Skip to main content
Dentistry Journal logoLink to Dentistry Journal
. 2020 Aug 3;8(3):83. doi: 10.3390/dj8030083

Potential Co-Factors of an Intraoral Contact Allergy—A Cross-Sectional Study

Constanze Olms 1,2,*, Jana Schor 3, Maryam Yahiaoui-Doktor 4
PMCID: PMC7559516  PMID: 32756376

Abstract

The aim of this cross-sectional study was to evaluate the frequency of dental allergens and potential co-factors, especially hypothyroidism, for patients with an intraoral contact allergy. From 2015 to 2016, patients with confirmed symptoms of an intraoral contact allergy (study group SG n = 50) were recruited in the dental clinic of the University of Leipzig. The participants of the control group (CG n = 103) were patients without oral diseases or intraoral symptoms of a contact allergy. For the data collection, a new “Allergy questionnaire” was developed. Information on allergies and general diseases were collected. The statistical analysis was carried out with SPSS 23.0. Sensitizations/allergies to metals and composites were higher in SG compared to CG. Of all study participants (n = 148), 14.2% (n = 21) had a nickel allergy. In 18% (n = 8) of the SG a cobalt allergy based on all metal allergens could be seen. In addition, an association between a nickel and cobalt allergy was found. Hypothyroidism occurred significantly more frequently (p = 0.049) in SG than in CG. Sensitizations and allergies can occur to metals in dental alloys. Hypothyroidism increased the risk of having an allergy threefold.

Keywords: contact allergy, metal sensitization, hypothyroidism

1. Introduction

Dental materials are among the most common artificial materials that are incorporated into the human body. Intolerances to dental materials can either be directly associated with toxic damage or occur as part of sensitization or allergy. In recent decades, an increase in allergies could be observed in the world population [1,2,3,4,5,6,7]. This increase is attributed to lifestyle and cultural, economic, ecological and other factors [1]. In the German population, the number of allergies has been growing continuously for years [8]. Almost a third of the population in Germany is affected by an allergic disease in the course of their life and allergic sensitization has been found in 50% of the German population [8]. In the 2013 study on Adult Health in Germany (DEGS1), nearly 20% of the respondents said that they had an allergic disease in the last 12 months. The most common allergic diseases were hay fever (14.8%), bronchial asthma (8.6%) and contact dermatitis (8.1%) [9]. Contact eczema is also increasingly observed in children [10,11,12], and is also increasingly prevalent among the elderly [13,14]. The most important risk factors for a contact allergy are: workload, age, gender, the handling of consumer goods and a genetic predisposition [15]. Allergic contact dermatitis has thus reached a frequency similar to that of diabetes mellitus [16].

The introduction of new materials into dentistry also increases the likelihood of an allergic intolerance reaction as a result of dental treatment [17]. Current epidemiological studies on dentistry are lacking. A previous clinical case report shows that multiple allergies can be associated with a lichenoid oral mucosa lesion. In this case, a L-Thyroxin substituted hypothyroidism was identified [18]. An increase in hypothyroidism has also been described in the clinical picture of oral lichen planus and oral lichenoid lesions [19,20]. An analysis of data from 2012 to 2016 showed that one of the most common diseases in patients with intraoral symptoms of contact allergy is a thyroid disorder (32,6% n = 28/86) [21]. In that study, of the patients with a thyroid disease, 20 patients, representing 71.4%, took thyroid hormone preparations [21].

The aim of this cross-sectional study was to evaluate the frequency of dental allergens and potential co-factors especially hypothyroidism for patients with intraoral contact allergy.

Our hypotheses were:

  1. There are no differences in the occurrence of metal or resin allergens in patients with symptoms of an intraoral contact allergy and those without.

  2. Patients with a nickel allergy more often also have a cobalt allergy.

  3. Patients with hypothyroidism have no higher risk of having a sensitization and/or allergy.

2. Material and Methods

The study was endorsed by the Ethics Committee of Leipzig University and is listed under the reference 075-15-09032015. The principles outlined in the Declaration of Helsinki in its latest version from the 64th WMA general meeting in October 2013 in Fortaleza (Brazil) were followed (World Medical Association 2013).

