Key result
Old age did not increase susceptibility to atherosclerosis in mice, with old and young mice developing comparable aortic lesion sizes (5,600 vs 6,457 microm2/section; p=0.77) on an atherogenic diet.
Why the study?
Does age directly affect susceptibility to atherosclerosis in a diet-induced mouse model?
Does age directly affect susceptibility to atherosclerosis in a diet-induced mouse model?
Absolute Event Rate: 5600% vs 6457%
p-value: p=0.77
Age does not have a direct effect on atherosclerosis susceptibility in C57BL/6 mice, suggesting that increased cardiovascular events with age are likely related to progressive plaque growth rather than increased susceptibility.
Questions direct age effect on atherogenesis in mice; hypothesis-generating for mechanisms of rising CV events with age in humans.
Age is considered to be a major risk factor for atherosclerosis, but it is unclear whether age has a direct effect on susceptibility to atherosclerosis. Wild-type mice develop fatty streak lesions in the aortic root only when fed a cholate-containing high fat/cholesterol diet. To investigate the influence of age on fatty streak formation, young (10 weeks) and old (53 weeks) female C57BL/6 mice were fed an atherogenic diet containing 15% fat, 1.25% cholesterol and 0.5% sodium cholate for 12 weeks. Atherosclerotic lesions at the aortic root were measured after cryosections were stained with oil red O. Results showed that old mice developed a comparable size of aortic lesions with young counterparts (5,600 +/- 2,480 vs. 6,457 +/- 1,537 microm2/section; p = 0.77), although old mice had significantly higher plasma cholesterol levels than young mice on the atherogenic diet (p < 0.05). Plasma levels of soluble vascular cell adhesion molecule 1 were significantly higher in old mice than in young mice on both chow and Western diets (p < 0.005). These data indicate that age has no direct effect on atherosclerosis susceptibility although it is accompanied by elevations in plasma cholesterol and vascular cell adhesion molecule 1 levels in C57BL/6 mice. Thus, increased cardiovascular events with age are probably related to a progressive increase in plaque size rather than to an increase in atherosclerosis susceptibility.
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Li et al. (2007) studied Atherosclerosis. Old age (53 weeks) vs. Young age (10 weeks) was evaluated on Atherosclerotic lesions at the aortic root (microm2/section) (p=0.77). Old age did not increase susceptibility to atherosclerosis in mice, with old and young mice developing comparable aortic lesion sizes (5,600 vs 6,457 microm2/section; p=0.77) on an atherogenic diet.
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