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Oral health-related quality of life of young people with mucopolysaccharidosis: a paired cross-sectional study

Abstract

The purpose of the present study was to compare the perceptions of the parents/ caregivers of young people with and without Mucopolysaccharidosis (MPS) with regards to their oral health-related quality of life (OHRQoL). A cross-sectional study was conducted with 29 individuals with MPS and 29 normotypic individuals aged three to 21 years and their parents/caregivers. All parents/caregivers of young people with MPS in follow-up at two reference hospitals in the city of Belo Horizonte, southeastern Brazil, were invited to participate in the study. Individuals without MPS were recruited from the pediatric clinics of both hospitals. Parents/caregivers answered a structured questionnaire addressing the sociodemographic characteristics, behavioral habits and medical and dental history of the children as well as the Brazilian short-form version of the Parental-Caregiver (P-CPQ). The individuals with and without MPS were examined for malocclusion, dental caries and oral hygiene by an examiner who had undergone training and calibration exercises. Mean age of the subjects was 12.1 years (± 4.2). Comparing total P-CPQ scores and scores on the oral symptoms, functional limitations and wellbeing domains, the parents/caregivers individuos with MPS reported a statistically significant greater negative impact on OS domain than their counterparts. Regarding the clinical variables, malocclusion was also associated a greater negative impact on OHRQoL of young people with MPS when compared to those of young people without MPS. Our findings show the great negative impact caused by the malocclusion of young people with MPS.

Mucopolysaccharidosis; Rare Diseases; Quality of Life; Oral Health; Dental Care for Disabled

Introduction

Mucopolysaccharidoses (MPS) are a group of rare genetic diseases caused by an enzyme inadequacy in the lysosomes of the organism. The absence or malfunctioning of these enzymes causes the non-degradation of glycosaminoglycans (GAG) and their consequent deposition within the lysosomes. The accumulation of GAG in the cell promotes progressive clinical manifestations that affect several organs.11. Neufeld EF, Muenzer J. The mucopolisaccharidosis. In: Scriver CR, Beandet AL, Sly S, Valle D, Childs B, Kinzler KW, editores. The metabolic and molecular basis of inherited disease. 8th ed. New York: McGraw-Hill; 2001. p. 3421-52.,22. Giugliani R, Federhen A, Muñoz Rojas MV, Vieira TA, Artigalás O, Pinto LL, et al. [Enzyme replacement therapy for mucopolysaccharidoses I, II and VI: recommendations from a group of Brazilian F experts]. Rev Assoc Med Bras (1992). 2010 May-Jun;56(3):271-7. Portuguese. https://doi.org/10.1590/S0104-42302010000300009
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,33. Khan SA, Peracha H, Ballhausen D, Wiesbauer A, Rohrbach M, Gautschi M, et al. Epidemiology of mucopolysaccharidoses. Mol Genet Metab. 2017 Jul;121(3):227-40. https://doi.org/10.1016/j.ymgme.2017.05.016
https://doi.org/10.1016/j.ymgme.2017.05....

MPS is a musculoskeletal disease, the classification of which is based on enzyme deficiency. The absence or malfunctioning of 11 enzymes is responsible for seven different types of the disease (MPS I, II, III, IV, VI, VII and IX). The overall incidence of MPS is estimated to range from 1:25,000 to 1:52,000 live births.11. Neufeld EF, Muenzer J. The mucopolisaccharidosis. In: Scriver CR, Beandet AL, Sly S, Valle D, Childs B, Kinzler KW, editores. The metabolic and molecular basis of inherited disease. 8th ed. New York: McGraw-Hill; 2001. p. 3421-52.,22. Giugliani R, Federhen A, Muñoz Rojas MV, Vieira TA, Artigalás O, Pinto LL, et al. [Enzyme replacement therapy for mucopolysaccharidoses I, II and VI: recommendations from a group of Brazilian F experts]. Rev Assoc Med Bras (1992). 2010 May-Jun;56(3):271-7. Portuguese. https://doi.org/10.1590/S0104-42302010000300009
https://doi.org/10.1590/S0104-4230201000...
,33. Khan SA, Peracha H, Ballhausen D, Wiesbauer A, Rohrbach M, Gautschi M, et al. Epidemiology of mucopolysaccharidoses. Mol Genet Metab. 2017 Jul;121(3):227-40. https://doi.org/10.1016/j.ymgme.2017.05.016
https://doi.org/10.1016/j.ymgme.2017.05....
In Brazil, 1069 individuals with MPS were identified between 2004 and 2013.33. Khan SA, Peracha H, Ballhausen D, Wiesbauer A, Rohrbach M, Gautschi M, et al. Epidemiology of mucopolysaccharidoses. Mol Genet Metab. 2017 Jul;121(3):227-40. https://doi.org/10.1016/j.ymgme.2017.05.016
https://doi.org/10.1016/j.ymgme.2017.05....
,44. Federhen A, Batista CC, Burin M, Leistner-Segal S, Matte U, Rafaelli C, et al. MPS I and MPS II: minimal estimated incidence in Brazil and comparison to the rest of the world. Mol Genet Metab. 2015;114(2):43. https://doi.org/10.1016/j.ymgme.2014.12.082
https://doi.org/10.1016/j.ymgme.2014.12....

