Khalil Abdelouahed, Orellana Marlene Rossibel Montesino, Fulop Tamas, Turcotte Eric E, Bentourkia M'hamed
Department of Medicine, Geriatrics Service, Faculty of Medicine and Health Sciences, University of Sherbrooke Canada.
Department of Nuclear Medicine and Radiobiology, Faculty of Medicine and Health Sciences, University of Sherbrooke Canada.
Am J Nucl Med Mol Imaging. 2014 Apr 25;4(3):283-92. eCollection 2014.
This study was aimed to investigate the usefulness of (18)F-FDG-PET to differentiate vascular inflammation and to determine the effect of rosuvastatin. Eight subjects were recruited and were divided according to their health status in three groups; 3 healthy subjects, 3 patients with hypercholesterolemia and 2 patients with stable angina pectoris. Hypercholesterolemic patients were submitted immediately after their recruitment to rosuvastatin treatment (20 mg/d). Two PET/CT measurements were made throughout the course of the study, one at baseline and the second 12 months later. Our results showed that the ratio of calcified arteries to total analyzed arteries segments were 23%, 36% and 44% for healthy, hypercholesterolemic and stable angina patients respectively. Healthy subjects present, at baseline, a high level of vascular inflammation as measured by (18)F-FDG uptake in both calcified and non-calcified segments of the arteries. This vascular inflammation increases as a function of the cardiovascular risk factors. After the 12-month follow-up period, non-calcified arteries showed a significant increase of (18)F-FDG uptake in both healthy, hypercholesterolemic and stable angina patients. However, the highest increase was noted for the healthy subjects; (50% increase, p<0.0001), while hypercholesterolemic patients under rosuvastatin showed only 25% increase of (18)F-FDG uptake (p<0.0001). This study confirms the usefulness of (18)F-FDG measurement to localize and quantify arterial inflammation in each artery segments and as a function of the CVD risk factors. Rosuvastatin may have a protective effect against arterial inflammation however; other studies with higher rosuvastatin doses (>20 mg/d) are needed to confirm this beneficial effect.
本研究旨在探讨(18)F-FDG-PET在鉴别血管炎症及确定瑞舒伐他汀疗效方面的作用。招募了8名受试者,并根据健康状况分为三组:3名健康受试者、3名高胆固醇血症患者和2名稳定型心绞痛患者。高胆固醇血症患者在招募后立即接受瑞舒伐他汀治疗(20mg/d)。在研究过程中进行了两次PET/CT测量,一次在基线时,另一次在12个月后。我们的结果显示,健康、高胆固醇血症和稳定型心绞痛患者的钙化动脉与总分析动脉段的比例分别为23%、36%和44%。健康受试者在基线时,通过动脉钙化和非钙化段的(18)F-FDG摄取量测量显示出高水平的血管炎症。这种血管炎症随着心血管危险因素的增加而增加。在12个月的随访期后,健康、高胆固醇血症和稳定型心绞痛患者的非钙化动脉(18)F-FDG摄取量均显著增加。然而,健康受试者的增加幅度最大(增加50%,p<0.0001),而接受瑞舒伐他汀治疗的高胆固醇血症患者(18)F-FDG摄取量仅增加25%(p<0.0001)。本研究证实了(18)F-FDG测量在定位和量化各动脉段动脉炎症以及作为心血管疾病危险因素函数方面的作用。然而,瑞舒伐他汀可能对动脉炎症有保护作用;需要其他使用更高瑞舒伐他汀剂量(>20mg/d)的研究来证实这种有益效果。