Next Article in Journal
Prenatal Exposure to Aluminum and Status of Selected Essential Trace Elements in Rural South African Women at Delivery
Next Article in Special Issue
Recommendations for Improving the Quality of Rare Disease Registries
Previous Article in Journal
Accounting for Fairness in a Two-Stage Stochastic Programming Model for Kidney Exchange Programs
Previous Article in Special Issue
The Occurrence of 275 Rare Diseases and 47 Rare Disease Groups in Italy. Results from the National Registry of Rare Diseases
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
IJERPH
Volume 15
Issue 7
10.3390/ijerph15071493
ijerph-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Oral Symptoms and Oral Health-Related Quality of Life in People with Rare Diseases in Germany: A Cross-Sectional Study

by
Sabrina Wiemann
1,
Nicolas Frenzel Baudisch
2,
Rainer A. Jordan
2,
Johannes Kleinheinz
1 and
Marcel Hanisch
1,*
1
Department of Cranio-Maxillofacial Surgery, Research Unit Rare Diseases with Orofacial Manifestations (RDOM), University Hospital Münster, Albert-Schweitzer-Campus 1, Building W 30, D-48149 Münster, Germany
2
Institute of German Dentists (IDZ), Research Focus: Sociology of medicine and Health Psychology, Universitätsstraße 73, D-50931 Köln, Germany
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2018, 15(7), 1493; https://doi.org/10.3390/ijerph15071493
Submission received: 15 June 2018 / Revised: 11 July 2018 / Accepted: 13 July 2018 / Published: 15 July 2018
(This article belongs to the Special Issue Current Situation and Distribution of Rare Diseases: Challenges, Prevention, Healthcare and Effects)
Browse Figure
Versions Notes

Abstract

:
Background: The aim of this study was to collect information on oral health-related quality of life (OHRQoL) in people with rare diseases. Methods: A questionnaire comprising free text questions and the German version of the standardized Oral Health Impact Profile-14 (OHIP-14) questionnaire on OHRQoL was developed. All participants who indicated oral symptoms in the questionnaire were included in a cluster analysis. Different cluster analyses were performed (Ward’s, k-Means) to find symptom profile groups in the data. Results: A total of 484 questionnaires with 96 rare diseases were included in the study. The most reported symptoms were anomalies of the tooth formation, dysgnathia, changes in number of the teeth, and malocclusions. The OHIP mean values of the five resulting symptom clusters ranged from 15.1 to 19.9, which is very high compared to the general population in Germany, which has a mean value of 4.09. Discussion: All investigated symptoms show a negative association with OHRQoL, but the strongest were for symptoms of the oral mucosa and periodontal diseases. All the symptoms described in this cluster analysis can lead to considerably higher mean values of the OHIP total score among people with rare disease and thus to worse OHRQoL than reported in the general population.

1. Introduction

Rare diseases are by definition ‘rare’. A disease is categorized as ‘rare’ if fewer than 2000 people suffer from it. In the European Union, between 27 and 36 million people have a rare disease [1,2], about four million of which live in Germany [3].
Studies have shown that about 15% of all known 6000–8000 rare diseases can manifest orofacially [4,5,6] and can affect oral health-related quality of life (OHRQoL) [7]. In 2009, the Council of the European Union issued a recommendation to member states to develop measures to improve medical care for people with rare diseases [8]. As a result, the National Action Plan for People with Rare Diseases, which is currently in the implementation phase, was launched in Germany in 2013 [9].
Thus far, there have been very few studies on the OHRQoL of people with rare diseases; the few previous analyses reports showed reduced OHRQoL in people with rare disease [7,10,11].
The Oral Health Impact Profile (OHIP) is a validated instrument to assess OHRQoL; with 14 items, the OHIP-14 measures the incidence of different functional and psychosocial influences on OHRQoL. The maximum number of points is 56 in the OHIP-14 version, which means a very high impact on OHRQoL for the patient [12]. Therefore, this serves as a suitable instrument for describing the influence of oral health on general health from the patient’s perspective [13].
On average, it takes seven years before a rare disease is correctly diagnosed [14]. In the process, oral manifestations of rare diseases seem to negatively influence OHRQoL [7]. With oral symptoms, the dentist can contribute towards reducing the time taken for a diagnosis. Dental checkups make up one of the most frequent reasons for contact between patients and health care professionals. In cases of oral symptoms, the dentist can be the first health care professional who is able to identify a rare disease by its oral manifestations [15]. This could in turn positively influence OHRQoL and also general quality of life, because dentists and physicians can start the appropriate therapy earlier. There is a low-frequency problem in the context of individual rare diseases. Due to that low frequency, analyses with a high number of cases for individual diseases are difficult, which is why a cluster analysis based on symptoms was considered appropriate for this study. With this method it is possible to investigate all diseases with oral manifestations in an overarching study and not every disease on its own. Symptom profile groups allow us to find out which symptoms have a negative impact on OHRQoL. A cluster analysis allows the possibility of finding symptom profile groups in the present data source.
Therefore, the aim of this study was to collect information on OHRQoL in people with rare diseases and to find out which symptoms were mostly reported and which symptoms had the highest impact on OHRQoL.

