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生物医学研究中常见的非人灵长类物种的比较寿命和健康寿命。

Comparative lifespan and healthspan of nonhuman primate species common to biomedical research.

作者信息

Huber Hillary F, Ainsworth Hannah C, Quillen Ellen E, Salmon Adam, Ross Corinna, Azhar Adinda D, Bales Karen, Basso Michele A, Coleman Kristine, Colman Ricki, Darusman Huda S, Hopkins William, Hotchkiss Charlotte E, Jorgensen Matthew J, Kavanagh Kylie, Li Cun, Mattison Julie A, Nathanielsz Peter W, Saputro Suryo, Scorpio Diana G, Sosa Paul-Michael, Vallender Eric J, Wang Yaomin, Zeiss Caroline J, Shively Carol A, Cox Laura A

机构信息

Texas Biomedical Research Institute, San Antonio, TX, USA.

Wake Forest University School of Medicine, Winston-Salem, NC, USA.

出版信息

Geroscience. 2025 Feb;47(1):135-151. doi: 10.1007/s11357-024-01421-8. Epub 2024 Nov 25.

Abstract

There is a critical need to generate age- and sex-specific survival curves to characterize chronological aging consistently across nonhuman primates (NHP) used in biomedical research. Sex-specific Kaplan-Meier survival curves were computed in 12 translational aging models: baboon, bonnet macaque, chimpanzee, common marmoset, coppery titi monkey, cotton-top tamarin, cynomolgus macaque, Japanese macaque, pigtail macaque, rhesus macaque, squirrel monkey, and vervet/African green. After employing strict inclusion criteria, primary results are based on 12,269 NHPs that survived to adulthood and died of natural/health-related causes. A secondary analysis was completed for 32,616 NHPs that died of any cause. Results show a pattern of reduced male survival among catarrhines (African and Asian primates), especially macaques, but not platyrrhines (Central and South American primates). For many species, median lifespans were lower than previously reported. An important consideration is that these analyses may offer a better reflection of healthspan than lifespan since research NHPs are typically euthanized for humane welfare reasons before their natural end of life. This resource represents the most comprehensive characterization of sex-specific lifespan and age-at-death distributions for 12 biomedically relevant species, to date. These results clarify relationships among NHP ages and provide a valuable resource for the aging research community, improving human-NHP age equivalencies, informing investigators of expected survival rates, providing a metric for comparisons in future studies, and contributing to understanding of factors driving lifespan differences within and among species.

摘要

迫切需要生成特定年龄和性别的生存曲线,以便在生物医学研究中使用的非人类灵长类动物(NHP)中一致地描述自然衰老过程。在12种转化衰老模型中计算了特定性别的Kaplan-Meier生存曲线:狒狒、冠毛猕猴、黑猩猩、普通狨猴、铜头伶猴、棉顶狨猴、食蟹猕猴、日本猕猴、猪尾猕猴、恒河猴、松鼠猴和绿猴/非洲绿猴。在采用严格的纳入标准后,主要结果基于12269只存活至成年并死于自然/健康相关原因的NHP。对32616只死于任何原因的NHP进行了二次分析。结果显示,狭鼻猴(非洲和亚洲灵长类动物),尤其是猕猴中,雄性生存率降低,但阔鼻猴(中美洲和南美洲灵长类动物)并非如此。对于许多物种来说,中位数寿命低于先前报道。一个重要的考虑因素是,这些分析可能比寿命更能反映健康寿命,因为出于人道福利原因,研究用的NHP通常在其自然生命结束前被安乐死。该资源代表了迄今为止对12种与生物医学相关物种特定性别的寿命和死亡年龄分布最全面的描述。这些结果阐明了NHP年龄之间的关系,为衰老研究界提供了宝贵的资源,改善了人类与NHP年龄的等效性,告知研究人员预期的生存率,为未来研究提供比较指标,并有助于理解驱动物种内部和物种之间寿命差异的因素。

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