Some signs and symptoms are characteristic and common to different types of MPS, such as typical facies, excessive body hair growth, short stature, visual impairment, cardiopathy, sleep apnea, neurological problems, skeletal distention, corneal opacification, inguinal and abdominal hernias, enlarged liver and spleen, hearing impairment, respiratory problems, progressive joint limitation, enlarged tongue and abnormalities in the number and shape of the teeth.11. Neufeld EF, Muenzer J. The mucopolisaccharidosis. In: Scriver CR, Beandet AL, Sly S, Valle D, Childs B, Kinzler KW, editores. The metabolic and molecular basis of inherited disease. 8th ed. New York: McGraw-Hill; 2001. p. 3421-52.,22. Giugliani R, Federhen A, Muñoz Rojas MV, Vieira TA, Artigalás O, Pinto LL, et al. [Enzyme replacement therapy for mucopolysaccharidoses I, II and VI: recommendations from a group of Brazilian F experts]. Rev Assoc Med Bras (1992). 2010 May-Jun;56(3):271-7. Portuguese. https://doi.org/10.1590/S0104-42302010000300009
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,55. Guimarães MC, de Farias SM, Costa AM, de Amorim RF. Maroteaux-Lamy syndrome: orofacial features after treatment by bone marrow transplant. Oral Health Prev Dent. 2010;8(2):139-42.,66. Gönüldaş B, Yılmaz T, Sivri HS, Güçer KŞ, Kılınç K, Genç GA, et al. Mucopolysaccharidosis: otolaryngologic findings, obstructive sleep apnea and accumulation of glucosaminoglycans in lymphatic tissue of the upper airway. Int J Pediatr Otorhinolaryngol. 2014 Jun;78(6):944-9. https://doi.org/10.1016/j.ijporl.2014.03.021
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The main oral problems described in individuals with MPS are abnormalities in the number and anatomy of the primary and permanent teeth, enamel defects (primary and permanent teeth), delayed eruption of permanent teeth, impacted teeth, diastema, malocclusion (especially anterior open bite and crossbite), protruding tongue, a lack of lip seal, mouth breathing, limited mouth opening, bruxism and dental caries.77. Ribeiro EM, Fonteles CS, Freitas AB, Alves KSS, Monteiro AJ, Silva CA. A clinical multicenter study of orofacial features in 26 brazilian patients with different types of mucopolysaccharidosis. Cleft Palate Craniofac J. 2015 May;52(3):352-8. https://doi.org/10.1597/13-204
https://doi.org/10.1597/13-204...
,88. Sarmento DJ, Araújo TK, Mesquita GQ, Diniz DN, Fonseca FRA, Medeiros PF, et al. Relationship between occlusal features and enzyme replacement therapy in patients with mucopolysaccharidoses. J Oral Maxillofac Surg. 2018 Apr;76(4):785-92. https://doi.org/10.1016/j.joms.2017.10.003
https://doi.org/10.1016/j.joms.2017.10.0...
,99. Almeida-Barros RQ, Medeiros PF, Azevedo MQA, Lira Ortega AO, Yamamoto AT, Dornelas SK, et al. Evaluation of oral manifestations of patients with mucopolysaccharidosis IV and VI: clinical and imaging study. Clin Oral Investig. 2018 Jan;22(1):201-8. https://doi.org/10.1007/s00784-017-2100-8
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,1010. Ballıkaya E, Eymirli PS, Yıldız Y, Avcu N, Sivri HS, Uzamış-Tekçiçek M. Oral health status in patients with mucopolysaccharidoses. Turk J Pediatr. 2018;60(4):400-6. https://doi.org/10.24953/turkjped.2018.04.007
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,1111. Prado HV, Carneiro NC, Perazzo MF, Abreu MH, Martins CC, Borges-Oliveira AC. Assessing a possible vulnerability to dental caries in individuals with rare genetic diseases that affect the skeletal development. Orphanet J Rare Dis. 2019 Jun;14(1):145. https://doi.org/10.1186/s13023-019-1114-5
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Oral health plays a fundamental role in the lives of individuals with MPS, as oral diseases may result in infection as well as nutritional, respiratory, chewing and speech problems, compounding their already severely weakened state of general health.55. Guimarães MC, de Farias SM, Costa AM, de Amorim RF. Maroteaux-Lamy syndrome: orofacial features after treatment by bone marrow transplant. Oral Health Prev Dent. 2010;8(2):139-42.,1111. Prado HV, Carneiro NC, Perazzo MF, Abreu MH, Martins CC, Borges-Oliveira AC. Assessing a possible vulnerability to dental caries in individuals with rare genetic diseases that affect the skeletal development. Orphanet J Rare Dis. 2019 Jun;14(1):145. https://doi.org/10.1186/s13023-019-1114-5
https://doi.org/10.1186/s13023-019-1114-...
,1212. Fonseca FR, de Santana Sarmento DJ, Vasconcelos Medeiros PF, Diniz DN, Santos MT. Patients with mucopolysaccharidosis have tendencies towards vertical facial growth. J Oral Maxillofac Surg. 2014 Dec;72(12):2539-46. https://doi.org/10.1016/j.joms.2014.07.006
https://doi.org/10.1016/j.joms.2014.07.0...
,1313. Soni-Jaiswal A, Mercer J, Jones SA, Bruce IA, Callery P. Mucopolysaccharidosis I; Parental beliefs about the impact of disease on the quality of life of their children. Orphanet J Rare Dis. 2016 Jul;11(1):96. https://doi.org/10.1186/s13023-016-0478-z
https://doi.org/10.1186/s13023-016-0478-...
,1414. Wiemann S, Baudisch NF, 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. Int J Environ Res Public Health. 2018 Jul;15(7):15-27. https://doi.org/10.3390/ijerph15071493
https://doi.org/10.3390/ijerph15071493...

