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PMID: 19718453 Published · epublish English Journal Article

The influence of radiographic phenotype and smoking status on peripheral blood biomarker patterns in chronic obstructive pulmonary disease.

PloS one ·Vol. 4 ·No. 8 ·2009-08-31 ·Pages e6865

Bon JM, Leader JK, Weissfeld JL, Coxson HO, Zheng B, Branch RA, Kondragunta V, Lee JS, Zhang Y, Choi AM, Lokshin AE, Kaminski N, Gur D, Sciurba FC

Abstract

Chronic obstructive pulmonary disease (COPD) is characterized by both airway remodeling and parenchymal destruction. The identification of unique biomarker patterns associated with airway dominant versus parenchymal dominant patterns would support the existence of unique phenotypes representing independent biologic processes. A cross-sectional study was performed to examine the association of serum biomarkers with radiographic airway and parenchymal phenotypes of COPD. Serum from 234 subjects enrolled in a CT screening cohort was analyzed for 33 cytokines and growth factors using a multiplex protein array. The association of serum markers with forced expiratory volume in one second percent predicted (FEV1%) and quantitative CT measurements of airway thickening and emphysema was assessed with and without stratification for current smoking status. Significant associations were found with several serum inflammatory proteins and measurements of FEV1%, airway thickening, and parenchymal emphysema independent of smoking status. The association of select analytes with airway thickening and emphysema was independent of FEV1%. Furthermore, the relationship between other inflammatory markers and measurements of physiologic obstruction or airway thickening was dependent on current smoking status. Airway and parenchymal phenotypes of COPD are associated with unique systemic serum biomarker profiles. Serum biomarker patterns may provide a more precise classification of the COPD syndrome, provide insights into disease pathogenesis and identify targets for novel patient-specific biological therapies.

MeSH Terms
Aged Biomarkers/blood Cohort Studies Female Forced Expiratory Volume Humans Male Middle Aged Pulmonary Disease, Chronic Obstructive/blood,diagnostic imaging,physiopathology Smoking/blood Tomography, X-Ray Computed
Chemicals
Biomarkers
Authors & Affiliations
14 authors, click to expand affiliations / ORCID
Bon Jessica M
Division of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America. [email protected]
Leader Joseph K
Weissfeld Joel L
Coxson Harvey O
Zheng Bin
Branch Robert A
Kondragunta Venkateswarlu
Lee Janet S
Zhang Yingze
Choi Augustine M K
Lokshin Anna E
Kaminski Naftali
Gur David
Sciurba Frank C
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Article Info
Journal
PloS one
Abbr.
PLoS One
ISSN
1932-6203
Published
2009-08-31
Epub
2009-00-31
Pages
e6865
Language
English
Region
United States
NLM ID
101285081
PMCID
PMC2730536
Subset
IM
Grants
NCI NIH HHS · P50 CA090440 · United States
NHLBI NIH HHS · P50 HL084948 · United States
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