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年龄相关性疾病临床前模型中年龄与性别的系统评价方案

Protocol for the systematic review of age and sex in preclinical models of age-correlated diseases.

作者信息

Diederich Kai, Steinfath Matthias, Bannach-Brown Alexandra, Bert Bettina, Butzke Daniel, Wildner Paul Lucas, Wurm Maximilian, Schadock Ines, Heinl Céline

机构信息

German Centre for the Protection of Laboratory Animals (Bf3R), German Federal Institute for Risk Assessment (BfR), Berlin, Berlin, Germany.

QUEST Center, Berlin Institute of Health at Charité - Universitätsmedizin Berlin, Berlin, Berlin, Germany.

出版信息

F1000Res. 2024 Nov 25;13:858. doi: 10.12688/f1000research.153466.2. eCollection 2024.

Abstract

The translation of animal-based biomedical research into clinical research is often inadequate. Maximizing translation should be central to animal research on human diseases, guiding researchers in study design and animal model selection. However, practical considerations often drive the choice of animal model, which may not always reflect key patient characteristics, such as sex and age, impacting the disease's course. Despite diseases affecting both sexes, researchers frequently use male mice. To address this imbalance, journals and funding agencies have begun questioning the sex of animals used in studies and issued new guidelines. Conversely, the age of rodents is rarely discussed, even though many diseases primarily affect older patients. Young mice are commonly used, even in studies of diseases affecting older adults. Systematic comparisons between the age of rodents used and the age of patients in clinical trials are lacking. In this review, we systematically analyze the age and sex of mice used to model the five leading causes of global disability-adjusted life-years over the age of 75. We compare the results with the age and sex of patients in clinical trials focusing on Alzheimer's disease, stroke, type 2 diabetes mellitus, ischemic heart disease, and chronic obstructive pulmonary disease. We also analyze whether the age of the mice used has changed over the past decade. By systematically assessing the age and sex of the mice, we aim to initiate a discussion on the appropriate choice of animal model to improve the translatability of research results.

摘要

基于动物的生物医学研究向临床研究的转化往往并不充分。最大化转化应成为人类疾病动物研究的核心,指导研究人员进行研究设计和动物模型选择。然而,实际考量常常驱动动物模型的选择,而这可能并不总能反映关键的患者特征,如性别和年龄,从而影响疾病的进程。尽管疾病对两性都会产生影响,但研究人员经常使用雄性小鼠。为解决这种不平衡,期刊和资助机构已开始质疑研究中所使用动物的性别,并发布了新的指导方针。相反,啮齿动物的年龄很少被讨论,即便许多疾病主要影响老年患者。即便在针对影响老年人的疾病研究中,也通常使用年轻小鼠。临床试验中所使用啮齿动物的年龄与患者年龄之间缺乏系统的比较。在本综述中,我们系统地分析了用于模拟全球75岁以上伤残调整生命年主要五大病因的小鼠的年龄和性别。我们将结果与专注于阿尔茨海默病、中风、2型糖尿病、缺血性心脏病和慢性阻塞性肺疾病的临床试验中患者的年龄和性别进行比较。我们还分析了过去十年中所使用小鼠的年龄是否发生了变化。通过系统地评估小鼠的年龄和性别,我们旨在引发关于合适动物模型选择的讨论,以提高研究结果的可转化性。

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