Abstract
Background:
Allergic contact dermatitis (ACD) is a delayed type of hypersensitivity from contact with a specific allergen to which the patients has developed a specific sensitivity. The aim of the study was to evaluate the results of epicutaneous patch testing with standard series of contact allergen in patients suspected to have ACD.
Methods:
355 cases of ACD were included in the study. Test substances were applied on the upper part of the patient’s back, on clinically uninvolved and untreated skin. All patients were free from therapy with oral antihistamines, steroids and immunosuppressants. The patch test was removed and reaction were evaluated after 48 h and 72 h. Grading of negative (-) to positive (+ to ++++) patch test was done according to the International Contact Dermatitis Research Group. Statistical data analysis was performed by using χ2–test.
Results:
Of the 355 cases, 146 patients were male (41.1%) and 209 were female (58.9%). The youngest patients in the study was 16 years of age and the oldest was 67 years of age. The commonest age group affected was 41-50 years. Hands were the most common site of involvement. The occupational character of skin lesions was find in 75 (21.1%). The most common positive reactions were recorded to nickel sulphate 99 (27.8%), cobalt chloride 46 (12.9%), thimerosal 31 (8.7%), colophony 23 (6.5%), carba mix 21 (5.9%), potassium dichromate 20 (5.6%), acid chromici 19 (5.3%), fragrance mix 18 (5%), balsam of Peru 13 (3.7%), formaldehyde 9 (2.5%), and other allergens 26 (7.3%). Females were significantly more likely to show a positive response to two or more allergens (p<0.05). There was no statistically significant impact of age, occupation and duration of disease on results of patch testing (p>0.05).
Conclusions:
Our results indicate that nickel sulphate, cobalt chloride and thimerosal are the most common allergens responsible for induction of ACD. These findings are crucial in the treatment, long term management, an education of patients with ACD.
Keywords: allergen, allergic contact dermatitis, epicutaneous patch test
1. INTRODUCTION
Allergic contact dermatitis (ACD) is a very common type of skin disorders seen among patients attending dermatology clinics. The prevalence of this disease in the general population ranges from 15% to 28% and is increasing (1, 2). It is a delayed type of hypersensitivity from contact with a specific allergen to which the patients has developed a specific sensitivity. When the antigen contacts the skin, it is processed and presented with HLA-DR on the surface of Langerhans cells, which act as antigen presenting cells in the skin (3). These cells migrate to the regional lymph nodes and the allergen is subsequently processed by the T-lymphocytes. It leads to proliferation of specific T cell clones that circulate through the body and back into the skin. Upon re-exposure of the allergen, CD8+ T-cells response is mediated by the CD4+ T-cell subset. Skin penetration of allergens is facilitated by skin barrier impairment due to dermatitis or trauma. Disruption the integrity of the epidermal barrier appears to be the first step in the events following contact with allergen (4). Clinically, acute ACD is characterized by erythema, swelling and blisters while the more chronic reaction features epidermal reactive changes including lichenification, thick scale and fissuring. A wide range of pictures may evolve representing between these two poles.
Epicutaneous patch tests are tools used in the identification of the etiological agents of allergic contact dermatitis. It is a scientific method of investigation, with internationally defined rules and well-established foundations. The function of the patch test is to produce, in a controlled manner, the elicitation phase of ACD, and thus determine the etiological agent of this dermatitis (5).It has been recommended that all patients with chronic dermatitis must be patch tested, keeping in view the indefinite course of disease (6). Therefore, the aim of the study was to evaluate the results of epicutaneous patch testing with standard series of contact allergen in patients suspected to have ACD.
2. PATIENTS AND METHODS
This was a descriptive case study conducted at Department of Dermatovenereology , University Clinical Centre Sarajevo, during the 2016-2017 period. 355 patients clinically diagnosed with contact dermatitis were included in the study. After informed consent, relevant history was taken and clinical examination was performed. The following factors were considered: sex, age, duration of disease, location of primary lesions and the relationship between the development of skin lesions and occupational work. All patients were free from therapy with oral antihistamines, steroids and immunosuppressants. Cases with any kind of food sensitivity or any other confirmed skin diseases were also excluded.