2. Methods

The present study was conceived as an epidemiological survey to collect information on OHRQoL in people with rare diseases in Germany. A questionnaire comprising free text questions and the German version of the standardized OHIP-14 questionnaire on OHRQoL was developed [16]. The free text questions were chosen so that the participants could provide their information without prescribed response options from the principal investigator. The questionnaire (Table S1) was sent digitally to all 125 member associations of the umbrella organization of self-help groups, the Alliance of Chronic Rare Diseases (ACHSE e.V.) in Germany in February 2016. All questionnaires received by July 2017 were considered. Approval obtained from the Ethics Commission of the General Medical Council of Westphalia-Lippe and the Westphalian Wilhelms University of Münster is available (Ref. No. 2106-006-f-S). Included in the study were all people in Germany with a rare disease aged 16 and above who could be reached via the ACHSE.

2.1. Questionnaire

The OHIP-14 questionnaire is the short form of the OHIP-49 and gathers information on the frequency of functional limitations, pain, psychological unease/discomfort, physical impairment, mental impairment, social impairment, and disadvantage/disability in the past month [16]. Each of the 14 items was coded as follows: 0 = never, 1 = hardly ever, 2 = now and then, 3 = often, and 4 = very often. In the open-ended questions, possible oral manifestations of the disease were also requested. To streamline analysis, the principal investigators translated the patient responses into medical terms and divided them into categories. For instance, the subjective patient statement ‘dry mouth’ was renamed xerostomia/hyposalivation.

2.2. Participants

There was no patient selection; all self-help groups listed with the ACHSE were contacted and all persons with a rare disease who are in contact with a self-help organization listed with the ACHSE could participate in the study. As a result, individual rare diseases, depending on the number of participants, are represented more strongly or less strongly in this study. The aim was to get as many questionnaires as possible during the study period. Due to the rarity of individual rare diseases, even rare diseases for which only one questionnaire was submitted were included in the study. Against this backdrop, the attempt was to focus on the symptoms and their effect on OHRQoL in order to also consider the dependency of the OHRQoL on the symptom constellation.

2.3. Data Source

All participants who indicated oral symptoms in the questionnaire were included in the cluster analysis. Participants who did not indicate oral symptoms were excluded (46.5%). The cluster analysis was executed using the following 12 symptoms, which were translated into medical terminology based on the data of the participants: dysgnathia, malocclusion, anomalies of tooth formation, mineralization disorders of the teeth, cleft lip or cleft palate, microstomia, temporomandibular dysfunction, diseases of the oral mucosa, diseases of the periodontium, changes in the number of teeth, neurological diseases, and vegetative disorders. These were coded as dichotomous variables suitable for a cluster analysis both in their incidence and in their medical relevance.

2.4. Statistical Methods

The statistics program SPSS was used for the analysis. The aim of a cluster analysis is that it forms groups of cases according to their similarities and dissimilarities in certain aspects. In the present study, these aspects were the participants’ oral symptoms so that the mathematical algorithms yielded symptom profile groups. Each group is very different from the others but is itself highly homogeneous [17].
First, a cluster analysis using the Ward algorithm was used with an indefinite number of clusters. With the Elbow criterion, 2–6 clusters seemed to be an adequate number of clusters. Based on this criterion, a cluster analysis applying the k-means algorithm with 2–6 clusters and another Ward’s analysis with 2–6 clusters were then carried out. Both analyzing methods were compared with regard to group belonging, group size, and the symptom groups in the individual clusters. The Kappa coefficient (4, 04) was also calculated. This coefficient shows the consensus of the cluster solutions [17]. Due to the data’s heterogeneity, the results were considered acceptable.
Several cluster analyses were performed with cases ordered randomly, and all analyses showed stable results independent of the order of cases and algorithm (Ward’s, k-Means) used. After comparing the symptom prevalence in each cluster of every cluster analysis solution and according to medical and/ or dental considerations, Ward’s method with five clusters was chosen for further analysis. For instance, dysgnathia and malocclusion both appear with high prevalence in cluster five; from a medical perspective, there is a logical connection between these two symptoms; therefore, this resulting cluster was deemed appropriate. Thus, the five-cluster Ward’s method revealed the most interpretable and consistent clusters. The five resulting clusters of the k-Means cluster solution showed nearly the same symptom profile groups with only slightly less marked symptom prevalences. Following this, for each cluster, the mean, median, 95% confidence interval, standard deviation, and minimum and maximum of the OHIP total score was calculated. We performed a cluster analysis on group symptoms and formed symptom profile groups to solve the low-frequency problem of rare diseases and to get an overview of which symptoms co-occur with each other.

