Source:http://linkedlifedata.com/resource/pubmed/id/16569340
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
2006-3-29
|
pubmed:abstractText |
Insulin-like growth factor-1 (IGF-1) is involved in regulating the Th-1/Th-2 balance, favoring the development of the Th-2 compartment which enhances fibrosis, one of the main characteristics of Chronic Lung Disease (CLD) in premature newborns. Limited data is available concerning a possible association between early epithelial lining fluid (ELF) concentrations of IGF-1 (total and free forms), IGF-binding protein-3 (IGFBP-3), beta2-microglobulin and subsequent development of CLD in preterm neonates. If neutropenic, preterm neonates are frequently treated with recombinant human granulocyte colony stimulating factor (rhG-CSF). The objective of the study was to correlate ELF concentrations of IGF-1 and beta2 microglobulin during the first week of life both in non-neutropenic and in rhGCSF-treated neutropenic preterm neonates, with subsequent development in CLD. Thirty preterm neonates with Respiratory Distress Syndrome (6 with neutropenia) were studied. Eleven out of 24 non-neutropenic preterm infants (46%) and all of the six neutropenic subjects (100%) developed CLD. With the exception of first day values, there was a clear similarity in the behaviors of assayed molecules between non-neutropenic and neutropenic patients developing CLD. Non-neutropenic patients without CLD showed significantly lower values of free IGF-1 and beta2M both on days 1 and 3. Total IGF-I and cell counts were different only on the 3rd day. Conclusions: 1) the mechanisms leading to CLD might be mediated by high levels of IGF-family molecules soon after birth 2) beta2M could be a marker of increased bronchoalveolar lavage fluid cellularity with potential inflammatory properties 3) G-CSF treatment induces an increased synthesis of IGF-1 molecules by cells recruited in the lung, with possible enhancement of the fibrogenic mechanisms.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Granulocyte Colony-Stimulating...,
http://linkedlifedata.com/resource/pubmed/chemical/Insulin-Like Growth Factor Binding...,
http://linkedlifedata.com/resource/pubmed/chemical/Insulin-Like Growth Factor I,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/beta 2-Microglobulin
|
pubmed:status |
MEDLINE
|
pubmed:issn |
0394-6320
|
pubmed:author |
pubmed-author:AmeglioFF,
pubmed-author:AntenucciMM,
pubmed-author:CapoluongoEE,
pubmed-author:CarrozzoMM,
pubmed-author:CastagnolaMM,
pubmed-author:GiardinaBB,
pubmed-author:LulliPP,
pubmed-author:MatassaP GPG,
pubmed-author:RomagnoliCC,
pubmed-author:SantiniS ASA,
pubmed-author:VenteMM,
pubmed-author:ZuppiCC
|
pubmed:issnType |
Print
|
pubmed:volume |
19
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
57-66
|
pubmed:dateRevised |
2011-11-17
|
pubmed:meshHeading |
pubmed-meshheading:16569340-Bronchoalveolar Lavage Fluid,
pubmed-meshheading:16569340-Cell Count,
pubmed-meshheading:16569340-Chlamydia Infections,
pubmed-meshheading:16569340-Chronic Disease,
pubmed-meshheading:16569340-Epithelial Cells,
pubmed-meshheading:16569340-Granulocyte Colony-Stimulating Factor,
pubmed-meshheading:16569340-Humans,
pubmed-meshheading:16569340-Infant, Newborn,
pubmed-meshheading:16569340-Infant, Premature,
pubmed-meshheading:16569340-Insulin-Like Growth Factor Binding Protein 3,
pubmed-meshheading:16569340-Insulin-Like Growth Factor I,
pubmed-meshheading:16569340-Neutropenia,
pubmed-meshheading:16569340-Pulmonary Fibrosis,
pubmed-meshheading:16569340-Recombinant Proteins,
pubmed-meshheading:16569340-Ureaplasma Infections,
pubmed-meshheading:16569340-Ureaplasma urealyticum,
pubmed-meshheading:16569340-beta 2-Microglobulin
|
pubmed:articleTitle |
Increased levels of IGF-1 and beta2-microglobulin in epithelial lining fluid of preterm newborns developing chronic lung disease. effects of rhG-CSF.
|
pubmed:affiliation |
Biochemistry and Clinical-Biochemistry Institute, Catholic University School of Medicine, Largo F. Vito 1, 00168 Rome, Italy. ecapoluongo@rm.unicatt.it
|
pubmed:publicationType |
Journal Article
|