Type I collagenases in bronchoalveolar lavage fluid from preterm babies at risk of developing chronic lung disease

被引:36
作者
Sweet, DG
McMahon, KJ
Curley, AE
O'Connor, CM
Halliday, HL
机构
[1] Royal Matern Hosp, Reg Neonatal Unit, Belfast BT12 6BB, Antrim, North Ireland
[2] Queens Univ Belfast, Dept Child Hlth, Belfast BT7 1NN, Antrim, North Ireland
[3] Univ Coll Dublin, Dept Med & Therapeut, Dublin 2, Ireland
来源
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION | 2001年 / 84卷 / 03期
关键词
chronic lung disease; lungs; collagen; extracellular matrix; matrix metalloproteinase; preterm;
D O I
10.1136/fn.84.3.F168
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective-To assess whether increased collagenolysis precedes severe chronic lung disease (CLD). Methods-Matrix metalloproteinase-1 (MMP-1) and MMP-8 (enzymes that degrade type I collagen, the main structural protein of lung extracellular matrix) were measured by enzyme linked immunosorbent assay in 100 bronchoalveolar lavage samples taken during the first 6 postnatal days fi om 45 ventilated preterm babies <33 weeks gestation. The median value for each baby was calculated. CLD was defined as an oxygen requirement after the 36th week after conception. Results-MMP-8 levels in bronchoalveolar lavage fluid were higher (median 13 ng/ml) in 20 babies who developed CLD than in 25 without CLD (median 2 ng/ml). No MMP-1 was detected in any sample. Conclusions-MMP-8 can be detected in bronchoalveolar ravage fluid from preterm babies, and higher levels are found in those who later develop CLD. MMP-8 may contribute to lung injury that occurs as a prelude to CLD.
引用
收藏
页码:F168 / F171
页数:4
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