3. Results

Of the 545 submitted questionnaires, 484 could be included in the study; 61 questionnaires could not be considered because the participants were less than 16 years old. Twelve self-help groups refused to participate in the study either due to lack of interest or because the self-help group believed that the study would be of no personal benefit to the members. The participants were predominantly female (64.7%), and their ages ranged from 16 to 80 years with an average of 44.6 years. The OHIP mean values of the resulting symptom clusters ranged from 15.1 to 19.9. In total, participants with 96 different rare diseases participated in the study.
All rare diseases analyzed in this study are listed in the Orphanet classification of rare diseases [18], and the most prevalent (n ≥ 10) are listed in Table 1. The diseases were recorded based on data given by the patients. The data of 257 participants who described an oral manifestation were analyzed by cluster analysis. Of the 95 named symptoms, which were indicated by the patients in their own words, the 12 symptoms that were represented most frequently and could have an impact on OHRQoL from a medical perspective were included in the cluster analysis (Table 2).
Cluster 1 included anomalies of tooth formation (conical shaped teeth, taurodontism, macrodontia, and microdontia) and mineralization disorders of the dental hard tissue (amelogenesis imperfecta, dentine dysplasia, and dentinogenesis imperfecta). The mean value of the OHIP total value was 15.9 (12.6; 19.2) points.
Cluster 2 included symptoms involving the oral mucosa (aphthae and stomatitis) and diseases of the periodontium (gingivitis, periodontitis, recessions, hyperplasia of the oral mucosa, tooth loss through periodontitis) and microstomia. The mean value of the OHIP total value was 19.7 (13.8; 25.7) points. It seems that symptoms related to the oral mucosa and diseases of the periodontium have the highest impact on OHRQoL.
Cluster 3 is characterized by the symptom changes in the number of teeth (hypodontia, oligodontia, anodontia, and hyperdontia), anomalies of tooth formation (form abnormalities, macrodontia, microdontia, and taurodontism), and cleft lip and palate. The mean value of the OHIP total value was 16.9 (13.0; 20.8) points.
Cluster 4 included temporomandibular dysfunctions (bruxism, luxations, cartilage displacement, ankylosis, and pain in the mandibular joint), vegetative disorders (hyposalivation, hypersalivation, and xerostomia), and neurological diseases (facial nerve paresis, trigeminal neuralgia, and somatosensory disorders of the trigeminal nerve). The mean value of the OHIP total value was 16.9 (13.0; 20.8) points.
Cluster 5 included dysgnathia (micrognathia, macrognathia, high palate, and mandibular retrognathia) and malocclusions (crossbite, edge-to-edge bite, overbite, impacted tooth, inclination, wide space, and overcrowding). The mean value of the OHIP total value was 15.1 (11.6; 18.8) points.
If symptoms appear involving the oral mucosa, the periodontium, and a restricted mouth opening (microstomia), as is the case in cluster 2, this results in the worst OHIP total scores. The OHIP mean values in the other clusters vary only marginally (Table 3). Figure 1 shows the cluster distribution.

4. Discussion

Not only can rare diseases negatively influence the general quality of life, they also negatively impact the OHRQoL [20]. The OHIP mean values in the present study among people with rare diseases had a mean value between 15.1 and 19.9 depending on the different symptom combinations. With cluster analysis techniques, we identified five symptom profile groups to analyze. The aim of this study was to group symptoms across all mentioned diseases and investigate the impact on OHRQoL.

4.1. Limitations

Because there are up to 8000 different rare diseases globally [21], it is impossible to generalize ‘rare diseases’ as ‘a’ disease, because each disease is peculiar, and furthermore, there are diverse manifestations within a rare disease [11,22].
Because the questionnaire was distributed using the snowball method, we cannot accurately say how many people were reached; however, we opted for this method due to the difficulty of reaching many people with rare diseases.
In addition, it is not possible to give evidence about the severity of the disease because the questionnaire only asks which diseases and symptoms the participants have. In a cluster analysis, it is difficult to group a large number of symptoms accordingly. The more symptoms included in a cluster analysis, the more difficult and unstable the cluster analysis becomes. Therefore, it is more insightful to limit the number of symptoms included in the analysis to enable a sensible formation of groups. This requires that symptoms that could also be significant to OHRQoL were not taken into consideration. In addition, a cluster analysis only groups symptoms and does not assess causal relationships. For this reason, no such assertions were made with respect to symptoms and OHRQoL [17].
This study therefore serves as an attempt to obtain a classification of symptoms across illnesses. Certain symptom combinations were found in the cluster analysis that are often mentioned together or possibly trigger each other. Coherence within a cluster was considered appropriate, because, for instance, microstomia complicates oral hygiene and hence promotes a disease of the periodontium. The mere presence of a symptom contains no information about its severity and intensity and therefore its effect on the OHRQoL.

