Details

Autor(en) / Beteiligte

• Takahashi, Norihito
• Dohi, Tomotaka
• Endo, Hirohisa
• Takeuchi, Mitsuhiro
• Doi, Shinichiro
• Kato, Yoshiteru
• Okai, Iwao
• Iwata, Hiroshi
• Okazaki, Shinya
• Isoda, Kikuo
• Miyauchi, Katsumi
• Minamino, Tohru

Titel

Coronary lipid-rich plaque characteristics in Japanese patients with acute coronary syndrome and stable angina: A near infrared spectroscopy and intravascular ultrasound study

Ist Teil von

• International journal of cardiology. Heart & vasculature, 2021-04, Vol.33, p.100747-100747, Article 100747

Ort / Verlag

Ireland: Elsevier B.V

Erscheinungsjahr

2021

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• •This study aimed to evaluate the characteristics of lipid-rich plaque (LRP) in Japanese.•The maxLCBI4mm significantly predicted acute coronary syndrome culprit lesion.•Almost 20% of patients had at least one high-risk LRP in non-culprit lesion segment in same vessel.•No surrogate maker (lipids and inflammation) for a high-risk LRP was found.•Direct intravascular evaluation of plaque characteristics remains important. Asians have a much lower incidence of adverse coronary events than Caucasians. We sought to evaluate the characteristics of coronary lipid-rich plaques (LRP) in Asian patients with acute coronary syndrome (ACS) and stable angina (SA). We also aimed to identify surrogate markers for the extent of LRP. We evaluated 207 patients (ACS, n = 75; SA, n = 132) who underwent percutaneous coronary intervention under near infrared spectroscopy intravascular ultrasound (NIRS-IVUS). Plaque characteristics and the extent of LRP [defined as a long segment with a 4-mm maximum lipid-core burden index (maxLCBI4mm)] on NIRS in de-novo culprit and non-culprit segments were analyzed. The ACS culprit lesions had a significantly higher maxLCBI4mm (median [interquartile range (IQR)]: 533 [385–745] vs. 361 [174–527], p < 0.001) than the SA culprit lesions. On multivariate logistic analysis, a large LRP (defined as maxLCBI4mm ≥ 400) was the strongest independent predictor of the ACS culprit segment (odds ratio, 3.87; 95% confidence interval, 1.95–8.02). In non-culprit segments, 19.8% of patients had at least one large LRP without a small lumen. No significant correlation was found between the extent of LRP and systematic biomarkers (hs-CRP, IL-6, TNF-α), whereas the extent of LRP was positively correlated with IVUS plaque burden (r = 0.24, p < 0.001). We confirmed that NIRS-IVUS plaque assessment could be useful to differentiate ACS from SA culprit lesions, and that a threshold maxLCBI4mm ≥ 400 was clinically suitable in Japanese patients. No surrogate maker for a high-risk LRP was found; consequently, direct intravascular evaluation of plaque characteristics remains important.