Human synovial fluid interleukin-6, but not type II collagen breakdown, positively correlated with pain after anterior cruciate ligament injury and reconstruction

Breanna Sullivan, Austin V. Stone, Caitlin E.W. Conley, Emily R. Hunt, Christian Lattermann, Cale Jacobs

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

Anterior cruciate ligament (ACL) injury initiates a biochemical cascade thought to contribute to the onset and progression of posttraumatic osteoarthritis (PTOA). Interleukin-1ß (IL-1ß), IL-6, and C-telopeptide fragments of type II collagen (CTX-II) are implicated in joint inflammation and cartilage degradation following ACL injury; however, their association with pain is still being explored. The purpose of this study was to evaluate the associations between synovial fluid concentrations of IL-1ß, IL-6, and CTX-II with pain following ACL injury and reconstruction. We hypothesized that greater IL-1ß, IL-6, and CTX-II would correlate with greater Pain Visual Analogue Scale (VAS) scores. This was a secondary analysis of 23 patients (mean age = 18.4 years, BMI = 27.4, 13 females/10 males) with acute ACL tears who participated in a pilot randomized trial. Synovial fluid and VAS scores were collected on the day of initial presentation, at ACL reconstruction, and 1 and 4 weeks after surgery. Synovial fluid concentrations of IL-1ß, IL-6, and CTX-II were assessed using enzyme-linked immunoabsorbent assays, and repeated measures correlations were used to assess the relationships between pain and synovial IL-1ß, IL-6, or CTX-II after ACL injury and reconstruction. Pain was positively correlated with synovial fluid IL-6 concentrations (r = 0.52, p < 0.001); however, pain was inversely correlated with CTX-II (r = −0.39, p = 0.002). IL-1ß had no significant correlation with pain. Statement of clinical relevance: PTOA has been described as a “silent killer” and these results suggest that early PTOA may have pro-inflammatory pathways that are not primarily associated with pain but still lead to progressive cartilage loss.

Original languageEnglish
Pages (from-to)300-306
Number of pages7
JournalJournal of Orthopaedic Research
Volume41
Issue number2
DOIs
StatePublished - Feb 2023

Bibliographical note

Publisher Copyright:
© 2022 Orthopaedic Research Society. Published by Wiley Periodicals LLC.

Funding

Funding was provided in part by the University of Kentucky College of Medicine MVP Grant; NIH National Center for Advancing Translational Sciences, Grant/Award Number: UL1TR001998. Disclosures: Austin Stone (3C‐Allosource, 3C‐Smith & Nephew, 5‐Allosource, 5‐Flexion Therapeutics, 9‐AOSSM, 9‐AANA), Christian Lattermann (3B‐Samumed, Vericel, Joint Restoration Foundation; 8‐Cartilage, J Sports Physiology, The Knee, OJSM; 9‐Biologic Association, International Cartilage Repair Society), Cale Jacobs (5‐Flexion Therapeutics, 5‐Smith & Nephew, 8‐VJSM). Funding was provided in part by the University of Kentucky College of Medicine MVP Grant; NIH National Center for Advancing Translational Sciences, Grant/Award Number: UL1TR001998. Disclosures: Austin Stone (3C-Allosource, 3C-Smith & Nephew, 5-Allosource, 5-Flexion Therapeutics, 9-AOSSM, 9-AANA), Christian Lattermann (3B-Samumed, Vericel, Joint Restoration Foundation; 8-Cartilage, J Sports Physiology, The Knee, OJSM; 9-Biologic Association, International Cartilage Repair Society), Cale Jacobs (5-Flexion Therapeutics, 5-Smith & Nephew, 8-VJSM).

FundersFunder number
9-Biologic Association
International Cartilage Repair Society8-VJSM
University of Kentucky College of Medicine
National Center for Advancing Translational Sciences (NCATS)UL1TR001998, 9-AANA, 9-AOSSM

    Keywords

    • anterior cruciate ligament
    • biomarker
    • cartilage
    • knee
    • pain

    ASJC Scopus subject areas

    • Orthopedics and Sports Medicine

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