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Eur Respir J 2006; 27:51-59
Copyright ©ERS Journals Ltd 2006

Increased injury and intramuscular collagen of the diaphragm in COPD: autopsy observations

A. Scott1, X. Wang1, J. D. Road2 and W. D. Reid1,3

1 School of Rehabilitation Sciences, 2 Respiratory Division, and 3 James Hogg iCAPTURE Centre for Cardiovascular and Pulmonary Research, University of British Columbia, BC, Canada.

CORRESPONDENCE: W. D. Reid, School of Rehabilitation Sciences, T325-2211 Wesbrook Mall, Vancouver, BC, V6T 2B5 Canada. Fax: 1 6048227624. E-mail: wdreid{at}interchange.ubc.ca

Keywords: Aged, diaphragm, human, lung diseases, obstructive, pathology/physiopathology

Received: December 14, 2004
Accepted October 4, 2005

Evidence for diaphragm injury in people with chronic obstructive pulmonary disease (COPD) has been reported, although the extent of injury and collagen accumulation post mortem have not previously been examined. In addition, it is not known whether the amount of injury and collagen are different in key regions of the diaphragm.

The cross-sectional area of collagen and the percentage of abnormal myofibres in the post mortem diaphragm and psoas major were determined by computer-assisted image analysis of stained cross-sections of the diaphragm for collagen with picrosirius red and with haematoxylin and eosin for morphology.

In the midcostal diaphragm of six subjects with COPD and six subjects with no significant respiratory disease, the COPD diaphragm displayed a greater cross-sectional area of collagen and percentage of abnormal myofibres (collagen: 24.2±1.0 versus 18.6±1.1%; injury: 28.4±7.2 versus 12.0±1.3%). In 18 patients with various respiratory conditions, the midcostal diaphragm displayed more collagen and abnormal myofibres than the crural diaphragm, while both costal and crural diaphragms displaying more collagen and abnormal myofibres than psoas major.

This study reveals extensive injury and collagen accumulation in the chronic obstructive pulmonary diseased diaphragm, and reveals a regional pattern of injury and intramuscular collagen which may correspond to variations in diaphragm loading.




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