Skip to main content

Prevalence and clinical presentation of molar incisor hypomineralisation among a population of children in the community of Madrid

Abstract

Objective

The main objective of this study was to estimate the prevalence of molar incisor hypomineralisation (MIH), an alteration of tooth enamel with an estimated worldwide prevalence rate of 14%, among children using primary care services in the Community of Madrid, Spain.

Materials and methods

This was a descriptive, cross-sectional and multicentre study. After calibrating all researchers and following the diagnostic criteria of the European Academy of Paediatric Dentistry (EAPD), children aged between 8 and 16 years who were users of the dental services at 8 primary oral health units of the Madrid Health Service (SERMAS) were included. The children underwent a dental examination, and the parents were asked to complete a questionnaire.

Results

The prevalence of MIH was 28.63% (CI: 24.61–32.65%). The age cohorts most affected by MIH were 8 years (21.4%) and 11 years (20.7%). The presence of MIH was greater among girls (85; 60.71%) than among boys (55; 39.28%). The mean number of affected teeth per patient was 4.46 ± 2.8. The most frequently affected molar was the upper right first molar (74.3%), and the upper left central incisor was the most affected incisor (37.85%). Opacities were the defects most frequently recorded (63.57%).

Conclusions

The prevalence of MIH in this study is the highest of all relevant studies conducted in Spain.

Peer Review reports

Introduction

Dental enamel alterations have been studied since 1895 [1]. One of these alterations is molar incisor hypomineralisation, described for the first time at the end of the 1970s in Sweden, when paediatric dentists began to detect changes in the enamel of first molars and permanent incisors, is an alteration of the tooth enamel of unknown aetiology and not related to dental caries [2]. In 2001, Weerjheim et al. suggested using the name molar incisor hypomineralisation (MIH), which was defined as “hypomineralisation of systemic origin of one to four permanent first molars frequently associated with affected incisors” and must be differentiated from other enamel pathologies, such as diffuse opacities, hypoplasia, amelogenesis imperfecta or non-MIH hypomineralisations, such as initial caries [3,4,5].

In 2003, the European Academy of Paediatric Dentistry (EAPD) established the diagnostic criteria for MIH: demarcated opacity, posteruptive enamel breakdown, atypical restauration and extracted molar due to MIH, and the first prevalence studies were carried out in Europe to establish strategies for the diagnosis, treatment and prevention of this pathology [6, 7].

Microscopically, compared with healthy enamel, the enamel of affected teeth shows porous areas with a higher carbon content and lower calcium and phosphorus concentrations. The borders between healthy and affected enamel are well defined. At the macroscopic level, affected teeth present alterations in enamel translucency, resulting in marked opacities, in addition to areas with fractured enamel and exposed dentin [8]. Clinically, patients affected by MIH present with several problems. Frequently, mild cases only show aesthetic defects, especially when anterior teeth are affected. More serious cases involve tooth sensitivity to changes in temperature and during brushing, resulting in inadequate oral hygiene, with a consequent increase in number and severity of caries and gingival problems. Dental professionals will observe rapid tooth decay, especially in posterior sectors, with lesions in unusual areas, making restorative treatment difficult and potentially causing premature tooth loss. In addition to the above, anaesthetic management of patients may be challenging due to chronic pulp inflammation resulting from continuous bacterial penetration from the porous enamel into the dentin, which can cause behavioural problems during dental treatment [6, 9, 10]. Aetiology of MIH is unknow and has been related with environmental factors presents from the last months of pregnancy to the first years of life that are capable of altering the enamel development, such as, maternal illness, early childhood diseases or use of drugs, included self-medication [11, 12].

Research on the prevalence of MIH began in 2000, but despite the popularisation of the use of the EAPD criteria, the results were substantially different among investigations; as such, several researchers highlighted the need to standardize the criteria among studies [13, 14]. In 2015, Ghanim et al. proposed a new evaluation system that takes into account both the clinical status of enamel lesions and their extent [15]. Currently, the prevalence of MIH is considered high. 2 recent reviews estimated worldwide prevalence rates of 13.1% and 14.2% [16, 17]. In Spain, the estimated prevalence rate is 20% [17, 18]. Regarding the Community of Madrid, the estimated prevalence is approximately 12% [19], but there are no published studies that follow the standardized assessment criteria recommended by the EAPD for MIH studies.

In our setting, public dental care in the Community of Madrid, which is provided through the Oral Health Units (OHUs) of Primary Care Health Centres, there are also no studies on the prevalence of MIH that meet the EAPD criteria. Considering that this pathology has a high prevalence and is a complex clinical problem and given that dental consultations in the Madrid public health system mainly involve preventive care, this study was designed with the aim of determining the prevalence of MIH among children users of public dental services in Madrid.