Each patient was patch tested with allergens of European Baseline Series (Table 1), manufactured by the Institute of Immunology, Zagreb, Croatia. Test substances were applied on the upper part of the patient’s back, on clinically uninvolved and untreated skin with adhesive strips for patch test (Curatest, Lohmann Rauscher, Germany). The patch test was removed and reaction were evaluated after 48 h and 72 h. Patients were instructed to wear the patch for 48 hours without removing it and to avoid contact with water. Grading of negative (-) to positive (+ to +++) patch test was done according to the International Contact Dermatitis Research Group Criteria (7). An irritant response was interpreted as a negative response. Positive patch test results were presented by frequency and percentage. Statistical data analysis was performed by using χ2–test.
Table 1. The series of allergens used for patch testing.
| Allergen | Dilution (%) vechicle | Allergen | Dilution (%) vechicle |
|---|---|---|---|
| Acid chromici | 1.0 aqua | Epoxy resin | 1.0 vaseline |
| Cobalt chlorid | 1.0 vaseline | Colophony | 20.0 vaseline |
| Asepsol | 0.5 aqua | Quaternium | 1.0 vaseline |
| Potassium dichromate | 0.5 vaseline | PPD-black rubber mix | 0.1 vadeline |
| Resorcini | 2.0 vaseline | Balsam of Peru | 25.0 vaseline |
| Lidocain | 1.0 vaseline | Fragrance mix | 8.0 vaseline |
| Nickel sulfate | 5.0 vaseline | Paraben mix | 15.0 vaseline |
| Paraphenylene diamine | 0.5 vaseline | Ammonium persulfate | 2.5 vaseline |
| Terpentini | 10.0 vaseline | Thimerosal | 0.1 vaseline |
| Carba mix | 3.0 vaseline | Neomycin sulfate | 20.0 vaseline |
| Mercapto mix | 2.0 vaseline | Formaldehyde | 1.0 aqua |
| Thiuram mix | 1.0 vaseline | Vaseline | As it is |
3. RESULTS
Of the 355 cases, 146 patients were male (41.1%) and 209 were female (58.9%). The youngest patients in the study was 16 years of age and the oldest was 67 years of age. The commonest age group affected was 41-50 years. Minimum duration of disease noted in our study was less than 6 weeks and maximum was 7 years. The majority of the patients had the disease for 6 to 12 months. Hands and face including ears and the neck were the most common site of involvement. The occupational character of skin lesions was find in 75 (21.1%).
Positive patch test results with at least one allergen were obtained for 221 (62.2%) patients, more frequently in women than in men (147 vs 74). The frequency of sensitization to allergens used for the study is shown in Table 2. The most common positive reactions were recorded to nickel sulphate 99 (27.8%), cobalt chloride 46 (12.9%), thimerosal 31 (8.7%), colophony 23 (6.5%), carba mix 21 (5.9%), potassium dichromate 20 (5.6%), acid chromici 19 (5.3%) , fragrance mix 18 (5%), balsam of Peru 13 (3.7), formaldehyde 9 (2.5%), Less common were: paraphenyle diamine 6 (1.7%), paraben mix 5 (1.4%) and epoxy resin 3 (0.8%). Reactivity against the rest of the panel was not remarkable. Regarding patch test reactivity, most of the patients had 2+ degree of reaction. Females were significantly more likely to show a positive response to two or more allergens (p<0.05). There was no statistically significant impact of age, occupation and duration of disease on results of patch testing (p>0.05). The adverse reaction during patch testing were pruritus and tape erythema.
