A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Association of epicardial adipose tissue with proteomics, coronary flow reserve, cardiac structure and function, and quality of life in heart failure with preserved ejection fraction: insights from the PROMIS-HFpEF study
Tekijät: Venkateshvaran Ashwin, Faxen Ulrika Ljung, Hage Camilla, Michaelsson Erik, Svedlund Sara, Saraste Antti, Beussink-Nelson Lauren, Fermer Maria Lagerstrom, Gan Li-Min, Tromp Jasper, Lam Carolyn SP, Shah Sanjiv J, Lund Lars H
Kustantaja: Wiley
Julkaisuvuosi: 2022
Journal: European Journal of Heart Failure
Tietokannassa oleva lehden nimi: EUROPEAN JOURNAL OF HEART FAILURE
Lehden akronyymi: EUR J HEART FAIL
Vuosikerta: 24
Numero: 12
Aloitussivu: 2251
Lopetussivu: 2260
Sivujen määrä: 10
ISSN: 1388-9842
eISSN: 1879-0844
DOI: https://doi.org/10.1002/ejhf.2709
Verkko-osoite: https://doi.org/10.1002/ejhf.2709
Rinnakkaistallenteen osoite: https://research.utu.fi/converis/portal/detail/Publication/177356555
Aim: Epicardial adipose tissue (EAT) may play a role in the pathophysiology of heart failure with preserved ejection fraction (HFpEF). We investigated associations of EAT with proteomics, coronary flow reserve (CFR), cardiac structure and function, and quality of life (QoL) in the prospective multinational PROMIS-HFpEF cohort.
Methods and results: Epicardial adipose tissue was measured by echocardiography in 182 patients and defined as increased if ≥9 mm. Proteins were measured using high-throughput proximity extension assays. Microvascular dysfunction was evaluated with Doppler-based CFR, cardiac structural and functional indices with echocardiography and QoL by Kansas City Cardiomyopathy Questionnaire (KCCQ). Patients with increased EAT (n = 54; 30%) had higher body mass index (32 [28-40] vs. 27 [23-30] kg/m2 ; p < 0.001), lower N-terminal pro-B-type natriuretic peptide (466 [193-1133] vs. 1120 [494-1990] pg/ml; p < 0.001), smaller indexed left ventricular (LV) end-diastolic and left atrial (LA) volumes and tendency to lower KCCQ score. Non-indexed LV/LA volumes did not differ between groups. When adjusted for body mass index, EAT remained associated with LV septal wall thickness (coefficient 1.02, 95% confidence interval [CI] 1.00-1.04; p = 0.018) and mitral E wave deceleration time (coefficient 1.03, 95% CI 1.01-1.05; p = 0.005). Increased EAT was associated with proteomic markers of adipose biology and inflammation, insulin resistance, endothelial dysfunction, and dyslipidaemia but not significantly with CFR.
Conclusion: Increased EAT was associated with cardiac structural alterations and proteins expressing adiposity, inflammation, lower insulin sensitivity and endothelial dysfunction related to HFpEF pathology, probably driven by general obesity. Potential local mechanical or paracrine effects mediated by EAT remain to be elucidated.
Ladattava julkaisu This is an electronic reprint of the original article. |