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Aging on a different scale – chronological versus pathology-related aging

机译:不同规模的衰老–与时间相关的衰老与与病理相关的衰老

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摘要

In the next decades the elderly population will increase dramatically, demanding appropriate solutions in health care and aging research focusing on healthy aging to prevent high burdens and costs in health care. For this, research targeting tissue-specific and individual aging is paramount to make the necessary progression in aging research. In a recently published study we have attempted to make a step interpreting aging data on chronological as well as pathological scale. For this, we sampled five major tissues at regular time intervals during the entire C57BL/6J murine lifespan from a controlled in vivo aging study, measured the whole transcriptome and incorporated temporal as well as physical health aspects into the analyses. In total, we used 18 different age-related pathological parameters and transcriptomic profiles of liver, kidney, spleen, lung and brain and created a database that can now be used for a broad systems biology approach. In our study, we focused on the dynamics of biological processes during chronological aging and the comparison between chronological and pathology-related aging.
机译:在接下来的几十年中,老年人口将急剧增加,要求在医疗保健和衰老研究中寻求适当的解决方案,重点是健康的衰老,以防止医疗保健的高负担和费用。为此,针对组织特异性衰老和个体衰老的研究对于使衰老研究取得必要进展至关重要。在最近发表的一项研究中,我们试图一步一步地按时间顺序和病理范围解释衰老数据。为此,我们从受控的体内衰老研究中,在整个C57BL / 6J鼠的整个生命周期中,以固定的时间间隔对五个主要组织进行了采样,测量了整个转录组,并将时间和身体健康方面纳入了分析。总的来说,我们使用了18种不同的年龄相关的病理参数以及肝,肾,脾,肺和脑的转录组谱,并创建了一个数据库,该数据库现在可用于广泛的系统生物学方法。在我们的研究中,我们着眼于按时间顺序老化的生物过程的动力学,以及按时间顺序和病理学相关的老化之间的比较。

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