Materials and methods

This was an observational, descriptive, cross-sectional and multicentre study to estimate the prevalence of MIH among children aged between 8 and 16 years in different oral health units (OHUs) of the Community of Madrid, Spain. We selected this age group because it is the group included in public oral health program. This study was approved by the Ethics Committee of the Hospital Clínico San Carlos following the Declaration of Helsinki’s ethical principles for medical research involving human subjects (Internal Code: 21/162-E_Tesis).

Study population and sample selection

Participation was voluntary; the guardians of the children were approached about participating in the study, and all those who agreed signed an informed consent form. The inclusion criteria were as follows: (1) children between 8 and 16 years of age, (2) complete eruption or eruption of at least 1/3 of the occlusal surface of the first 4 permanent molars, and (3) signed informed consent form (guardians).

The exclusion criteria were as follows: (1) no first permanent molars or eruption less than 1/3 of the occlusal surface of molars, (2) fixed orthodontic appliances, (3) systemic diseases or under treatment with drugs that could alter enamel development, and (4) lack of cooperation during the examination.

The sample size was calculated for an estimated prevalence of 12%, referencing a previous study carried out in a population similar to ours [14], with a precision of 3% and a confidence level of 95%, which resulted in a sample size of 451 children.

The OHUs of the Madrid Health Service (SERMAS) were divided into two groups to facilitate randomization:

  • 40 metropolitan OHUs located in the city of Madrid.

  • 46 OHUs located in other municipalities of the Community of Madrid. Those located in towns with fewer than 20,000 inhabitants were considered rural OHUs.

Ultimately, 8 OHUs were selected: 4 in the city of Madrid and another 4 in the municipalities of Parla, Alcobendas and Algete (rural).

Training and calibration

Prior to data collection, the 8 participating dentists received a training session on the diagnosis of MIH using the EAPD criteria [10] (Fig. 1). Subsequently, calibration was carried out. A questionnaire with 29 photographs of teeth was sent to each dentist; the dentists provided diagnoses using the EAPD diagnostic criteria on which they were previously trained. Each dentist completed the questionnaire twice, within a week between each session. The kappa coefficient was used to calculate inter-examiner agreement. All kappa values were between 0.74 and 0.94; therefore, according to the Landis and Koch scale, the degree of agreement was classified as good and very good.

Fig. 1
figure 1

EAPD diagnostic criteria for MIH

Data collection

Data collection consisted of 2 steps: a dental examination and a questionnaire to be completed by the parents. The oral examination was performed by the dentists in an office dental chair. The light source was the equipment light. Cotton balls were used to dry oral surfaces; an air syringe was not used. Ball-ended probes were used to detect irregularities in the enamel surface. Each dentist completed a data collection sheet for each patient.

Data analysis

IBM SPSS Statistics version 27.0 was used for statistical analyses. Quantitative variables are described using means and standard deviations, and categorical variables are described as frequencies and percentages. The prevalence of MIH was calculated as a percentage, and estimations are reported using confidence intervals. The Mann‒Whitney U test and the Wilcoxon test were used to analyse significant differences between different samples, and the chi-square test was used to determine the differences between percentages. Differences were considered statistically significant when p < 0.05.

Results

The sample comprised 489 children between 8 and 16 years of age, of whom 258 (52.76%) were girls and 231 were boys (47.23%). A total of 140 children were affected by MIH; therefore, the estimated prevalence of MIH in this study was 28.63% (CI: 24.61–32.65%). Regarding sex, 55 boys (39.28%) and 85 girls (60.71%) were affected by MIH. Girls were affected more than boys and difference was significant (chi-square test, p < 0.05).

The mean age of the children (N = 489) at the time of the examination was 11.01 ± 2.3 years, and that of children affected by MIH (N = 140) was 10.5 ± 2.11 years. The age cohorts most affected by MIH were 8 years (21.4%), 11 years (20.7%) and 10 years (17.1%); notably, in the 16-year-old cohort, no patients presented MIH. There were significant differences between the 10-year-old cohort and 11-year-old cohort and other cohorts with regard to the presence of MIH (chi-square test, p < 0.05). Figure 2 shows the distribution of the sample and the prevalence of MIH by sex and age at the time of the examination.

Fig. 2
figure 2

Distribution of MIH in the sample. Age and Sex

A total of 1,672 permanent index teeth were studied. The number of affected teeth in each patient with MIH varied between 1 and 12; the mean number of affected teeth was 4.46 ± 2.8. In the upper arch, 55.6% (n = 347) of the teeth presented hypomineralisation, and the average number of affected teeth was 2.47 ± 1.66. In the lower arch, the percentage of affected teeth was lower, 44.39% (n = 277), with a mean of 1.99 ± 1.55 affected teeth. In both arches, the most common number of affected teeth was 2, and 6 patients had 12 affected index teeth. Significant differences were found between the upper and lower arches with regard to the mean number of affected teeth (Wilcoxon signed rank test, p = 0.001).

