Bacterial infections of the dental pulp result in tissue destruction and pe
riapical bone resorption. The availability of genetically engineered mouse
strains is a major advantage in the use of this model system for studies of
periapical pathogenesis. The main limitation of the mouse model is its sma
ll size, and the necessity for laborious histologic analyses to quantify pe
riapical bone destruction. In the present study, we evaluated the use of a
new technology, high-resolution micro-computed tomography (micro-CT), for t
he rapid and non-invasive quantification of periapical bone destruction. Pe
riapical lesions were induced in the lower first molars of mice by exposing
the pulp to the oral environment. Mandibles were harvested on day 21 after
pulp exposure, and were subjected to micro-CT analysis, with 17-mu m-thick
radiographic sections. Samples were then decalcified, embedded, and sectio
ned for histolology. The cross-sectional area of periapical lesions was det
ermined by image analysis of corresponding micro-CT and histologic sections
. The results showed a highly significant correlation between micro-CT and
histology (p < 0.0001), with mean differences of 4.1% (range, 0.9 to 7.2%)
between the two methods. The mean error associated with image analysis was
4.9% for images obtained by both micro-CT and histology. The variability of
replicate (n = 5) independent micro-CT determinations was 3.4%, less than
that associated with the image analysis error. These results demonstrate th
at micro-CT imaging is a rapid, reproducible, and non-invasive method, that
gives results that an closely comparable with those obtained by histology.
Micro-CT appears to have utility for the accurate quantification of change
s in bone architecture in small biological specimens.