Open AccessPlasma P-Selectin Is Inversely Associated with Lung Function and Corticosteroid Responsiveness in Asthma
Author(s) -
Mats W. Johansson,
Brandon M Grill,
Karina T. Barretto,
Molly C Favour,
Hazel Marie Schira,
Calvin M. Swanson,
Kristine E. Lee,
Ronald L. Sorkness,
Deane F. Mosher,
Loren C. Denlinger,
Nizar N. Jarjour
Publication year - 2020
Publication title -
international archives of allergy and immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.696
H-Index - 100
eISSN - 1423-0097
pISSN - 1018-2438
DOI - 10.1159/000509600
Subject(s) - medicine , exacerbation , asthma , air trapping , endotype , exhaled nitric oxide , lung volumes , biomarker , corticosteroid , immunology , nitrogen washout , bronchial hyperresponsiveness , cardiology , gastroenterology , pulmonary function testing , lung , respiratory disease , functional residual capacity , spirometry , chemistry , biochemistry
Background: Severe asthma has multiple phenotypes for which biomarkers are still being defined. Plasma P-selectin reports endothelial and/or platelet activation. Objective: To determine if P-selectin is associated with features of asthma in a longitudinal study. Methods: Plasmas from 70 adult patients enrolled in the Severe Asthma Research Program (SARP) III at the University of Wisconsin-Madison were analyzed for concentration of P-selectin at several points over the course of 3 years, namely, at baseline (BPS), after intramuscular triamcinolone acetonide (TA) injection, and at 36 months after baseline. Thirty-four participants also came in during acute exacerbation and 6 weeks after exacerbation. Results: BPS correlated inversely with forced expiratory volume in 1 s (FEV 1 ) and with residual volume/total lung capacity, an indicator of air trapping. BPS was inversely associated with FEV 1 change after TA, by regression analysis. FEV 1 did not change significantly after TA if BPS was above the median, whereas patients with BPS below the median had significantly increased FEV 1 after TA. BPS was higher in and predicted assignment to SARP phenotype cluster 5 (“severe fixed-airflow asthma”). P-selectin was modestly but significantly increased at exacerbation but returned to baseline within 3 years. Conclusions: High BPS is associated with airway obstruction, air trapping, the “severe fixed-airflow” cluster, and lack of FEV 1 improvement in response to TA injection. P-selectin concentration, which is a stable trait with only modest elevation during exacerbation, may be a useful biomarker for a severe asthma pheno- or endotype characterized by low pulmonary function and lack of corticosteroid responsiveness.