The study recruited participants from the university dental hospital allergy patients from April 2015 to April 2016. A healthy control group (CG) was formed comprising patients who visited their dentist for their annual dental check-up. Normally, we receive around 60–70 allergy patients in one year and decided to recruit twice as many controls, as this seemed practicable. Subjects in the study group (SG) were patients who had sensitization and/or allergies to dental materials with intraoral symptoms of a contact allergy. Exclusion criteria were: caries lesions, acute periodontics disorders or other pathological oral diseases. Additionally, patients who were dissatisfied with their dentures or who could not cope as well as those who developed symptoms, due to toxic, mechanical or microbiological stimuli, were excluded.

The subjects of the CG had no symptoms of an intraoral contact allergy to dental materials, neither diseases of the oral mucosa nor acute complaints, caries lesions or acute periodontics disorders. All participants were at least 18 years of age and of both sexes. Participation was voluntary and the participants were informed about the study and its aims. Once they gave their consent, the subjects were sent the questionnaires via post and could send them back to study management using an addressed pre-stamped envelope (see Figure 1).

Figure 1.

Figure 1

Modified Consort flow diagram.

For the data collection, a newly designed “Allergy questionnaire” was developed. The questionnaire mostly dealt with the collection of allergen-specific data (allergy test, allergens) and information on the participant′s restorations [17,21]. Data on dentures and their materials used were collected based on the dental status, the material pass or the declaration of conformity of the laboratory-produced dentures. In addition to the collection of personal data, the general medical history was collected [21]. The anonymized data were divided into the following categories: dental status, allergen-specific data and medical history.

The statistical evaluation was carried out with SPSS 23.0 (SPSS Inc., Chicago, IL, USA). The frequency distributions were descriptive. Differences between the SG and CG were tested with the t-test or Mann–Whitney U-test. Associations were determined using regression analyses and Fisher′s Exact test. A type I (alpha) error of p < 0.05 was considered statistically significant and p < 0.001 was considered highly significant. As this study was of an exploratory nature, in order to generate hypotheses for possible future studies, no correction for multiple-testing was carried-out.

3. Results

The study included 50 subjects in the SG, of which 45 had complete data which could be used for the analysis (Figure 1). Data from the 103 participants in the CG were complete and all were used for this analysis (Figure 1). Table 1 shows the sociodemographic and dental restorations data. There were 38 (84.4%) females in the SG and 59 (57.3%) in the CG, and the median age was 65 (IQR: 55–71) in the SG and 50 (IQR: 39–59) in the CG.

Table 1.

Sociodemographic and dental restorations data.

Personal Data Study Group (n = 45) Control Group (n = 103)
Sex
Female
38 (84.4%) 59 (57%)
Age in years—Median (IQR) 65 (55–71) 50 (39–59)
Profession
Pensioners 23 (51%) 18 (17%)
Non-academics 14 (31%) 48 (47%)
Academics 3 (7%) 11 (11%)
no profession 0 4 (4%)
no information 5 (11%) 22 (21%)
Dental Restorations (not Mutually Exclusive)
direct restoration 31 (69%) 97 (94%)
indirect restoration 7 (16%) 11 (11%)
crowns 27 (60%) 52 (50%)
fixed partial dentures 20 (44%) 27 (26%)
dental implants 6 (13%) 4 (4%)
removable dentures (partial or complete) 25 (56%) 22 (21%)

The most commonly used direct restoration material was composite in both groups. The material amalgam was used in approximately 37% of cases in the CG. High-gold alloys were often used as a material for indirect restorations. In the area of fixed restorations, it was mainly ceramic veneer crowns with a base made of a non-noble metal alloy that had been used. Noble metal alloys were used much more frequently in the SG. In the SG, a fixed partial denture made of a noble-metal alloy and one of polyetheretherketone (PEEK) were used.

Table 2 shows the overview of the frequently found allergens in both groups. From the evaluation of the allergen-specific data, 33 of the patients in the SG show several different allergens. Dentally-relevant allergens, especially metals dominated in the SG. Looking at the metal allergies of all subjects of the SG and CG together, a total of 14.2% (21/148) of the subjects had a known nickel allergy. At the same time 6% (9) had a cobalt allergy and 2% (3) a palladium allergy. The Fisher′s Exact test showed that a nickel allergy was associated with a cobalt allergy (p < 0.001). A Palladium allergy also tended to occur more often together with a nickel allergy.

Table 2.

Allergens.

