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Source data are available as a Source Data file. Pro-atherogenic lipids and atherosclerosis are greater in XX than XY mice, indicating a primary effect of sex chromosomes. Our findings may have important ramifications for human health, particularly following menopause, when protective effects of female sex hormones are lost, and the effects of an XX sex chromosome genotype may contribute to pro-atherogenic lipid profiles and CAD. However, there were no differences in serum testosterone concentrations between XX and XY mice, regardless of sex. Introduction Sex chromosomes and sex hormones are the primary determinants of biological sex. Moreover, greater body weights Fig. At baseline and following 1 week of the Western diet, males had significantly higher body weights than females, regardless of sex chromosome genotype Fig. Our data suggest that the greater atherosclerosis susceptibility in XX compared to XY mice is associated with enhanced absorption and bioavailability of dietary fat, which likely influences serum lipid levels and adiposity. Source data are available as a Source Data file Full size image Female mice had significant increases in food intake and activity compared to males, regardless of sex chromosome genotype, while males of each genotype had higher energy expenditure than females Fig. Notably, some studies report that postmenopausal females exhibit a pro-atherogenic lipid profile and an increase in CAD to a level that not only catches up to, but exceeds that of age-matched males 11 , 12 , Serum testosterone concentrations were higher in male than female mice, regardless of sex chromosome genotype Male, XX:

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Source data are available as a Source Data file. Pro-atherogenic lipids and atherosclerosis are greater in XX than XY mice, indicating a primary effect of sex chromosomes. Our findings may have important ramifications for human health, particularly following menopause, when protective effects of female sex hormones are lost, and the effects of an XX sex chromosome genotype may contribute to pro-atherogenic lipid profiles and CAD. However, there were no differences in serum testosterone concentrations between XX and XY mice, regardless of sex. Introduction Sex chromosomes and sex hormones are the primary determinants of biological sex. Moreover, greater body weights Fig. At baseline and following 1 week of the Western diet, males had significantly higher body weights than females, regardless of sex chromosome genotype Fig. Our data suggest that the greater atherosclerosis susceptibility in XX compared to XY mice is associated with enhanced absorption and bioavailability of dietary fat, which likely influences serum lipid levels and adiposity. Source data are available as a Source Data file Full size image Female mice had significant increases in food intake and activity compared to males, regardless of sex chromosome genotype, while males of each genotype had higher energy expenditure than females Fig. Notably, some studies report that postmenopausal females exhibit a pro-atherogenic lipid profile and an increase in CAD to a level that not only catches up to, but exceeds that of age-matched males 11 , 12 , Serum testosterone concentrations were higher in male than female mice, regardless of sex chromosome genotype Male, XX: Sex sex sex only sex

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  1. Generally, results from these studies suggest that estrogens have beneficial effects on circulating lipid profiles e. Moreover, higher serum lipids and atherosclerosis are evident in XX female and male mice under different experimental paradigms e. Source data are available as a Source Data file Full size image Female mice had significant increases in food intake and activity compared to males, regardless of sex chromosome genotype, while males of each genotype had higher energy expenditure than females Fig.

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