AI Article Synopsis

  • The study aimed to investigate the anti-inflammatory effects of theophylline on airway inflammation in COPD patients.
  • A randomized double-blind trial was conducted with 11 patients, where 6 received theophylline and 5 received a placebo over 4 weeks.
  • Results showed that theophylline significantly reduced certain inflammatory markers (neutrophil elastase and myeloperoxidase) but did not lead to significant changes in overall cell counts, indicating a potential benefit in reducing airway inflammation, though clinical implications still need further exploration.

Article Abstract

Objective: Recent studies have shown that theophylline may exert anti-inflammatory effects on neutrophils. We undertook to assess the effect of theophylline on airway inflammation in COPD.

Methodology: We performed a 4-week randomized double-blind, placebo-controlled study in 11 theophylline-naive patients with mild to moderate COPD. After a 1-week run-in period, six subjects were administered 400 mg/day theophylline (Theodur; Nikken Chemicals Co. Ltd, Tokyo, Japan) for 4 weeks, while five subjects were administered a placebo. Induced sputum was obtained before and after the run-in period and then after 2 and 4 weeks of treatment. Cell differential count and levels of interleukin-8, matrix metalloproteinase-9, neutrophil elastase (NE), myeloperoxidase (MPO), alpha1-antitrypsin (alpha1-AT), leukotriene B4 and tissue inhibitor of metalloproteinases-1 (TIMP-1) were assessed.

Results: No variable was significantly different during the run-in period or with placebo treatment. In contrast, theophylline treatment significantly decreased NE and MPO levels at 4 weeks, although the cell differential count did not change appreciably as a result of treatment.

Conclusion: These results suggest that 4 weeks of theophylline treatment attenuates neutrophil-associated inflammation in the airways of mild to moderate COPD patients. However, the clinical benefits remain to be determined.

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Source
http://dx.doi.org/10.1111/j.1440-1843.2004.00573.xDOI Listing

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