Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1995-9-14
pubmed:abstractText
The purpose of this study was to determine if the measurement of surfactant protein A (SP-A) in bronchoalveolar lavage (BAL) fluid predicts survival in patients with idiopathic pulmonary fibrosis (IPF). We performed BAL on 44 patients with IPF and 33 healthy volunteers. SP-A and total phospholipid (PL) were measured in the surfactant pelleted by centrifugation and expressed as a ratio to account for differences in the alveolar surface area sampled. The mean SP-A/PL was lower in patients with IPF than in healthy volunteers (31.8 +/- 2.8 versus 63.9 +/- 6.4 micrograms/mumol, p = 0.006) and in patients who died within 2 yr than in those who survived (23.4 +/- 2.6 versus 37.5 +/- 4.2 micrograms/mumol, p = 0.015). Using Cox's proportional hazard model, we found that SP-A/PL modeled continuously was associated with survival time (p = 0.002). The 5-yr survival of patients with SP-A/PL above the median level for all patients with IPF (29.7 micrograms/mumol) was more than twice that of patients below the median (68 versus 30%, p = 0.007). SP-A/PL improved upon prediction of survival modeled by most routine physiologic variables with the exception of percent predicted TLC or the multifarious clinical-radiographic-physiologic score (CRP). Cellular analysis of lavage did not predict survival in this cohort of patients. We conclude that SP-A/PL is a biochemical marker in lavage that predicts survival in patients with IPF.
pubmed:grant
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1073-449X
pubmed:author
pubmed:issnType
Print
pubmed:volume
152
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
751-9
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:7633738-Adult, pubmed-meshheading:7633738-Aged, pubmed-meshheading:7633738-Biological Markers, pubmed-meshheading:7633738-Bronchoalveolar Lavage Fluid, pubmed-meshheading:7633738-Case-Control Studies, pubmed-meshheading:7633738-Cause of Death, pubmed-meshheading:7633738-Cohort Studies, pubmed-meshheading:7633738-Female, pubmed-meshheading:7633738-Follow-Up Studies, pubmed-meshheading:7633738-Forced Expiratory Volume, pubmed-meshheading:7633738-Forecasting, pubmed-meshheading:7633738-Glycoproteins, pubmed-meshheading:7633738-Humans, pubmed-meshheading:7633738-Male, pubmed-meshheading:7633738-Middle Aged, pubmed-meshheading:7633738-Phospholipids, pubmed-meshheading:7633738-Proportional Hazards Models, pubmed-meshheading:7633738-Proteolipids, pubmed-meshheading:7633738-Pulmonary Fibrosis, pubmed-meshheading:7633738-Pulmonary Surfactant-Associated Protein A, pubmed-meshheading:7633738-Pulmonary Surfactant-Associated Proteins, pubmed-meshheading:7633738-Pulmonary Surfactants, pubmed-meshheading:7633738-Smoking, pubmed-meshheading:7633738-Survival Rate, pubmed-meshheading:7633738-Total Lung Capacity, pubmed-meshheading:7633738-Vital Capacity
pubmed:year
1995
pubmed:articleTitle
Surfactant protein A predicts survival in idiopathic pulmonary fibrosis.
pubmed:affiliation
Department of Medicine, National Jewish Center for Immunology and Respiratory Medicine, Denver, CO 80206, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.