Quantification of perivascular inflammation does not provide incremental prognostic value over myocardial perfusion imaging and calcium scoring.
Autor: | Bengs S; Department of Nuclear Medicine, University Hospital Zurich, 8091, Zurich, Switzerland.; Center for Molecular Cardiology, University of Zurich, 8952, Schlieren, Switzerland., Haider A; Department of Nuclear Medicine, University Hospital Zurich, 8091, Zurich, Switzerland.; Center for Molecular Cardiology, University of Zurich, 8952, Schlieren, Switzerland., Warnock GI; Department of Nuclear Medicine, University Hospital Zurich, 8091, Zurich, Switzerland.; Center for Molecular Cardiology, University of Zurich, 8952, Schlieren, Switzerland., Fiechter M; Department of Nuclear Medicine, University Hospital Zurich, 8091, Zurich, Switzerland.; Center for Molecular Cardiology, University of Zurich, 8952, Schlieren, Switzerland.; Swiss Paraplegic Center, 6207, Nottwil, Switzerland., Pargaetzi Y; Department of Nuclear Medicine, University Hospital Zurich, 8091, Zurich, Switzerland.; Center for Molecular Cardiology, University of Zurich, 8952, Schlieren, Switzerland., Rampidis G; Department of Nuclear Medicine, University Hospital Zurich, 8091, Zurich, Switzerland., Etter D; Department of Nuclear Medicine, University Hospital Zurich, 8091, Zurich, Switzerland.; Center for Molecular Cardiology, University of Zurich, 8952, Schlieren, Switzerland., Wijnen WJ; Department of Nuclear Medicine, University Hospital Zurich, 8091, Zurich, Switzerland.; Center for Molecular Cardiology, University of Zurich, 8952, Schlieren, Switzerland., Portmann A; Department of Nuclear Medicine, University Hospital Zurich, 8091, Zurich, Switzerland.; Center for Molecular Cardiology, University of Zurich, 8952, Schlieren, Switzerland., Osto E; Institute of Clinical Chemistry, University of Zurich, 8091, Zurich, Switzerland.; University Heart Center, University Hospital Zurich, 8006, Zurich, Switzerland., Treyer V; Department of Nuclear Medicine, University Hospital Zurich, 8091, Zurich, Switzerland.; Institute for Regenerative Medicine, University of Zurich, 8952, Schlieren, Switzerland., Benz DC; Department of Nuclear Medicine, University Hospital Zurich, 8091, Zurich, Switzerland., Meisel A; Department of Nuclear Medicine, University Hospital Zurich, 8091, Zurich, Switzerland.; Center for Molecular Cardiology, University of Zurich, 8952, Schlieren, Switzerland., Fuchs TA; Department of Nuclear Medicine, University Hospital Zurich, 8091, Zurich, Switzerland., Gräni C; Department of Nuclear Medicine, University Hospital Zurich, 8091, Zurich, Switzerland., Buechel RR; Department of Nuclear Medicine, University Hospital Zurich, 8091, Zurich, Switzerland., Kaufmann PA; Department of Nuclear Medicine, University Hospital Zurich, 8091, Zurich, Switzerland., Pazhenkottil AP; Department of Nuclear Medicine, University Hospital Zurich, 8091, Zurich, Switzerland.; University Heart Center, University Hospital Zurich, 8006, Zurich, Switzerland., Gebhard C; Department of Nuclear Medicine, University Hospital Zurich, 8091, Zurich, Switzerland. Catherine.gebhard@usz.ch.; Center for Molecular Cardiology, University of Zurich, 8952, Schlieren, Switzerland. Catherine.gebhard@usz.ch. |
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Jazyk: | angličtina |
Zdroj: | European journal of nuclear medicine and molecular imaging [Eur J Nucl Med Mol Imaging] 2021 Jun; Vol. 48 (6), pp. 1806-1812. Date of Electronic Publication: 2020 Nov 16. |
DOI: | 10.1007/s00259-020-05106-0 |
Abstrakt: | Aims: Perivascular fat attenuation index (FAI) has emerged as a novel coronary computed tomography angiography (CCTA)-based biomarker predicting cardiovascular outcomes by capturing early coronary inflammation. It is currently unknown whether FAI adds prognostic value beyond that provided by single-photon emission computed tomography myocardial perfusion imaging (SPECT-MPI) and CCTA findings including coronary artery calcium scoring (CACS). Methods and Results: A total of 492 patients (mean age 62.5 ± 10.8 years) underwent clinically indicated multimodality CCTA and electrocardiography (ECG)-gated 99m Tc-tetrofosmin SPECT-MPI between May 2005 and December 2008 at our institution, and follow-up data on major adverse cardiovascular events (MACE) was obtained for 314 patients. FAI was obtained from CCTA images and was measured around the right coronary artery (FAI[RCA]), the left anterior descending artery (FAI[LAD]), and the left main coronary artery (FAI[LMCA]). During a median follow-up of 2.7 years, FAI[RCA] > - 70.1 was associated with an increased rate of MACE (log rank p = 0.049), while no such association was seen for FAI[LAD] or FAI[LMCA] (p = NS). A multivariate Cox regression model accounting for cardiovascular risk factors, CCTA and SPECT-MPI findings identified FAI[RCA] as an independent predictor of MACE (HR 2.733, 95% CI: 1.220-6.123, p = 0.015). However, FAI[RCA] was no longer a significant predictor of MACE after adding CACS (p = 0.279). A first-order interaction term consisting of sex and FAI[RCA] was significant in both models (HR 2.119, 95% CI: 1.218-3.686, p = 0.008; and HR 2.071, 95% CI: 1.111-3.861, p = 0.022). Conclusion: FAI does not add incremental prognostic value beyond multimodality MPI/CCTA findings including CACS. The diagnostic value of FAI[RCA] is significantly biased by sex. |
Databáze: | MEDLINE |
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