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Objective <p>Knee osteoarthritis (OA) is a leading cause of disability globally, with previous injury a key risk factor. This study investigates the relationship between the risk of progression and incidence of knee radiographic OA (rOA) and pain (KP) with major traumatic injury and identify potential predictors for rOA and KP.</p> Design <p>The longitudinal ADVANCE cohort study observes UK male military personnel, n=579 sustained combat-injury and n=565 uninjured, frequency-matched for age, rank, role, service, and deployment, in Afghanistan (2003-2014). Participants had bilateral radiographs (unless amputated), pain questionnaires, six-minute walk-tests, and serum collected, 8- and 11-years post-injury (Baseline and Follow-up). We compared rates and risk of rOA and KP incidence and progression and assessed the performance of twenty potential demographic, joint-specific and molecular predictors.</p> Results <p>Knee rOA and KP incidence and progression rates increased between Baseline and Follow-up. rOA progression did not differ between trauma-exposed and unexposed groups; however, KP progression increased for those sustaining a specific knee injury (IRR:2.53, 95% CI:1.08-5.92. Increased rOA incidence was seen in those with lower-limb loss (IRR:1.98, 95% CI:1.21-2.95), and KP incidence in trauma-exposed participants with no limb-loss or knee injury (IRR:1.45, 95% CI:1.05-2.01). No predictive model explained a large proportion of variance for rOA or KP incidence or progression. </p> Conclusions <p>Our results are consistent with a short post-injury window of increased rOA incidence, followed by a plateau. Comparatively, individuals with lower-limb loss experience a similar increase due to trauma, and then continue a steeper decline in joint-health due to altered joint biomechanics and mechanoinflammation.</p>

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Influence of major trauma and lower limb loss on radiographic progression and incidence of knee osteoarthritis and pain: a comparative and predictive analysis from the ADVANCE study

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年1月26日

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  • Oliver O’Sullivan,
  • Fraje Watson,
  • Anthony M J Bull,
  • Susie Schofield,
  • Emma C Coady,
  • Christopher J Boos,
  • Paul Cullinan,
  • Nicola T Fear,
  • Stefan Kluzek,
  • Alexander N. Bennett,
  • Ana M. Valdes

摘要

Objective

Knee osteoarthritis (OA) is a leading cause of disability globally, with previous injury a key risk factor. This study investigates the relationship between the risk of progression and incidence of knee radiographic OA (rOA) and pain (KP) with major traumatic injury and identify potential predictors for rOA and KP.

Design

The longitudinal ADVANCE cohort study observes UK male military personnel, n=579 sustained combat-injury and n=565 uninjured, frequency-matched for age, rank, role, service, and deployment, in Afghanistan (2003-2014). Participants had bilateral radiographs (unless amputated), pain questionnaires, six-minute walk-tests, and serum collected, 8- and 11-years post-injury (Baseline and Follow-up). We compared rates and risk of rOA and KP incidence and progression and assessed the performance of twenty potential demographic, joint-specific and molecular predictors.

Results

Knee rOA and KP incidence and progression rates increased between Baseline and Follow-up. rOA progression did not differ between trauma-exposed and unexposed groups; however, KP progression increased for those sustaining a specific knee injury (IRR:2.53, 95% CI:1.08-5.92. Increased rOA incidence was seen in those with lower-limb loss (IRR:1.98, 95% CI:1.21-2.95), and KP incidence in trauma-exposed participants with no limb-loss or knee injury (IRR:1.45, 95% CI:1.05-2.01). No predictive model explained a large proportion of variance for rOA or KP incidence or progression.

Conclusions

Our results are consistent with a short post-injury window of increased rOA incidence, followed by a plateau. Comparatively, individuals with lower-limb loss experience a similar increase due to trauma, and then continue a steeper decline in joint-health due to altered joint biomechanics and mechanoinflammation.