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Published ahead of print on May 19, 2004, doi:10.1164/rccm.200308-1100OC
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American Journal of Respiratory and Critical Care Medicine Vol 170. pp. 541-546, (2004)
© 2004 American Thoracic Society
doi: 10.1164/rccm.200308-1100OC


Original Article

Upper Airway Muscle Inflammation and Denervation Changes in Obstructive Sleep Apnea

John H. Boyd, Basil J. Petrof, Qutayba Hamid, Richard Fraser and R. John Kimoff

Respiratory Division and Sleep Laboratory, McGill University Health Center; Meakins-Christie Laboratories; and Department of Pathology, McGill University, Montreal, Quebec, Canada

Correspondence and requests for reprints should be addressed to R. John Kimoff, M.D., Room L4.08, 687 Pine Avenue West, McGill University Health Center, Montreal, PQ, Canada H3A 1A1. E-mail: john.kimoff{at}muhc.mcgill.ca

Inflammatory cell infiltration and afferent neuropathy have been shown in the upper airway (UA) mucosa of subjects with obstructive sleep apnea (OSA). We hypothesized that inflammatory and denervation changes also involve the muscular layer of the pharynx in OSA. Morphometric analysis was performed on UA tissue from nonsnoring control subjects (n = 7) and patients with OSA (n = 11) following palatal surgery. As compared with control subjects, inflammatory cells were increased in the muscular layer of patients with OSA, with CD4+ and activated CD25+ T cells (both increased ~ threefold) predominating. Inflammation was also present in UA mucosa, but with a different pattern consisting of CD8+ (2.8-fold increase) and activated CD25+ (3.2-fold increase) T cell predominance. As ascertained by immunoreactivity for the panneuronal marker PGP9.5, there was a dramatic (5.7-fold) increase in intramuscular nerve fibers in OSA patients compared with control subjects, as well as direct evidence of denervation based on positive immunostaining of the muscle fiber sarcolemmal membrane for the neural cell adhesion molecule in patients with OSA. These data suggest that inflammatory cell infiltration and denervation changes affect not only the mucosa, but also the UA muscle of patients with OSA. This may have important implications for the ability to generate adequate muscular dilating forces during sleep.

Key Words: immunohistochemistry • muscular diseases • neural cell adhesion molecule




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