The most frequently affected molar was the upper right first molar (74.3%, n = 104), followed by the upper left first molar (68.6%, n = 96), the lower left first molar (65%, n = 91) and the lower right first molar (61.4%, n = 86); the least frequently affected tooth was the upper left lateral incisor (14.3%, n = 20).

Regarding the number of affected molars in each patient with MIH, the mean number of affected molars was 2.69 ± 1.15. A total of 36.4% (n = 52) showed involvement of the 4 molars, 30% (n = 42) had 2 affected molars, 18.6% (n = 26) had a single affected molar, and 14.3% (n = 20) had 3 affected molars. The mean number of affected incisors in patients with MIH was 1.76 ± 2.1. 36,4% of these patients (n = 51) showed no affected incisors and had hypomineralisation only on the first permanent molars or molar hypomineralisation (MH). On average, 1.03 ± 1.31 incisors were affected in the upper arch, and 0.75 ± 1.13 were affected in the lower arch. Significant differences were found in the number of affected upper and lower incisors (Wilcoxon signed rank test, p = 0.004). The distribution of incisor involvement by the number of affected molars is shown in Table 1.

Table 1 Distribution of MH and MIH affected incisor and molars

Regarding types of defects due to MIH, those proposed by the EAPD— demarcated opacities, post-eruptive enamel breakdown, atypical restorations, atypical caries and missing teeth—were analysed. Of the 1,672 teeth analysed, 624 (37.32%) showed some type of enamel defect. A total of 519 (31%) presented opacities, 47 (2.8%) presented atypical restorations, 33 (2%) presented post-eruptive enamel breakdown, 24 (1.4%) presented atypical caries, and 1 tooth (0.1%) had been extracted because of MIH.

In patients with MIH (n = 140), opacity was the most frequent defect (n = 76) in the upper first molars. Tooth loss associated with MIH was detected only in 1 lower left first molar.

Regarding primary molars, 97 patients (69.3%, n = 140) had at least 1 s primary molar present at the time of the examination, and 74 (52.9%) had all 4. Of those who had a primary molar (n = 97), 73 (75.3%) did not present any alteration in the molars present, 9 (9.3%) had 1 molar affected by hypomineralised lesions on second primary molars (HSPM), 9 (9.3%) had 2 affected molars, 2 (2.1%) had 3 affected molars, and 4 (4.1%) had 4 affected molars. Regarding the type of defect, 341 primary second molars were analysed. A total of 39 teeth (11.4%) had opacities, 6 (1.8%) had atypical caries, 3 (0.9%) had atypical restorations, and 1 (0.3%) had post-eruptive enamel breakdown. Table 2 shows the percentages of affected index teeth by defect type.

Table 2 Distribution of defect types in permanent index teeth

The extent of the defects and their severity were evaluated using the EAPD criteria: Type I was considered when defect extension was less than 1/3 of the affected tooth, type II when at least 1/3 but less than 2/3 of the affected tooth and type III when 2/3 or more of the tooth was affected. Of the teeth analysed in which the size of the defect was recorded (n = 613), 51.71% of the defects showed type I extension, 35.7% showed type II extension, and 12.56% showed type III extension.

With regard to the severity of the affected teeth (n = 624), 83.17% (n = 519) of teeth only showed changes in colour, i.e., mild severity, and 16.82% (n = 105) of the teeth presented severe disease, i.e., post-eruptive enamel breakdown, atypical caries or restorations or loss due to MIH. Of the 140 patients diagnosed with MIH, 61 (43.57%) had severe disease in at least 1 tooth, and in 79 patients (56.42%), all the teeth presented mild disease. In the children with mild disease, an average of 3.84 teeth were affected, and in the children with severe disease, an average of 5.28 teeth were affected. The difference in the mean number of affected teeth as a function of severity was significant (Mann‒Whitney U test for independent samples, p = 0.003). The most severe lesions were found in older children (mean age of 11.15 years for severe lesions versus 10.25 years for mild lesions (Mann‒Whitney U test for independent samples, p = 0.014). No relationship was found between lesion severity and sex.

Regarding defect colour, most of the teeth with opacities were white. Colour alterations were analysed in 515 teeth. A total of 60.97% (n = 314) of teeth had white defects, 21.16% (n = 109) had yellow defects, and 17.86% (n = 92) had brown defects. Yellow and brown defects occurred more frequently in molars than in incisors. Figure 3 shows the percentage of opacities by defect colour and tooth type.

