Liu Shuai, Lin Xue, Shi Ximin, Fang Ligang, Huo Li, Shang Fei, Knuuti Juhani, Han Chunlei, Wu Xiaomeng, Guo Rui, Ding Haiyan, Zhang Runhua, Duan Huimin, Ding Jie, Xing Haiqun, Zhao Xihai
Center for Biomedical Imaging Research, Department of Biomedical Engineering, Tsinghua University School of Medicine, Haidian District, Beijing, 100084, China.
Department of Cardiology, Peking Union Medical College Hospital, Chinese Academy of Medical Science, Beijing, China.
J Cardiovasc Magn Reson. 2020 Apr 16;22(1):23. doi: 10.1186/s12968-020-00614-2.
Chronic alcohol consumption initially leads to asymptomatic left ventricular dysfunction, but can result in myocardial impairment and heart failure if ongoing. This study sought to characterize myocardial tissues and oxidative metabolism in asymptomatic subjects with chronic alcohol consumption by quantitative cardiovascular magnetic resonance (CMR) and 11C-acetate positron emission tomography (PET)/computed tomography (CT).
Thirty-four male subjects (48.8 ± 9.1 years) with alcohol consumption > 28 g/day for > 10 years and 35 age-matched healthy male subjects (49.5 ± 9.7 years) underwent CMR and 11C-acetate PET/CT. Native and post T1 values and extracellular volume (ECV) from CMR and Kmono and K1 from PET imaging were measured. Quantitative measurements by CMR and PET imaging were compared between subjects with moderate to heavy alcohol consumption and healthy controls, and their correlations were also analyzed.
Compared to healthy controls, subjects with alcohol consumption showed significantly shorter native T1 (1133 ± 65 ms vs. 1186 ± 31 ms, p < 0.001) and post T1 (477 ± 42 ms vs. 501 ± 38 ms, p = 0.008) values, greater ECV (28.2 ± 2.2% vs. 26.9 ± 1.3%, p = 0.003), marginally lower Kmono (57.6 ± 12.1 min × 10 vs. 63.0 ± 11.7 min × 10, p = 0.055), and similar K1 (0.82 ± 0.13 min vs. 0.83 ± 0.15 min, p = 0.548) after adjusting for confounding factors. There were no significant differences in CMR measurements and K1 between subjects with heavy and moderate alcohol consumption (all p > 0.05). In contrast, subjects with heavy alcohol consumption showed significantly lower Kmono values compared to those with moderate alcohol consumption (52.9 ± 12.1 min × 10 vs. 63.7 ± 9.2 min × 10, p = 0.012). Strong and moderate correlations were found between K1 and ECV in healthy controls (r = 0.689, p = 0.013) and subjects with moderate alcohol consumption (r = 0.518, p = 0.048), respectively.
Asymptomatic men with heavy alcohol consumption have detectable structural and metabolic changes in myocardium on CMR and 11C-acetate PET/CT. Compared with quantitative CMR, 11C-acetate PET/CT imaging may be more sensitive for detecting differences in myocardial damage among subjects with moderate to heavy alcohol consumption.
长期饮酒最初会导致无症状性左心室功能障碍,但如果持续饮酒,可能会导致心肌损伤和心力衰竭。本研究旨在通过定量心血管磁共振成像(CMR)和11C-乙酸正电子发射断层扫描(PET)/计算机断层扫描(CT)对长期饮酒的无症状受试者的心肌组织和氧化代谢进行特征分析。
34名男性受试者(48.8±9.1岁),每日饮酒量>28 g,持续时间>10年,以及35名年龄匹配的健康男性受试者(49.5±9.7岁)接受了CMR和11C-乙酸PET/CT检查。测量CMR的固有T1值、T1加权后值和细胞外容积(ECV)以及PET成像的Kmono和K1值。比较中度至重度饮酒受试者与健康对照者的CMR和PET成像定量测量结果,并分析它们之间的相关性。
与健康对照者相比,饮酒受试者的固有T1值(1133±65 ms对1186±31 ms,p<0.001)和T1加权后值(477±42 ms对501±38 ms,p=0.008)显著缩短,ECV更高(28.2±2.2%对26.9±1.3%,p=0.003),Kmono略低(57.6±12.1 min×10对63.0±11.7 min×10,p=0.055),调整混杂因素后K1相似(0.82±0.13 min对0.83±0.15 min,p=0.548)。重度饮酒和中度饮酒受试者之间的CMR测量值和K1无显著差异(所有p>0.05)。相比之下,重度饮酒受试者的Kmono值显著低于中度饮酒受试者(52.9±12.1 min×10对63.7±9.2 min×10,p=0.012)。在健康对照者(r=0.689,p=0.013)和中度饮酒受试者(r=0.518,p=0.048)中,K1与ECV之间分别存在强相关性和中度相关性。
长期大量饮酒的无症状男性在CMR和11C-乙酸PET/CT上可检测到心肌结构和代谢变化。与CMR定量分析相比,1-乙酸PET/CT成像在检测中度至重度饮酒受试者心肌损伤差异方面可能更敏感。