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      Gelatinase activities in the airways of premature infants and development of bronchopulmonary dysplasia.

      American Journal of Physiology - Lung Cellular and Molecular Physiology
      Bronchopulmonary Dysplasia, physiopathology, Enzyme Activation, Gelatinases, metabolism, Humans, Hyaline Membrane Disease, enzymology, Infant, Newborn, Infant, Premature, Matrix Metalloproteinase 2, Matrix Metalloproteinase 9, Muscle, Smooth, Respiratory Function Tests, Time Factors, Tissue Inhibitor of Metalloproteinase-1, Trachea

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          Abstract

          Matrix-degrading metalloproteinases may play a role in the pathophysiology of bronchopulmonary dysplasia (BDP). We, therefore, evaluated correlations between gelatinase activities [metalloproteinase (MMP)-2 and MMP-9] or tissue inhibitor of metalloproteinase (TIMP)-1 levels present in the airways during the initial phase of hyaline membrane disease and the onset of BPD. Tracheal aspirates were obtained within 6 h of birth (day 0) from 64 intubated neonates with a gestational age < or =30 wk. Forty-five neonates were resampled on day 3 or 5. Total MMP-2 level measured by zymography fell with time, whereas total MMP-9 level and TIMP-1 levels, assayed by ELISA, increased; the MMP-9 increase correlated with the increase in airway inflammatory cell numbers. Among the parameters measured on day 0, 3, or 5, lower total MMP-2 level, lower birth weight, and higher fraction of inspired oxygen on day 0 were significantly and independently associated with the development of BPD. In conclusion, MMP-9 level and TIMP-1 levels increased after birth but are not linked to BPD outcome. In contrast, low MMP-2 level at birth is strongly associated with the development of BPD.

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