Oral health-related quality of life (OHRQoL) regards the impact of oral problems on aspects of daily living.1515. Jokovic A, Locker D, Stephens M, Kenny D, Tompson B, Guyatt G. Measuring parental perceptions of child oral health-related quality of life. J Public Health Dent. 2003;63(2):67-72. https://doi.org/10.1111/j.1752-7325.2003.tb03477.x
https://doi.org/10.1111/j.1752-7325.2003...
The magnitude of impact in terms of frequency, severity or duration can affect an individual’s perception of his or her life in general. The presence of oral problems can negatively affect the OHRQoL of MPS patients. Many of problems can also impair the performance of their daily activities. This happens because these conditions are often associated with pain, discomfort and aesthetic change.1010. Ballıkaya E, Eymirli PS, Yıldız Y, Avcu N, Sivri HS, Uzamış-Tekçiçek M. Oral health status in patients with mucopolysaccharidoses. Turk J Pediatr. 2018;60(4):400-6. https://doi.org/10.24953/turkjped.2018.04.007
https://doi.org/10.24953/turkjped.2018.0...
,1616. Raluy-Callado M, Chen WH, Whiteman DA, Fang J, Wiklund I. The impact of Hunter syndrome (mucopolysaccharidosis type II) on health-related quality of life. Orphanet J Rare Dis. 2013 Jul;8(1):101. https://doi.org/10.1186/1750-1172-8-101
https://doi.org/10.1186/1750-1172-8-101...

Radiological and oral changes are very common in individuals with MPS. These changes in individual with MPS may impair mouth opening, chewing and eating. These changes can negatively impact the quality of life of these individuals. Regular follow-up, preventive applications and dental treatments must be included in the approach of the multidisciplinary team of patients with MPS. These actions can provide better oral health.1010. Ballıkaya E, Eymirli PS, Yıldız Y, Avcu N, Sivri HS, Uzamış-Tekçiçek M. Oral health status in patients with mucopolysaccharidoses. Turk J Pediatr. 2018;60(4):400-6. https://doi.org/10.24953/turkjped.2018.04.007
https://doi.org/10.24953/turkjped.2018.0...

To the best of our knowledge, there are no previous reports addressing the impact of the nature and severity of MPS on OHRQoL. As individuals with MPS have systemic characteristics of motor and neurological impairment, it is important to know how these characteristics affect quality of life.55. Guimarães MC, de Farias SM, Costa AM, de Amorim RF. Maroteaux-Lamy syndrome: orofacial features after treatment by bone marrow transplant. Oral Health Prev Dent. 2010;8(2):139-42.,1313. Soni-Jaiswal A, Mercer J, Jones SA, Bruce IA, Callery P. Mucopolysaccharidosis I; Parental beliefs about the impact of disease on the quality of life of their children. Orphanet J Rare Dis. 2016 Jul;11(1):96. https://doi.org/10.1186/s13023-016-0478-z
https://doi.org/10.1186/s13023-016-0478-...
,1515. Jokovic A, Locker D, Stephens M, Kenny D, Tompson B, Guyatt G. Measuring parental perceptions of child oral health-related quality of life. J Public Health Dent. 2003;63(2):67-72. https://doi.org/10.1111/j.1752-7325.2003.tb03477.x
https://doi.org/10.1111/j.1752-7325.2003...
,1616. Raluy-Callado M, Chen WH, Whiteman DA, Fang J, Wiklund I. The impact of Hunter syndrome (mucopolysaccharidosis type II) on health-related quality of life. Orphanet J Rare Dis. 2013 Jul;8(1):101. https://doi.org/10.1186/1750-1172-8-101
https://doi.org/10.1186/1750-1172-8-101...
,1717. Needham M, Packman W, Quinn N, Rappoport M, Aoki C, Bostrom A, et al. MPS II: adaptive behavior of patients and impact on the family system. J Genet Couns. 2015;24(4):635-44. https://doi.org/10.1007/s10897-013-9665-4
https://doi.org/10.1007/s10897-013-9665-...
,1818. Hendriksz CJ, Lavery C, Coker M, Ucar SK, Jain M, Bell L, et al. The burden endured by caregivers of patients with morquio a syndrome: results from an international patient-reported outcomes survey. J Inborn Errors Metab Screen. 2014;2:e140003. https://doi.org/10.1177/2326409814540872
https://doi.org/10.1177/2326409814540872...

To fill this gap in knowledge, the aim of the present study was to compare the perceptions of parents/caregivers regarding the OHRQoL of young people with and without MPS.

Methods

Study design and sample characteristics

A paired cross-sectional study was carried out with 58 individuals divided into two groups (29 with MPS and 29 without MPS) and their respective parents/caregivers. The individuals with MPS was recruited from two public hospitals in the city of Belo Horizonte, southeastern Brazil. Both hospitals are reference centers for the disease. The diagnosis of MPS was recorded on medical records made available for the present study. All parents and caregivers of these individuals were contacted either in person or by telephone, received clarifications regarding the objectives of the study and were invited to participate. Individuals without MPS were recruited from among patients awaiting routine appointments at the pediatric outpatient clinics of the same hospitals. These individuals had no chronic diseases or physical or mental disabilities.

The OpenEpi® statistical software (Dean, Sullivan and Soe; OpenEpi: Open Source Epidemiological Statistics for Public Health, http://www.OpenEpi.com) was used to calculate the test power for the sample of 29 individuals with MPS. For such, a significance level of 0.05 and test power of 0.80 were considered. Moreover, prevalence values of occlusal problems were obtained from the pilot study (68.0% among individuals with MPS and 32.0% among those without MPS).

Non-clinical data collection

Parents/caregivers who agreed to participate in the study with their children provided written informed consent. This study received approval from the Human Research Ethics Committee of the 255.475.

The parents/caregivers answered a pre-structured questionnaire addressing the sociodemographic characteristics (sex, age, economic status, parent’s/caregiver’s age and parent’s/caregiver’s schooling). The economic status of the family and educational level (years of study) of the parents/caregivers were evaluated using the Brazilian line Economic Classification,1919. Associação Brasileira de Empresas de Pesquisa – ABEP. Critério de classificação econômica Brasil. São Paulo: Associação Brasileira de Empresas de Pesquisa; 2015 [cited 2019 Dec]. Available from: http://www.abep.org/codigos-e-guias-da-abep
http://www.abep.org/codigos-e-guias-da-a...
grouping the participants into higher (classes A and B), middle (class C) and lower (classes D and E) economic classes.

