BACKGROUND: Inflammation plays a pivotal role in atherogenesis and is a causal risk factor for atherosclerotic cardiovascular disease. Non-invasive coronary CT angiography (CCTA) enables evaluation of coronary plaque phenotype. This study investigates the relationship between a comprehensive panel of inflammatory markers and short-term plaque progression on serial CCTA imaging, hypothesising that inflammation is associated with increased plaque volume. METHODS: A total of 161 patients aged â¥40 years with stable multivessel coronary artery disease were included, who underwent CCTA at baseline and 12 months follow-up. Baseline plasma levels of interleukin 6 (IL-6), high-sensitivity C-reactive protein and other inflammatory markers were measured. Plaque volumes were assessed using semiautomated software, calculating total, noncalcified, calcified and low-attenuation noncalcified plaque volumes. Linear regression models, adjusted for ASSIGN score, segment involvement score and body mass index, evaluated associations between inflammatory markers and plaque volume changes. RESULTS: The mean±SDâage was 65.4±8.4 years, with 129 (80.6%) male participants. Baseline total plaque volume was 1394 (1036, 1993) mm³. After 12 months, total plaque volume changed by 78 (-114, 244) mm³. IL-6 levels were associated with a 4.9% increase in total plaque volume (95%âCI: 0.9 to 8.9, p=0.018) and a 4.8% increase in noncalcified plaque volume (95%âCI: 0.7 to 8.9, p=0.022). No significant associations were observed for other inflammatory markers. CONCLUSIONS: Plasma IL-6 levels are significantly associated with increased total and noncalcified short-term plaque progression in patients with stable coronary artery disease. This supports the potential of IL-6 as a target for reducing plaque progression and cardiovascular risk.
Interleukin 6 plasma levels are associated with progression of coronary plaques.
血浆白细胞介素 6 水平与冠状动脉斑块的进展有关
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作者:Kraaijenhof Jordan M, Nurmohamed Nick S, Tzolos Evangelos, Meah Mo, Geers Jolien, Kaiser Yannick, Kroon Jeffrey, Hovingh G Kees, Stroes Erik S G, Dweck Marc R
| 期刊: | Open Heart | 影响因子: | 2.800 |
| 时间: | 2024 | 起止号: | 2024 Sep 19; 11(2):e002773 |
| doi: | 10.1136/openhrt-2024-002773 | 研究方向: | 细胞生物学 |
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