NETosis is associated with the severity of aortic stenosis: Links with inflammation.
Aged
Aortic Valve
/ diagnostic imaging
Aortic Valve Stenosis
/ diagnosis
Biomarkers
/ metabolism
Disease Progression
Echocardiography
Enzyme-Linked Immunosorbent Assay
Extracellular Traps
/ metabolism
Female
Follow-Up Studies
Histones
/ blood
Humans
Immunoturbidimetry
Inflammation
/ metabolism
Interleukin-6
/ blood
Leukocyte Elastase
/ blood
Male
Middle Aged
Neutrophils
/ metabolism
Peroxidase
/ blood
Prognosis
Retrospective Studies
Aortic stenosis
Citrullinated histones
Myeloperoxidase
Neutrophil elastase
Neutrophil extracellular traps
Journal
International journal of cardiology
ISSN: 1874-1754
Titre abrégé: Int J Cardiol
Pays: Netherlands
ID NLM: 8200291
Informations de publication
Date de publication:
01 07 2019
01 07 2019
Historique:
received:
08
11
2018
revised:
18
03
2019
accepted:
24
03
2019
pubmed:
7
4
2019
medline:
13
2
2020
entrez:
7
4
2019
Statut:
ppublish
Résumé
An involvement of neutrophil extracellular traps (NETs) in the aortic stenosis (AS) pathogenesis is unknown. We enrolled 50 patients, median age 66.5 years with isolated severe AS, after aortic valve replacement and 20 healthy sex/age-matched controls. Autopsy-derived aortic valves from 5 healthy donors served as controls. Valvular expression of citrullinated histone H3 (citH3), myeloperoxidase (MPO), and neutrophil elastase (NE) and macrophages (CD68) were evaluated by immunostaining. Plasma citH3 and interleukin 6 (IL-6) were also determined. All stenotic and healthy valves expressed citH3 in the leaflets' endothelial and sub-endothelial layers at the aortic side. Amount of valvular citH3-positive cells was higher in AS patients compared with controls (53.5 [33-62]% vs. 5.7 [4.1-9.0]%, p < 0.0001) and correlated with aortic valve area (AVA; r = -0.69, p < 0.0001) and mean transvalvular gradient (r = 0.6, p < 0.0001). Double-staining revealed that in AS valves 27.2 ± 9.8% of cells were citH3/MPO- and 25.3 ± 8.9% citH3/NE-positive. Within stenotic valves, 6.4 ± 2.5% of cells showed citH3/CD68 double-positivity and were identified as macrophages. AS patients compared to controls had 83% higher plasma citH3 (p < 0.0001). In AS, plasma citH3 correlated with IL-6 (r = 0.39, p = 0.0054) levels and AVA (r = -0.45, p = 0.0009). The presence of NETs in stenotic valves and association with AS severity suggest novel mechanisms involved in the disease progression.
Sections du résumé
BACKGROUND
An involvement of neutrophil extracellular traps (NETs) in the aortic stenosis (AS) pathogenesis is unknown.
METHODS
We enrolled 50 patients, median age 66.5 years with isolated severe AS, after aortic valve replacement and 20 healthy sex/age-matched controls. Autopsy-derived aortic valves from 5 healthy donors served as controls. Valvular expression of citrullinated histone H3 (citH3), myeloperoxidase (MPO), and neutrophil elastase (NE) and macrophages (CD68) were evaluated by immunostaining. Plasma citH3 and interleukin 6 (IL-6) were also determined.
RESULTS
All stenotic and healthy valves expressed citH3 in the leaflets' endothelial and sub-endothelial layers at the aortic side. Amount of valvular citH3-positive cells was higher in AS patients compared with controls (53.5 [33-62]% vs. 5.7 [4.1-9.0]%, p < 0.0001) and correlated with aortic valve area (AVA; r = -0.69, p < 0.0001) and mean transvalvular gradient (r = 0.6, p < 0.0001). Double-staining revealed that in AS valves 27.2 ± 9.8% of cells were citH3/MPO- and 25.3 ± 8.9% citH3/NE-positive. Within stenotic valves, 6.4 ± 2.5% of cells showed citH3/CD68 double-positivity and were identified as macrophages. AS patients compared to controls had 83% higher plasma citH3 (p < 0.0001). In AS, plasma citH3 correlated with IL-6 (r = 0.39, p = 0.0054) levels and AVA (r = -0.45, p = 0.0009).
CONCLUSIONS
The presence of NETs in stenotic valves and association with AS severity suggest novel mechanisms involved in the disease progression.
Identifiants
pubmed: 30952530
pii: S0167-5273(18)36512-4
doi: 10.1016/j.ijcard.2019.03.047
pii:
doi:
Substances chimiques
Biomarkers
0
Histones
0
Interleukin-6
0
Peroxidase
EC 1.11.1.7
Leukocyte Elastase
EC 3.4.21.37
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
121-126Commentaires et corrections
Type : CommentIn
Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.