Logo

American Heart Association

  2
  0


Final ID: MDP1310

Electrochemical Impedance Spectroscopy Unmasks High-Risk Atherosclerotic Features in Human Coronary Artery Disease

Abstract Body (Do not enter title and authors here): Background
Coronary plaque rupture remains the prominent mechanism of myocardial infarction. Accurate identification of rupture-prone plaque may improve clinical management. This study assessed the discriminatory performance of electrochemical impedance spectroscopy (EIS) in human cardiac explants to detect high-risk atherosclerotic features that portend rupture risk.

Methods
In this single-center, prospective study, n=26 cardiac explants were collected for EIS interrogation of the three major coronary arteries. Vessels in which advancement of the EIS catheter without iatrogenic plaque disruption was rendered impossible were not assessed. N=61 vessels underwent EIS measurement and histological analyses. Plaques were dichotomized according to previously established high rupture-risk parameter thresholds. Diagnostic performance was determined via receiver operating characteristic areas-under-the-curve (AUC).

Results
Necrotic cores were identified in n=19 vessels (median area 1.53 mm2) with median fibrous cap thickness of 62 μm. Impedance was significantly greater in plaques with necrotic core area ≥1.75 mm2 vs <1.75 mm2 (19.8±4.4 kΩ vs 7.2±1.0 kΩ, P=0.019), fibrous cap thickness ≤65 μm vs >65 μm (19.1±3.5 kΩ vs 6.5±0.9 kΩ, P=0.004), and ≥20 macrophages per 0.3 mm-diameter high-power field (HPF) vs <20 macrophages per HPF (19.8±4.1 kΩ vs 10.2±0.9 kΩ, P=0.002). Impedance identified necrotic core area ≥1.75 mm2, fibrous cap thickness ≤65 μm, and ≥20 macrophages per HPF with AUCs of 0.889 (95% CI: 0.716–1.000) (P=0.013), 0.852 (0.646—1.000) (P=0.025), and 0.835 (0.577—1.000) (P=0.028), respectively. Further, phase delay discriminated severe stenosis (≥70%) with an AUC of 0.767 (0.573—0.962) (P=0.035).

Conclusions
EIS discriminates high-risk atherosclerotic features that portend plaque rupture in human coronary artery disease and may serve as a complementary modality for angiography-guided atherosclerosis evaluation.
  • Chen, Michael  ( UCLA DGSOM , Los Angeles , California , United States )
  • Suwanaphoom, Krit  ( UCLA DGSOM , Los Angeles , California , United States )
  • Sanaiha, Yas  ( UCLA DGSOM , Los Angeles , California , United States )
  • Luo, Yuan  ( State Key Laboratory of Transducer Technology, Shanghai Institute of Microsystem and Information Technology, Chinese Academy of Sciences , Shanghai , China )
  • Benharash, Peyman  ( UCLA DGSOM , Los Angeles , California , United States )
  • Fishbein, Michael  ( UCLA DGSOM , Los Angeles , California , United States )
  • Packard, Rene  ( UCLA DGSOM , Los Angeles , California , United States )
  • Author Disclosures:
    Michael Chen: DO NOT have relevant financial relationships | Krit Suwanaphoom: No Answer | Yas Sanaiha: No Answer | Yuan Luo: No Answer | Peyman Benharash: No Answer | Michael Fishbein: DO NOT have relevant financial relationships | Rene Packard: DO have relevant financial relationships ; Consultant:GE Healthcare:Active (exists now)
Meeting Info:

Scientific Sessions 2024

2024

Chicago, Illinois

Session Info:

Cardiovascular Imaging

Monday, 11/18/2024 , 12:50PM - 02:15PM

Moderated Digital Poster Session

More abstracts on this topic:
Age- and Sex-Related Coronary Atherosclerosis by Artificial Intelligence Quantitative Coronary CT Angiography from the INVICTUS Registry

Okubo Ryo, Ichikawa Keishi, Abe Mitsunori, Kitagawa Toshiro, Ikenaga Hiroki, Osawa Kazuhiro, Saji Mike, Iguchi Nobuo, Nakazawa Gaku, Takahashi Kuniaki, Ijichi Takeshi, Matsuo Hitoshi, Mikamo Hiroshi, Kurata Akira, Moroi Masao, Iijima Raisuke, Crabtree Tami, Min James, Earls James, Nakanishi Rine, Sobue Yoshihiro, Kaneko Umihiko, Sato Hideyuki, Fujimoto Shinichiro, Nozaki Yui, Kajiya Takashi, Miyoshi Toru

A major uremic toxin indoxyl sulfate impairs macrophage efferocytosis and accelerates atherogenesis: a potential mechanism for cardiovascular risk in chronic kidney disease

Jha Prabhash, Kasai Taku, Vromman Amelie, Holden Rachel, Libby Peter, Tabas Ira, Singh Sasha, Aikawa Elena, Aikawa Masanori, Lupieri Adrien, Sonawane Abhijeet, Le Thanh-dat, Becker-greene Dakota, Chelvanambi Sarvesh, Turner Mandy, Nakamura Yuto, Passos Livia

You have to be authorized to contact abstract author. Please, Login
Not Available