Table 2. Results of epicutaneous patch testing. n= number of positive test results.
| Allergen | n | % |
|---|---|---|
| Nickel sulfate | 99 | 27.8 |
| Cobalt chloride | 46 | 12.9 |
| Thimerosal | 31 | 8.7 |
| Colophony | 23 | 6.5 |
| Carba mix | 21 | 5.9 |
| Potassium dichromate | 20 | 5.6 |
| Acid chromici | 19 | 5.3 |
| Fragrance mix | 18 | 5.0 |
| Balsam of Peru | 13 | 3.7 |
| Formaldehyde | 9 | 2.5 |
| Others | 26 | 7.3 |
4. DISCUSSION
Epicutaneous patch tests along with history and clinical features are very important steps in the identification of specific causative allergen in patients with ACD. Today, about 3000 antigens are known to act as contact allergens (8). Based on the patch test results, our study identified metals as the most common allergens. In addition to metals, the other common allergens identified included thimerosal, colophony, carba mix, fragrance mix, balsam of Peru and formaldehyde. The frequency of positive patch test results in the patients (62.2%) as well as clear predominance of women among applicants with eczema, are within the range of results available in literature (9, 10).
Nickel is ubiquitous metal used in a wide variety of products and is the most common allergen encountered worldwide (11). Dermatitis due to contact with nickel was initially described among workers in the nickel-plating industry and was documented as an allergic response in 1925 (12). Frequency on nickel allergy is reported to be continuously increasing in several countries, and represents a major health and socioeconomic problem (13). In our study, 99 (27.8%) patients showed an allergic response to nickel, making it the most prevalent of the allergens identified in this study. Nickel sensitivity was found to be more common in females compared to males with the male female ratio of 1:3. This is in accordance to the studies done by Thilak et al (14). Jewellery, spectacle frames, watches and metal components of clothing were the frequent sources of nickel in the study due to prolonged contact with the skin. Nickel salts being soluble in water and sweat easily cause sensitization. The reason for the relatively high prevalence of nickel ACD could be the use of nickel in consumer items that come in direct and prolonged contact with the skin (15). However, exposure may also occur in certain occupational settings generally associated with soluble nickel salts. Oral/intestinal exposure to sufficient doses of nickel ions may trigger systemic allergic dermatitis, with large inter-individual variation related to the elicitation threshold (16). European Union Nickel directive (17) has passed certain legislation with the intention of controlling the use of nickel releasing objects in contact with the skin.
The second most common allergen identified in our series was cobalt. Cobalt is a metal found in nature. It is commonly used with nickel for metal plating, and added to alloys to make more robust tools and parts (18). In addition, cobalt may also be found in hair dyes, detergents, antiperspirants, solid soaps, and cosmetics. As some pigments are salts of cobalt, exposure via these may cause ACD. Positive reaction to this allergen occurred in 12.9% of people tested, and this percentage was greater than in other European countries (19). Most patients with positive cobalt chloride tests also had allergies to nickel and potassium dichromate. Approximately 80% of individuals with cobalt sensitivity have co-sensitivity to other metals, with the predominant co-sensitivity being nickel (20). It has been postulated that nickel sensitization and preexisting dermatitis are often prerequisites for cobalt sensitization.
In our study it was a high rate of sensitization to thimerosal. It is an organic mercurial compound of thyosalic acid. Thimerosal has antibacterial and antifungal properties, without irritating the skin and mucous membranes. It is commonly found in cosmetics such as eye shadows, mascaras, lotions, contact lens solution and ophthalmic preparations. This preservative is also used in vaccines and many other products (21). However, many studies clearly indicate that the incidence of positive patch test results with thimerosal is very high (22). Its widespread use may explain the high rate of positive patch test reactions.
Allergic contact dermatitis to colophony was seen in 23 (6.5%) cases. Colophony is a mixture of approximately 100 chemical compounds, 95% of which is abietic acid, the main allergen of rosin. It is used in a wide variety of medical and personal care products. Bajaj et al estimated the prevalence of colophony allergy to be 5.7% among 590 patients with a positive skin patch test (23).