The parents/caregivers were answered using the short form of the Parental-Caregiver Perceptions Questionnaire (P-CPQ)1515. Jokovic A, Locker D, Stephens M, Kenny D, Tompson B, Guyatt G. Measuring parental perceptions of child oral health-related quality of life. J Public Health Dent. 2003;63(2):67-72. https://doi.org/10.1111/j.1752-7325.2003.tb03477.x
https://doi.org/10.1111/j.1752-7325.2003...
,2020. Goursand D, Ferreira MC, Pordeus IA, Mingoti SA, Veiga RT, Paiva SM. Development of a short form of the Brazilian Parental-Caregiver Perceptions Questionnaire using exploratory and confirmatory factor analysis. Qual Life Res. 2013 Mar;22(2):393-402. https://doi.org/10.1007/s11136-012-0145-3
https://doi.org/10.1007/s11136-012-0145-...
for the determination of OHRQoL in the individuals with and without MPS. This proxy-report instrument was selected because the majority of the participants with MPS had mental disabilities and could have had difficulty answering the questions.

The P-CPQ is used to evaluate the perceptions of parents/caregivers regarding the OHRQoL of children in the previous three months and has 13 questions distributed among three domains: oral symptoms (three items), functional limitations (four items) and wellbeing (six items). The questions follow a scale from 0 to 4 points. Each item has five response options: never=0; once or twice = 1; sometimes = 2; often = 3; every day or almost every day = 4. The total score ranges from zero to 52 points, with higher scores indicating a greater negative impact on OHRQoL. A “do not know” response option is also included on all items. This response option scored 0 point.1515. Jokovic A, Locker D, Stephens M, Kenny D, Tompson B, Guyatt G. Measuring parental perceptions of child oral health-related quality of life. J Public Health Dent. 2003;63(2):67-72. https://doi.org/10.1111/j.1752-7325.2003.tb03477.x
https://doi.org/10.1111/j.1752-7325.2003...
,2020. Goursand D, Ferreira MC, Pordeus IA, Mingoti SA, Veiga RT, Paiva SM. Development of a short form of the Brazilian Parental-Caregiver Perceptions Questionnaire using exploratory and confirmatory factor analysis. Qual Life Res. 2013 Mar;22(2):393-402. https://doi.org/10.1007/s11136-012-0145-3
https://doi.org/10.1007/s11136-012-0145-...

Clinical data collection

The examination of the oral cavity of each participant (young person with or without MPS) was performed after the administration of the questionnaire to the parents/caregivers. The participants were examined under artificial light in a dental chair, on a cot or in a wheelchair. The team was composed of an examiner and assistant (scorer/organizer). The examinations were performed with the aid of a mouth mirror (PRISMA®, São Paulo, Brazil) and Community Periodontal Probe (WHO-621; Trinity, Campo Mourão, Brazil).

Dental caries experience was recorded based on the diagnostic criteria of the World Health Organization (WHO). The DMFT (permanent dentition) and dmft (deciduous dentition) indices were used to identify the number of decayed (D/d), missing or indicated for extraction (M/m) and filled (F/f) teeth (T/t).2121. World Health Organization – WHO. Oral health surveys. Geneva: World Health Organization; 2013 [cited 2019Dec]. Available from: http://apps.who.int/iris/bitstream/10665/97035/1/9789241548649_eng.pdf?ua=1
http://apps.who.int/iris/bitstream/10665...

Oral hygiene was analyzed using the Simplified Oral Hygiene Index (OHI-S), for which six dental surfaces are used to represent the entire buccal cavity. Each surface receives a code ranging from zero to three based on the amount of calculus and bacterial plaque.2222. Greene JC, Vermillion JR. The simplified oral hygiene index. J Am Dent Assoc. 1964 Jan;68(1):7-13. https://doi.org/10.14219/jada.archive.1964.0034
https://doi.org/10.14219/jada.archive.19...
,2323. Teixeira SA, Santos PC, Batista AR, Albuquerque BN, Vasconcelos M, Borges-Oliveira AC. Assessment of oral hygiene in mentally disabled children. Rev Odonto Ciênc. 2015;30(3):65-70. https://doi.org/10.15448/1980-6523.2015.3.12849.
https://doi.org/10.15448/1980-6523.2015....

Malocclusion was recorded based on Oliveira et al.2424. Oliveira AC, Paiva SM, Campos MR, Czeresnia D. Factors associated with malocclusions in children and adolescents with Down syndrome. Am J Orthod Dentofacial Orthop. 2008 Apr;133(4):489.e1-8. https://doi.org/10.1016/j.ajodo.2007.09.014
https://doi.org/10.1016/j.ajodo.2007.09....
and the WHO criteria:2121. World Health Organization – WHO. Oral health surveys. Geneva: World Health Organization; 2013 [cited 2019Dec]. Available from: http://apps.who.int/iris/bitstream/10665/97035/1/9789241548649_eng.pdf?ua=1
http://apps.who.int/iris/bitstream/10665...
horizontal overjet (increased/diminished, negative/anterior crossbite), vertical overjet/overbite (increased/deep bite, diminished, negative, top-to-top) and posterior crossbite. When at least one condition was diagnosed, the subject was classified as having an occlusal problem resulting from an abnormal vertical or transverse occlusion. No child or adolescent selected for the study had a history of orthodontic treatment.