Allergen-Specific Data Study Group (n = 45) Control Group (n = 103)
Allergy pass 33 (73%) 23 (22%)
Allergy test 40 (89%) 49 (48%)
Patch test 32 (71%) 18 (17%)
Prick test 15 (33%) 44 (43%)
Allergens Dental Restorations Materials
Nickel 11 (24%) 10(10%)
Mercury 10 (22%) 0
Cobalt 8 (18%) 1 (1%)
Palladium 3 (7%) 0
Copper 3 (7%) 0
Methacrylate 12 (27%) 1 (1%)
Composite 9 (20%) 0
Ceramic 2 (4%) 0
Allergens Drugs
Antibiotics 13 (29%) 9 (9%)
Local anaesthetic 5 (11%) 1 (1%)
Allergens other
Pollen (plants/grasses) 14 (31%) 28 (27%)
Food 11 (24%) 10 (10%)
Latex 8 (18%) 2 (2%)
House dust 8 (18%) 14 (14%)
Animal hair 4 (9%) 14 (14%)

Data on the medical history show that although the average age in the SG was ten years higher, cardiovascular diseases were similarly distributed in both groups. Statistical differences were observed for fungal infections and thyroid diseases (Table 3). The analysis of the data shows a relationship between hypothyroidism and having an allergy. The evaluation of the data of the allergy consultation had previously suggested a connection between hypothyroidism and an allergy [21]. In the present study, 16 subjects (35.6%) in the SG were diagnosed with hypothyroidism. One subject did not provide any information and 28 subjects had no known thyroid dysfunction. In the SG, all subjects with a positive medical history of hypothyroidism were female. In the CG, 19 subjects (18.4%) had hypothyroidism, of which 17 (16.5%) were female and two (2%) were male. Thus, hypothyroidism occurred significantly more frequently (p = 0.049) in the SG than in the CG.

Table 3.

Results of medical history (SG…Study Group, CG…Control Group).

Diseases SG n = 45
CG n = 103
Total Female Male No Information p-Value
Cardiovascular diseases SG 20
44.4%
16
35.6%
4
8.9%
-
-
0.454
CG 39
37.9%
25
24.3%
14
13.6%
-
-
Thyroid disease
(Hypothyroidism)
SG 16
35.6%
16
35.6%
-
-
1
2.2%
0.047
CG 19
18.4%
17
16.5%
2
2%
-
-
Fungal infections SG 9
20%
9
20%
-
-
1
2.2%
<0.001
CG 2
2%
1
1%
1
1%
-
-
Pneumopathy SG 7
15.6%
7
15.6%
-
-
-
-
0.118
CG 6
5.8%
5
4.9%
1
1%
-
-
Autoimmune diseases SG 7
15.6%
7
15.6%
-
-
2
4.4%
0.218
CG 5
4.9%
5
4.9%
-
-
-
Diseases of the internal organs SG 7
15.6%
7
15.6%
-
-
-
-
0.023
CG 5
4.9%
2
2%
3
2.9%
-
-
Neurological diseases SG 5
11.1%
3
6.7%
2
4.4%
-
-
0.004
CG 1
1%
-
-
1
1%
-
-
Blood disorders SG 4
8.9%
4
8.9%
-
-
-
-
0.015
CG 1
1%
- 1
1%
-
Diabetes mellitus SG 3
6.7%
2
4.4%
1
2.2%
-
-
0.444
CG 11
10.7%
6
6.8%
5
4.9%
-
Insulin-dependent diabetes mellitus SG -
-
-
-
-
-
-
-
<0.001
CG 6
5.8%
3
2.9%
3
2.9%
-
Infectious diseases SG -
-
-
-
-
-
-
-
0.509
CG 1
1%
1
1%
- -

If the datasets of SG and CG are summed up, the data of 148 subjects can be analyzed. Of those, 82 (55.4%) reported at least one allergy (SG 37/82.2%, CG 45/43.7%). Overall, 68 (83%) with allergies were female and 14 (17%) were male. This difference was significant (p = 0.033). In total, 35 subjects of SG and CG had hypothyroidism. An association between thyroid dysfunction (hypothyroidism) and the occurrence of allergy was seen. A logistic binary regression analysis, adjusting for sex and age, showed that patients with hypothyroidism had a three times higher risk of having an allergy than patients without hypothyroidism (odds ratio = 2.994, 95% confidence interval 1.288–6.961, p = 0.011).

4. Discussion

The lack of information on the association between an intraoral contact allergy and hypothyroidism motivated us to carry out this cross-sectional observational study. The main aim was to find out whether there are co-factors for an intraoral contact allergy that are different between the two groups (study and control). The ratio of patients in the two groups was approximately 2:1.