Carba mix was the fifth most common allergen in our patients, with a positive reaction recorded in 21 patients (5.9%). The prevalence of carba mix sensitization has also been reported from other countries and have ranged between 2.2 % to 4.4% (24, 25). Carba mix serves as a rubber accelerator added to natural rubber to speed its polymerization. It is used in the manufacture of many rubber products. Examples of such products include health care equipment (medical and utility gloves, tubing, bed sheeting), industrial and safety products (masks, respirators, ear plugs, headphones), office products and sport equipment (16). In addition to rubber products, carba mix may also be found in fungicides, pesticides, hairbrushes, and in some soaps, shampoos, and disinfectants.
Potassium dichromate reactivity was observed in 5.6% of the patients in the present study. Exposure to potassium dichromate is considered to be occupational as it is a major component used in the cement and tile industry. Notably higher prevalence rate of potassium dichromate sensitization of 51% have been reported from India (26)
A mix of eight common fragrances, Fragrance Mix, is commonly used for testing fragrance contact allergy. The mix consists of the cinnamic aldehyde and alcohol, eugenol and isoeugenol, geraniol, hydroxycitronellal, amyl cinnamaldehide, and oak moss (27). In our study, ACD to fragrance mix was seen in 5% cases. A study conducted in Denmark on about 10 000 patients with eczema showed that 5.5% of respondents reported positive reaction after exposure to the mix (28).
Balsam of Peru is also the addition of fragrance in many cosmetics, and its use is wide due to fixative properties. It is a complex substance that contains many potential allergens such as benzoic acid, benzyl acetate, benzyl benzoate, vanillin, nerolidol, and cinnamic acid among others. In addition to its use in fragrances, balsam of Peru can also be found in foods, drinks and medicines. The most common balsam-related foods deemed responsible for causing dermatitis included tomatoes, citrus and spices (29). Among our patients positive patch test with balsam of Peru were found in 3.7% of patients. Most patients with positive balsam of Peru tests also had allergies to fragrance mix.
While formaldehyde itself is not used much as preservative, so-called formaldehyde-releasers are widely used in many cosmetic products, topical medications and household products. Moreover, formaldehyde is found in aminoplastics and phenolic resins, various glues, and textiles. Therefore, the low concentrations of formaldehyde often found in skincare products are sufficient to worsen an existing dermatitis. The prevalence of formaldehyde sensitization has also been reported from other countries and have ranged between 2% and 9% (30). For consumers allergic to formaldehyde and suffering from any kind of dermatitis, it is very important to know the potential for formaldehyde exposure in order to avoid ACD (31).
ACD is a chain of complex processes of the immune system with response to chemical substances present in the environment. The clinical relevance of positive tests is important in interpreting patch test results, as this enables the differentiation of ACD and contact sensitization. Furthermore, monitoring patients after patch testing is important as regards clinical relevance and treatment evaluation.
5. CONCLUSIONS
Our results indicate that nickel sulphate, cobalt chloride and thimerosal are the most common allergens responsible for induction of ACD. Patch tests are essential for the diagnosis of contact sensitization. These findings are crucial in the treatment, long term management, an education of patients with ACD. In view of more than one-quarter of general population being allergic, improvements of primary prevention of contact allergy need to be enforced.
Author’s contribution:
Each author participated in each step of research. Articles was revised and final approval for publishing was given.
Conflict of interest:
none declared.
Financial support and sponsorship:
None.