4.2. Interpretation

In a representative study of the whole German population, an OHIP value of 4.09 points was established [19]. The participants of our study show a considerably worse OHRQoL than the general population.
If one considers the confidence intervals of the total German population, there is a significant difference from the people with rare diseases in our study. The confidence interval among patients with implanted dentures was between 10 and 12 points in the 90%. In our study, the confidence intervals only start at 12.6 points in clusters 1–4. Therefore, there are no overlaps of the intervals, which means significantly worse OHIP scores among people with rare diseases and oral symptoms.
The confidence intervals very slightly overlap in the lower boundary in cluster 5. The values tend to approach the 90th percentile of patients with removable dentures. The confidence interval there is between 15 and 19 points. It should be noted here that these are the worst 10% values in the total population, while these only correspond to the average values among people with rare diseases. However, maximum values of 56 points were also indicated in the current sample, which shows how strongly people with rare diseases can be impaired in their OHRQoL.
Our values also display strong scattering. For instance, the standard deviation in cluster 2 is 17 points. This means people in this cluster differ from the mean of 20 OHIP points by 17 points on average, which means 3–37 points. The participants with 3 points report a somewhat low impact on OHRQoL, while participants with 37 points report a high impact on OHRQoL [19].
The average OHIP total score was an average of between 15.1 and 19.9 of 56 possible OHIP points across all clusters. It is useful to understand what 1 OHIP point stands for. Reissmann et al. [23] have investigated how many events are necessary for 1 more OHIP point to be added by participants. The OHIP-49 questionnaire was used for their study, which does not allow for a direct comparison to the present study, but it does give an impression of the considerably reduced OHRQoL. They concluded that a total of 15.2 events are required in a month on average for the OHIP total score to increase by one point. Therefore, a person must interrupt a meal, feel unwell, or have pain an average of 15.2 times per month for the OHIP score to rise by 1 point. This means that the person must struggle with this constraint every two days.
Clearly, all symptoms are accompanied by reduced OHRQoL. The method of cluster analysis was chosen so that, without the influence of the principal investigators, it could be discovered which symptom combinations were indicated together in order to then describe varying OHRQoL between the groups.
Cluster analysis seems to be a suitable option for finding symptomatically homogeneous groups in larger samples regarding rare diseases [17]. In all the formed clusters, the OHIP total score has a mean value between 15.1 and 16.9 points; only in cluster 2 (diseases of the oral mucosa, diseases of the periodontium, and microstomia) is the mean value considerably above that at 19.9 and thus describes worse OHRQoL. This can be explained by the fact that diseases of the periodontium and diseases involving the oral mucosa, such as recurrent aphtous stomatitis [24] or epidermolysis bullosa, which is also accompanied by a restricted mouth opening, lead to pain and functional limitations and thus negatively influence the OHRQoL [25]. A microstomia, as can appear in scleroderma for instance, complicates oral hygiene in turn and thus favors the occurrence of periodontal diseases. A small mouth opening can also complicate or limit food intake and even make dental treatment problematic [25]. It is therefore plausible that rare diseases involving the oral mucosa, the periodontium, and a limited mouth opening may be accompanied by reduced OHRQoL.
