Basement membrane biomarkers in very low birth weight premature infants - Association with length of NICU stay and bronchopulmonary dysplasia

被引:5
作者
Aghai, ZH
Arevalo, R
Lumicao, L
Lesser, M
Shi, QH
Jain, A
Krauss, AN
Auld, PAM
Hanauske-Abel, HM
机构
[1] Cornell Univ, Dept Pediat, New York Presbyterian Hosp, Weill Med Coll, New York, NY 10021 USA
[2] Jamaica Hosp, Div Neonatol, New York, NY USA
[3] N Shore Univ Hosp, Dept Res, Manhasset, NY 11030 USA
来源
BIOLOGY OF THE NEONATE | 2002年 / 81卷 / 01期
关键词
infant; very low birth weight; biomarker; basement membrane; bronchopulmonary dysplasia; economics; medical;
D O I
10.1159/000047179
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Basement membranes, critical for vital organs like the lungs, consist of two interwoven homopolymers, one assembled by type IV collagens and one by laminins. We hypothesized their serum antigens C-IV and P1, respectively, to be global measures for the maturity of these organs. In 39 very low birth weight premature neonates (means: gestational age, 25.8 weeks; birth weight, 779 g) requiring intensive care, we analyzed these biomarkers during the first two months post partum. Median C-IV and P1 exceeded adult levels by one order of magnitude. The individuals with the lowest first week C-IV values (mean: 667 ng/ml) required significantly longer neonatal intensive care unit stays than those with the highest values (mean: 2,467 ng/ml), on average 109 vs. 80 days (p = 0.008) irrespective of gestational age. Patients diagnosed with bronchopulmonary dysplasia (BPD) at 36 weeks postconceptional age, already in their first week of life displayed C-IV levels lower than in controls, suggesting a defect in pulmonary basement membrane remodeling. This is the first identification by a matrix biomarker of a BPD-antecedent state. Copyright (C) 2002 S. Karger AG, Basel.
引用
收藏
页码:16 / 22
页数:7
相关论文
共 25 条
[1]  
Burri PH, 1999, LUNG DEV, P122, DOI DOI 10.1007/978-1-4614-7537-8_5
[2]   Laminin E8 alveolarization site: Heparin sensitivity, cell surface receptors, and role in cell spreading [J].
Chen, LL ;
Shick, V ;
Matter, ML ;
Laurie, SM ;
Ogle, RC ;
Laurie, GW .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1997, 272 (03) :L494-L503
[3]  
Colorado PC, 2000, CANCER RES, V60, P2520
[4]  
FRANK L, 1992, FETAL NEONATAL PHYSL, P914
[5]  
*FUJ CHEM IND, 1992, TECHN MAN PAN, V4
[6]  
*FUJ CHEM IND, 1997, TECHN MAN HLM KIT
[7]   TYPE-IV COLLAGEN IN DEVELOPING HUMAN LUNG - A COMPARISON BETWEEN NORMAL AND HYPOPLASTIC FETAL LUNGS [J].
HAIDAR, A ;
WIGGLESWORTH, JS ;
KRAUSZ, T .
EARLY HUMAN DEVELOPMENT, 1990, 21 (03) :175-180
[8]  
Hanauske-Abel H. M., 1996, HEPATOLOGY TXB LIVER, P465
[9]  
Hanauske-Abel HM, 2000, PEDIATR RES, V47, p131A
[10]   Role of distinct type IV collagen networks in glomerular development and function [J].
Harvey, SJ ;
Zheng, KQ ;
Sado, Y ;
Naito, I ;
Ninomiya, Y ;
Jacobs, RM ;
Hudson, BG ;
Thorner, PS .
KIDNEY INTERNATIONAL, 1998, 54 (06) :1857-1866