Training and calibration process

The first step was a thorough reading of the clinical diagnostic criteria used. The theoretical training was performed using images and slides analyzed on two separate occasions separated by a 10-day interval for the determination of intra-examiner diagnostic variability. The next step was the practical calibration of the examiner. Inter-examiner agreement was determined by comparing the results to those of an experienced specialist with a doctoral degree in pediatric dentistry on two separate occasions separated by an eight-day interval. Due to the limited number of individuals with MPS, children and adolescents without MPS were examined during the calibration exercise (n = 20). The students from a public school in Belo Horizonte participated in this stage. Kappa values ranged from 0.76 to 0.98 for the conditions investigated (dental caries = 0.83; oral hygiene = 0.76 and malocclusion = 0.93). The participants in the calibration exercise were not included in the main study.

Pilot study

Five individuals with MPS and five without MPS from one of the previously selected hospitals participated in this phase along with their parents/caregivers. The results of the pilot study revealed no need for any change to the methods. The participants in this phase were included in the final sample of the study.

Data analysis

The data were analyzed using the Statistical Package for Social Sciences (SPSS for Windows, version 22.0, IBM Inc., Armonk, USA). First, the Shapiro-Wilk test was performed to verify the sample distribution. There was a non-normal distribution, and non-parametric tests were performed. After the descriptive analysis, bivariate analysis was performed with the chi-square, Student’s t, Mann-Whitney and Wilcoxon tests (p < 0.05).

Results

Among the 34 individuals recruited with MPS, five were not included in the study (refusal, death, transportation difficulty and advanced disease conditions). Thus, the final sample consisted of 29 individuals with MPS and 29 individuals without MPS and their parents/caregivers.

The age of the young people ranged from three to 21 years (mean: 12.1 ± 4.2 years; median: 14.5 years). Most were in the favored economic class (56.5%). The age of the parents/caregivers ranged from 23 to 59 years (mean: 40.9 ± 9.0 years; median: 40.0 years). No significant difference between the two groups were found regarding sex, age, economic status, parent’s/caregiver’s age or parent’s/caregiver’s schooling (p > 0.05) (Table 1).

Table 1
Distribution of independent variables according to presence/absence of MPS (n = 58).

The distribution of individuals according to the type of MPS is displayed in Figure. MPS I: 24,2%; MPS II: 20,6%; MPS III: 10,3%; MPS IV: 3,4%; MPS VI: 34,6% and two patients with MPS did not have a defined diagnosis at the time of the data collection (6,9%).

Figure 1
Distribution of individuals with MPS by type (n = 29).

Table 2 displays the total P-CPQ scores as well as the scores on the oral symptoms, functional limitations and wellbeing domains for the groups with and without MPS. Statistically significant differences were found for the total score and all domain scores (p < 0.001). The parents/caregivers of the young people with MPS had more negative perceptions of the impact of oral conditions on quality of life compared to those of the young people without MPS.

Table 2
Mean total P-CPQ score and domain scores (n = 58).

Table 3 displays the associations between the P-CPQ scores and the clinical variables investigated. According to the parents/caregivers, the occurrence of malocclusion was correlated with more negative impact on the OHRQoL of the individuals with MPS, as demonstrated by the total P-CPQ score and scores on the oral symptoms, functional limitations and wellbeing domains (p < 0.05).

Table 3
P-CPQ scores among individuals with and without MPS according to independent variables (n = 58).

Discussion

In the present study, the young people with MPS had greater negative impacts on OHRQoL compared to those without MPS, as demonstrated by the total P-CPQ and domain scores. Thus, the inherent health problems of individuals with MPS may have detrimental effects on OHRQoL. Living with a rare disease and disability exerts a negative influence on the lives of affected individuals and their families due mainly to the medical care and rehabilitation that most of these individuals need on day-to-day basis. This routine is associated with financial expenses that greatly affect the family’s economic situation, priorities and quality of life.1313. Soni-Jaiswal A, Mercer J, Jones SA, Bruce IA, Callery P. Mucopolysaccharidosis I; Parental beliefs about the impact of disease on the quality of life of their children. Orphanet J Rare Dis. 2016 Jul;11(1):96. https://doi.org/10.1186/s13023-016-0478-z
https://doi.org/10.1186/s13023-016-0478-...
,1717. Needham M, Packman W, Quinn N, Rappoport M, Aoki C, Bostrom A, et al. MPS II: adaptive behavior of patients and impact on the family system. J Genet Couns. 2015;24(4):635-44. https://doi.org/10.1007/s10897-013-9665-4
https://doi.org/10.1007/s10897-013-9665-...
,1818. Hendriksz CJ, Lavery C, Coker M, Ucar SK, Jain M, Bell L, et al. The burden endured by caregivers of patients with morquio a syndrome: results from an international patient-reported outcomes survey. J Inborn Errors Metab Screen. 2014;2:e140003. https://doi.org/10.1177/2326409814540872
https://doi.org/10.1177/2326409814540872...
,2525. Johansen H, Dammann B, Andresen IL, Fagerland MW. Health-related quality of life for children with rare diagnoses, their parents’ satisfaction with life and the association between the two. Health Qual Life Outcomes. 2013 Sep;11(1):152. https://doi.org/10.1186/1477-7525-11-152
https://doi.org/10.1186/1477-7525-11-152...

Despite the low values found in the total score for groups with MPS and without MPS. Parents and caregivers of individuals with MPS perceive the impact of oral conditions on OHRQoL more than the group without MPS. Parents and caregivers of individuals with MPS perceive this impact on OHRQoL, because the oral conditions of individuals with MPS are worse (hygiene, greater presence of malocclusion, greater experience with caries) than individuals without MPS.77. Ribeiro EM, Fonteles CS, Freitas AB, Alves KSS, Monteiro AJ, Silva CA. A clinical multicenter study of orofacial features in 26 brazilian patients with different types of mucopolysaccharidosis. Cleft Palate Craniofac J. 2015 May;52(3):352-8. https://doi.org/10.1597/13-204
https://doi.org/10.1597/13-204...
,1414. Wiemann S, Baudisch NF, 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. Int J Environ Res Public Health. 2018 Jul;15(7):15-27. https://doi.org/10.3390/ijerph15071493
https://doi.org/10.3390/ijerph15071493...