In the present study, females had more adverse reactions to dental materials, which is also shown in the study by Vamnes et al. where 70% (208/296) of those affected were females [22]. Richter and Geier showed that in the stomatitis patients and in those who were tested for the clarification of a denture incompatibility, females and older patients predominated [23]. Patients with allergic complaints or material intolerances often have a long history of dental problems. Any existing restorations and the materials used for them are helpful for a clinical diagnosis. For instance, in our study, we saw that older, predominantly female patients with long-term dental history, had developed oral intolerance. In the SG, the median age was 65 years, and crowns, fixed partial dentures, removable partial dentures and complete dentures were more common, while in the CG (median age 50 years), direct restorations dominated. In the most recent German Oral Health Study (DMS V), 77.3% (747/966) had no removable partial nor complete dentures, and in the group of younger adults (35–45 years) only 2.7% were supplied with a removable denture [24,25]. Up to around 30 years ago, more high-gold alloys were used for fixed and removable partial dentures with a metal framework; however today, due to costs, non-noble alloys composed of cobalt-chromium are used. This can be seen from the information on dentures of the CG. Thus, younger adults (35–45 years) are coming into contact with cobalt-chromium alloys, e.g., for crowns and fixed partial dentures more often. This is also reflected in the increased contact sensitivities to cobalt compared to past data surveys [21]. Our hypothesis that there are no differences in the occurrence of metal or resin allergens in patients with symptoms of an intraoral contact allergy and those without, can therefore be rejected.

4.1. Occurrence of Cross-Allergies

Allergies to several substances can occur at the same time. A cross-allergy of nickel and palladium has been known to exist for a long time [26]. In the periodic table, both metals are in the same subgroup (VIII). Furthermore, reactions to palladium are observed in about 50% of patients with an allergy to nickel [27,28,29,30]. In the study by Rachmawati et al., 80% of patients (25) with a positive test reaction to nickel also showed sensitization to palladium salts [31]. In the study by Raap et al., (2009), all patients (100%, 10) with nickel sensitization also showed a positive patch-test response to palladium [32]. In the study by Muris et al., (2015), a cross-allergy between nickel and palladium was found only in patients with amalgam fillings and crowns. In particular, patients (10.2%, 91/906) with oral symptoms and other complaints had significant sensitizations to palladium and nickel. Dry mouth (xerostomia) and metallic taste were strongly associated with palladium and nickel sensitization in this study [33].

One third of all nickel allergy sufferers also show reactions to cobalt chloride, which is called a coupling allergy [34]. In the present study, allergic reactions to cobalt also occurred in SG′s nickel allergy sufferers. Cobalt is an element of the same subgroup (VIII) in the periodic table as nickel. In nature, cobalt and nickel coexist [35]. Cobalt is a potent allergen and is often described as a contact allergen [36]. As a result, sensitization to nickel and cobalt can occur simultaneously [37]. Whether this is a genuine, cross-allergic reaction has not yet been clearly clarified [37]. The study by Lidén et al. (2016) showed that 14% (92/656) of patients with contact dermatitis had a contact allergy to cobalt. Of these, 50% (46/92) had a solitary cobalt allergy [38]. Similar results have been reported in other studies [39,40,41].

Rarely have reactions to nickel, copper and chromium been observed [42]. In a separate meta-analysis, metallic allergens such as nickel, palladium and cobalt were common [43].

Isolated reactions to cobalt without simultaneous reactions to nickel and chromium are rather rare [34].

In the present study, the most frequent allergens in SG were metals. Allergies to metals and composites were higher in the SG compared to the CG. For instance, 14.2% (21) of all study participants (n = 148) had a nickel allergy, and in 18% of the SG a cobalt allergy based on all metal allergens could be detected. Our second hypothesis that patients with a nickel allergy have more often a cobalt allergy also, is supported by this study.

4.2. Allergies and Systemic Diseases

The hypothesis that patients with hypothyroidism had no higher risk of having an allergy is rejected. The occurrence of thyroid disease associated with allergic rhinitis, asthma and chronic urticaria has been described previously [44,45,46,47]. Recent studies also assume immunological interactions. Chronic idiopathic urticaria and autoimmune thyroid disease are characterized by the presence of anti-IgE and/or anti-IgE receptor antibodies and thyroid antibodies in some patients [48]. An increase in hypothyroidism has also been described in the clinical picture of oral lichen planus and oral lichenoid lesions. In the study by Rachmawati et al. (2015), there was an association between autoimmune diseases and sensitization to the dental metals nickel, palladium, gold, and mercury. No thyroid antibodies were found on sensitization to palladium, gold and mercury. In contrast, thyroid antibodies were detected in patients with nickel sensitization [31]. In the study by Muris et al. (2014), patients with palladium-containing dental alloys showed an increased epicutaneous test response and lymphocyte proliferation [49]. We saw a direct association between the occurrence of allergies and hypothyroidism in the present study (p = 0.047).

