Structural and functional properties of bone are compromised in amyotrophic lateral sclerosis mice

Abstract

In addition to muscle weakness, amyotrophic lateral sclerosis (ALS) is associated with an increased incidence of skeletal fractures. The SOD1^G93A mouse model recapitulates many features of human ALS. These mice also exhibit decreased bone mass. However, the functional, or biomechanical, behavior of the skeleton in SOD1^G93A mice has not been investigated. To do so, we examined skeletal phenotypes in end-stage (16-week-old) SOD1^G93A female mice and healthy littermate female controls (N = 9–10/group). Outcomes included trabecular and cortical bone microarchitecture by microcomputed tomography; stiffness and strength via three-point bending; resistance to crack growth by fracture toughness testing; and cortical bone matrix properties via cyclic reference point indentation. SOD1^G93A mice had similar bone size, but significantly lower trabecular bone mass (–54%), thinner trabeculae (–41%) and decreased cortical bone thickness (–17%) and cortical area (–18%) compared to control mice (all p < 0.01). In line with these bone mass and microstructure deficits, SOD1^G93A mice had significantly lower femoral bending stiffness (–27%) and failure moment (–41%), along with decreased fracture toughness (–18%) (all p < 0.001). This is the first study to demonstrate functional deficits in the skeleton of end-stage ALS mice, and imply multiple mechanisms for increased skeletal fragility and fracture risk in patients in ALS. Importantly, our results provide strong rationale for interventions to reduce fracture risk in ALS patients with advanced disease.

Keywords:

• ALS mouse model
• bone strength
• bone biomechanics
• fracture toughness
• microCT

Acknowledgements

We thank Dimitrios Psaltos for assistance during microCT scanning and analysis.

Declaration of interest

The authors have nothing to disclose.

This work was supported by NASA [NNX16AL36G] and NIH [R01-NS055099].

Additional information

Funding

This work was supported by NASA [NNX16AL36G] and NIH [R01-NS055099].