Tytuł pozycji:
Epicardial, paracardial, and perivascular fat quantity, gene expressions, and serum cytokines in patients with coronary artery disease and diabetes
- Tytuł:
-
Epicardial, paracardial, and perivascular fat quantity, gene expressions, and serum cytokines in patients with coronary artery disease and diabetes
- Autorzy:
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Gąsior, Zbigniew
Kowalówka, Adam
Haberka, Maciej
Deja, Marek
Biedroń, Małgorzata
Okopień, Bogusław
Gajos, Grzegorz
Manka, Robert
Skudrzyk, Estera
Machnik, Grzegorz
Regulska-Ilow, Bożena
- Data publikacji:
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2019
- Słowa kluczowe:
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perivascular fat
epicardial fat
diabetes
adipose tissue dysfunction
- Język:
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angielski
- ISBN, ISSN:
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00323772
- Prawa:
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Udzielam licencji. Uznanie autorstwa - Użycie niekomercyjne - Na tych samych warunkach 4.0 Międzynarodowa
http://creativecommons.org/licenses/by-nc-sa/4.0/legalcode.pl
- Dostawca treści:
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Repozytorium Uniwersytetu Jagiellońskiego
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INTRODUCTION Obesity and diabetes mellitus (DM) are common disorders that increase cardiovascular
risk and lead to coronary artery disease (CAD).
OBJECTIVES The aim of our study was to assess the link between epicardial fat (EF) volume and paracardial
fat (PF) volume, relative expressions of several genes in epicardial, paracardial, and perivascular
fat and corresponding serum cytokines in patients with CAD in relation to DM.
PATIENTS AND METHODS A total of 66 consecutive patients (33 with DM) with multivessel CAD were
included. We obtained cardiac magnetic resonance, serum cytokines levels, and their relative mRNA expressions
in EF, PF, and perivascular fat samples of the following: adrenomedullin (ADM), fibroblast growth
factor 21 (FGF21), transforming growth factor β (TGFβ), phospholipid transfer protein (PLTP), receptor for
advanced glycation endproducts (RAGE), thrombospondin 1 (THSB1), and uncoupling protein 1 (UCP1).
RESULTS There were no differences in the anthropometric parameters or fat depots, except for higher
epicardial fat volume in patients with DM (mean [SD], 105.6 [38.5] ml vs 84 [29.2] ml; P = 0.02). Patients
with DM exhibited a significantly increased RAGE expression in EF (median [Q1–Q3], 0.17 [0.06–1.48]
AU vs 0.08 [0.02–0.24] AU, P = 0.03). Diabetes was also associated with increased expression of ADM
in EF and PF and decreased expression of FGF21 compared with patients without DM.
CONCLUSIONS Patients with multivessel CAD and DM revealed increased volume and more dysfunctional
profile of gene expressions in EF and significantly decreased expression of cardioprotective FGF21.