The other clusters vary only marginally in the OHIP mean values. The symptom anomalies of tooth formation and mineralization disorders of the dental hard tissue grouped in cluster 1 resulted in an average OHIP total score of 15.9 (Table 3). Anomalies of tooth formation, such as microdontia, macrodontia, conical teeth, and taurodontism, lead to aesthetic restrictions, which negatively impact social life [26] and may require dento-aesthetic rehabilitation [27]. Mineralization disorders of the dental hard tissue, such as amelogenesis imperfecta and dentinogenesis imperfecta, not only lead to higher susceptibility to caries but may also cause pain and aesthetic limitations and negatively impact the confidence of the patients thus resulting in reduced OHRQoL [28].
The mean value of 16.9 was seen in cluster 3, where anomalies of tooth formation appear in conjunction with changes in the number of teeth and cleft lip and palate. The combination of multiple dental agenesis, anomalies of tooth formation, and cleft lip and palate has often been reported [29] and occurs generically in the Ectrodactyly–Ectodermal Dysplasia–Cleft Lip/Palate (EEC) syndrome [30]. Patients with congenital dental agenesis thus benefit with regard to their OHRQoL from dento-prosthetic rehabilitation, especially if the dentures are anchored to dental implants [31]. It is well documented that improvement of OHRQoL can be achieved through dental implants [32,33]. By contrast, if there has been no dento-prosthetic treatment for multiple dental agenesis, OHRQoL is considerably worse [34]. Cleft lip and palate lead to aesthetic and functional impairments, especially in food intake and articulation and negatively affect OHRQoL [35]. It therefore seems plausible that, among people with anomalies of tooth formation, dental agenesis, and cleft lip and palate, not only aesthetic and psychosocial impairments but also functional limitations can negatively influence OHRQoL.
The symptoms of temporomandibular dysfunction, vegetative disorders, and neurological diseases are presented in cluster 4. Shooting pain several times daily, as occurs in trigeminal neuralgia, negatively impacts OHRQoL just like temporomandibular dysfunctions, with the resulting pain and functional limitations [36,37]. A reduced rate of saliva flow (hyposalivation) or the absence of saliva flow (xerostomia) also has a negative effect on OHRQoL [38]. Rare diseases such as Sjögren syndrome, which are accompanied by a reduced rate of saliva flow, also show high rates of caries, which are caused wholly or partly by reduced saliva flow [39]. The OHIP total score was an average of 16.9 in cluster 4. Due to the considerable severity of some of the symptoms (shooting pain in the area surrounding the trigeminal nerve in trigeminal neuralgia, as well as food intake complicated by mouth dryness and the often-existing mucositis), it would have been expected that particularly high OHIP values would be seen in this cluster. However, the mean value of 16.9 is only slightly higher than that in clusters 1, 3, and 5 (15.9, 16.9, 15.1) and is lower than the values of cluster 2. A possible reason for this is data heterogeneity. Another possible reason is symptom specificity. There was no question about the severity of the symptom, which is a subjective statement from the participants.
Dysgnathia, in combination with malocclusions, displayed the lowest mean value of the OHIP total score at 15.19, as seen in cluster 5. Therefore, in this sample, dysgnathia and malocclusions affect OHRQoL less negatively than symptoms in other clusters. A possible explanation could be that only slight forms of dysgnathia or malocclusion were present among the participants of the study, because the negative influence on OHRQoL increases with the severity of the malocclusion [40].
In general, worse oral health of people with rare diseases could be reported in this study, as it is known in single rare diseases such as lysosomal storage disease [41].
In the future, more nuanced surveys, with higher numbers of cases for individual rare diseases and estimates for the severity of the symptoms, are still necessary in order to evaluate the OHRQoL more specifically.

