Macrophages in epicardial adipose tissue and serum NT-proBNP in patients with stable coronary artery disease
https://doi.org/10.15789/0000-0003-4049-8715
Abstract
Coronary artery disease (CAD) is widely considered a chronic inflammatory disorder, and dysfunction of epicardial adipose tissue could be an important source of the inflammation. Amino-terminal fragment of pro-B-type natriuretic peptide (NT-proBNP) is a known marker of cardiovascular disorders of cardiac origin. Recent studies show that inflammatory stimuli may influence its secretion. Our purpose was to evaluate NT-proBNP serum concentration in relation to immune cell ratios in epicardial adipose tissue (EAT), and cytokine levels in the patients with stable CAD. Patients with stable CAD and heart failure classified into classes II–III, according to the New York Heart Association (NYHA) scale, scheduled for the coronary artery bypass graft (CABG) surgery, were recruited into the study (n = 10; 59.5 (53.0-65.0) y. o.; 50% males). The EAT and subcutaneous adipose tissue (SAT) specimens were harvested in the course of CABG surgery. Immunostaining with anti-CD68, anti-CD45, antiIL-1β and anti-TNFα monoclonal antibodies was performed to evaluate cell composition by differential counts per ten fields (400 magnification). Fasting venous blood was obtained from patients before CABG. Blood was centrifuged at 1500g, aliquots were collected and stored frozen at -40 °С until final analysis. Concentrations of NT-proBNP, IL-1β, IL-6, IL-10, TNFα were determined in serum samples by enzyme-linked immunosorbent assay (ELISA). We have found increased production of IL-1β and TNFα cytokines in EAT compared to SAT. Concentrations of NT-proBNP exceeded 125 pg/ml in 4 patients, and correlations between the CD68+ macrophage counts in both EAT and SAT samples (rs = 0.762; p = 0.010 and rs = 0.835; p = 0.003, respectively). NT-proBNP levels showed positive relations with CD45+ leukocyte counts (rs = 0.799; p = 0.006), and with IL-1β+ cell numbers (rs = 0.705; p = 0.023) in EAT samples only. As for the serum biomarkers, NT-proBNP levels showed negative correlation with fasting glucose levels (rs = -0.684; p = 0.029), and positive correlation with serum IL-6 concentrations (rs = 0.891; p = 0.001). Increased serum concentrations of NT-proBNP in CAD patients correlate with accumulation of macrophages in EAT, which is associated with increased production of IL-1β in EAT and correlates with some metabolic parameters.
About the Authors
I. V. KologrivovaRussian Federation
Kologrivova Irina V., PhD (Medicine), Research Associate, Department of Clinical Laboratory Diagnostics
634012, Tomsk, Kievskaya str., 111a.
Competing Interests:
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T. E. Suslova
Russian Federation
Suslova Tatiana E., PhD (Medicine), Head, Department of Clinical Laboratory Diagnostics
Tomsk
Competing Interests:
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O. A. Koshelskaya
Russian Federation
Koshelskaya Olga A., PhD, MD (Medicine), Professor, Leading Research Associate, Department of Atherosclerosis and Coronary Artery Disease
Tomsk
Competing Interests:
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M. S. Rebenkova
Russian Federation
Rebenkova Maria S., Junior Research Associate, Laboratory of Molecular and Cellular Pathology and Genetic Testing
Tomsk
Competing Interests:
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O. A. Kharitonova
Russian Federation
Kharitonova Olga A., Junior Research Associate, Department of Atherosclerosis and Coronary Artery Disease
Tomsk
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O. N. Dymbrylova
Dymbrylova Ochirma N., PhD (Medicine), Junior Research Associate, Department of Clinical Laboratory Diagnostics
Tomsk
S. L. Andreev
Russian Federation
Andreev Sergey L., PhD (Medicine), Senior Research Associate, Department of Cardiovascular Surgery
Tomsk
Competing Interests:
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References
1. Altun I., Unal Y., Basaran O., Akin F., Emir G.K., Kutlu G., Biteker M. Increased epicardial fat thickness correlates with aortic stiffness and N-terminal pro-brain natriuretic peptide levels in acute ischemic stroke patients. Tex. Heart Inst. J., 2016, Vol. 43, no. 3, pp. 220-226.
2. Arjamaa O. Physiology of natriuretic peptides: The volume overload hypothesis revisited. World J. Cardiol., 2014, Vol. 6, no. 1, pp. 4-7.