Studies with a higher number of participants need to be conducted to confirm our findings. Whether this is a true cross-allergy between nickel and cobalt should be clarified and to make a conclusive statement about which allergens might set off hypothyroidism and vice versa.

5. Conclusions

In the present study, not only was the common occurrence of nickel and palladium allergies together observed, but also that of nickel and cobalt allergies. We also saw an association (adjusted for sex and age) between hypothyroidism and an allergy. Patients with hypothyroidism were three times more likely to be allergic. Theoretically, sensitizations and allergies can occur to any ingredient in dental materials. It is therefore important for the dentist to know potential allergens in dental materials.

Acknowledgments

We would like to thank Katharina Ogrodowski for her help with the coordination of patients.

Author Contributions

Conceptualization, C.O. and M.Y.-D.; Methodology, C.O.; Software, J.S.; Validation, C.O., J.S. and M.Y.-D.; Formal Analysis, M.Y.-D.; Investigation, C.O.; Resources, C.O.; Data Curation, C.O.; Writing—Original Draft Preparation, C.O. and M.Y.-D.; Writing—Review & Editing, C.O., J.S. and M.Y.-D.; Visualization, C.O. and J.S.; Supervision, J.S.; Project Administration, C.O. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Conflicts of Interest

The authors declare no conflict of interest.

