Publication: Evaluation of lung parenchyma, blood vessels, and peripheral blood lymphocytes as a potential source of acute phase reactants in patients with COPD.
dc.contributor.author | Arellano-Orden, Elena | |
dc.contributor.author | Calero, Carmen | |
dc.contributor.author | López-Ramírez, Cecilia | |
dc.contributor.author | Sánchez-López, Verónica | |
dc.contributor.author | López-Villalobos, José Luis | |
dc.contributor.author | Abad Arranz, María | |
dc.contributor.author | Blanco-Orozco, Ana | |
dc.contributor.author | Otero-Candelera, Remedios | |
dc.contributor.author | López-Campos, José Luis | |
dc.date.accessioned | 2023-01-25T13:39:16Z | |
dc.date.available | 2023-01-25T13:39:16Z | |
dc.date.issued | 2019-06-20 | |
dc.description.abstract | Background: Previous studies have shown that the arterial wall is a potential source of inflammatory markers in COPD. Here, we sought to compare the expression of acute phase reactants (APRs) in COPD patients and controls both at the local (pulmonary arteries and lung parenchyma) and systemic (peripheral blood leukocytes and plasma) compartments. Methods: Consecutive patients undergoing elective surgery for suspected primary lung cancer were eligible for the study. Patients were categorized either as COPD or control group based on the spirometry results. Pulmonary arteries and lung parenchyma sections, peripheral blood leukocytes, and plasma samples were obtained from all participants. Gene expression levels of C-reactive protein (CRP) and serum amyloid A (SAA1, SAA2, and SAA4) were evaluated in tissue samples and peripheral blood leukocytes by reverse transciption-PCR. Plasma CRP and SAA protein levels were measured by enzyme-linked immunosorbent assays. Proteins were evaluated in paraffin-embedded lung tissues by immunohistochemistry. Results: A total of 40 patients with COPD and 62 controls were enrolled. We did not find significant differences in the gene expression between COPD and control group. Both CRP and SAA were overexpressed in the lung parenchyma compared with pulmonary arteries and peripheral blood leukocytes. The expression of SAA was significantly higher in the lung parenchyma than in the pulmonary artery (2-fold higher for SAA1 and SAA4, P=0.015 and P | |
dc.identifier.doi | 10.2147/COPD.S188567 | |
dc.identifier.essn | 1178-2005 | |
dc.identifier.pmc | PMC6592023 | |
dc.identifier.pmid | 31417249 | |
dc.identifier.pubmedURL | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6592023/pdf | |
dc.identifier.unpaywallURL | https://www.dovepress.com/getfile.php?fileID=50621 | |
dc.identifier.uri | http://hdl.handle.net/10668/14399 | |
dc.journal.title | International journal of chronic obstructive pulmonary disease | |
dc.journal.titleabbreviation | Int J Chron Obstruct Pulmon Dis | |
dc.language.iso | en | |
dc.organization | Instituto de Biomedicina de Sevilla-IBIS | |
dc.organization | Hospital Universitario Virgen del Rocío | |
dc.page.number | 1323-1332 | |
dc.pubmedtype | Journal Article | |
dc.rights | Attribution-NonCommercial 4.0 International | |
dc.rights.accessRights | open access | |
dc.rights.uri | http://creativecommons.org/licenses/by-nc/4.0/ | |
dc.subject | C-reactive protein | |
dc.subject | COPD | |
dc.subject | arterial wall | |
dc.subject | inflammation | |
dc.subject | parenchyma | |
dc.subject | serum amyloid A | |
dc.subject.mesh | Acute-Phase Proteins | |
dc.subject.mesh | Acute-Phase Reaction | |
dc.subject.mesh | Correlation of Data | |
dc.subject.mesh | Female | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Lung | |
dc.subject.mesh | Lymphocytes | |
dc.subject.mesh | Male | |
dc.subject.mesh | Middle Aged | |
dc.subject.mesh | Pulmonary Artery | |
dc.subject.mesh | Pulmonary Disease, Chronic Obstructive | |
dc.subject.mesh | Serum Amyloid A Protein | |
dc.subject.mesh | Spirometry | |
dc.title | Evaluation of lung parenchyma, blood vessels, and peripheral blood lymphocytes as a potential source of acute phase reactants in patients with COPD. | |
dc.type | research article | |
dc.type.hasVersion | VoR | |
dc.volume.number | 14 | |
dspace.entity.type | Publication |
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