Fig. 3
figure 3

Healthy and demarcated opacity teeth. Color of the opacities according to the type of index tooth (%)

Discussion

The main objective of this study was to estimate the prevalence of MIH among users of public dental services in Madrid, Spain. Worldwide, the prevalence of MIH is highly variable, ranging from 0.5 to 40% () [17, 20, 21]. In Spain, it ranges from 12 to 24.8% [17,18,19, 22, 23], higher than the prevalence in other areas of Europe such as Croatia (13%) [24], Germany (13.5%) [25], Sarajevo (11.5%) [26], Switzerland (14.8%) [27]and Belgium (18.6%) [28]. Although EAPD was the first to unify diagnostic criteria for MIH, others are currently accepted [29]. In our case, we decided to use EAPD criteria because we were more interested in knowing prevalence of MIH than in treatment needs.

In this study, the first to be carried out in Madrid using the EAPD criteria, the estimated prevalence of MIH among children aged between 8 and 16 years was 28.63%. This result is higher than expected based on studies carried out in our country; however, the results were similar to those reported in other studies in Caracas (Venezuela) (25.35%) [30], Brazil (28.7%) [31], Mexico (35.4%) [32] and Lebanon (26.7%) [33]. Similar to our study, others have also investigated the presence of MIH among public health care users. Rodriguez-Rodriguez et al. (Venezuela) and López Jordi et al. (Argentina and Uruguay) studied the prevalence of MIH among public and private health care users and found higher prevalence rates in the private system. These authors explain these higher rates as follows: in their countries, only people from the lowest socioeconomic level and who do not receive social security benefits seek dental care through the public system [30, 34]. In contrast, in our study, conducted only with participants who use the public system, we obtained higher prevalence rates than those obtained in any other study conducted in our country. We believe that this is because more children with dental pathologies are seen through the public system in Madrid because the Madrid health system, which provides universal and fully subsidized medical coverage, provides free dental treatment for permanent teeth in children between 7 and 16 years of age [35].

With regard to sex, although several recent meta-analyses have not found differences [16, 17, 20], in our study, we found a higher prevalence of MIH among girls, a finding that is similar to the results reported in other published studies [24, 26, 36, 37]. Schwendicke et al., in a meta-analysis carried out in 2018, did not find differences between sexes; however, they acknowledge that in certain areas, the prevalence among girls is significantly higher than among boys, but the causes could not be determined [16]. Chawla et al. [38] suggest that this higher prevalence may be observed because dental maturity usually occurs earlier in girls, and therefore, their teeth would have been erupted for longer, with more post-eruptive enamel breakdown detected. Being MIH an alteration in which there may be an aesthetic affectation, especially when the incisor group is affected, we believe that the greater presence of MIH n girls in our study can be explained because girls tend to show more concern about their physical appearance. All participants in this research were users of a free access preventive program and, affected girls, would attend dental check-ups more frequently than those who are not affected.

In studies in which different age groups were analysed, the prevalence of MIH seems to be influenced by the age of the participants. According to other studies, the prevalence of MIH appears to be higher in younger patient cohorts. This may be because at 8 years of age, the age recommended by the EAPD for conducting MIH prevalence studies [21], the first permanent molars erupt, and most are still intact without enamel breakdown; this allows the visualization of opacities, facilitating the diagnosis of MIH. In older children, it is possible that more post-eruptive enamel breakdown occurs, and if conservative treatment is administered, these molars may not be identified as affected by MIH, resulting in the underdiagnosis of this condition [10, 21]. In our study, the highest prevalence of MIH corresponded to the youngest children, 8 years of age (21.4%), similar to the studies by Grieshaber et al. [27] and Arslanagic-Muratbegovic et al. [26]; however, in this study, the age of participants in the youngest cohort was 6 years. Our study found significant differences between the 10-year-old and 11-year-old cohorts and the other cohorts; however, this may have been influenced by the sample size because some studies propose that each cohort should be made up of at least 100 children [21]; in this study, the size of the cohorts was less than 100.

On the other hand, youngest children who still have primary molars may present defects in the enamel of these teeth, comparable to MIH, which is called hypomineralisation of second primary molars (HSPM). It has been shown to be a pathology predictive of MIH [5].

Regarding the possibility of greater MIH involvement in the upper or lower arch, studies are not conclusive. Several investigations have shown greater involvement in the upper arch than in the lower arch [26, 31, 39,40,41] but found no significant differences; in this study, the number of teeth affected by MIH was also greater in the upper arch than in the lower arch, but the difference was significant. Chawla et al. (2008) provided various reasons for greater maxillary molar involvement. The lower molars tend to erupt earlier than the upper molars; therefore, as the former have been exposed to the oral environment for longer, they can be affected earlier by enamel breakdown, with such patients receiving conservative treatment, leading to underestimations of the diagnosis of MIH in the lower molars. Additionally, examinations performed in the lower arch may be influenced by the presence of the tongue, which can make it difficult to detect MIH lesions in the lower molars [38].

