Arthroscopy is a minimally invasive surgical approach to the diagnosis and treatment of patients with persistent, recalcitrant symptoms related to temporomandibular joint (TMJ) pathology. Synovial fluid analysis combined with arthroscopy has provided a research model designed to identify pathogenic mechanisms of TMJ disease. It is our purpose to study IgA, IgG, and beta-glucuronidase levels in order to find a correlation between biochemical markers and joint pathology which will allow us to better understand intra-articular pathology. Our working hypothesis was that those joints with the highest levels of osteoarthritis and synovitis, would have elevated levels of inflammatory by products in the synovial fluid. Our patient population included 20 patients (18 female, 2 male) with severe pain and limitation of mandibular movement that failed to improve with at least 3 months of a full course of nonsurgical therapy. Arthroscopic surgery was performed on 29 temporomandibular joints in these 20 patients. Immediately prior to the arthroscopic procedure, a synovial fluid aspirate was obtained by injecting then aspirating 2 mL of 0.9% saline from the superior joint space. Synovial fluid aspirates of TMJs from 13 control subjects (6 female and 7 males), with no history of TMJ pain/dysfunction, were obtained. These subjects underwent flexible fiberoptic arthroscopy through a No. 15 gauge needle and a 0.86 mm flexible endoscope and were recruited for the study with full IRB approval. Arthroscopic examination of the patient and control groups involved classification of joints for osteoarthritis (OA) and synovitis (syn) using a visual grading system. All synovial fluid samples were analyzed for beta-glucuronidase, IgA, and IgG using fluorometric assay and ELISA. The results in the symptomatic group revealed the following arthroscopic findings: non-OA in 11 joints, OA grade I in 7 joints, and OA grade II in 11 joints. In the asymptomatic control group, all 13 joints showed non-OA (P < .05 nonparametric variance). The symptomatic group demonstrated the following: non-syn in 1 joint, syn grade 1 in 1 joint, syn grade 2 in 11 joints, syn grade 3 in 13 joints, and syn grade 4 in 3 joints. The asymptomatic control group demonstrated non-syn in 8 joints, syn grade 1 in 2 joints, and syn grade 2 in 3 joints (P < .05, nonparametric variance). Beta-glucuronidase was significantly elevated (P < .05, t test) in the patient group when compared to the control group (4.13 plus minus 8.30 versus 0.9 ±0.83) (mean ± standard deviation). The difference in the IgG level was also statistically significant (31,638 ± 70,714 versus 4,407 ± 1,324; P < .05, t test). IgA level showed a similar trend between the patient and the control group (6,315 ± 19,037 versus 425 ± 192; P =.10, t test).