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Mimicking and Measuring Occlusal Erosive Tooth Wear with the "Rub&Roll" and Non-contact Profilometry
Published on: February 2, 2018
Severe tooth wear in Prader-Willi syndrome. A case-control study
Ronnaug Saeves1, Ivar Espelid, Kari Storhaug
1TAKO-centre, Lovisenberg Diakonale Hospital, Lovisenberggt 17, 0440 Oslo, Norway. Ronnaug.Saeves@tako.no
Insights
Individuals with Prader-Willi syndrome (PWS) experience severe tooth wear due to erosion and attrition. This highlights a significant need for dental rehabilitation in affected young adults.
Area of Science:
- Genetics
- Dentistry
- Endocrinology
Background:
- Prader-Willi syndrome (PWS) is a rare genetic disorder with multisystemic effects, including oral abnormalities.
- Individuals with PWS often exhibit severe hypotonia, endocrine issues, hyperphagia, obesity, and cognitive impairments.
Purpose of the Study:
- To investigate the prevalence of tooth wear in individuals with Prader-Willi syndrome.
- To identify potential risk factors associated with tooth wear in the PWS population.
Main Methods:
- A case-control study involving 49 individuals with PWS (aged 6-40) and an age/sex-matched control group.
- Tooth wear assessed using the Visual Erosion Dental Examination (VEDE) and individual tooth wear index (IA) from dental casts, photographs, and clinical evaluation.
- Whole saliva collection and analysis.
Main Results:
- Significantly higher tooth wear (VEDE and IA scores) in the PWS group compared to controls (p < 0.001).
- Tooth wear in PWS correlated with age, reduced saliva secretion, and tooth grinding.
- Multivariate analysis confirmed PWS, age, and tooth grinding as significant predictors of tooth wear.
Conclusions:
- Tooth wear, encompassing both erosion and attrition, is a critical issue in Prader-Willi syndrome.
- Young adults with PWS demonstrate a substantial requirement for prosthodontic rehabilitation due to severe tooth wear.
Background:
Prader-Willi syndrome (PWS) is a rare complex multsystemic genetic disorder characterized by severe neonatal hypotonia, endocrine disturbances, hyperphagia and obesity, mild mental retardation, learning disabilities, facial dysmorphology and oral abnormalities. The purpose of the present study was to explore the prevalence of tooth wear and possible risk factors in individuals with Prader-Willi syndrome.
Methods:
Forty-nine individuals (6-40 years) with PWS and an age- and sex-matched control group were included. Tooth wear was evaluated from dental casts and intraoral photographs and rated by four examiners using the Visual Erosion Dental Examination (VEDE) scoring system and the individual tooth wear index IA. In accordance with the VEDE scoring system, tooth wear was also evaluated clinically. Whole saliva was collected.
Results:
Mean VEDE score was 1.70 ± 1.44 in the PWS group and 0.46 ± 0.36 in the control group (p < 0.001). Median IA was 7.50 (2.60-30.70) in the PWS group and 2.60 (0.90-4.70) among controls (p < 0.001). In the PWS group tooth wear correlated significantly with age (VEDE; r = 0.79, p < 0.001, IA; r = 0.82, p < 0.001) and saliva secretion (VEDE; r = 0.46, p = 0.001, IA; r = 0.43, p = 0.002). Tooth grinding was also associated with tooth wear in the PWS group, as indicated by the mean VEDE 2.67 ± 1.62 in grinders and 1.14 ± 0.97 in non-grinders (p = 0.001) and median IA values 25.70 (5.48-68.55) in grinders and 5.70 (1.60-9.10) in non-grinders (p = 0.003). Multivariate linear regression analysis was performed with tooth wear as the dependent variable and PWS (yes/no), age, tooth grinding and saliva secretion as independent variables. PWS (yes/no), age and tooth grinding retained a significant association with tooth wear, VEDE (p < 0.001) and log IA (p < 0.001). The only factor significantly associated with tooth wear in the control group was age.
Conclusions:
Our study provides evidence that tooth wear, in terms of both erosion and attrition, is a severe problem in Prader-Willi syndrome. There is therefore considerable need for prosthodontic rehabilitation in young adults with PWS.
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