ERYTHROCYTIC GLUTATHIONE IN CYSTIC-FIBROSIS - A POSSIBLE MARKER OF PULMONARY DYSFUNCTION

Citation
S. Mangione et al., ERYTHROCYTIC GLUTATHIONE IN CYSTIC-FIBROSIS - A POSSIBLE MARKER OF PULMONARY DYSFUNCTION, Chest, 105(5), 1994, pp. 1470-1473
Citations number
20
Categorie Soggetti
Respiratory System
Journal title
ChestACNP
ISSN journal
00123692
Volume
105
Issue
5
Year of publication
1994
Pages
1470 - 1473
Database
ISI
SICI code
0012-3692(1994)105:5<1470:EGIC-A>2.0.ZU;2-E
Abstract
To evaluate the role of red blood cell (RBC) antioxidants as clinical markers of oxidative exposure, we measured RBC glutathione (GSH) conce ntrations in 32 adult patients with cystic fibrosis (CF), and 8 health y age-matched control subjects. We chose patients with CF because this disease is characterized by severe bronchial inflammation and marked oxidant-antioxidant imbalance. Although the GSH concentration of the t wo study groups was not significantly different, the RBC GSH concentra tion of patients with CF had a greater variability (p=0.01) and was al so inversely and significantly correlated to tests of pulmonary functi on (p<0.05). These data indicate a large and significant interindividu al variability of erythrocytic antioxidants in patients with CF, with a compensatory, but probably inadequate, increase in patients with mor e severe respiratory deterioration. Red blood cell GSH concentration m ay thus provide a biologic marker for disease severity and a rationale for antioxidant manipulation in these patients.