Aging alters the subchondral bone response 7 days after noninvasive traumatic joint injury in C57BL/6JN mice

Posttraumatic osteoarthritis (PTOA) commonly develops following anterior cruciate ligament (ACL) injuries, affecting around 50% of individuals within 10–20 years. Recent studies have highlighted early changes in subchondral bone structure after ACL injury in adolescent or young adult mice, which could contribute to the development of PTOA. However, ACL injuries do not only occur early in life. Middle‐aged and older patients also experience ACL injuries and PTOA, but whether the aged subchondral bone also responds rapidly to injury is unknown. This study utilized a noninvasive, single overload mouse injury model to assess subchondral bone microarchitecture, turnover, and material properties in both young adults (5 months) and early old age (22 months) female C57BL/6JN mice at 7 days after injury. Mice underwent either joint injury (i.e., produces ACL tears) or sham injury procedures on both the loaded and contralateral limbs, allowing evaluation of the impacts of injury versus loading. The subchondral bone response to ACL injury is distinct for young adult and aged mice. While 5‐month mice show subchondral bone loss and increased bone resorption postinjury, 22‐month mice did not show loss of bone structure and had lower bone resorption. Subchondral bone plate modulus increased with age, but not with injury. Both ages of mice showed several bone measures were altered in the contralateral limb, demonstrating the systemic skeletal response to joint injury. These data motivate further investigation to discern how osteochondral tissues differently respond to injury in aging, such that diagnostics and treatments can be refined for these demographics. Early subchondral bone changes after injury may contribute to posttraumatic osteoarthritis. This study assessed subchondral bone 7 days after noninvasive single overload injury for young adult and aged female mice. In aging, the subchondral bone plate thickens and stiffens. For young mice, injury provokes subchondral bone loss and increased resorption. However, for aged mice, injury does not induce bone loss and, instead, decreases bone resorption. Several contralateral subchondral bone measures indicated a systemic response to joint injury for both ages.