3. Caro-Codón J., Rey J.R., Buño A., Iniesta A.M., Rosillo S.O., Castrejon-Castrejon S., Rodriguez-Sotelo L., Martinez L.A., Marco I., Merino C., Martin-Polo L., Garcia-Veas J.M., Martinez-Cossiani M., Gonzalez-Valle L., Herrero A., López-de-Sa E., Merino J.L. Characterization of NT-proBNP in a large cohort of COVID-19 patients. Eur. J. Heart Fail., 2021, Vol. 23, pp. 456-464.
4. Fish-Trotter H., Ferguson J.F., Patel N., Arora P., Allen N.B., Bachmann K.N., Daniels L.B., Reilly M.P., Lima J.A.C., Wang T.J., Gupta D.K. Inflammation and circulating natriuretic peptide levels. Circ. Heart Fail., 2020, Vol. 13, no. 7, e006570. doi: 10.1161/CIRCHEARTFAILURE.119.006570.
5. Gruden G., Landi A., Bruno G. Natriuretic peptides, heart, and adipose tissue: new findings and future developments for diabetes research. Diabetes Care, 2014, Vol. 37, no. 11, pp. 2899-2908.
6. Heinisch B.B., Vila G., Resl M., Riedl M., Dieplinger B., Mueller T., Luger A., Pacini G., Clodi M. B-type natriuretic peptide (BNP) affects the initial response to intravenous glucose: a randomised placebo-controlled cross-over study in healthy men. Diabetologia, 2012, Vol. 55, no. 5, pp. 1400-1405.
7. Hirata Y., Kurobe H., Akaike M., Chikugo F., Hori T., Bando Y., Nishio C., Higashida M., Nakaya Y., Kitagawa T., Sata M. Enhanced inflammation in epicardial fat in patients with coronary artery disease. Int. Heart J., 2011, Vol. 52, no. 3, pp. 139-142.
8. Iacobellis G., Corradi D., Sharma A.M. Epicardial adipose tissue: anatomic, biomolecular and clinical relationships with the heart. Nat. Clin. Pract. Cardiovasc. Med., 2005, Vol. 2, no. 10, pp. 536-543.
9. Luedike P., Alatzides G., Papathanasiou M., Heisler M., Pohl J., Lehmann N., Rassaf T. Predictive potential of macrophage migration inhibitory factor (MIF) in patients with heart failure with preserved ejection fraction (HFpEF). Eur. J. Med. Res., 2018, Vol. 23, no. 1, 22. doi: 10.1186/s40001-018-0321-1.
10. Madamanchi C., Alhosaini H., Sumida A., Runge M.S. Obesity and natriuretic peptides, BNP and NTproBNP: mechanisms and diagnostic implications for heart failure. Int. J. Cardiol., 2014, Vol. 176, no. 3, pp. 611-617.
11. National Guidelines OSSN, RCO and RNMOT for the diagnosis and treatment of chronic heart failure (fourth revision). Journal of Cardiac Failure, 2013, Vol. 81, no. 7, pp. 379-472. (In Russ.)
12. Obokata M., Reddy Y.N.V., Pislaru S.V., Melenovsky V., Borlaug B.A. Evidence supporting the existence of a distinct obese phenotype of heart failure with preserved ejection fraction. Circulation, 2017, Vol. 136, no. 1, pp. 6-19.
13. Park Y.M., Myers M., Vieira-Potter V.J. Adipose tissue inflammation and metabolic dysfunction: role of exercise. Mo Med., 2014, Vol. 111, no. 1, pp. 65-72.
14. Solus J., Chung C.P., Oeser A., Avalos I., Gebretsadik T., Shintani A., Raggi P., Sokka T., Pincus T., Stein C.M. Amino-terminal fragment of the prohormone brain-type natriuretic peptide in rheumatoid arthritis. Arthritis Rheum., 2008, Vol. 58, no. 9, pp. 2662-2669.
15. van Tassell B.W., Trankle C.R., Canada J.M., Carbone S., Buckley L., Kadariya D., del Buono M.G., Billingsley H., Wohlford G., Viscusi M., Oddi-Erdle C., Abouzaki N.A., Dixon D., Biondi-Zoccai G., Arena R., Abbate A. IL-1 blockade in patients with heart failure with preserved ejection fraction. Results from DHART2. Circ. Heart Fail., 2018, Vol. 11, no. 8, e005036. doi:10.1161/CIRCHEARTFAILURE.118.005036.
Supplementary files
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For citations:
Kologrivova I.V., Suslova T.E., Koshelskaya O.A., Rebenkova M.S., Kharitonova O.A., Dymbrylova O.N., Andreev S.L. Macrophages in epicardial adipose tissue and serum NT-proBNP in patients with stable coronary artery disease. Medical Immunology (Russia). 2022;24(2):389-394. https://doi.org/10.15789/0000-0003-4049-8715