REFERENCES
- 1.Tyssen JP, Linnenberg A, Manne T, Johansen JD. The epidemiology of contact allergy in the general population-prevalence and main findings. Contact Dermatitis. 2007;57(5):287–299. doi: 10.1111/j.1600-0536.2007.01220.x. [DOI] [PubMed] [Google Scholar]
- 2.Czarnobilska E, Obtulowicz K, Dyga W, Spiewak R. A half of schoolchildren with “ISAAK eczema” are ill with allergic contact dermatitis. J Eur Acad dermatol venereal. 2011;25(9):1104–1107. doi: 10.1111/j.1468-3083.2010.03885.x. [DOI] [PubMed] [Google Scholar]
- 3.Marks JG, DeLeo VA. Allergic and irritant contact dermatitis. Contact and occupational dermatology. In: Marks JG Jr, editor; Deleo VA, editor. 2nd ed. Mosby: St. Louis; 1997. pp. 3–14. [Google Scholar]
- 4.De Benedetto A, Kubo A, Beck LA. Skin barrier disruption: a requirement for allergen sensitisation? J Invest dermatol. 2012;132(3):949–963. doi: 10.1038/jid.2011.435. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Lazzarini R, Duarte I. Lindmayer Ferreira A. Patch tests. An Bras Dermatol. 2013;88(6):879–888. doi: 10.1590/abd1806-4841.20132323. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Carlsen Bc, Menne T, Johonsen JD. 20 years of standard patch testing in eczema population with focus on patients with multiple contact allergies. Contact Dermatitis. 2007;57(2):76–83. doi: 10.1111/j.1600-0536.2007.01155.x. [DOI] [PubMed] [Google Scholar]
- 7.Pongpairoj K, Ale I, Andersen KE, Brize M, Diepgen TL. Elsner PU, et al. Proposed ICDRG classification of the clinical presentation of contact allergy. Dermatitis. 2016;27(5):248–258. doi: 10.1097/DER.0000000000000222. [DOI] [PubMed] [Google Scholar]
- 8.Kuljanac I, Knezevic E, Cvitanovic H. Epicutaneous patch test result in children and adults with allergic contact dermatitis in Karlovac county: a retrospective survey. acta Dermatovenereol Croat. 2011;19(2):91–97. [PubMed] [Google Scholar]
- 9.Reduta T, Bacharewicz J, Pawlos A. Patch test result in patients with allergic contact dermatitis in the Podlasie region. Postep derm Alergol. 2013;6:350–357. doi: 10.5114/pdia.2013.39433. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Shakoor Z, Al-Mutairi AS, Al-Shenaifi AF, Al-Abdulsalam AM, Al-Shirah BZ. Al-Harbi S. Screening for skin-sensitizing allergens among patients with clinically suspected allergic contact dermatitis. saudi Med J. 2017;38(9):922–927. doi: 10.15537/smj.2017.9.19864. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Zug KA, Warshav EM, Fowler JF, Jr, Maibach HI, Belsito DL. Pratt MD, et al. Patch-test results of the North American Contact Dermatitis Group 2005-2006. Dermatitis. 2009;20(3):149–160. [PubMed] [Google Scholar]
- 12.Counts AL, Miller MA, Khakhria ML, Strange S. Nickel allergy associated with a transpalatal arch appliance. J Orofac Orthop. 2002;63(6):509–515. doi: 10.1007/s00056-002-0128-z. [DOI] [PubMed] [Google Scholar]
- 13.Wojciechowska M, Czajkowski R, Kowaliszyn B, Zbikowska-Gotz M, Bartuzi Z. Analysis of skin patch results and metalloproteinase-2 levels in a patients with contact dermatitis. Postep Derm Alergol. 2015;32(3):154–161. doi: 10.5114/pdia.2014.40979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Thilak S, Meera G, Brindha T. A study of 300 cases of allergic contact dermatitis. Int J Res Dermatol. 2017;3(1):13–19. [Google Scholar]
- 15.Almutairi N, Almutava F. Allergic contact dermatitis pattern in Kuwait: nickel leads the pack. In-depth analysis of nickel allergy based on the results from a large prospective patch test series report. Adv Dermatol Allergol. 2017;3(3):207–215. doi: 10.5114/ada.2017.67843. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Uter W, Werfel T, White JR, Johansen JD. Contact allergy: a review of current problems from a clinical perspective. Int J Environ Res Health. 2018;15(6):E1108. doi: 10.3390/ijerph15061108. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.European Parliament and Council Directive 94/27EEC. Official Journal of the European Communities. 22-07-1994;(L 188/1-2) (nickel) [Google Scholar]
