Lifespan of male and female APP/PS1 and APP <sup>NL-F/NL-F</sup> mouse models of Alzheimer's disease

Alzheimer's disease (AD) disproportionately affects women, yet most preclinical research studies are male-centric. We performed lifespan analyses of male and female AD mouse models (APP/PS1 and APP<sup>NL-F/NL-F</sup>) and their shared genetic background control (C57BL/6). Survival curves support significant sex differences between genotypes. Minimal longevity revealed increased age in male APP/PS1, and decreased age in male APP<sup>NL-F/NL-F</sup> mice. Maximal longevity revealed an increased average age in males. Furthermore, median lifespan differed between sex and genotype. This study supports dimorphic survival in two mouse models of AD, emphasizing the need to examine mechanisms and treatments in both sexes.

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Publication Details

Journal
Journal of Alzheimer s Disease
Published
2025-03-26
DOI
https://doi.org/10.1177/13872877251325878
Citations
3
Primary Topic
Nuclear Receptors and Signaling
Type
article
Field-Weighted Citation Impact
2.73

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article

Lifespan of male and female APP/PS1 and APP NL-F/NL-F mouse models of Alzheimer's disease

Kevin N. Hascup, Kathleen Quinn, Andrzej Bartke, Yimin Fang et al.
3 citations
Journal of Alzheimer s Disease
Nuclear Receptors and Signaling
2.73
article

Lifespan of male and female APP/PS1 and APP NL-F/NL-F mouse models of Alzheimer's disease

Kevin N. Hascup, Kathleen Quinn, Andrzej Bartke, Yimin Fang, Erin R. Hascup, Mackenzie R. Peck, Hannah Roberts, Tiarra Hill
article en
3 citations

Abstract

Alzheimer's disease (AD) disproportionately affects women, yet most preclinical research studies are male-centric. We performed lifespan analyses of male and female AD mouse models (APP/PS1 and APP<sup>NL-F/NL-F</sup>) and their shared genetic background control (C57BL/6). Survival curves support significant sex differences between genotypes. Minimal longevity revealed increased age in male APP/PS1, and decreased age in male APP<sup>NL-F/NL-F</sup> mice. Maximal longevity revealed an increased average age in males. Furthermore, median lifespan differed between sex and genotype. This study supports dimorphic survival in two mouse models of AD, emphasizing the need to examine mechanisms and treatments in both sexes.

Journal of Alzheimer s DiseaseVol. 105(1)
Southern Illinois University School of Medicine (US)
National Institute on Aging
Good health and well-being
Openalex Percentile: Top 11%
Nuclear Receptors and Signaling
2.73
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Lifespan of male and female APP/PS1 and APP <sup>NL-F/NL-F</sup> mouse models of Alzheimer's disease — Kevin N. Hascup, Kathleen Quinn, et al. · Journal of Alzheimer s Disease (2025) | TGRS Research Map | TGRS