Circulation Journal
Online ISSN : 1347-4820
Print ISSN : 1346-9843
ISSN-L : 1346-9843
Images in Cardiovascular Medicine
Clinical Utility of Near-Infrared Spectroscopy Intravascular Ultrasound in the Assessment of Rapidly Progressive Cardiac Allograft Vasculopathy
Sakae TakenakaTakuma SatoToshiyuki Nagai Toshihisa Anzai
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Supplementary material

2025 Volume 89 Issue 2 Pages 255-

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The patient was a 47-year-old male diagnosed with the dilated phase of hypertrophic cardiomyopathy. He had undergone heart transplantation (HTx) at the age of 43 years, and postoperative coronary angiography had shown no significant stenosis. However, intravascular ultrasound (IVUS) revealed that the maximal intimal thickness (MIT) of the left anterior descending artery (LAD) had progressed from 0.63 mm (at 1 month) to 1.15 mm (at 2 years) (Supplementary Figure A,B), and near-infrared spectroscopy (NIRS) IVUS at 2 years showed yellow signals with a maximum lipid core burden index in a 4-mm segment (max-LCBI) of 71 (Figure A). Based on these findings, we switched the immunosuppressive agent from mycophenolate mofetil to everolimus to suppress endometrial hyperplasia. IVUS at 3 years showed regression of the MIT in the LAD from 1.15 mm to 0.89 mm (Supplementary Figure C), and NIRS-IVUS demonstrated a significant reduction in yellow signals (Figure B). At 4 years, IVUS showed no evidence of progression of cardiac allograft vasculopathy (CAV) (Figure C, Supplementary Figure D).

Figure.

Serial changes on NIRS-IVUS: (A) 2 years, (B) 3 years, and (C) 4 years after heart transplantation (HT). LCBI, lipid core burden index; NIRS-IVUS, near-infrared spectroscopy intravascular ultrasound.

NIRS-IVUS was originally developed to assess the composition of atherosclerotic plaques.1 A previous study showed that even a very low max-LCBI value (<100) was associated with accelerated plaque burden, which in patients with HTx might reflect an immunologic reaction, when compared with patients with atherosclerosis.2 Our case demonstrates that NIRS-IVUS may be useful for assessing the therapeutic effect of changing immunosuppressive agents to control CAV.

Disclosures

Drs. Anzai and Nagai are members of Circulation Journal’s Editorial Team.

Supplementary Files

Please find supplementary file(s);

https://doi.org/10.1253/circj.CJ-24-0024

References
 
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