References

  • 1.Park H.J., Lim H.S., Park K.H., Lee J.H., Park J.W., Hong C.S. Changes in allergen sensitization over the last 30 years in Korea respiratory allergic patients: A single-center. Allergy Asthma Immunol. Res. 2014;6:434–443. doi: 10.4168/aair.2014.6.5.434. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Suh M., Kim H.H., Sohn M.H., Kim K.E., Kim C., Shin D.C. Prevalenceof allergic diseases among Korean school-age children: A nationwide cross-sectional questionnaire study. J. Korean Med. Sci. 2011;26:332–338. doi: 10.3346/jkms.2011.26.3.332. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Zar H.J., Ehrlich R.I., Workman L., Weinberg E.G. The changing prevalence of asthma, allergic rhinitis and atopic eczema in African adolescents from 1995 to 2002. Pediatr. Allergy Immunol. 2007;18:60–65. doi: 10.1111/j.1399-3038.2007.00554.x. [DOI] [PubMed] [Google Scholar]
  • 4.Maziak W., Behrens T., Brasky T.M., Duhme H., Rzehak P., Weiland S.K., Keil U. Are asthma and allergies in children and adolescents in- creasing? Results from ISAAC phase I and phase III surveys in Münster, Germany. Allergy. 2003;58:572–579. doi: 10.1034/j.1398-9995.2003.00161.x. [DOI] [PubMed] [Google Scholar]
  • 5.Lee S.L., Wong W., Lau Y.L. Increasing prevalence of allergic rhinitis but not asthma among children in Hong Kong from 1995 to 2001 (Phase 3 International Study of Asthma and Allergies in Child- hood) Pediatr. Allergy Immunol. 2004;15:72–78. doi: 10.1046/j.0905-6157.2003.00109.x. [DOI] [PubMed] [Google Scholar]
  • 6.Pearce N., Aït-Khaled N., Beasley R., Mallol J., Keil U., Mitchell E., Robertson C. ISAAC Phase Three Study Group. Worldwide trends in the prevalence of asthma symptoms: Phase III of the International Study of Asthma and Allergies in Childhood (ISAAC) Thorax. 2007;62:758–766. doi: 10.1136/thx.2006.070169. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Williams H., Stewart A., von Mutius E., Cookson W., Anderson H.R. International Study of Asthma and Allergies in Childhood (ISAAC) Phase One and Three Study Groups. Is eczema really on the in-crease worldwide? J. Allergy Clin. Immunol. 2008;121:947–954. doi: 10.1016/j.jaci.2007.11.004. [DOI] [PubMed] [Google Scholar]
  • 8.Bergmann K.C., Heinrich J., Niemann H. Current status of allergy prevalence in Germany: Position paper of the Environmental Medicine Commission of the Robert Koch Institute. Allergo J. Int. 2016;25:6–10. doi: 10.1007/s40629-016-0092-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Langen U., Schmitz R., Steppuhn H. Häufigkeit allergischer Erkrankungen in Deutschland Ergebnisse allergischer Erkrankungen in Deutschland (DEGS1) Bundesgesundheitsblatt-Gesundh. -Gesundh. 2013;56:698–706. doi: 10.1007/s00103-012-1652-7. [DOI] [PubMed] [Google Scholar]
  • 10.Lee P.W., Elsaie M.L., Jacob S.E. Allergic contact dermatitis in children: Common allergens and treatment: A review. Curr. Opin. Pediatr. 2009;21:491–498. doi: 10.1097/MOP.0b013e32832d2008. [DOI] [PubMed] [Google Scholar]
  • 11.Pigatto P., Martelli A., Marsili C., Fiocchi A. Contact dermatitis in children. Ital. J. Pediatr. 2010;36:2. doi: 10.1186/1824-7288-36-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Simonsen A.B., Deleuran M., Johansen J.D., Sommerlund M. Contact allergy and allergic contact dermatitis in children—A review of current data. Contact Derm. 2011;65:254–265. doi: 10.1111/j.1600-0536.2011.01963.x. [DOI] [PubMed] [Google Scholar]
  • 13.Jacob S.E., Elsaie M.L., Castanedo-Tardan M.P., Stechschulte S., Kaufman J. Aging and contact dermatitis: A review. Curr. Aging Sci. 2009;2:121–126. doi: 10.2174/1874609810902020121. [DOI] [PubMed] [Google Scholar]
  • 14.Prakash A.V., Davis M.D. Contact dermatitis in older adults: A review of the literature. Am. J. Clin. Dermatol. 2010;11:373–381. doi: 10.2165/11319290-000000000-00000. [DOI] [PubMed] [Google Scholar]