According to the literature, GAGs progressively accumulate in bones, cartilage, muscles and ligaments, generating an inflammatory process and tissue damage that result in functional limitations and pain.1313. Soni-Jaiswal A, Mercer J, Jones SA, Bruce IA, Callery P. Mucopolysaccharidosis I; Parental beliefs about the impact of disease on the quality of life of their children. Orphanet J Rare Dis. 2016 Jul;11(1):96. https://doi.org/10.1186/s13023-016-0478-z
https://doi.org/10.1186/s13023-016-0478-...
,1616. Raluy-Callado M, Chen WH, Whiteman DA, Fang J, Wiklund I. The impact of Hunter syndrome (mucopolysaccharidosis type II) on health-related quality of life. Orphanet J Rare Dis. 2013 Jul;8(1):101. https://doi.org/10.1186/1750-1172-8-101
https://doi.org/10.1186/1750-1172-8-101...
,1717. Needham M, Packman W, Quinn N, Rappoport M, Aoki C, Bostrom A, et al. MPS II: adaptive behavior of patients and impact on the family system. J Genet Couns. 2015;24(4):635-44. https://doi.org/10.1007/s10897-013-9665-4
https://doi.org/10.1007/s10897-013-9665-...
, 88. Sarmento DJ, Araújo TK, Mesquita GQ, Diniz DN, Fonseca FRA, Medeiros PF, et al. Relationship between occlusal features and enzyme replacement therapy in patients with mucopolysaccharidoses. J Oral Maxillofac Surg. 2018 Apr;76(4):785-92. https://doi.org/10.1016/j.joms.2017.10.003
https://doi.org/10.1016/j.joms.2017.10.0...
A study conducted in Norway involving 209 parents of children and adolescents (six to 18 years) with rare congenital disorders showed that health-related quality of life was lower among the children with rare disorders than children from the general population; the greatest reduction in quality of life was found for physical functioning, whereas the smallest was found for emotional functioning.2525. Johansen H, Dammann B, Andresen IL, Fagerland MW. Health-related quality of life for children with rare diagnoses, their parents’ satisfaction with life and the association between the two. Health Qual Life Outcomes. 2013 Sep;11(1):152. https://doi.org/10.1186/1477-7525-11-152
https://doi.org/10.1186/1477-7525-11-152...

Cognitive impairment can also exert a negative impact on OHRQoL by limiting one’s independence with regards to oral hygiene, which, when neglected, can lead to consequences such as periodontal disease and dental caries.1111. Prado HV, Carneiro NC, Perazzo MF, Abreu MH, Martins CC, Borges-Oliveira AC. Assessing a possible vulnerability to dental caries in individuals with rare genetic diseases that affect the skeletal development. Orphanet J Rare Dis. 2019 Jun;14(1):145. https://doi.org/10.1186/s13023-019-1114-5
https://doi.org/10.1186/s13023-019-1114-...
,1313. Soni-Jaiswal A, Mercer J, Jones SA, Bruce IA, Callery P. Mucopolysaccharidosis I; Parental beliefs about the impact of disease on the quality of life of their children. Orphanet J Rare Dis. 2016 Jul;11(1):96. https://doi.org/10.1186/s13023-016-0478-z
https://doi.org/10.1186/s13023-016-0478-...
,1414. Wiemann S, Baudisch NF, 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. Int J Environ Res Public Health. 2018 Jul;15(7):15-27. https://doi.org/10.3390/ijerph15071493
https://doi.org/10.3390/ijerph15071493...
,1515. Jokovic A, Locker D, Stephens M, Kenny D, Tompson B, Guyatt G. Measuring parental perceptions of child oral health-related quality of life. J Public Health Dent. 2003;63(2):67-72. https://doi.org/10.1111/j.1752-7325.2003.tb03477.x
https://doi.org/10.1111/j.1752-7325.2003...
,1616. Raluy-Callado M, Chen WH, Whiteman DA, Fang J, Wiklund I. The impact of Hunter syndrome (mucopolysaccharidosis type II) on health-related quality of life. Orphanet J Rare Dis. 2013 Jul;8(1):101. https://doi.org/10.1186/1750-1172-8-101
https://doi.org/10.1186/1750-1172-8-101...
,1717. Needham M, Packman W, Quinn N, Rappoport M, Aoki C, Bostrom A, et al. MPS II: adaptive behavior of patients and impact on the family system. J Genet Couns. 2015;24(4):635-44. https://doi.org/10.1007/s10897-013-9665-4
https://doi.org/10.1007/s10897-013-9665-...
,2323. Teixeira SA, Santos PC, Batista AR, Albuquerque BN, Vasconcelos M, Borges-Oliveira AC. Assessment of oral hygiene in mentally disabled children. Rev Odonto Ciênc. 2015;30(3):65-70. https://doi.org/10.15448/1980-6523.2015.3.12849.
https://doi.org/10.15448/1980-6523.2015....
In the present study, only malocclusion exerted a significant negative impact on the OHRQoL of the individuals with MPS, as evidenced by the total P-CPQ score and scores on the oral symptoms, functional limitations and wellbeing domains. Malocclusion may be due to the skeletal and joint abnormalities these individuals have due to the deposition of GAGs in the head and neck region. Occlusal problems, such as dental crowding, open bite and tooth impaction, can lead to functional, respiratory and esthetic problems, which can exert a negative impact on OHRQoL.88. Sarmento DJ, Araújo TK, Mesquita GQ, Diniz DN, Fonseca FRA, Medeiros PF, et al. Relationship between occlusal features and enzyme replacement therapy in patients with mucopolysaccharidoses. J Oral Maxillofac Surg. 2018 Apr;76(4):785-92. https://doi.org/10.1016/j.joms.2017.10.003
https://doi.org/10.1016/j.joms.2017.10.0...
,99. Almeida-Barros RQ, Medeiros PF, Azevedo MQA, Lira Ortega AO, Yamamoto AT, Dornelas SK, et al. Evaluation of oral manifestations of patients with mucopolysaccharidosis IV and VI: clinical and imaging study. Clin Oral Investig. 2018 Jan;22(1):201-8. https://doi.org/10.1007/s00784-017-2100-8
https://doi.org/10.1007/s00784-017-2100-...
,1010. Ballıkaya E, Eymirli PS, Yıldız Y, Avcu N, Sivri HS, Uzamış-Tekçiçek M. Oral health status in patients with mucopolysaccharidoses. Turk J Pediatr. 2018;60(4):400-6. https://doi.org/10.24953/turkjped.2018.04.007
https://doi.org/10.24953/turkjped.2018.0...

