What do we currently need to know about molar incisor hypomineralisation (MIH) and hypomineralized second primary molars (HSPM)? / Que faut-il savoir, à l'heure actuelle, sur les hypominéralisations molaires incisives (MIH) et les hypominéralisations des secondes molaires temporaires (HSPM) ?

Introduction: Molar incisor hypomineralization (MIH) and hypomineralized second primary molars (HSPM) are qualitative and asymmetric enamel defects. MIH affect at least one permanent first molar and can also be associated with permanent incisors. HSPM affect at least one primary second molar and possibly primary canines. Hypomineralized enamel is characteristic: the enamel prisms are disorganized, less distinct, the interprismatic space is more marked, the mineral density is decreased and the protein content is increased. Currently, etiologies remain unknown but the various studies tend towards a multifactorial model with several systemic, genetic and/or epigenetic factors, acting in a synergistic or additive way. Material and Method: The authors highlight the various factors involved in diagnosing MIH and HSPM. A review of the prevalence (French and worldwide) and etiologies of these pathologies is also provided, to enable practitioners to answer any questions parents may have. Conclusion: The knowledge of these different elements on diagnosis, structure, prevalence and etiologies will allow the orthodontist to better collaborate with the dentist but also with the parents in order to ensure an adequate dental and orthodontic management.

Introduction: L'hypominéralisation molaire incisive (MIH) et l'hypominéralisation des secondes molaires temporaires (HSPM) sont des défauts qualitatifs et asymétriques de l'émail. Les MIH affectent au moins une première molaire permanente et peuvent également être associées aux incisives permanentes. Les HSPM affectent au moins une deuxième molaire temporaire et éventuellement les canines temporaires. L'émail hypominéralisé est caractéristique : les prismes d'émail sont désorganisés, moins distincts, l'espace interprismatique est plus marqué, la densité minérale est diminuée et la teneur en protéines augmentée. Actuellement, les étiologies restent méconnues mais les différentes études tendent vers un modèle multifactoriel avec plusieurs facteurs systémiques, génétiques et/ou épigénétiques, agissant de manière synergique ou additive. Matériel et méthode: Les auteurs mettent en avant les différents éléments permettant le diagnostic des MIH et des HSPM. Un point sur les prévalences (française et mondiale) et sur les étiologies de ces pathologies est également proposé afin de permettre aux praticiens de répondre aux éventuelles interrogations des parents. Conclusion: La connaissance de ces différents éléments sur le diagnostic, la structure, les prévalences et les étiologies permettra à l'orthodontiste une meilleure collaboration avec le chirurgien-dentiste, mais également avec les parents afin d'assurer une prise en charge dentaire et orthodontique adéquate.

The prevalence and characteristics of and the association between MIH and HSPM in South-Western France.

BACKGROUND: Molar-incisor hypomineralisation (MIH) and hypomineralised second primary molars (HSPM) involve qualitative structural developmental anomalies of tooth enamel, affecting the first permanent molars (FPM) and the second primary molars, respectively. This developmental anomaly of systemic origin has important consequences for oral health. AIM: To determine the prevalence of MIH and HSPM in south-western France and explore the distribution of hypomineralised lesions on permanent and primary molars. DESIGN: Amongst 856 children (aged 7-9 years) in schools randomly selected by the Academy of Bordeaux (Ministry of Education), the FPM, permanent incisors and the second primary molars were examined by two examiners trained and calibrated for the diagnostic criteria for MIH and HSPM of the European Academy of Paediatric Dentistry. RESULTS: Molar-incisor hypomineralisation was present in 160 children (18.7%) and HSPM in 81 children (9.5%); 4.9% had both HSPM and MIH (42 of 856). Hypomineralised lesions were present in 1-4 FPM in affected individuals (mean = 2.4) and were distributed in an asymmetrical manner with widely varying severity at the tooth and individual level. A child with HSPM was more likely to have MIH than a child without HSPM (95% CI OR = 6.0 [3.7-9.7]; p < .0001). CONCLUSION: Molar-incisor hypomineralisation and HSPM have three main asymmetrical characteristics: tooth location, severity of hypomineralisation and number of teeth affected.

Prevalence of talon cusp: Systematic literature review, meta-analysis and new scoring system.

OBJECTIVES: Talon cusp is a developmental anomaly consisting of a vertical ridge or cusp projecting labially or lingually from an anterior permanent or primary tooth. A range of prevalence between 0.06 % and 40.8 % has been reported in the literature. Although many epidemiological studies have been conducted, no synthesis of these data has been performed to date. The aim of this paper was to determine the prevalence of talon cusp and to investigate the link between sex and talon cusp. SOURCE: A systematic search was undertaken using the PubMed/Medline, Embase and Cochrane Library electronic databases for publications from 1981 to 2020 investigating the prevalence of talon cusp and the link between talon cusp and sex. STUDY SELECTION: Three reviewers selected the studies independently, extracted the data in accordance with the PRISMA statement, and assessed the risk of bias via the GRADE & Cochrane approaches. RESULTS: From 39 potentially eligible studies, 9 were selected for full text analysis and 8 were included in the meta-analysis, representing 35,224 participants. The meta-analyses were performed with a random model, calculating a weighted-mean prevalence (at least one talon cusp per individual) of 1.67 %. Sex and talon cusp were not statistically significantly associated in our study (OR = 1.10; 95 % CI [0.82-1.47]; p > 0.05). DISCUSSION: We report the first prevalence of talon cusp provided by meta-analysis in a non-syndromic sample. A non-statistically significant association between sex and talon cusp is relevant in terms of genetic etiology. In order to improve the homogeneity and accuracy of the results of further studies, we propose a new universal scoring system for talon cusp. CLINICAL SIGNIFICANCE: Talon cusp is a developmental anomaly with various clinical implications. Therapeutics may vary from simple monitoring to extraction of the supporting tooth. This condition occurs in approximately 1.67 % of the population.