  • 15.Peiser M., Tralau T., Heidler J., Api A.M., Arts J.H.E., Basketter D.A., English J., Diepgen T.L., Fuhlbrigge R.C., Gaspari A.A., et al. Allergic contact dermatitis: Epidemiology, molecular mechanisms, in vitro methods and regulatory aspects. Current knowledge assembled at an international workshop at BfR, Germany. Cell. Mol. Life Sci. 2012;69:763–781. doi: 10.1007/s00018-011-0846-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Brasch J., Becker D., Aberer W., Bircher A., Kranke B., Jung K., Przybilla B., Biedermann T., Werfel T., John S.M., et al. Guideline contact dermatitis: S1-Guidelines of the German Contact Allergy Group (DKG) of the German Dermatology Society (DDG), the Information Network of Dermatological Clinics (IVDK), the German Society for Allergology and Clinical Immunology (DGAKI), the Working Group for Occupational and Environmental Dermatology (ABD) of the DDG, the Medical Association of German Allergologists (AeDA), the Professional Association of German Dermatologists (BVDD) and the DDG. Allergo J. Int. 2014;23:126–138. doi: 10.1007/s40629-014-0013-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Stoll S. Ph.D. Thesis. Albert-Ludwigs-Universität; Freiburg i. Br., Germany: 2007. Allergien in aller Munde?: -Eine Untersuchung der Epikutantests der Zahn-, Mund- und Kieferklinik Freiburg von 1993 bis 2001. [Google Scholar]
  • 18.Olms C., Remmerbach T.W. Allergen-getriggerte lichenoide Mundschleimhautläsionen: Diagnose und Therapie anhand eines Fallbeispiels. Swiss Dent. J. 2017;127:27–37. doi: 10.61872/sdj-2017-01-03. [DOI] [PubMed] [Google Scholar]
  • 19.Garcia-Pola M.J., Llorente-Pendás S., Seoane-Romero J.M., Berasaluce M.J., García-Martín J.M. Thyroid Disease and Oral Lichen Planus as Comorbidity: A Prospective Case-Control Study. Dermatology. 2016;232:214–219. doi: 10.1159/000442438. [DOI] [PubMed] [Google Scholar]
  • 20.Siponen M., Huuskonen L., Läärä E., Salo T. Association of oral lichen planus with thyroid disease in a Finnish population: A retrospective case-control study. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. Endod. 2010;110:319–324. doi: 10.1016/j.tripleo.2010.04.001. [DOI] [PubMed] [Google Scholar]
  • 21.Olms C., Yahiaoui-Doktor M., Remmerbach T.W. Contact allergies to dental materials. Swiss Dent. J. 2019;129:571–579. doi: 10.61872/sdj-2019-07-08-555. [DOI] [PubMed] [Google Scholar]
  • 22.Vamnes J.S., Lygre G.B., Gronningsaeter A.G., Gjerdet N.R. Four years of clinical experience with an adverse reaction unit for dental biomaterials. Community Dent. Oral Epidemiol. 2004;32:150–157. doi: 10.1111/j.0301-5661.2004.00148.x. [DOI] [PubMed] [Google Scholar]
  • 23.Richter G., Geier J. Dentalwerkstoffe–Problemsubstanzen in der allergologischen Diagnostik?: Teil I: Analyse der Testergebnisse bei Patienten mit Mundschleimhaut/Dentalwerkstoff-Problemen. Der Hautarzt. 1996;47:839–843. doi: 10.1007/s001050050517. [DOI] [PubMed] [Google Scholar]
  • 24.Institut der Deutschen Zahnärzte . Fünfte Deutsche Mundgesundheitsstudie (DMS V) Institut der Deutschen Zahnärzte; Cologne, Germany: 2016. [(accessed on 2 August 2020)]. Im Auftrag von Bundeszahnärztekammer und Kassenzahnärztlicher Bundesvereinigung. Available online: http://www.kzbv.de/dms-v.8.de.html. [Google Scholar]
  • 25.Jordan A.R., Micheelis W. Fünfte Deutsche Mundgesundheitsstudie DMSV. Volume 35 Deutscher Zahnärzte Verlag DÄV; Köln, Germany: 2016. [Google Scholar]
  • 26.Watsky K.L. Occupational allergic contact dermatitis to platinum, palladium, and gold. Contact Derm. 2007;57:382–383. doi: 10.1111/j.1600-0536.2007.01144.x. [DOI] [PubMed] [Google Scholar]
  • 27.Aberer W., Holub H., Strohal R., Slavicek R. Palladium in dental alloys—The dermatologists’ responsibility to warn? Contact Derm. 1993;28:163–165. doi: 10.1111/j.1600-0536.1993.tb03379.x. [DOI] [PubMed] [Google Scholar]
  • 28.Schmalz G., Garhammer P. Biological interactions of dental cast alloys with oral tissues. Dent. Mater. 2002;18:396–406. doi: 10.1016/S0109-5641(01)00063-X. [DOI] [PubMed] [Google Scholar]
  • 29.Wataha J.C., Hanks C.T. Biological effects of palladium and risk of using palladium in dental casting alloys. J. Oral Rehabil. 1996;23:309–320. doi: 10.1111/j.1365-2842.1996.tb00858.x. [DOI] [PubMed] [Google Scholar]
  • 30.Garhammer P., Schmalz G., Hiller K.A., Reitinger T., Stolz W. Patients with local adverse effects from dental alloys: Frequency, complaints, symptoms, allergy. Clin. Oral Investig. 2001;5:240–249. doi: 10.1007/s007840100127. [DOI] [PubMed] [Google Scholar]
  • 31.Rachmawati D., Muris J., Scheper R.J., Rustemeyer T., Kleverlaan C.J., Feilzer A.J., von Blomberg B.M., van Hoogstraten I.M.W. Continuing the quest for autoimmunity due to oral metal exposure. Autoimmunity. 2015;48:494–501. doi: 10.3109/08916934.2015.1033688. [DOI] [PubMed] [Google Scholar]