Individuals with MPS have a smaller nasopharyngeal space, which causes mouth breathing and may lead to open bite. Open bite can have a negative effect on phonation, which makes communication difficult and affects quality of life.66. Gönüldaş B, Yılmaz T, Sivri HS, Güçer KŞ, Kılınç K, Genç GA, et al. Mucopolysaccharidosis: otolaryngologic findings, obstructive sleep apnea and accumulation of glucosaminoglycans in lymphatic tissue of the upper airway. Int J Pediatr Otorhinolaryngol. 2014 Jun;78(6):944-9. https://doi.org/10.1016/j.ijporl.2014.03.021
https://doi.org/10.1016/j.ijporl.2014.03...
,1010. Ballıkaya E, Eymirli PS, Yıldız Y, Avcu N, Sivri HS, Uzamış-Tekçiçek M. Oral health status in patients with mucopolysaccharidoses. Turk J Pediatr. 2018;60(4):400-6. https://doi.org/10.24953/turkjped.2018.04.007
https://doi.org/10.24953/turkjped.2018.0...
This situation may result in less participation in school, at work and in one’s social life.88. Sarmento DJ, Araújo TK, Mesquita GQ, Diniz DN, Fonseca FRA, Medeiros PF, et al. Relationship between occlusal features and enzyme replacement therapy in patients with mucopolysaccharidoses. J Oral Maxillofac Surg. 2018 Apr;76(4):785-92. https://doi.org/10.1016/j.joms.2017.10.003
https://doi.org/10.1016/j.joms.2017.10.0...
,1212. Fonseca FR, de Santana Sarmento DJ, Vasconcelos Medeiros PF, Diniz DN, Santos MT. Patients with mucopolysaccharidosis have tendencies towards vertical facial growth. J Oral Maxillofac Surg. 2014 Dec;72(12):2539-46. https://doi.org/10.1016/j.joms.2014.07.006
https://doi.org/10.1016/j.joms.2014.07.0...
,1313. Soni-Jaiswal A, Mercer J, Jones SA, Bruce IA, Callery P. Mucopolysaccharidosis I; Parental beliefs about the impact of disease on the quality of life of their children. Orphanet J Rare Dis. 2016 Jul;11(1):96. https://doi.org/10.1186/s13023-016-0478-z
https://doi.org/10.1186/s13023-016-0478-...
,1414. Wiemann S, Baudisch NF, 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. Int J Environ Res Public Health. 2018 Jul;15(7):15-27. https://doi.org/10.3390/ijerph15071493
https://doi.org/10.3390/ijerph15071493...
,1717. Needham M, Packman W, Quinn N, Rappoport M, Aoki C, Bostrom A, et al. MPS II: adaptive behavior of patients and impact on the family system. J Genet Couns. 2015;24(4):635-44. https://doi.org/10.1007/s10897-013-9665-4
https://doi.org/10.1007/s10897-013-9665-...
,2626. Shapiro EG, Rudser K, Ahmed A, Steiner RD, Delaney KA, Yund B, et al. A longitudinal study of emotional adjustment, quality of life and adaptive function in attenuated MPS II. Mol Genet Metab Rep. 2016 Apr;7:32-9. https://doi.org/10.1016/j.ymgmr.2016.03.005
https://doi.org/10.1016/j.ymgmr.2016.03....
Moreover, such individuals may have difficulty chewing food properly due to open bite and deficient molar occlusion. Consequently, chewing and swallowing occur less effectively, which could lead to asphyxia and choking episodes.55. Guimarães MC, de Farias SM, Costa AM, de Amorim RF. Maroteaux-Lamy syndrome: orofacial features after treatment by bone marrow transplant. Oral Health Prev Dent. 2010;8(2):139-42.

