Orthodontic force induces local bone resorption in mild-type hypophosphatasia mouse model.

OBJECTIVES: Hypophosphatasia (HPP) is a congenital disease caused by mutations in the tissue non-specific alkaline phosphatase gene. HPP is characterized by impaired hard tissue mineralization and premature tooth loss. Mild-type HPP includes childhood-, adult, and odonto-HPP. Mild-type HPP is difficult to diagnose because individuals with mild-type HPP do not have characteristic symptoms. The effects of applying mechanical stress, such as that caused by orthodontic force, on the teeth and jawbones of patients with mild-type HPP are unknown; therefore, in this study these effects were examined in mild-type HPP model mice.

METHODS: A 10 gf nickel-titanium closed-coil spring was placed on the maxillary incisors and left first molar (M1) of mild-type HPP model mice (Akp2+/-). The M1 moved mesially to the maxillary incisors 14 days before sampling.

RESULTS: Tooth movement distance, serum alkaline phosphatase (ALP) and serum C-terminal telopeptide of Type I collagen (CTX-1) levels did not differ between Akp2+/- and normal (Akp2+/+) mice. However, alveolar bone resorption on the compressed side was higher in Akp2+/- mice than that in normal mice. The cancellous bone quality on the compressed was side was lower in Akp2+/- than in Akp2+/+ mice. Fibrous structures infiltrated the bone resorption sites, and the number of osteoclasts was markedly higher in Akp2+/- mice.

CONCLUSIONS: The application of orthodontic force to mice with mild-type HPP did not affect the serum ALP and bone resorption marker CTX-1 levels, or tooth movement. However, compression induced alveolar bone resorption due to an increase in osteoclasts. These findings support the importance of differentially diagnosing mild-type HPP before initiating treatment.