The results of this study agree with those reported in many other studies, i.e., opacities are the most frequent lesions [25, 26, 41, 42]. In our study, atypical restorations ranked second, which differs from other studies, which found post-eruptive enamel breakdown more frequently) [26, 39, 43]. Given that the children who participated in our study were users of an oral health programme that includes restorative treatment of permanent molars, we believe that the reason for the presence of atypical restorations as the second most frequent lesion is that teeth with post-eruptive enamel breakdown received restorative treatment. Similar to García-Margarit et al. [22], we believe that longitudinal designs are needed to assess the progression of lesions over time.

To analyse lesion extension, the scale proposed by Ghanim et al. [15] was used, and less than 1/3 of the tooth surface affected was the most frequently observed extension, similar to results reported in the studies by Argote et al. [41] and Sidhu et al. [44]. The lesion severity most frequently found in our study was mild, with results comparable to those obtained in other studies [30, 42,43,44].

Patients with more severe lesions had a greater number of affected teeth and were older than patients with mild lesions, findings that are consistent with the results of other studies [26, 41]. In this study, examinations were performed in an office dental chair, which is why we believe that the results may be more reliable than those reported in studies in which examinations were performed in schools and without the chair light. The limitations of our study include the use of the short data form suggested by the EAPD, which is why only the index teeth were analysed, and the fewer number of participants in the oldest age groups, which decreases the representativeness of the sample.

Conclusions

The prevalence of MIH among children using public dental services in Madrid was 28.63%, the highest among the studies that have been carried out in Spain. The prevalence of MIH was highest among female patients between the ages of 8 and 11 years. Opacities were the most frequent lesions, followed by atypical restorations. Regarding the extent of the defects, most of the teeth showed less than 1/3 of the tooth surface affected. Brown defects were more prevalent in molars, and the incisors showed white or yellow defects. Longitudinal studies are needed to measure lesion progression. Given the high prevalence of MIH, it is necessary to promote multidisciplinary awareness and prevention programs for primary health care personnel, including nurses and paediatricians.

Data availability

All collected data from patients analysed during this study are included in this published article.

Abbreviations

EAPD:

European Academy of Paediatric Dentistry

MIH:

Molar Incisor Hypomineralisation

OHUs:

Oral health units

References

  1. Berten J. Hypoplasie Des Schmelzes. Dtsch Mschr Zahnheilkd. 1895;13:425–600.

  2. Weerheijm KL, Mejàre I. Molar incisor hypomineralization: a questionnaire inventory of its occurrence in member countries of the European Academy of Paediatric Dentistry (EAPD). Int J Paediatr Dent [Internet]. 2003;13(6):411–6. Available from: http://www.ncbi.nlm.nih.gov/pubmed/14984047.

  3. Weerheijm KL. Molar incisor hypomineralisation (MIH). Eur J Paediatr Dent [Internet]. 2003 Sep [cited 2019 Sep 7];4(3):114–20. Available from: http://www.ncbi.nlm.nih.gov/pubmed/14529330.

  4. Weerheijm KL, Jalevik B, Alaluusua S. Molar-incisor hypomineralisation. Caries Res 2001;Sept/Oct(35):390–1.

  5. Lygidakis NA, Garot E, Somani C, Taylor GD, Rouas P, Wong FSL. Best clinical practice guidance for clinicians dealing with children presenting with molar-incisor-hypomineralisation (MIH): an updated European Academy of Paediatric Dentistry policy document. European Archives of Paediatric Dentistry [Internet]. 2022;23(1):3–21. https://doi.org/10.1007/s40368-021-00668-5.

  6. Schneider PM, Silva M. Endemic Molar Incisor Hypomineralization: a Pandemic Problem That Requires Monitoring by the Entire Health Care Community. Curr Osteoporos Rep [Internet]. 2018;16(3):283–8. Available from: http://link.springer.com/https://doi.org/10.1007/s11914-018-0444-x.

  7. Weerheijm KL, Duggal M, Mejàre I, Papagiannoulis L, Koch G, Martens LC, et al. Judgement criteria for Molar Incisor Hypomineralisation (MIH) in epidemiologic studies: a summary of the European meeting on MIH held in Athens, 2003. Eur J Paediatr Dent. 2003;4(3):110–3.

