Osteoarthritis and Cartilage
Volume 20, Issue 4 , Pages 271-278, April 2012

Effects of intraarticular IL1-Ra for acute anterior cruciate ligament knee injury: a randomized controlled pilot trial (NCT00332254)

  • V.B. Kraus

      Affiliations

    • Department of Medicine, Duke University Medical Center, Durham, NC, USA
    • Corresponding Author InformationAddress correspondence and reprint requests to: V.B. Kraus, Box 3416, Duke University Medical Center, Durham, NC 27710. Tel: 1-919-681-6652; Fax: 1-919-684-8907.
  • ,
  • J. Birmingham

      Affiliations

    • Department of Medicine, Duke University Medical Center, Durham, NC, USA
  • ,
  • T.V. Stabler

      Affiliations

    • Department of Medicine, Duke University Medical Center, Durham, NC, USA
  • ,
  • S. Feng

      Affiliations

    • Biostatistics and Bioinformatics, Duke University Medical Center, Durham, NC, USA
  • ,
  • D.C. Taylor

      Affiliations

    • Orthopaedic Surgery, Duke University Medical Center, Durham, NC, USA
  • ,
  • C.T. Moorman III

      Affiliations

    • Orthopaedic Surgery, Duke University Medical Center, Durham, NC, USA
  • ,
  • W.E. Garrett

      Affiliations

    • Orthopaedic Surgery, Duke University Medical Center, Durham, NC, USA
  • ,
  • A.P. Toth

      Affiliations

    • Orthopaedic Surgery, Duke University Medical Center, Durham, NC, USA

Received 31 July 2011; accepted 21 December 2011. published online 03 February 2012.

Summary 

Objective

To evaluate the clinical effectiveness of intraarticular IL-1 receptor antagonist (IL-1Ra) for anterior cruciate ligament (ACL) tear.

Methods

Eleven patients with acute ACL tear confirmed by magnetic resonance imaging (MRI) were randomized to receive a single intraarticular injection of IL-1Ra (anakinra 150 mg, n = 6) or equal volume of saline placebo (1 ml, n = 5). The double-blinded treatment was administered a mean 2 weeks after injury. Synovial fluid (SF) (n = 9 patients) and sera (all patients) were available at baseline (prior to injection) and immediately prior to surgery (mean 35 days later) and analyzed for SF IL-1α, IL-1β, IL-1Ra and serum hyaluronan (HA), an indicator of synovial inflammation. The primary outcome, standardized Knee Injury and Osteoarthritis Outcome Score (KOOS) questionnaire, was obtained at 0 (baseline), 4, and 14 days after injection.

Results

Compared with placebo, the IL-1Ra group had substantially greater improvement in key outcomes over 14 days (KOOS pain P = 0.001; activities of daily living P = 0.0015; KOOS sports function P = 0.0026; KOOS quality of life (QOL) P = 0.0048; and total KOOS P < 0.0001). There were no adverse reactions in either group. SF IL-1α (P = 0.05) and serum HA (P = 0.03), but not IL-1β, or IL-1Ra, decreased significantly in the IL-1Ra but not the placebo treated patients. Compared with placebo, IL-1α was borderline significantly different in the IL-1Ra treated group (P = 0.06).

Conclusions

Administered within the first month following severe knee injury, IL-1Ra reduced knee pain and improved function over a 2-week interval. This promising proof of concept study provides a new paradigm for studies of acute joint injury and suggests that a larger follow-up study is warranted.

Keywords: Joint injury, IL-1Ra, Biomarkers, Clinical trial, Anterior cruciate ligament, Post-traumatic arthritis

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PII: S1063-4584(12)00012-X

doi:10.1016/j.joca.2011.12.009

Osteoarthritis and Cartilage
Volume 20, Issue 4 , Pages 271-278, April 2012