The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Fatty acid composition MRI of epicardial adipose tissue: methods and detection of proinflammatory biomarkers in ST-segment elevation myocardial infarction patients
Abstract
Purpose: To develop a method for quantifying the fatty acid composition (FAC) of human epicardial adipose tissue (EAT) using accelerated MRI and identify its potential for detecting proinflammatory biomarkers in patients with ST‐segment elevation myocardial infarction (STEMI). Methods: A multi‐echo radial gradient‐echo sequence was developed for accelerated imaging during a breath hold using a locally low‐rank denoising technique to reconstruct undersampled images. FAC mapping was achieved by fitting the multi‐echo images to a multi‐resonance complex signal model based on triglyceride characterization. Validation of the method was assessed using a phantom comprised of multiple oils. In vivo imaging was performed in STEMI patients (n = 21; 14 males/seven females). FAC was quantified in EAT, subcutaneous AT, and abdominal visceral AT. Results: Phantom validation demonstrated strong correlations (r > 0.97) and statistical significance (p < 0.0001) between measured and reference proton density fat fraction and FAC values. In vivo imaging of STEMI patients revealed a distinct EAT FAC profile compared to subcutaneous AT and abdominal visceral AT. EAT FAC parameters had significant correlations with left ventricular (LV) end‐diastolic volume index (p < 0.05), LV end‐systolic volume index (p < 0.05), and LV mass index (p < 0.05). Conclusions: Accelerated MRI enabled accurate quantification of human EAT FAC. The relationships between the EAT FAC profile and LV structure and function in STEMI patients suggest the potential of EAT FAC MRI as a biomarker for adipose tissue quality and inflammatory status in cardiovascular disease.
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Investigators have demonstrated the ability to use CMR to assess fatty acid composition (saturated vs unsaturated) within EAT, and this may better differentiate HFpEF subtypes and response to therapy than volume alone.
“Investigators have demonstrated the ability to use CMR to assess fatty acid composition (saturated vs unsaturated) within EAT,23,24 and this may better differentiate HFpEF subtypes and response to therapy than volume alone.”
From Tirzepatide Reduces LV Mass and Paracardiac Adipose Tissue in Obesity-Related Heart Failure (2025) · cites this paper as [24]
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Packer, M. (2018) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2018.03.509 · Cited by 656 · cited 1×
“7,8 The FAC of the EAT, delineating the respective levels of saturated fatty acids (SFAs), monounsaturated fatty acids (MUFAs), and polyunsaturated fatty acids (PUFAs), has been proposed as a possible mediator of its proinflammatory properties.”
Epicardial adipose tissue and cardiovascular diseases
Ansaldo, A. M., Montecucco, F., Sahebkar, A., Dallegri, F., & Carbone, F. (2019) · International Journal of Cardiology · doi:10.1016/j.ijcard.2018.09.089 · Cited by 247
Patel, V. B., Shah, S., Verma, S., & Oudit, G. Y. (2017) · Heart Failure Reviews · doi:10.1007/s10741-017-9644-1 · Cited by 218
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Tirzepatide Reduces LV Mass and Paracardiac Adipose Tissue in Obesity-Related Heart Failure
Kramer, C. M., Borlaug, B. A., Zile, M. R., Ruff, D., DiMaria, J. M., Menon, V., Ou, Y., Zarante, A. M., Hurt, K. C., Murakami, M., et al. (2025) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2024.11.001 · Cited by 200
Metadata
- Authors
- Echols, J. T., Wang, S., Patel, A. R., Hogwood, A. C., Abbate, A., & Epstein, F. H.
- Affiliations
- Biomedical Engineering University of Virginia Charlottesville Virginia USA
- Division of Cardiovascular Medicine University of Virginia Charlottesville Virginia USA
- Robert M. Berne Cardiovascular Research Center University of Virginia Charlottesville Virginia USA
- Venue
- Magnetic Resonance in Medicine
- Publisher
- Wiley
- Published
- 2024-09-25
- Volume
- 93
- Issue
- 2
- Pages
- 519-535
- ISSN
- 0740-3194
- 1522-2594
- PMC
- PMC11604849
- Cited by
- 9
- References
- 3
- Language
- en
- Funders
- National Institute on Aging (R01 AG076360)
- National Heart, Lung, and Blood Institute (R01 HL162872)
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