5. Conclusions

All investigated symptoms are associated with relatively low OHRQoL. The symptoms related to diseases of the periodontium, diseases of the oral mucosa, and microstomia are associated with lower OHRQoL in people with rare diseases. Cluster analysis is a suitable method for creating symptom groups. All symptoms described in this cluster analysis may lead to considerably higher mean values of the OHIP total score among people with rare diseases and thus to worse OHRQoL than are described in the average population.

Supplementary Materials

The following are available online at https://www.mdpi.com/1660-4601/15/7/1493/s1, Table S1: Original version of the questionnaire.

Author Contributions

Conception and study design: S.W., M.H., and J.K; Evaluation of the questionnaires and statistical analysis: S.W.; Statistical advice: N.F.B., R.A.J., M.H., and J.K. helped in the interpretation of data. S.W. and M.H. participated in the design and drafting of the manuscript. All the authors read and approved the final manuscript.

Funding

This research received no external funding.

Acknowledgments

The authors thank all the support groups and the umbrella organization ACHSE e.V. for their study participation.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Regulation (EC) No 141/2000 of the European Parliament and of the Concil of 16 December 1999 on Orphan Medical Products. Available online: http://ec.europa.eu/health/files/eurdralex/vol.1/reg_2004141cons-2009-07/reg200141cons-2009-07en.pdf (accessed on 2 April 2018).
  2. European Commission on Rare Diseases. Available online: https://ec.europa.eu/health/rare_diseases/policy_en (accessed on 27 March 2018).
  3. Bundesministerium für Gesundheit. Prävention: Seltene Erkrankungen. 2013. Available online: http://www.bmg.bund.de/praevention/gesundheitsgefahren/selteneerkrankungen.html (accessed on 27 March 2018).
  4. Online Mendeline Inheritance of Man. Available online: https://www.omin.org (accessed on 2 April 2018).
  5. Jackowski, J.; Hanisch, M. Orofacial manifestations in 2006 rare diseases—A preliminary systematiy review of the literature. J. Ger. Soc. Dent. Oral Med. 2012, 67, D10. [Google Scholar]
  6. Hennekam, R.C.M.; Allanson, J.E.; Krantz, I.D.; Gorlin, R.J. Gorlin’s Syndromes of the Head and Neck, 5th ed.; Oxford University Press: New York, NY, USA, 2010. [Google Scholar]
  7. Hanisch, M.; Jung, S.; Kleinheinz, J. Oral Health-Related Quality of Life in Rare Diseases with Oral Manifestations. Gesundheitswesen 2018. [Google Scholar] [CrossRef]
  8. The Council of the European Union. Council Recommendation of 8 June 2009 on an Action in the Field of Rare Diseases (2009/C 151/02). Official Journal of the European Union. Available online: http://eur-lex.europe.eu/LEXUriServ.do?uri=OJ.C:2009:151:0007:0010:EN:PDF (accessed on 3 March 2018).
  9. Nationaler Aktionsplan für Menschen mit Seltenen Erkrankungen: Handlungsfelder, Empfehlungen und Maßnahmenvorschläge. BMG, BMBF, ACHSEe.V. 2013. Available online: http://www.namse.de/images/stories/Dokumente/Aktionsplan/national%20plan%20of %20action.pdf (accessed on 30 March 2018).
  10. Berglund, B.; Björck, E. Women with Ehlers-Danlos Syndrome Experience Low Oral Health-Related Quality of Life. J. Orofac. Pain 2012, 26, 307–314. [Google Scholar] [PubMed]
  11. Toupenay, S.; Razanamihaja, N.; Berdal, A.; Boy-Lefevre, M.L. Rare diseases with oral components: Care course and quality of life. Community Dent. Health 2013, 30, 10–14. [Google Scholar] [PubMed]
  12. Slade, G.D. Derivation and validation of a short-Form oral health impact profile. Community Dent. Oral Epidemiol. 1997, 25, 284–290. [Google Scholar] [CrossRef] [PubMed]
  13. John, M.T.; Micheelis, W. Mundgesundheitsbezogene Lebensqualität in der Bevölkerung: Grundlagen und Ergebnisse des OHIP aus einer repräsentativen Stichprobe in Deutschland. IDZ-Inf. 2003, 1, 1–28. [Google Scholar]
  14. Schmitt-Sausen, N. Tag der Seltenen Erkrankungen: Mehr Aufmerksamkeit für Waisenkinder der Medizin. Dtsch. Arztebl. 2010, 107, A-430/B-381/C-373. [Google Scholar]
  15. Hanisch, M.; Fröhlich, L.F.; Kleinheinz, J. Gingival hyperplasia as first sign of recurrence of granulomatosis with polyangiitis (Wegener´s granulomatosis): Case report and review of the literature. BMC Oral Health 2017, 17, 33. [Google Scholar] [CrossRef] [PubMed]
  16. John, M.T.; Miglioretti, D.L.; LeResche, L.; Koepsell, T.D.; Hujoel, P.; Micheelis, W. German short forms of the Oral Health Impact Profile. Community Dent. Oral Epidemiol. 2006, 34, 277–288. [Google Scholar] [CrossRef] [PubMed]
