Literature DB >> 20378076

The dynamic nature of coronary artery lesion morphology assessed by serial virtual histology intravascular ultrasound tissue characterization.

Takashi Kubo1, Akiko Maehara, Gary S Mintz, Hiroshi Doi, Kenichi Tsujita, So-Yeon Choi, Osamu Katoh, Kenya Nasu, Andreas Koenig, Michael Pieper, Jason H Rogers, William Wijns, Dirk Böse, M Pauliina Margolis, Jeffrey W Moses, Gregg W Stone, Martin B Leon.   

Abstract

OBJECTIVES: We used virtual histology intravascular ultrasound (VH-IVUS) to investigate the natural history of coronary artery lesion morphology.
BACKGROUND: Plaque stability is related to its histological composition.
METHODS: We performed serial (baseline and 12-month follow-up) VH-IVUS studies and examined 216 nonculprit lesions (plaque burden >or=40%) in 99 patients. Lesions were classified into pathological intimal thickening (PIT), VH-IVUS-derived thin-capped fibroatheroma (VH-TCFA), thick-capped fibroatheroma (ThCFA), fibrotic plaque, and fibrocalcific plaque.
RESULTS: At baseline, 20 lesions were VH-TCFAs; during follow-up, 15 (75%) VH-TCFAs "healed," 13 became ThCFAs, 2 became fibrotic plaque, and 5 (25%) VH-TCFAs remained unchanged. Compared with VH-TCFAs that healed, VH-TCFAs that remained VH-TCFAs located more proximally (values are median [interquartile range]) (16 mm [15 to 18 mm] vs. 31 mm [22 to 47 mm], p = 0.013) and had larger lumen (9.1 mm(2) [8.2 to 10.7 mm(2)] vs. 6.9 mm(2) [6.0 to 8.2 mm(2)], p = 0.021), vessel (18.7 mm(2) [17.3 to 28.6 mm(2)] vs. 15.5 mm(2) [13.3 to 16.6 mm(2)]; p = 0.010), and plaque (9.7 mm(2) [9.6 to 15.7 mm(2)] vs. 8.4 mm(2) [7 to 9.7 mm(2)], p = 0.027) areas; however, baseline VH-IVUS plaque composition did not differ between VH-TCFAs that healed and VH-TCFAs that remained VH-TCFAs. Conversely, 12 new VH-TCFAs developed; 6 late-developing VH-TCFAs were PITs, and 6 were ThCFAs at baseline. In addition, plaque area at minimum lumen sites increased significantly in PITs (7.8 mm(2) [6.2 to 10.0 mm(2)] to 9.0 mm(2) [6.5 to 12.0 mm(2)], p < 0.001), VH-TCFAs (8.6 mm(2) [7.3 to 9.9 mm(2)] to 9.5 mm(2) [7.8 to 10.8 mm(2)], p = 0.024), and ThCFAs (8.6 mm(2) [6.8 to 10.2 mm(2)] to 8.8 mm(2) [7.1 to 11.4 mm(2)], p < 0.001) with a corresponding decrease lumen areas, but not in fibrous or fibrocalcific plaque.
CONCLUSIONS: Most VH-TCFAs healed during 12-month follow-up, whereas new VH-TCFAs also developed. PITs, VH-TCFAs, and ThCFAs showed significant plaque progression compared with fibrous and fibrocalcific plaque. Copyright (c) 2010 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20378076     DOI: 10.1016/j.jacc.2009.07.078

Source DB:  PubMed          Journal:  J Am Coll Cardiol        ISSN: 0735-1097            Impact factor:   24.094


  65 in total

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2.  Optimal boundary detection method and window settings for coronary atherosclerotic plaque volume analysis in coronary computed tomography angiography: comparison with intravascular ultrasound.

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Review 3.  Genome-wide significant loci: how important are they? Systems genetics to understand heritability of coronary artery disease and other common complex disorders.

Authors:  Johan L M Björkegren; Jason C Kovacic; Joel T Dudley; Eric E Schadt
Journal:  J Am Coll Cardiol       Date:  2015-03-03       Impact factor: 24.094

4.  Impact of tissue characteristics on luminal narrowing of mild angiographic coronary stenosis: assessment of integrated backscatter intravascular ultrasound.

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Review 5.  Intravascular imaging of vulnerable coronary plaque: current and future concepts.

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Journal:  Nat Rev Cardiol       Date:  2011-01-25       Impact factor: 32.419

6.  Predicting Locations of High-Risk Plaques in Coronary Arteries in Patients Receiving Statin Therapy.

Authors:  Ling Zhang; Andreas Wahle; Zhi Chen; John J Lopez; Tomas Kovarnik; Milan Sonka
Journal:  IEEE Trans Med Imaging       Date:  2017-07-11       Impact factor: 10.048

7.  From inflammation to calcification in atherosclerosis.

Authors:  Takehiro Nakahara; H William Strauss
Journal:  Eur J Nucl Med Mol Imaging       Date:  2017-05       Impact factor: 9.236

8.  Quantification of the focal progression of coronary atherosclerosis through automated co-registration of virtual histology-intravascular ultrasound imaging data.

Authors:  Lucas H Timmins; David S Molony; Parham Eshtehardi; Emad Rasoul-Arzrumly; Adrian Lam; Olivia Y Hung; Michael C McDaniel; John N Oshinski; Don P Giddens; Habib Samady
Journal:  Int J Cardiovasc Imaging       Date:  2016-11-14       Impact factor: 2.357

9.  Plaque modification and stabilization after paclitaxel-coated balloon treatment for de novo coronary lesions.

Authors:  Ae-Young Her; Eun-Seok Shin; Ju-Hyun Chung; Yong Hoon Kim; Scot Garg; Joo Myung Lee; Joon-Hyung Doh; Chang-Wook Nam; Bon-Kwon Koo
Journal:  Heart Vessels       Date:  2019-01-30       Impact factor: 2.037

Review 10.  Reassessing the Mechanisms of Acute Coronary Syndromes.

Authors:  Peter Libby; Gerard Pasterkamp; Filippo Crea; Ik-Kyung Jang
Journal:  Circ Res       Date:  2019-01-04       Impact factor: 17.367

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