Biochemical, clinical, and morphologic studies on lungs of infants with bronchopulmonary dysplasia

Pediatr Pulmonol. 1996 Oct;22(4):215-29. doi: 10.1002/(SICI)1099-0496(199610)22:4<215::AID-PPUL1>3.0.CO;2-L.

Abstract

We correlated clinical, biochemical, and morphologic findings in the lungs of 48 infants dying of either bronchopulmonary dysplasia (BPD) or hyaline membrane disease (HMD) to obtain a better idea of the disease process. The infants ranged from 24 weeks of gestation to 1 1/2 postnatal years. The lungs of BPD and HMD infants had higher contents of DNA, alkalisoluble protein, hydroxyproline, and desmosine, as well as increased concentrations of DNA, hydroxyproline, and desmosine when compared with the lungs of 72 control infants. BPD was classified histologically into 4 groups: Group I was a phase of acute lung injury, Group II the proliferative phase; Group III the phase of early repair, and Group IV the phase of late repair. We saw a significant increase in hydroxyproline concentration in Groups II and III. The ratio of type I/III collagen decreased in BPD Groups II to IV. Desmosine was significantly higher only in Group III than in controls. When the pathological classification was related to biochemical and clinical features of BPD, the classification showed dependence on the number of days the infant survived postnatally and not on the gestational age of the infant. The number of days on assisted ventilation was a slightly better predictor of the disease classification than days on > 60% oxygen. A statistical model correctly predicted the pathologic classification 83% of the time.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bronchopulmonary Dysplasia / classification
  • Bronchopulmonary Dysplasia / metabolism*
  • Bronchopulmonary Dysplasia / pathology*
  • Case-Control Studies
  • Collagen / analysis
  • DNA / analysis
  • Desmosine / analysis
  • Humans
  • Hyaline Membrane Disease / metabolism
  • Hyaline Membrane Disease / pathology
  • Hydroxyproline / analysis
  • Infant
  • Infant, Newborn
  • Lung / chemistry*
  • Lung / pathology*

Substances

  • Desmosine
  • Collagen
  • DNA
  • Hydroxyproline