tors, their residual risks for CAD remain very high. 5- 7 We and others have clarified that other classical coronary risk factors, including hypertension, diabetes, and smoking, appear to be the residual risk factors for CAD in patients with FH. 8-11 In contrast, recent studies have shown that cholesterol efflux capacity (CEC), which reflects the initial step of the reverse cholesterol transport mediated by highdensity lipoprotein (HDL), is associated with probability of CAD independently of HDL cholesterol (HDL-C) levels. 12 However, there are few data regarding this issue F amilial hypercholesterolemia (FH) is among the most common causes of coronary artery disease (CAD) worldwide, with an estimated frequency of 1 in 300 among the general population, and 1 in 31 among patients with CAD. 1,2 Patients with FH have an extremely elevated risk for CAD due to a very high level of lowdensity lipoprotein cholesterol (LDL-C). 3,4 Although there are many approaches to reduce LDL-C levels in patients with FH, including the use of statins, ezetimibe, and proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibi-