Table 2.
Mice (60 Weeks) | Rabbit (8 Months) | Swine (~ 12 Months) | |
---|---|---|---|
Pathology of atherosclerosis similar to humans | + | ++ | +++ |
Prominent necrotic core | ++ | + | +++ |
Positive vascular remodeling | +++ | ++ | +++ |
Thinned fibrous cap | +++ | ++ | ++ |
Evidence of plaque rupture | +++ | + | ++* |
Known genetic background | +++ | ++† | ++† |
Simple development method | ++ | ++ | ++ |
Metabolic profile similar to humans | + | + | +++‡ |
Short development time (<6 months) | ++ | +++ | ++§ |
Ability to perform noninvasive imaging | ++ | ++ | ++ |
Ability to perform invasive imaging | — | ++ | +++ |
Ability to perform systemic therapeutic interventions | ++ | ++ | ++ |
Ability to perform invasive therapeutic procedures | — | ++ | +++ |
Development cost | + | ++ | +++ |
Usually evident as intraplaque hemorrhage.
The Watanabe rabbit and the FH swine have well-characterized genetic backgrounds.
Except for persistently low triglyceride levels.
Lesions develop in the diabetic swine between 5 and 9 months.