Neutrophil count as the centerpiece in the joined association networks of inflammatory and cell damage markers, and neuroendocrine stress markers in patients with stable angina pectoris following stenting.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2019
Historique:
received: 26 07 2018
accepted: 28 03 2019
entrez: 12 4 2019
pubmed: 12 4 2019
medline: 30 1 2020
Statut: epublish

Résumé

The primary aim of this study was to examine whether markers of cell damage and of the psycho-neuroendocrino-inflammatory/immune (PNI) system could be associated in patients with stable coronary artery disease (CAD) on the next day following percutaneous coronary intervention (PCI). Blood samples of 23 patients (18 men and five women, mean age 62.9 ± 10.6 years), were collected immediately before (pre-PCI), immediately after (post-PCI), and on the day following PCI (1d-PCI). Lactoferrin, LL-37 and interleukin-6 (IL-6) were assayed in plasma, in addition to cortisol and chromogranin A (CgA), as well as CK, ASAT and ALAT. Total and differential leukocyte counts were also analysed. At all the three time points, the monocyte fractions, the monocyte-to-lymphocyte and the neutrophil-to-lymphocyte ratios and CgA levels were elevated. We detected significant peri-procedural changes in the plasma levels of our PNI markers: IL-6 (p<0.05), lactoferrin, LL-37 (both: p <0.0001), CgA, (p<0.05), and cortisol (p<0.01). On the first day after PCI, highly significant associations were found of ASAT with IL-6 and neutrophil count (both: r>0.75, p<0.0001), and of CgA with neutrophil count and monocyte count (both: r>0.79, p<0.0001); furthermore, cortisol was also associated with neutrophil count (r>0.7, p<0.0001). The findings suggest that myocardial damage could correlate not only with an inflammatory reaction but, via neutrophil count, also with increased level of stress in stable CAD after PCI. Furthermore, 1d-PCI neutrophil count may serve as an easy-to-obtain integrative PNI measure in stable CAD.

Identifiants

pubmed: 30973928
doi: 10.1371/journal.pone.0215209
pii: PONE-D-18-22142
pmc: PMC6459524
doi:

Substances chimiques

Antimicrobial Cationic Peptides 0
Biomarkers 0
CHGA protein, human 0
Chromogranin A 0
IL6 protein, human 0
Interleukin-6 0
LTF protein, human 0
Aspartate Aminotransferases EC 2.6.1.1
Alanine Transaminase EC 2.6.1.2
Creatine Kinase EC 2.7.3.2
Lactoferrin EC 3.4.21.-
Hydrocortisone WI4X0X7BPJ
Cathelicidins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0215209

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Tamás Horváth (T)

Invasive Cardiology Unit, Centre of Cardiology, Medical Faculty, University of Szeged, Szeged, Hungary.

Gyöngyi Serfőző (G)

Department of Biochemistry, Medical Faculty, University of Szeged, Szeged, Hungary.

Ádám Györkei (Á)

Synthetic and Systems Biology Unit, Biological Research Centre, Szeged, Hungary.
PhD School of Biology, Faculty of Sciences, University of Szeged, Szeged, Hungary.

Imre Földesi (I)

Department of Laboratory Medicine, Medical Faculty, University of Szeged, Szeged, Hungary.

Tamás Forster (T)

Centre of Cardiology, Medical Faculty, University of Szeged, Szeged, Hungary.

Margit Keresztes (M)

Department of Biochemistry, Medical Faculty, University of Szeged, Szeged, Hungary.

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Classifications MeSH