Occlusal problems can also compromise the esthetics of one’s facial appearance, generating low self-esteem and psychological conditions, such as anxiety and depression.1010. Ballıkaya E, Eymirli PS, Yıldız Y, Avcu N, Sivri HS, Uzamış-Tekçiçek M. Oral health status in patients with mucopolysaccharidoses. Turk J Pediatr. 2018;60(4):400-6. https://doi.org/10.24953/turkjped.2018.04.007
https://doi.org/10.24953/turkjped.2018.0...
,1414. Wiemann S, Baudisch NF, 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. Int J Environ Res Public Health. 2018 Jul;15(7):15-27. https://doi.org/10.3390/ijerph15071493
https://doi.org/10.3390/ijerph15071493...
,1616. Raluy-Callado M, Chen WH, Whiteman DA, Fang J, Wiklund I. The impact of Hunter syndrome (mucopolysaccharidosis type II) on health-related quality of life. Orphanet J Rare Dis. 2013 Jul;8(1):101. https://doi.org/10.1186/1750-1172-8-101
https://doi.org/10.1186/1750-1172-8-101...
,2626. Shapiro EG, Rudser K, Ahmed A, Steiner RD, Delaney KA, Yund B, et al. A longitudinal study of emotional adjustment, quality of life and adaptive function in attenuated MPS II. Mol Genet Metab Rep. 2016 Apr;7:32-9. https://doi.org/10.1016/j.ymgmr.2016.03.005
https://doi.org/10.1016/j.ymgmr.2016.03....
According to the literature, patients acquire good occlusion and chewing function after an orthodontic intervention. The negative impact that malocclusion can have on quality of life is mitigated when the diagnosis is made early and dental care is available.88. Sarmento DJ, Araújo TK, Mesquita GQ, Diniz DN, Fonseca FRA, Medeiros PF, et al. Relationship between occlusal features and enzyme replacement therapy in patients with mucopolysaccharidoses. J Oral Maxillofac Surg. 2018 Apr;76(4):785-92. https://doi.org/10.1016/j.joms.2017.10.003
https://doi.org/10.1016/j.joms.2017.10.0...
,99. Almeida-Barros RQ, Medeiros PF, Azevedo MQA, Lira Ortega AO, Yamamoto AT, Dornelas SK, et al. Evaluation of oral manifestations of patients with mucopolysaccharidosis IV and VI: clinical and imaging study. Clin Oral Investig. 2018 Jan;22(1):201-8. https://doi.org/10.1007/s00784-017-2100-8
https://doi.org/10.1007/s00784-017-2100-...
,1212. Fonseca FR, de Santana Sarmento DJ, Vasconcelos Medeiros PF, Diniz DN, Santos MT. Patients with mucopolysaccharidosis have tendencies towards vertical facial growth. J Oral Maxillofac Surg. 2014 Dec;72(12):2539-46. https://doi.org/10.1016/j.joms.2014.07.006
https://doi.org/10.1016/j.joms.2014.07.0...
,1414. Wiemann S, Baudisch NF, 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. Int J Environ Res Public Health. 2018 Jul;15(7):15-27. https://doi.org/10.3390/ijerph15071493
https://doi.org/10.3390/ijerph15071493...
,1818. Hendriksz CJ, Lavery C, Coker M, Ucar SK, Jain M, Bell L, et al. The burden endured by caregivers of patients with morquio a syndrome: results from an international patient-reported outcomes survey. J Inborn Errors Metab Screen. 2014;2:e140003. https://doi.org/10.1177/2326409814540872
https://doi.org/10.1177/2326409814540872...

The major limitation of this study was the use of a convenience sample, which restricts the ability to generalize the results to other groups of patients with MPS. Despite the small sample size, it can be considered representative of individuals with MPS in the state of Minas Gerais, as this is a rare disease and the vast majority of affected individuals registered in the state participated in the study (90.0%). However, one of the strengths of this study is the matching of the groups for sex and age. This made the intergroup comparisons of clinical, socioeconomic and behavioral variables more reliable by eliminating possible confounding factors and bias.

The results of the present study can serve as a source of knowledge and assist in disseminating information on the disease to health professionals, because no previous study was found in the literature evaluating the perceptions of parents/caregivers regarding OHRQoL. Such information is of extreme importance to an early diagnosis and the treatment of the disease, resulting in improvements in signs and symptoms and, consequently, the quality of life of affected individuals.

It is evident that the path to improving the quality of life of individuals with MPS is multidisciplinary care and good communication among health professionals. This is the starting point for the promotion of oral health, more effective multidisciplinary care and a more democratic policy directed at this population. The importance of the participation of a dentist on the multidisciplinary team that provides care and follow-up for individuals with MPS is evident. Dentists can provide such individuals with a better oral health status. The early identification of signs and symptoms can lead to the timely establishment of appropriate therapy and have a positive influence on both OHRQoL as well as general quality of life.55. Guimarães MC, de Farias SM, Costa AM, de Amorim RF. Maroteaux-Lamy syndrome: orofacial features after treatment by bone marrow transplant. Oral Health Prev Dent. 2010;8(2):139-42.,1111. Prado HV, Carneiro NC, Perazzo MF, Abreu MH, Martins CC, Borges-Oliveira AC. Assessing a possible vulnerability to dental caries in individuals with rare genetic diseases that affect the skeletal development. Orphanet J Rare Dis. 2019 Jun;14(1):145. https://doi.org/10.1186/s13023-019-1114-5
https://doi.org/10.1186/s13023-019-1114-...
,1414. Wiemann S, Baudisch NF, 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. Int J Environ Res Public Health. 2018 Jul;15(7):15-27. https://doi.org/10.3390/ijerph15071493
https://doi.org/10.3390/ijerph15071493...
,2727. Almeida TD, Santos PM, Angelo GL, Teixeira SA, Oliveira AC. Assistance to people with mental disabilities: a discussion from the social integration. Rev Odonto Ciênc. 2016;31(2):95-100. https://doi.org/10.15448/1980-6523.2016.2.13224
https://doi.org/10.15448/1980-6523.2016....

Conclusions

Parents/caregivers of young people with MPS reported a greater negative impact on OHRQoL when compared to those of young people without MPS. Malocclusion in individuals with MPS was also associated with poorer quality of life.

Acknowledgments

This study was funded in part by the Brazilian fostering agencies Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq [Council of Scientific and Technological Development]), Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES [Coordination for the Advancement of Higher Education Personnel]) –(Finance Code 001), Fundação de Amparo a Pesquisa do Estado de Minas Gerais (FAPEMIG [State of Minas Gerais Research Foundation]) and Pró-Reitoria de Pesquisa da Universidade Federal de Minas Gerais (PRPq/UFMG [Dean’s Office for Research Projects of the Federal University of Minas Gerais]).

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Publication Dates

  • Publication in this collection
    28 Aug 2020
  • Date of issue
    2020

History

  • Received
    28 Jan 2020
  • Accepted
    10 July 2020
  • Reviewed
    21 July 2020
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