory nerve was slower, and the amplitude decreased 24 VAS: Visual analog scale; EMG: Electromyography; HAMD: Hamilton Depression Scale. Mercury ions replace tyrosinase enzyme anions, which inhibit the formation of melanin and produce the whitening and anti-freckle effects.[1] Some products are added with the mercury content, which exceeds bid badly in thousands or even millions of times, in order to make the lightening effect remarkable. The long-term usage of these unqualified products would induce chronic mercury poisoning. The common symptoms of chronic mercury poisoning are irritability, tremor, and gingivitis, while the onset of pain is rare. Furthermore, it has been reported that it causes memory loss, dizziness, insomnia, dreams, edema, proteinuria, abdominal pain, nausea, hyperthyroidism, and abortion. Studies on mercury poisoning, which leads to peripheral nerve damage, are rare. Patients in the present study prominently complained of pain, but rarely referred to limb weakness. Distal extremity hypoalgesia was not observed, and all patients had no severe central nervous system symptoms, such as lags in response, seizures, confusion, difficulty in swallowing, glossolalia, deafness, narrow field of vision, strabismus, or photophobia, which were similar with Minamata disease.[2] Mercury damages the nerves in several ways: it interferes with membrane and receptor functions, and neurotransmitter transport and metabolism; it interrupts cytoskeletal proteins, and interferes with axoplasmic flow and signal transduction; it interferes with cell respiration, energy metabolism and others.[3] Among the 16 patients, six patients presented with proteinuria, but without edema. After 3–5 courses of chelation treatment, urine mercury returned to normal levels. Then, after approximately 4–8 weeks, pain was alleviated, urine protein was negative, and HAMD scale scores returned to normal. Unqualified products that contain toxic substances such as mercury are not rare. These substances usually damage the nervous and renal systems. Hence, history taking is all important, and mercury chelation treatment should be given after diagnosis as soon as possible. Furthermore, the public should be warned about this danger. Declaration of patient consent The authors certify that they have obtained all appropriate patient consent forms. In the form, the patients/patients’ guardians have given their consent for their images and other clinical information to be reported in the present study. The patients/patients’ guardians understand that their names and initials will not be published, and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed. Supplementary information is linked to the online version of the paper on the Chinese Medical Journal website. Financial support and sponsorship This study was supported by grants from the National Natural Science Foundation of China (No. 81501111), and the Henan Provincial Major Scientific College Project (No. 18A320065). Conflicts of interest There are no conflicts of interest.

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          Most cited references3

          • Record: found
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          Widespread use of toxic skin lightening compounds: medical and psychosocial aspects.

          Hyperpigmentation disorders and skin lightening treatments have a significant impact on the dermatologic, physiologic, psychologic, economic, social, and cultural aspects of life. Skin lightening compounds, such as hydroquinone and topical corticosteroids, are often used to treat hyperpigmentation disorders, such as melasma, or lighten skin for cosmetic purposes. Despite their established effectiveness, a multitude of dermatologic and systemic complications have been associated with these agents. Regulatory agencies have also recognized the adverse effects of skin lighteners and many countries around the world now forbid the production and sale of these compounds, although this prohibition has not significantly curtailed distribution. Dermatologists and users of cosmetic products should be aware of the various components in bleaching compounds, their potential adverse effects, and alternative options for skin lightening. Copyright © 2011 Elsevier Inc. All rights reserved.
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            Neurotoxicological effects of low-dose methylmercury and mercuric chloride in developing offspring mice.

            Mercury is a well-known toxic metal and potently induces severe neurotoxicological effects, especially in infants and children. The purpose of this study was to explore the underlying mechanisms of neurotoxic effects of mercurial compounds on the different stages of developing mice. Low-doses (the probability of human exposure in mercury-contaminated areas) of methylmercury (MeHg) (M, 0.02mg/kg/day) and mercury chloride (HgCl(2)) (H, 0.5mg/kg/day) were administered to mice of the following groups: (1) treatment with distilled water for 7 consecutive weeks after weaning (control-vehicle (CV)); exposure to mercurial compounds at different stages; (2) for 7 consecutive weeks after weaning (control-MeHg (CM) and control-HgCl(2) (CH)); (3) only during perinatal and weaning stages (MeHg-vehicle (MV) and HgCl-vehicle (HV)); and (4) in all experimental stages (MeHg-MeHg (MM) and HgCl(2)-HgCl(2) (HH)). Results revealed the neurobehavioral defects (increased locomotor activities, motor equilibrium impairment, and auditory dysfunction) that correlated with increasing Hg accumulation in CM and CH groups. However, it revealed a decrease and an increase in locomotor activities in MV and HV groups, respectively; these became more severe in MM and HH groups than in MV and HV groups. Motor equilibrium performance in MV and HV groups remained normal, while that in MM and HH groups was decreased. The most severe auditory defects (altered auditory brainstem response, ABR test) found in MM and HH groups than those in the respective CM and CH, MV and HV, including absolute wave III delays and interwave I-III latencies, which suggested that the irreversible auditory dysfunction caused by mercurial compounds. Furthermore, the alteration of lipid peroxidation (LPO), Na(+)/K(+)-ATPase activities, and nitric oxide (NO(x)) in the brain tissues contributed to the observed neurobehavioral dysfunction and hearing impairment. These findings provide evidence that fetuses were much more susceptible to the effects of mercurial compounds with regard to inducing severely neurotoxicological injuries as that found in human beings. The signaling of ROS/Na(+)-K(+)-ATPase/NO(x) plays a crucial role in the underlying mechanism for mercurial compound-induced toxic effects in offspring. Copyright © 2011. Published by Elsevier Ireland Ltd.
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              [Pathological and biochemical studies of 30 Niigata autopsy cases related to Minamata disease].

              To reevaluate pathologically and biochemically 30 autopsy cases related to Minamata disease (MD) in Niigata Prefecture (NP) and compare the findings with those of autopsy cases related to MD in Kumamoto Prefecture (KP).
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                Author and article information

                Journal
                Chin Med J (Engl)
                Chin. Med. J
                CMJ
                Chinese Medical Journal
                Medknow Publications & Media Pvt Ltd (India )
                0366-6999
                20 December 2017
                : 130
                : 24
                : 3003-3004
                Affiliations
                [1 ]Department of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450052, China
                [2 ]Department of Emergency, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450052, China
                Author notes
                Address for correspondence: Dr. Hong Lu, Department of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450052, China E-Mail: snluhong@ 123456163.com
                Article
                CMJ-130-3003
                10.4103/0366-6999.220312
                5742931
                29237936
                f989e0d2-fe3b-4751-8153-a02d1187bb53
                Copyright: © 2017 Chinese Medical Journal

                This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.

                History
                : 01 September 2017
                Categories
                Clinical Observation

                mercury,pain,psychiatric symptoms,renal damage,skin-lightening products

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