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The ACL injury response: A collagen-based analysis.

Joshua S Everhart1, John H Sojka2, Christopher C Kaeding3

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PubMed
Summary

Torn anterior cruciate ligaments (ACL) show rapid collagen turnover, indicating active healing processes. This high tissue turnover occurs regardless of injury type and persists over time.

Keywords:
ACL injuryBiopsyCollagen turnoverContact injuryNon-contact injury

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Area of Science:

  • Orthopedics
  • Sports Medicine
  • Biochemistry

Background:

  • Anterior cruciate ligament (ACL) injuries have poor healing potential.
  • Tendon grafts used in ACL reconstruction undergo significant tissue turnover ('ligamentization').
  • The fate of native torn ACL tissue, specifically collagen turnover and influencing factors like injury mechanism and chronicity, remains unclear.

Purpose of the Study:

  • To investigate whether native torn anterior cruciate ligament (ACL) tissue exhibits significant collagen turnover.
  • To determine if injury mechanism (contact vs. non-contact) or time since injury affects collagen turnover in torn ACLs.

Main Methods:

  • Biopsies from 33 mid-substance ACLs obtained during arthroscopic reconstruction and 2 uninjured cadaveric ACLs.
  • Quantification of immature collagen cross-links using ninhydrin reagent assays as a marker for collagen turnover.
  • Histochemical analysis of ACL tears at different stages of chronicity.

Main Results:

  • Collagen cross-link content was consistently low across all ACL samples, irrespective of injury mechanism.
  • This low content suggests high tissue turnover occurred between injury and surgical intervention.
  • No significant demographic differences were observed between contact and non-contact injury groups.

Conclusions:

  • Collagen turnover in the anterior cruciate ligament (ACL) is rapid following injury.
  • This robust tissue turnover begins within weeks of injury and continues throughout the lifespan of the torn ligament.
  • The rate of turnover is not influenced by whether the injury was contact or non-contact.