  • 32.Raap U., Stiesch M., Reh H., Kapp A., Werfel T. Investigation of contact allergy to dental metals in 206 patients. Contact Derm. 2009;60:339–343. doi: 10.1111/j.1600-0536.2009.01524.x. [DOI] [PubMed] [Google Scholar]
  • 33.Muris J., Goossens A., Goncalo M., Bircher A.J., Gimenez-Arnau A., Foti C., Rustemeyer T., Feilzer A.J., Kleverlaan C.J. Sensitization to palladium and nickel in Europe and the relationship with oral disease and dental alloys. Contact Derm. 2015;72:286–296. doi: 10.1111/cod.12327. [DOI] [PubMed] [Google Scholar]
  • 34.Trautmann A., Kleine-Tebbe J. Allergologie in Klinik und Praxis. Volume 2 Georg Thieme Verlag; Stuttgart, Germany: New York, NY, USA: 2013. [Google Scholar]
  • 35.Scansetti G., Botta G.C., Spinelli P., Reviglione L., Ponzetti C. Absorption and excretion of cobalt in the hard metal industry. Sci. Total Environ. 1994;150:141–144. doi: 10.1016/0048-9697(94)90141-4. [DOI] [PubMed] [Google Scholar]
  • 36.Thyssen J.P. Cobalt sensitization and dermatitis: Considerations for the clinician. Dermatitis. 2012;23:203–209. doi: 10.1097/DER.0b013e31826e4591. [DOI] [PubMed] [Google Scholar]
  • 37.Thyssen J.P., Johansen J.D., Carlsen B.C., Menne T. Prevalence of nickel and cobalt allergy among female patients with dermatitis before and after Danish government regulation: A 23-year retrospective study. J. Am. Acad. Dermatol. 2009;61:799–805. doi: 10.1016/j.jaad.2009.03.030. [DOI] [PubMed] [Google Scholar]
  • 38.Liden C., Andersson N., Julander A., Matura M. Cobalt allergy: Suitable test concentration, and concomitant reactivity to nickel and chromium. Contact Derm. 2016;74:360–367. doi: 10.1111/cod.12568. [DOI] [PubMed] [Google Scholar]
  • 39.Hegewald J., Uter W., Pfahlberg A., Geier J., Schnuch A. A multifactorial analysis of concurrent patch-test reactions to nickel, cobalt, and chromate. Allergy. 2005;60:372–378. doi: 10.1111/j.1398-9995.2005.00693.x. [DOI] [PubMed] [Google Scholar]
  • 40.Lagrelius M., Wahlgren C.-F., Matura M., Kull I., Liden C. High prevalence of contact allergy in adolescence: Results from the population-based BAMSE birth cohort. Contact Derm. 2016;74:44–51. doi: 10.1111/cod.12492. [DOI] [PubMed] [Google Scholar]
  • 41.Uter W., Gefeller O., Geier J., Schnuch A. Contact sensitization to cobalt--multifactorial analysis of risk factors based on long-term data of the Information Network of Departments of Dermatology. Contact Derm. 2014;71:326–337. doi: 10.1111/cod.12284. [DOI] [PubMed] [Google Scholar]
  • 42.Tschernitschek H., Geurtsen W. Kreuzallergie Kobalt-Nickel. Dtsch. Zahnärztl. Z. 2008;63:462–463. [Google Scholar]
  • 43.Sieber A., Olms C. Häufigkeiten von Allergien auf Zahnärztliche Materialien–Eine Metaanalyse. Volume 13 Springer; Berlin, Germany: 2014. Abstract Book, Research Festival for Life Science. [Google Scholar]
  • 44.Bush R.K., Ehrlich E.N., Reed C.E. Thyroid disease and asthma. J. Allergy Clin. Immunol. 1977;59:398–401. doi: 10.1016/0091-6749(77)90025-2. [DOI] [PubMed] [Google Scholar]
  • 45.Degirmenci P.B., Kirmaz C., Oz D., Bilgir F., Ozmen B., Degirmenci M., Colak H., Yilmaz H., Ozyurt B. Allergic rhinitis and its relationship with autoimmune thyroid diseases. Am. J. Rhinol. Allergy. 2015;29:257–261. doi: 10.2500/ajra.2015.29.4189. [DOI] [PubMed] [Google Scholar]
  • 46.Pan X.F., Gu J.Q., Shan Z.Y. The prevalence of thyroid autoimmunity in patients with urticaria: A systematic review and meta-analysis. Endocrine. 2015;48:804–810. doi: 10.1007/s12020-014-0367-y. [DOI] [PubMed] [Google Scholar]
  • 47.Reisacher W.R. Prevalence of autoimmune thyroid disease in chronic rhinitis. Ear Nose Throat J. 2008;87:524–527. doi: 10.1177/014556130808700912. [DOI] [PubMed] [Google Scholar]
  • 48.Rottem M. Allergy and systemic diseases: The case of chronic urticaria and thyroid disease. Isr. Med. Assoc. J. 2002;4:889–890. [PubMed] [Google Scholar]
  • 49.Muris J., Scheper R.J., Kleverlaan C.J., Rustemeyer T., van Hoogstraten I.M., von Blomberg M.E., Feilzer A.J. Palladium-based dental alloys are associated with oral disease and palladium-induced immune responses. Contact Derm. 2014;71:82–91. doi: 10.1111/cod.12238. [DOI] [PubMed] [Google Scholar]

Articles from Dentistry Journal are provided here courtesy of Multidisciplinary Digital Publishing Institute (MDPI)

RESOURCES