Literature DB >> 7554923

The mineral and protein content of enamel in amelogenesis imperfecta.

J T Wright1, T G Deaton, K I Hall, M Yamauchi.   

Abstract

The purpose of this investigation was to characterize the enamel composition of teeth affected with the hereditary enamel disorders known as amelogenesis imperfecta. Teeth from 10 individuals representing all 3 major AI types (hypocalcified, n = 3; hypomaturation, n = 3; hypoplastic, n = 4) and 10 normal teeth were studied. Half of each tooth was used for histological and biochemical studies. The enamel protein content was estimated by amino acid analysis. The enamel mineral content (volume %) was determined from the calcium and/or phosphorus content. Calcium was measured using atomic absorption and phosphorus was determined colorimetrically. The mean enamel mineral content was reduced for all hypomaturation and hypocalcified AI teeth while hypoplastic AI enamel varied from normal to reduced compared with normal enamel. The enamel protein content was increased in all but one AI case (7 cases were examined for protein) compared with the normal enamel. The mineral and protein content in AI enamel showed a significant inverse relationship (R = -0.939, P = 0.001). This study shows that all three of the major AI groups can have subtypes associated with substantial decreases in the enamel mineral content, although hypomineralization appears most severe in the hypomaturation and hypocalcified AI types. The decreased mineral content was associated with an increased protein content in AI enamel. These findings provide further evidence that altered enamel mineralization in AI teeth likely involves abnormal post-secretory processing of the enamel proteins.

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Year:  1995        PMID: 7554923     DOI: 10.3109/03008209509013730

Source DB:  PubMed          Journal:  Connect Tissue Res        ISSN: 0300-8207            Impact factor:   3.417


  6 in total

1.  Relationships between protein and mineral during enamel development in normal and genetically altered mice.

Authors:  Charles E Smith; Yuanyuan Hu; Amelia S Richardson; John D Bartlett; Jan C-C Hu; James P Simmer
Journal:  Eur J Oral Sci       Date:  2011-12       Impact factor: 2.612

2.  Phenotypic variation in FAM83H-associated amelogenesis imperfecta.

Authors:  J T Wright; S Frazier-Bowers; D Simmons; K Alexander; P Crawford; S T Han; P S Hart; T C Hart
Journal:  J Dent Res       Date:  2009-04       Impact factor: 6.116

3.  Assessment of restorative treatment of patients with amelogenesis imperfecta.

Authors:  Chiung-Fen Chen; Jan Ching Chun Hu; Maria Regina Padilla Estrella; Mathilde C Peters; Eduardo Bresciani
Journal:  Pediatr Dent       Date:  2013 Jul-Aug       Impact factor: 1.874

4.  Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta.

Authors:  Maria C L G Santos; P Suzanne Hart; Mukundhan Ramaswami; Cláudia M Kanno; Thomas C Hart; Sergio R P Line
Journal:  Head Face Med       Date:  2007-01-31       Impact factor: 2.151

5.  The Enamel Phenotype in Homozygous Fam83h Truncation Mice.

Authors:  Shih-Kai Wang; Yuanyuan Hu; Charles E Smith; Jie Yang; Chunhua Zeng; Jung-Wook Kim; Jan C-C Hu; James P Simmer
Journal:  Mol Genet Genomic Med       Date:  2019-05-06       Impact factor: 2.183

6.  The effect of different surface treatments of demineralised enamel on microleakage under metal orthodontic brackets.

Authors:  Horieh Moosavi; Farzaneh Ahrari; Hamideh Mohamadipour
Journal:  Prog Orthod       Date:  2013-05-20       Impact factor: 2.750

  6 in total

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