Ischemic-reperfusion injury is thought to be a cause of idiopathic carpal tunnel syndrome (CTS). The purpose of this study was to determine whether oxidative stress caused by ischemia-reperfusion injury in subsynovial connective tissue is associated with idiopathic CTS and its symptoms. Bioptic samples of tenosynovial tissue were collected from 20 idiopathic CTS patients during surgery. Control specimens of tenosynovial tissue were collected from eight non-CTS patients. Analysis included histological and immunohistochemical examination for the distribution of endothelial nitric oxide synthase (eNOS), nuclear factor (NF)-, and transforming growth factor (TGF)- RI in subsynovial connective tissues. Histological examinations showed a marked increase in fibroblast density and vascular proliferation in specimens from CTS patients. The expressions of eNOS, NF-, and TGF- RI in fibroblasts and vascular endothelial cells of subsynovial connective tissues of patients were significantly higher than in those of controls. A significant positive correlation was found between the subjective symptom severity of CTS, and the immunoreactivities of eNOS and NF-. This study suggests that oxidative stress in subsynovial connective tissue is related to CTS and its symptoms. © 2010 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J. Orthop. Res. 28: 1463Res. 28: -1468Res. 28: , 2010 Keywords: idiopathic carpal tunnel syndrome; oxidative stress; subsynovial connective tissueThe disease mechanism of idiopathic carpal tunnel syndrome (CTS) involves an elevated carpal tunnel pressure due to a reduction in the size of the tunnel or an increase in the volume of its content. 1,2 Previous studies demonstrated that no significant differences exist between patients with and without CTS in terms of transverse carpal ligament, 3,4 and, therefore, suggested that CTS is likely caused by an increase in carpal tunnel volume. This hypothesis is supported by recent MRI studies that showed evidence of tenosynovial swelling. 5,6 A number of researchers attempted to identify pathological changes in idiopathic CTS. Most reported that inflammatory cells are rare and that edema and nonspecific fibrosis are the most common histological findings of tenosynovium. 7 However, some authors pointed out that these pathological findings do not well correlate with the symptoms of CTS. 2,8 Freeland et al. 9 suggested that ischemia-reperfusion injury is an important cause of idiopathic CTS. This injury type would increase the levels of several types of proinflammatory cytokines in tenosynovium, and possibly cause the pathologic changes observed in idiopathic CTS. The purpose of our study was to seek evidence of the oxidative stress caused by ischemia-reperfusion injury in subsynovial connective tissue of idiopathic CTS and to investigate the extent of the association between oxidative stress and the symptoms of idiopathic CTS.
MATERIALS AND METHODSThis study was approved by our institutional review board, and informed consent for spec...