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Microsatellite DNA instability and COPD exacerbations

¹ Dept of Thoracic Medicine, University Hospital, Medical School, University of Crete, Heraklion, and ² Dept of Pulmonology, Agios Georgios General Hospital, Chania, Greece.

CORRESPONDENCE: N. M. Siafakas, Department of Thoracic Medicine, Medical School, University of Crete, 71110 Heraklion Crete, Greece. Fax: 30 2810542650. E-mail: siafak{at}med.uoc.gr

Keywords: Chronic bronchitis, emphysema, microsatellite DNA, smoking, somatic mutation, sputum

Received: December 16, 2007
Accepted May 5, 2008

Increased frequency of microsatellite DNA instability (MSI) has been detected in the sputum of chronic obstructive pulmonary disease (COPD) patients. The aim of the present study was to investigate the relationship between MSI in sputum cells and exacerbation frequency, which is an important parameter in the clinical course of the disease.

Induced sputum samples and peripheral blood obtained from 36 patients with COPD at stable state were analysed. The control group consisted of 30 nonsmoking healthy subjects. DNA was extracted and analysed for MSI using the following microsatellite markers: RH70958, D5S207, D6S2223, D6S344, D6S263, G29802 [GenBank] , D13S71, D14S588, D14S292 and D17S250. Following MSI analysis, exacerbations were recorded for 3 yrs in total.

No MSI was detected in healthy nonsmokers. A total of 18 (50%) out of 36 patients exhibited MSI in their sputum cells. Patients who exhibited MSI showed significantly increased frequency of exacerbations compared with patients that did not. In addition, a significantly increased frequency of purulent and of severe type exacerbations was found in patients exhibiting MSI. Patients positive for marker G29802 [GenBank] , D13S71 or D14S588 presented increased exacerbation frequency.

The significant association between microsatellite DNA instability and chronic obstructive pulmonary disease exacerbations indicates that somatic mutations could be involved in the pathogenesis and natural history of the disease.

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