- 18.Aleid NM, Fertig R, Maddy A, Tosti A. Common allergens identified based on patch test result in patients with suspected contact dermatitis of the scalp. Skin Appendage Disord. 2017;3(1):7–14. doi: 10.1159/000453530. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Uter W, Ramsch C, Aberer W, Ayala F, Balato A. Beliauskiene A, et al. The European baseline series in 10 European countries, 2005/2006-results of the European Surveillance System on Contact Allergies (ESSCA) Contact Dermatitis. 2009;61(1):31–38. doi: 10.1111/j.1600-0536.2009.01572.x. [DOI] [PubMed] [Google Scholar]
- 20.Marks JG, Elsner P. DeLeo VA. ed 3. Philadelphia, Mosby: 2002. Standard allergens, in Contact and occupational dermatology; pp. 65–69. [Google Scholar]
- 21.Breithaupt A, Jacob SE. Thiomersal and the relevance of patch-test reactions in children. Dermatitis. 2008;19(5):275–277. [PubMed] [Google Scholar]
- 22.Wohrl S, Hammer W, Focke M. Gotz M, Jarisch R. Patch testing in children, adults ant the elderly: Influence of age and sex on sensitization patterns. Pediatr Dermatol. 2003;20(2):119–123. doi: 10.1046/j.1525-1470.2003.20204.x. [DOI] [PubMed] [Google Scholar]
- 23.Bajaj AK, Saraswat A, Mukhija G. Patch testing expirience with 1000 patients. Indian J Dermatol VenerolLeprol. 2007;73(5):313–318. doi: 10.4103/0378-6323.34008. [DOI] [PubMed] [Google Scholar]
- 24.Warburton KL, Bauer A, Chowdhury MM, Cooper S, Krecisz B, Chomiczewska-Skora D, et al. ESSCA results with the baseline series, 2009-2012: rubber allergens. Contact Dermatitis. 2015;73(5):305–312. doi: 10.1111/cod.12454. [DOI] [PubMed] [Google Scholar]
- 25.Warshaw EM, Raju S, DeKoven JG, Belsito DV, Zug KA, Zirwas MJ. Maibach HI, et al. Positive patch test reactions to carba mix and iodopropynyl butylcarbamate: data from the North American Contact Dermatitis Group, 1998-2008. Dermatitis. 2013;24(5):241–245. doi: 10.1097/DER.0b013e3182a5a1d4. [DOI] [PubMed] [Google Scholar]
- 26.Parthap P, Kumar KA, Asokan N. Betsy Binesh VG. Occupational allergic contact dermatitis: a clinical study in a tertiary care centre in central Kerala. Indian J Dermatol. 2012;57(5):409–410. doi: 10.4103/0019-5154.100508. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Zukiewitz-Sobczak W, Adamczuk P, Wroblewska P, Zvolinski J, Chmielewska-Badora J. Krasowska E, et al. Allergy to selected cosmetic ingredients. Postep Derm Alergol. 2013;30(5):307–310. doi: 10.5114/pdia.2013.38360. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Johansen J, Menne T. The fragrance mix and its constituents: a 14-year material. Contact Dermatitis. 1999;32(1):18–23. doi: 10.1111/j.1600-0536.1995.tb00834.x. [DOI] [PubMed] [Google Scholar]
- 29.Salam TN, Flower JF. Balsam-related systemic contact dermatitis. J Am Acad Dermatol. 2001;45(3):377–381. doi: 10.1067/mjd.2001.114738. [DOI] [PubMed] [Google Scholar]
- 30.de Groot AC, Flyvholm MA, Lensen G, Menne T, Coenraads PJ. Formaldehyde-releasers: relationship to formaldehyde contact allergy. Contact allergy to formaldehyde and inventory of formaldehyde-releasers. Contact Dermatitis. 2009;61(2):63–85. doi: 10.1111/j.1600-0536.2009.01582.x. [DOI] [PubMed] [Google Scholar]
- 31.Malinauskiene L, Blaziene A, Chomiciene A, Isaksson M. Formaldehyde may be found in cosmetic products even when unlabellel. Open Med. 2015;10(1):323–328. doi: 10.1515/med-2015-0047. [DOI] [PMC free article] [PubMed] [Google Scholar]