    CAS  PubMed  Google Scholar 

  8. Weerheijm K, The European Academy of Paediatric Dentistry and Molar Incisor Hypomineralisation. Eur Arch Paediatr Dent [Internet]. 2015;16(3):233–4. Available from: http://link.springer.com/https://doi.org/10.1007/s40368-015-0189-5.

  9. Weerheijm KL. Molar incisor hypomineralization (MIH): clinical presentation, aetiology and management. Dent Update. 2004;31(1):9–12.

    Article  CAS  PubMed  Google Scholar 

  10. Ghanim A, Silva MJ, Elfrink MEC, Lygidakis NA, Mariño RJ, Weerheijm KL et al. Molar incisor hypomineralisation (MIH) training manual for clinical field surveys and practice. Eur Arch Paediatr Dent [Internet]. 2017;18(4):225–42. Available from: http://link.springer.com/https://doi.org/10.1007/s40368-017-0293-9.

  11. Zeb S, Mushtaq M, Ahmad M, Saleem W, Rabaan AA, Naqvi BSZ et al. Self-Medication as an Important Risk Factor for Antibiotic Resistance: A Multi-Institutional Survey among Students. Antibiotics. 2022;11(7).

  12. Alaluusua S. Aetiology of Molar-Incisor Hypomineralisation: A systematic review. Eur Arch Paediatr Dent [Internet]. 2010;11(2):53–8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/20403298.

  13. Elfrink MEC, Ghanim A, Manton DJ, Weerheijm KL. Standardised studies on Molar Incisor Hypomineralisation (MIH) and Hypomineralised Second Primary Molars (HSPM): a need. Eur Arch Paediatr Dent [Internet]. 2015;16(3):247–55. Available from: http://link.springer.com/https://doi.org/10.1007/s40368-015-0179-7.

  14. Hernandez M, Boj J, Espasa E. Do We Really Know the Prevalence of MIH? Journal of Clinical Pediatric Dentistry [Internet]. 2016;40(4):259–63. https://doi.org/10.17796/1053-4628-40.4.259.

  15. Ghanim A, Elfrink M, Weerheijm K, Mariño R, Manton D. A practical method for use in epidemiological studies on enamel hypomineralisation. Eur Arch Paediatr Dent [Internet]. 2015;16(3):235–46. Available from: http://link.springer.com/https://doi.org/10.1007/s40368-015-0178-8.

  16. Schwendicke F, Elhennawy K, Reda S, Bekes K, Manton DJ, Krois J. Global burden of molar incisor hypomineralization. J Dent [Internet]. 2018;68(December):10–8. https://doi.org/10.1016/j.jdent.2017.12.002.

  17. Zhao D, Dong B, Yu D, Ren Q, Sun Y. The prevalence of molar incisor hypomineralization: evidence from 70 studies. Int J Paediatr Dent [Internet]. 2018;28(2):170–9. https://doi.org/10.1111/ipd.12323.

  18. Bravo Pérez M, Almerich Silla J, Gómez Santos G, Hidalgo Olivares G, Lamas Oliveira M, Martínez Beneyto Y, et al. Encuesta De Salud oral Española. Revista del consejo Gen de Colegios de Odontologos y Estomatologos de España [Internet]. 2020;25(4):12–69. Available from: www.rcoe.es.

    Google Scholar 

  19. Comes Martínez Á, Puente Ruiz C, de la. Rodríguez Salvanés F. Prevalencia De Hipomineralización en primeros molares permanentes (MIH) en población infantil del Área 2 De Madrid. RCOE. 2007;12(3):129–34.

    Google Scholar 

  20. Lopes LB, Machado V, Mascarenhas P, Mendes JJ, Botelho J. The prevalence of molar-incisor hypomineralization: a systematic review and meta-analysis. Sci Rep [Internet]. 2021;11(1):22405. Available from: http://www.ncbi.nlm.nih.gov/pubmed/34789780.

  21. Jälevik B. Prevalence and diagnosis of molar-incisor- hypomineralisation (MIH): a systematic review. Eur Arch Paediatr Dent. 2010;11(2):59–64.

    Article  PubMed  Google Scholar 

  22. Garcia-Margarit M, Catalá-Pizarro M, Montiel-Company JM, Almerich-Silla JM. Epidemiologic study of molar-incisor hypomineralization in 8-year-old Spanish children. Int J Paediatr Dent [Internet]. 2014;24(1):14–22. Available from: https://onlinelibrary.wiley.com/doi/https://doi.org/10.1111/ipd.12020.

  23. Negre-Barber A, Montiel-Company JM, Catalá-Pizarro M, Almerich-Silla JM. Degree of severity of molar incisor hypomineralization and its relation to dental caries. Sci Rep [Internet]. 2018;8(1):1248. Available from: http://www.ncbi.nlm.nih.gov/pubmed/29352193.