  17. Janssen, J.; Laatz, W. Statistische Analyse mit SPSS-Eine Anwendungsorientierte Einführung in das Basissystem und das Modul Exakte Tests; Springer: Berlin/Heidelberg, Germany, 2017; p. 281. ISBN 978-3-662-534779. [Google Scholar]
  18. List of Rare Diseases and Synonyms in Alphabetical Order. January 2018 Version. Available online: http://www.orpha.net/consor4.01/www/cgibin/Education_Home.php?lng=DE#REPORT_RARE_DISEASES (accessed on 28 March 2018).
  19. John, M.T.; Micheelis, W.; Biffar, R. Norrmwerte Mundgesundheitsbezogener Lebensqualität für Kurzversionen des OHIP. Schweiz. Monatsschr. Zahnmed. 2004, 114, 784–791. [Google Scholar] [PubMed]
  20. Bogart, K.R.; Irvin, V.L. Health-realted quality of life among adults with diverse rare disorders. Orphanet J. Rare Dis. 2017, 12, 177. [Google Scholar] [CrossRef] [PubMed]
  21. Wetterauer, B.; Schuster, R. Seltene Krankheiten: Probleme, Stand und Entwicklung der nationalen und europäischen Forschungsförderung. Bundesgesundheitsblatt 2008, 51, 519. [Google Scholar] [CrossRef] [PubMed]
  22. Rare Diseases: Understanding this Public Health Priority. Available online: https://www.eurordis.org/IMG/pdf/princeps_document-EN.pdf (accessed on 29 March 2018).
  23. Reissmann, D.R.; Sierwald, I.; Heydecke, G.; John, M.T. Interpreting one oral health impact profile point. Health Qual. Life Outcomes 2013, 11, 12. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Tabolli, S.; Bergamo, F.; Alessandroni, L.; Di Pietro, C.; Sampogna, F.; Abeni, D. Quality of Life and psychological problems of patients with oral mucosal disease in dermatological practice. Dermatology 2009, 218, 314–320. [Google Scholar] [CrossRef] [PubMed]
  25. Fine, J.D. Inherited epidermolysis bullosa. Orphanet J. Rare Dis. 2010, 5, 12. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Faekonja, A. Prevalence of dental developmental anomalies of permanent teeth in children and their influence on esthetics. J. Esthet. Restor. Dent. 2017, 29, 276–283. [Google Scholar] [CrossRef] [PubMed]
  27. Samorodnitzky-Naveh, G.R.; Geiger, S.B.; Levin, L. Patients satisfaction with dental esthetics. J. Dent. 2012, 40, 624–631. [Google Scholar] [CrossRef]
  28. Lundgren, G.P.; Karsten, A.; Dahllöf, G. Oral health-related quality of life beforeand after crown therapy in young patients with amelogenesis imperfect. Health Qual. Life Outcomes 2015, 13, 197. [Google Scholar] [CrossRef] [PubMed]
  29. Hausamen, J.E.; Machtens, E.; Reuther, J.F.; Eufinger, H.; Kübler, A.; Schliephake, H. Mund-Kiefer-Gesichtschirurgie-Operationslehre und Atlas, 4th ed.; Springer: Berlin/Heidelberg, Germany, 2012; pp. 309–364. ISBN 978-3-642-17801-6. [Google Scholar]
  30. Sharma, G.; Nagpal, A. Oral health considerations in a patient with oligosymptomatic ectrodactyly-ectodermal dysplasia-cleft syndrome. Gen. Dent. 2017, 65, 66–69. [Google Scholar] [PubMed]
  31. Terheyden, H.; Wüsthoff, F. Occlusal rehabilitation in patients with congenitally missing teeth-dental implants, conventional prosthetics, tooth autotransplants, and preservation of deciduous teeth-a systematic review. Int. J. Implant Dent. 2015, 1, 30. [Google Scholar] [CrossRef] [PubMed]
  32. Fischer, K.R.; Lindner, I.; Fickl, S. Implant treatment in periodontally compromised subjety-quality of life and patient satisfaction. Clin. Oral Investig. 2016, 20, 697–702. [Google Scholar] [CrossRef] [PubMed]
  33. Filius, M.A.; Vissink, A.; Cune, M.S.; Raghoebar, G.M.; Visser, A. Long-term implant performance and patients’ satisfaction in oligodontia. J. Dent. 2018, 71, 18–24. [Google Scholar] [CrossRef] [PubMed]
  34. Hashem, A.; Kelly, A.; O’Connell, B.; O’Sullivan, M. Impact of moderate and severe hypodontia and amelogenesis imperfecta on quality of life and self-esteem of adult patients. J. Dent. 2013, 41, 689–694. [Google Scholar] [CrossRef] [PubMed]
  35. Stelzle, F.; Rohde, M.; Oetter, N.; Krug, K.; Riemann, M.; Adler, W.; Neukam, F.W.; Knipfer, C. Gingival esthetics and oral health-related quality of life in patients with cleft lip and palate. Int. J. Oral Maxillofac. Surg. 2017, 46, 993–999. [Google Scholar] [CrossRef] [PubMed]
  36. Shueb, S.S.; Nixdorf, D.R.; John, M.T.; Alonso, B.F.; Durham, J. What is the impact of acute and chronic orofacial pain on quality of life? J. Dent. 2015, 43, 1203–1210. [Google Scholar] [CrossRef] [PubMed]
  37. Lemos, G.A.; Paulino, M.R.; Forte, F.D.S.; Beltrão, R.T.S.; Batista, A.U.D. Influence of temporomandibular disorder presence an severity on oral- health- related Quality of Life. Rev. Dor 2015, 16, 10–14. [Google Scholar] [CrossRef]
