Il-18 Level in Patients Undergoing Coronary Artery Bypass Grafting Surgery or Valve Replacement: Which Link with Epicardial Fat Depot?

Author:

Dozio E.1,Dogliotti G.1,Malavazos A.E.2,Bandera F.3,Cassetti G.4,Vianello E.1,Zelaschi R.2,Barassi A.5,Pellissero G.6,Solimene U.17,Morricone L.2,Sigruener A.8,Tarabin V.8,Schmitz G.8,Menicanti L.4,Romanelli M.M. Corsi16

Affiliation:

1. Dipartimento di Scienze Biomediche per la Salute, Cattedra di Patologia Clinica, Università degli Studi di Milano, Milan, Italy

2. Unità Operativa di Diabetologia e Malattie Metaboliche, Servizio di Dietetica, Nutrizione Clinica e Prevenzione Cardiometabolica, IRCCS Policlinico San Donato, Milan, Italy

3. Unità Operativa di Cardiologia, IRCCS Policlinico San Donato, Milan, Italy

4. Unità Operativa di Cardiochirurgia, IRCCS Policlinico San Donato, Milan, Italy

5. Unità di Chimica e Biochimica Analitica, Dipartimento di Scienze della Salute, Università degli Studi di Milano, Milan, Italy

6. Unità Operativa Laboratorio di Patologia Clinica, Dipartimento dei Servizi Sanitari di Diagnosi e Cura - Medicina di Laboratorio, IRCCS Policlinico San Donato, Milan, Italy

7. Centro di Ricerca in Bioclimatologia Medica, Università degli Studi di Milano, Milan, Italy

8. Istituto di Chimica Clinica e Medicina di Laboratorio, Università di Regensburg, Regensburg, Germany

Abstract

Interleukin-18 (IL-18) is a member of the interleukin-1 family of cytokines produced constitutively by different cell types and by adipose tissue. Due to the link between obesity, inflammation and cardiovascular diseases, we aimed to measure IL-18 circulating level in patients undergoing open-heart surgery both for elective coronary artery bypass grafting (CABG) or for valve replacement (VR), and we also evaluated whether epicardial adipose tissue (EAT) depot may be a potential source of IL-18. Circulating IL-18 protein was quantified by enzyme-linked immunosorbent assay. IL-18, IL-18 receptor 1 (IL-18 Rl) and IL-18 receptor accessory protein (IL-18-RAP) gene expression in EAT depot were evaluated by one colour microarray platform. EAT thickness was measured by echocardiography. In this study we found that all cardiovascular patients (CABG and VR) have increased circulating IL-18 level compared to healthy control subjects (p < 0.0001), but no statistical significant difference was observed between CABG and VR groups (p = 0.35). A great increase in the gene expression of IL-18 (p < 0.05), IL-18 R1 (p < 0.01) and IL-18 RAP (p < 0.001) was observed in EAT samples obtained from CABG vs VR patients. In conclusion, CABG and VR patients had similar increased level of circulating IL-18 protein, but in EAT depots isolated from CABG gene expression of IL-18, IL-18 R1 and IL-18-RAP resulted higher than in VR patients. Future investigation on local IL-18 protein production, its autocrine-paracrine effect and its correlation with plasmatic IL-18 level could give more information on the relationship between IL-18 and coronary artery disease.

Publisher

SAGE Publications

Subject

Pharmacology,Immunology,Immunology and Allergy

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