Are hypomineralised lesions on second primary molars (HSPM) a predictive sign of molar incisor hypomineralisation (MIH)? A systematic review and a meta-analysis.

OBJECTIVES: Molar Incisor Hypomineralisation (MIH) and Hypomineralised Second Primary Molars (HSPM) involve qualitative structural developmental anomalies of tooth enamel affecting the first permanent molars (and often incisors) and the second primary molars, respectively. A putative relationship between HSPM and MIH has been reported in the scientific literature. The aim was to determine whether children with HSPM are more likely to develop MIH. SOURCE: A systematic search using PubMed/Medline, Embase and Cochrane Library electronic databases for publications from 2001 to August 2017 investigating the link between MIH and HSPM was undertaken. STUDY SELECTION: Four reviewers selected the studies independently, extracted the data according to PRISMA statement, and assessed the bias risk with the Newcastle-Ottawa Scale (NOS) criteria. RESULTS: From 645 potentially eligible studies, 14 were selected for full text analysis and 5 were included in the meta-analysis. Cross-sectional and cohort studies were reported and 4662 participants were included. The meta-analyses were performed with a random model calculated an OR total of 4.66 (95% CI 2.11-10.26; P < 0.001). The weighted mean of the co-occurrence of HSPM and MIH prevalence was 19.94%. DISCUSSION: The high heterogeneity (I2 = 88%) can be explained by the great variation present in number of participants and variable caries risk. Despite the limitations of the study, the presence of HSPM is predictive for MIH, with greater MIH prevalence in the presence of mild HSPM. CLINICAL SIGNIFICANCE: Early detection and preventive intervention could reduce MIH complications.

Analytical evidence of enamel hypomineralisation on permanent and primary molars amongst past populations.

Molar Incisor Hypomineralisation (MIH) and Hypomineralised Second Primary Molars (HSPM) involve prevalent qualitative structural developmental anomalies of tooth enamel affecting the first permanent molars (and often incisors) and the second primary molars, respectively. These demarcated hypomineralised lesions of enamel manifest as white-cream or yellow-brown opacities, with possible post-eruptive localised loss of enamel. Aetiological hypotheses have involved contemporary life factors (i.e. environmental pollutant exposure or early childhood medications) in contrast to factors not limited to a specific time period (i.e. hypoxia at birth or genetic predisposition). Evidence of MIH in ancient populations would reinforce aetiological factors present for many centuries. By means of microtomographic and X-ray fluorescence analyses the present study provides evidence that (i) two archaeological specimens: "S407" (Sains-en-Gohelle, France, 12th-16th centuries) and "B335" (Beauvais, France, 15th-18th centuries) were MIH-affected, and (ii) one individual "S323" was affected by HSPM and MIH (Sains-en-Gohelle, France, 7th-11th centuries).

Diagnostic guide enabling distinction between taphonomic stains and enamel hypomineralisation in an archaeological context.

OBJECTIVE: Molar Incisor Hypomineralisation (MIH) is a structural anomaly that affects the quality of tooth enamel and has important consequences for oral health. The developmentally hypomineralised enamel has normal thickness and can range in colour from white to yellow or brown with or without surface breakdown. The possibility of finding MIH in 'ancient populations' could downplay several current aetiological hypotheses (e.g., dioxin derivatives, bisphenols, antibiotics) without excluding the possible multifactorial aspect of the anomaly. In an archaeological context, chemical elements contained in the burial ground can stain teeth yellow or brown and therefore might create a taphonomic bias. The purpose of the present study is to test a proposed diagnostic guide enabling determination of the pathological or taphonomic cause of enamel discolouration and defects that resemble MIH present on 'ancient teeth'. DESIGN: Two sample groups including MIH discoloration (n=12 teeth) from living patients, taphonomic discoloration (n=9 teeth) and unknown discoloration (n=2 teeth) from medieval specimens were tested. Three non-destructive methods-Raman spectroscopy, X-ray micro-computed tomography and X-ray fluorescence were utilised. RESULTS: Hypomineralised enamel has decreased mineral density (p<0.0001) and increased phosphate/ß-carbonate ratio (p<0.01) compared to normal enamel whereas relative concentrations of manganese, copper, iron and lead are similar. In taphonomic discoloration, relative concentrations of these elements are significantly different (p<0.05) to normal enamel whereas mineral density and Raman spectra profile are comparable. CONCLUSIONS: Enamel hypomineralisation can be distinguished from taphonomic staining in archaeological teeth.

Mineral density of hypomineralised and sound enamel.

Molar Incisor Hypomineralisation (MIH) is a structural anomaly that affects the quality of tooth enamel and has important consequences for oral health. The developmentally hypomineralised enamel has normal thickness and can range in colour from white to yellow or brown. The purpose of the present study is to compare the mineral density of hypomineralised and normal enamel. The sample included eight MIH teeth from seven patients. MIH teeth were scanned using high resolution microtomography. Non-parametric statistical tests (Wilcoxon test for paired samples) were carried out. Hypomineralised enamel has decreased mineral density (mean 19%; p < 0.0001) compared to normal enamel. This weak enamel has implications in clinical management of MIH lesions.