  38. Niklander, S.; Veas, L.; Barrera, C.; Fuentes, F.; Chiappini, G. Marshall, M. Risk factors, hyposalivation and impact of xerostomia on oral health-related quality of life. Braz. Oral Res. 2017, 31, e14. [Google Scholar] [CrossRef] [PubMed]
  39. Xin, W.; Leung, K.C.M.; Lo, E.C.M.; Mok, M.Y.; Leung, M.H. A randomized, double-blind, placebo-controlled clinical trial of fluoride varnish in preventing dental caries of Sjögren’s syndrome patients. BMC Oral Health 2016, 16, 102. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  40. Sun, L.; Wong, H.M.; McGrath, C.P.; Sun, L.; Wong, H.M. Relationship between the Severity of Malocclusion and Oral Health Related Quality of Life: A Systematic Review and Meta-analysis. Oral Health Prev. Dent. 2017, 15, 503–517. [Google Scholar] [PubMed]
  41. Drążewski, D.; Grzymisławska, M.; Korybalska, K.; Czepulis, N.; Grzymisławski, M.; Witowski, J.; Surdacka, A. Oral Health Status of Patients with Lysosomal Storage Diseases in Poland. Int. J. Environ. Res. Public Health 2017, 14, 281. [Google Scholar] [CrossRef] [PubMed]
Ijerph 15 01493 g001 550
Figure 1. Boxplots of OHIP total score in each cluster.
Figure 1. Boxplots of OHIP total score in each cluster.
Ijerph 15 01493 g001
Table
Table 1. Commonly presented diseases in the present study (n ≥10).
Table 1. Commonly presented diseases in the present study (n ≥10).
Name of DiseaseOMIM NumberNumber of Individuals
Marfan Syndrome15470051
Ectodermal Dysplasia30510046
Achalasia23155044
Sarcoidosis18100036
Ehlers–Danlos Syndrome12018032
Lymphangioleiomyomatosis60669017
Alpha-1-Antitrypsin Deficiency61349015
Syringomyelia11842013
X-linked Hypophosphatemia30780013
Table
Table 2. Prevalences of the analyzed symptoms in the sample (%).
Table 2. Prevalences of the analyzed symptoms in the sample (%).
SymptomsPrevalence (%)
Anomalies of the Tooth Formation 24.4
Dysgnathia18.4
Changes in Number of the Teeth13.6
Malocclusion12.4
Oral Mucosa Disease9.5
Mineralization Disorders of the Hard Tissue of the Teeth9.3
Temperomandibular Dysfunction5.4
Disease of the Periodontium5.4
Vegetative Disorders3.1
Neurological Disease2.1
Cleft Lip and Palate1.7
Microstomia1.2
Table
Table 3. Categorization of the five clusters with symptom prevalence in each cluster in % and Oral Health Impact Profile-14 (OHIP-14) mean, standard deviation, minimum, and maximum. For reference: mean OHIP total score of the general German population is 4.09 [19].
Table 3. Categorization of the five clusters with symptom prevalence in each cluster in % and Oral Health Impact Profile-14 (OHIP-14) mean, standard deviation, minimum, and maximum. For reference: mean OHIP total score of the general German population is 4.09 [19].
ClustersSymptom Prevalence in Each Cluster (%)Number of Individuals in Each ClusterOHIP Mean (Minimum; Maximum)OHIP Standard Deviation
Cluster 1Anomalies of the Tooth Formation: 98%
Mineralization Disorders of the Hard Tissue of the Teeth: 70%		6315.9 (0;52)13.1
Cluster 2Oral Mucosa Disease: 83%
Disease of the Periodontium: 34%
Microstomia: 14%		3519.7 (0;56)17.1
Cluster 3Changes in the Number of the Teeth: 100%
Anomalies of the Tooth Formation: 96%
Cleft Lip/Palate: 7%		5616.9 (0;56)14.5
Cluster 4Temporomandibular Dysfunctions: 31%
Vegetative Disorders: 16%
Neurological Diseases: 15%		5516.9 (0;56)14.3
Cluster 5Dysgnathia: 100%
Malocclusion: 54%		4815.1 (0;56)12.4

Share and Cite

MDPI and ACS Style

Wiemann, S.; Frenzel Baudisch, N.; Jordan, R.A.; Kleinheinz, J.; Hanisch, M. Oral Symptoms and Oral Health-Related Quality of Life in People with Rare Diseases in Germany: A Cross-Sectional Study. Int. J. Environ. Res. Public Health 2018, 15, 1493. https://doi.org/10.3390/ijerph15071493

AMA Style

Wiemann S, Frenzel Baudisch N, Jordan RA, Kleinheinz J, Hanisch M. Oral Symptoms and Oral Health-Related Quality of Life in People with Rare Diseases in Germany: A Cross-Sectional Study. International Journal of Environmental Research and Public Health. 2018; 15(7):1493. https://doi.org/10.3390/ijerph15071493

Chicago/Turabian Style

Wiemann, Sabrina, Nicolas Frenzel Baudisch, Rainer A. Jordan, Johannes Kleinheinz, and Marcel Hanisch. 2018. "Oral Symptoms and Oral Health-Related Quality of Life in People with Rare Diseases in Germany: A Cross-Sectional Study" International Journal of Environmental Research and Public Health 15, no. 7: 1493. https://doi.org/10.3390/ijerph15071493

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop