TY - JOUR
T1 - Impact of noninsulin-dependent type 2 diabetes on carotid wall 18F-fluorodeoxyglucose positron emission tomography uptake
AU - Bucerius, Jan
AU - Mani, Venkatesh
AU - Moncrieff, Colin
AU - Rudd, James H.F.
AU - MacHac, Josef
AU - Fuster, Valentin
AU - Farkouh, Michael E.
AU - Fayad, Zahi A.
PY - 2012/6/5
Y1 - 2012/6/5
N2 - Objectives: In this study, the impact of noninsulin-dependent type 2 diabetes mellitus on carotid wall 18F-fluorodeoxyglucose (FDG) uptake in patients with documented or suspected cardiovascular disease was evaluated. Background: Inflammation is a pivotal process in the progression of atherosclerosis, which can be noninvasively imaged by FDG positron emission tomography (FDG-PET). Methods: Carotid artery wall FDG uptake was quantified in 134 patients (age 60.2 ± 9.7 years; diabetic subjects, n = 43). The pre-scan glucose (gluc) level corrected mean of the maximum standardized uptake value (SUV) values ( meanSUV gluc), mean of the maximum target-to-background ratio ( meanTBR gluc), and single hottest segment (SHS gluc) of FDG uptake in the artery wall were calculated. Associations between FDG uptake, the presence of risk factors for atherosclerosis, and diabetes were then assessed by multiple regression analysis with backward elimination. Results: The study demonstrated a significant association between diabetes and FDG uptake in the arterial wall (diabetes meanSUV gluc β = 0.324, meanTBR gluc β = 0.317, and SHS gluc β = 0.298; for all, p < 0.0001). In addition, in diabetic patients, both body mass index <30 kg/m 2 ( meanSUV gluc β = 0.4, meanTBR gluc β = 0.357, and SHS gluc β = 0.388; for all, p < 0.015) and smoking ( meanTBR gluc, β = 0.312; SHS gluc, β = 0.324; for all, p < 0.04) were significantly associated with FDG uptake. Conclusions: Type 2 diabetes was significantly associated with carotid wall FDG uptake in patients with known or suspected cardiovascular disease. In diabetic patients, obesity and smoking add to the risk of increased FDG uptake values.
AB - Objectives: In this study, the impact of noninsulin-dependent type 2 diabetes mellitus on carotid wall 18F-fluorodeoxyglucose (FDG) uptake in patients with documented or suspected cardiovascular disease was evaluated. Background: Inflammation is a pivotal process in the progression of atherosclerosis, which can be noninvasively imaged by FDG positron emission tomography (FDG-PET). Methods: Carotid artery wall FDG uptake was quantified in 134 patients (age 60.2 ± 9.7 years; diabetic subjects, n = 43). The pre-scan glucose (gluc) level corrected mean of the maximum standardized uptake value (SUV) values ( meanSUV gluc), mean of the maximum target-to-background ratio ( meanTBR gluc), and single hottest segment (SHS gluc) of FDG uptake in the artery wall were calculated. Associations between FDG uptake, the presence of risk factors for atherosclerosis, and diabetes were then assessed by multiple regression analysis with backward elimination. Results: The study demonstrated a significant association between diabetes and FDG uptake in the arterial wall (diabetes meanSUV gluc β = 0.324, meanTBR gluc β = 0.317, and SHS gluc β = 0.298; for all, p < 0.0001). In addition, in diabetic patients, both body mass index <30 kg/m 2 ( meanSUV gluc β = 0.4, meanTBR gluc β = 0.357, and SHS gluc β = 0.388; for all, p < 0.015) and smoking ( meanTBR gluc, β = 0.312; SHS gluc, β = 0.324; for all, p < 0.04) were significantly associated with FDG uptake. Conclusions: Type 2 diabetes was significantly associated with carotid wall FDG uptake in patients with known or suspected cardiovascular disease. In diabetic patients, obesity and smoking add to the risk of increased FDG uptake values.
KW - FDG-PET
KW - atherosclerosis
KW - carotid arteries
KW - diabetes mellitus
KW - inflammation
UR - http://www.scopus.com/inward/record.url?scp=84861615576&partnerID=8YFLogxK
U2 - 10.1016/j.jacc.2011.11.069
DO - 10.1016/j.jacc.2011.11.069
M3 - Article
C2 - 22651864
AN - SCOPUS:84861615576
SN - 0735-1097
VL - 59
SP - 2080
EP - 2088
JO - Journal of the American College of Cardiology
JF - Journal of the American College of Cardiology
IS - 23
ER -