  24. Jurlina D, Uzarevic Z, Ivanisevic Z, Matijevic N, Matijevic M. Prevalence of molar–incisor hypomineralization and caries in eight-year-old children in Croatia. Int J Environ Res Public Health. 2020;17(17):1–10.

    Article  Google Scholar 

  25. Amend S, Nossol C, Bausback-Schomakers S, Wleklinski C, Scheibelhut C, Pons-Kühnemann J et al. Prevalence of molar-incisor-hypomineralisation (MIH) among 6-12-year-old children in Central Hesse (Germany). Clin Oral Invest [Internet]. 2021;25:2093–100. https://doi.org/10.1007/s00784-020-03519-7.

  26. Arslanagic-Muratbegovic A, Markovic N, Zukanovic A, Tiro A, Dzemidzic V. Molar Incisor Hypomineralization: Prevalence and severity in six to nine-year-old Sarajevo children. Eur J Paediatr Dent [Internet]. 2020;21(3):243–7. Available from: http://www.ncbi.nlm.nih.gov/pubmed/32893660.

  27. Grieshaber A, Waltimo T, Haschemi AA, Erb J, Steffen R, Bornstein MM et al. Prevalence of and factors associated with molar-incisor hypomineralisation in schoolchildren in the canton of Basel-Landschaft, Switzerland. Clin Oral Investig [Internet]. 2022;27(2):871–7. Available from: https://link.springer.com/https://doi.org/10.1007/s00784-022-04648-x.

  28. Vanhée T, Poncelet J, Cheikh-Ali S, Bottenberg P, Prevalence. Caries, Dental Anxiety and Quality of Life in Children with MIH in Brussels, Belgium. J Clin Med [Internet]. 2022;11(11):3065. Available from: https://www.mdpi.com/2077-0383/11/11/3065.

  29. Steffen R, Krämer N, Bekes K. The Würzburg MIH concept: the MIH treatment need index (MIH TNI): a new index to assess and plan treatment in patients with molar incisior hypomineralisation (MIH). Eur Archives Pediatr Dentistry. 2017;18(5):355–61.

    Article  CAS  Google Scholar 

  30. Rodríguez-Rodríguez M, Carrasco-Colmenares W, Ghanim A, Natera A, Acosta-Camargo MG. Prevalence and Distribution of Molar Incisor Hypomineralization in children receiving dental care in Caracas Metropolitan Area, Venezuela. Acta Odontol Latinoam [Internet]. 2021;34(2):104–1112. Available from: http://www.ncbi.nlm.nih.gov/pubmed/34570857.

  31. Reis PPG, Jorge RC, Americano GCA, Thiago Pontes N, de Peres S, Silva Oliveira AMAM et al. AGE,. Prevalence and Severity of Molar Incisor Hypomineralization in Brazilian Children. Pediatr Dent [Internet]. 2021;43(4):270–5. Available from: https://onlinelibrary.wiley.com/doi/https://doi.org/10.1111/ipd.12327.

  32. Villanueva-Gutiérrez T, Irigoyen-Camacho MME, Castaño-Seiquier A, Zepeda-Zepeda MA, Sanchez-Pérez L, Frechero NMN. Prevalence and Severity of Molar–Incisor Hypomineralization, Maternal Education, and Dental Caries: A Cross-Sectional Study of Mexican Schoolchildren with Low Socioeconomic Status. J Int Soc Prevent Communit Den [Internet]. 2019;9(5):513–21. Available from: http://www.ncbi.nlm.nih.gov/pubmed/31620386.

  33. Elzein R, Chouery E, Abdel-Sater F, Bacho R, Ayoub F. Molar incisor hypomineralisation in Lebanon: prevalence and clinical characteristics. European Archives of Paediatric Dentistry [Internet]. 2020;21(5):609–16. Available from: http://link.springer.com/https://doi.org/10.1007/s40368-019-00505-w.

  34. Lopez Jordi M, del Cortese C, Alvarez SG, Salveraglio L, Ortolani I, Biondi AM. [Comparison of the prevalence of molar incisor hypomineralization among children with different health care coverage in the cities of Buenos Aires (Argentina) and Montevideo (Uruguay)]. Salud Colect. 2014;10(2):243–51.

    PubMed  Google Scholar 

  35. de Madrid C. Ley 7 /. 2018, de 26 de diciembre, de Atención a la Salud Bucodental y de creación del Programa de Atencion Dental Infantil. BOCM 2018.

