PMID- 21905256 OWN - NLM STAT- MEDLINE DCOM- 20120117 LR - 20151119 IS - 2151-4658 (Electronic) IS - 2151-464X (Linking) VI - 63 IP - 12 DP - 2011 Dec TI - Association between skeletal muscle inflammatory markers and walking pattern in people with knee osteoarthritis. PG - 1715-21 LID - 10.1002/acr.20625 [doi] AB - OBJECTIVE: Patients with knee osteoarthritis (OA) are characterized by increased muscle inflammation and altered gait. We investigated the association between proinflammatory mediators in the vastus lateralis and physical function and gait in patients with knee OA. METHODS: Nineteen patients with knee OA underwent gait analysis, assessment of self-reported pain and physical function (Western Ontario and McMaster Universities Osteoarthritis Index [WOMAC]), and a muscle biopsy that was taken during their knee replacement surgery. Muscle was analyzed for cellular protein inflammatory mediators, interleukin-6, monocyte chemotactic protein 1 (MCP-1), p65 NF-kappaB, signal transducer and activator of transcription 3 (STAT-3), and JNK-1. Sagittal plane knee function, including early stance knee range of motion (ROM) and knee sagittal plane impulse, was measured using a motion analysis system. Pearson's correlation was used to assess relationships between selected variables. RESULTS: Significant positive correlations were found between MCP-1 and self-perceived stiffness, physical function, and the total WOMAC score (P < 0.05). MCP-1 was also negatively correlated with early stance knee ROM (r = -0.52, P = 0.023). Reduced velocity was associated with elevated levels of p65 NF-kappaB and STAT-3 (P < 0.05). Knee sagittal plane impulse was negatively correlated with JNK-1 (P = 0.02), indicating reduction in knee impulse with an increased level of JNK-1. CONCLUSION: Increased levels of several proinflammatory mediators were correlated with altered knee function during walking as well as greater physical disability and slower gait velocity. Identification of the cellular and molecular mechanisms associated with muscle inflammation is important to better understand the underlying mechanism responsible for altered gait and function in patients with knee OA. CI - Copyright (c) 2011 by the American College of Rheumatology. FAU - Levinger, Pazit AU - Levinger P AD - La Trobe University, Bundoora, Victoria, Australia. p.levinger@latrobe.edu.au FAU - Caldow, Marissa K AU - Caldow MK FAU - Feller, Julian A AU - Feller JA FAU - Bartlett, John R AU - Bartlett JR FAU - Bergman, Neil R AU - Bergman NR FAU - McKenna, Michael J AU - McKenna MJ FAU - Cameron-Smith, David AU - Cameron-Smith D FAU - Levinger, Itamar AU - Levinger I LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - Arthritis Care Res (Hoboken) JT - Arthritis care & research JID - 101518086 RN - 0 (Biomarkers) RN - 0 (CCL2 protein, human) RN - 0 (Chemokine CCL2) RN - 0 (IL6 protein, human) RN - 0 (Inflammation Mediators) RN - 0 (Interleukin-6) RN - 0 (RELA protein, human) RN - 0 (STAT3 Transcription Factor) RN - 0 (STAT3 protein, human) RN - 0 (Transcription Factor RelA) RN - EC 2.7.11.24 (Mitogen-Activated Protein Kinase 8) SB - IM MH - Aged MH - Biomarkers/analysis MH - Biomechanical Phenomena MH - Biopsy MH - Chemokine CCL2/analysis MH - Cross-Sectional Studies MH - Disability Evaluation MH - Female MH - *Gait MH - Humans MH - Inflammation Mediators/*analysis MH - Interleukin-6/analysis MH - Male MH - Middle Aged MH - Mitogen-Activated Protein Kinase 8/analysis MH - Osteoarthritis, Knee/diagnosis/*immunology/*physiopathology MH - Pain Measurement MH - Quadriceps Muscle/*immunology/*physiopathology MH - Range of Motion, Articular MH - STAT3 Transcription Factor/analysis MH - Self Report MH - Transcription Factor RelA/analysis MH - Victoria MH - *Walking EDAT- 2011/09/10 06:00 MHDA- 2012/01/18 06:00 CRDT- 2011/09/10 06:00 PHST- 2011/09/10 06:00 [entrez] PHST- 2011/09/10 06:00 [pubmed] PHST- 2012/01/18 06:00 [medline] AID - 10.1002/acr.20625 [doi] PST - ppublish SO - Arthritis Care Res (Hoboken). 2011 Dec;63(12):1715-21. doi: 10.1002/acr.20625.