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    Sex-specific components of frailty in C57BL/6 mice.

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    License
    Attribution 3.0 Unported
    Date Issued
    2019-07-29
    Publisher Version
    10.18632/aging.102114
    Author(s)
    Baumann, Cory W.
    Kwak, Dongmin
    Thompson, LaDora V.
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    Permanent Link
    https://hdl.handle.net/2144/40040
    Version
    Published version
    Citation (published version)
    Cory W. Baumann, Dongmin Kwak, LaDora V. Thompson. 2019. "Sex-specific components of frailty in C57BL/6 mice.." Aging (Albany NY), Volume 11, Issue 14, pp. 5206 - 5214. https://doi.org/10.18632/aging.102114
    Abstract
    Many age-related biochemical, physiological and behavioral changes are known to be sex-specific. However, how sex influences frailty status and mortality risk in frail rodents has yet to be established. The purpose of this study was therefore to characterize sex differences in frail mice across the lifespan. Male (n=29) and female (n=27) mice starting at 17 months of age were assessed using a frailty phenotype adjusted according to sex, which included body weight, walking speed, strength, endurance and physical activity. Regardless of sex, frail mice were phenotypically dysfunctional compared to age-matched non-frail mice, while non-frail females generally possessed a higher body fat percentage and were more physically active than non-frail males (p≤0.05). The prevalence of frailty was greater in female mice at 26 months of age (p=0.05), but if normalized to mean lifespan, no sex differences remained. No differences were detected in the rate of death or mean lifespan between frail male and female mice (p≥0.12). In closing, these data indicate that sexual differences exist in aging C57BL/6 mice and if the frailty criteria are adjusted according to sex, the prevalence of frailty increases across age with frail mice dying early in life, regardless of sex.
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    Attribution 3.0 Unported
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    • BU Open Access Articles [3730]


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