  36. Hernández M, Boj JR, Espasa E, Peretz B. First Permanent Molars and Permanent Incisors Teeth by Tooth Prevalence of Molar–Incisor–Hypomineralisation in a Group of Spanish Schoolchildren. Acta Stomatol Croat [Internet]. 2018;52(1):4–11. Available from: http://www.ascro.hr/fileadmin/user_upload/2018/Number_2018-1/Hernandez_2018-1.pdf.

  37. Bahrololoomi Z, Amrollahi N, Mostafaloo N. The prevalence and extent of molar-incisor hypo-mineralization by gender in a group of Iranian children. Iran J Public Health. 2020;49(8):1585–7.

    PubMed  PubMed Central  Google Scholar 

  38. Chawla N, Messer LB, Silva M. Clinical studies on molar-incisor-hypomineralisation part 1: distribution and putative associations. Eur Arch Paediatr Dent [Internet]. 2008;9(4):180–90. Available from: http://www.ncbi.nlm.nih.gov/pubmed/19054471.

  39. Abdalla HE, Abuaffan AH, Kemoli AM. Molar incisor hypomineralization, prevalence, pattern and distribution in Sudanese children. BMC Oral Health [Internet]. 2021;21(1):9. Available from: https://bmcoralhealth.biomedcentral.com/articles/https://doi.org/10.1186/s12903-020-01383-1.

  40. Temilola OD, Folayan MO, Oyedele T. The prevalence and pattern of deciduous molar hypomineralization and molar-incisor hypomineralization in children from a suburban population in Nigeria. BMC Oral Health [Internet]. 2015;15(1):73. Available from: https://bmcoralhealth.biomedcentral.com/articles/https://doi.org/10.1186/s12903-015-0059-x.

  41. Argote Quispe DM, de Priego GPM, Leon Manco RA, Portaro CP. Molar incisor hypomineralization: Prevalence and severity in schoolchildren of Puno, Peru. J Indian Soc Pedod Prev Dent [Internet]. 2021;39(3):246–50. Available from: http://www.ncbi.nlm.nih.gov/pubmed/34810339.

  42. Glodkowska N, Emerich K. Molar Incisor Hypomineralization: prevalence and severity among children from Nothern Poland. Eur J Paediatr Dent [Internet]. 2019;20(1):59–66. Available from: http://www.ncbi.nlm.nih.gov/pubmed/30919647.

  43. Damares Lago J, Restrepo M, Girotto Bussaneli D, Patrícia Cavalheiro J, Feltrin de Souza J, Santos-Pinto L et al. Molar-Incisor Hypomineralization: Prevalence Comparative Study in 6 Years of Interval. ScientificWorldJournal [Internet]. 2022;2022:4743252. Available from: http://www.ncbi.nlm.nih.gov/pubmed/36530554.

  44. Sidhu N, Wang Y, Barrett E, Casas M. Prevalence and presentation patterns of enamel hypomineralisation (MIH and HSPM) among paediatric hospital dental patients in Toronto, Canada: a cross-sectional study. European archives of paediatric dentistry [Internet]. 2020;21(2):263–70. Available from: http://www.ncbi.nlm.nih.gov/pubmed/31586297.

Download references

Acknowledgements

We are grateful for the patients and their legal guardians for their participation in this study and their contribution to science. As well as Madrid Health Service for promoting research and always giving us their unconditional support. To the dentists and dental hygienists who participated in this study.

Funding

“This project received a grant for the publication of this paper from the Foundation for Biosanitary Research and Innovation in Primary Care (FIIBAP)”.

Author information

Authors and Affiliations

Authors

Contributions

S.O-L. contributed to conceptualization, methodology, formal analysis, data curation, investigation, writing-original draft. G.F-G.conceptualization, investigation, resources, validation, writing-review and editing, supervision. M.M.-H. conceptualization, investigation, resources, validation, writing-review and editing, supervision. N.G-L. contributed to investiga tion, resources, writing-review and editing.A.M.C. conceptualization, investigation, resources, validation, writing-review and editing, supervision. All authors read and approved the fnal manuscript.

Corresponding author

Correspondence to Antonia M. Caleya-Zambrano.

Ethics declarations

Ethics approval and consent to participate

This study was approved by the Ethics Committee of the Hospital Clínico San Carlos following the Declaration of Helsinki’s ethical principles for medical research involving human subjects (Internal Code: 21/162-E_Tesis). The parent/legal guardian of the patients signed a written consent for the use of records for purposes investigations.

Consent for publication

Not applicable.

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Ortega-Luengo, S., Feijóo-Garcia, G., Miegimolle-Herrero, M. et al. Prevalence and clinical presentation of molar incisor hypomineralisation among a population of children in the community of Madrid. BMC Oral Health 24, 229 (2024). https://doi.org/10.1186/s12903-024-04003-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12903-024-04003-4

Keywords