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将 AFRAID 和 FRIGHT 时钟应用于多药治疗的新型临床前小鼠模型。

Applying the AFRAID and FRIGHT Clocks to Novel Preclinical Mouse Models of Polypharmacy.

机构信息

Laboratory of Ageing and Pharmacology, Kolling Institute of Medical Research, Faculty of Medicine and Health, Royal North Shore Hospital, The University of Sydney, St Leonards, Sydney, New South Wales, Australia.

Blavatnik Institute, Department of Genetics, Paul F. Glenn Center for Biology of Aging Research at Harvard Medical School, Boston, Massachusetts, USA.

出版信息

J Gerontol A Biol Sci Med Sci. 2022 Jul 5;77(7):1304-1312. doi: 10.1093/gerona/glac067.

Abstract

The Frailty Inferred Geriatric Health Timeline (FRIGHT) and Analysis of Frailty and Death (AFRAID) clocks were developed to predict biological age and lifespan, respectively, in mice. Their utility within the context of polypharmacy (≥5 medications), which is very common in older adults, is unknown. In male C57BL/6J(B6) mice administered chronic polypharmacy, monotherapy, and undergoing treatment cessation (deprescribing), we aimed to compare these clocks between treatment groups; investigate whether treatment affected correlation of these clocks with mortality; and explore factors that may explain variation in predictive performance. Treatment (control, polypharmacy, or monotherapy) commenced from age 12 months. At age 21 months, each treatment group was subdivided to continue treatment or have it deprescribed. Frailty index was assessed and informed calculation of the clocks. AFRAID, FRIGHT, frailty index, and mortality age did not differ between continued treatment groups and control. Compared to continued treatment, deprescribing some treatments had inconsistent negative impacts on some clocks and mortality. FRIGHT and frailty index, but not AFRAID, were associated with mortality. The bias and precision of AFRAID as a predictor of mortality varied between treatment groups. Effects of deprescribing some drugs on elements of the clocks, particularly on weight loss, contributed to bias. Overall, in this cohort, FRIGHT and AFRAID measures identified no treatment effects and limited deprescribing effects (unsurprising as very few effects on frailty or mortality), with variable prediction of mortality. These clocks have utility, but context is important. Future work should refine them for intervention studies to reduce bias from specific intervention effects.

摘要

虚弱推断老年健康时间线(FRIGHT)和虚弱与死亡分析(AFRAID)时钟旨在分别预测小鼠的生物年龄和寿命。它们在老年人中非常常见的多药物治疗(≥5 种药物)背景下的实用性尚不清楚。在接受慢性多药物治疗、单药治疗和停药(去药物治疗)的雄性 C57BL/6J(B6)小鼠中,我们旨在比较这些时钟在治疗组之间的差异;研究治疗是否影响这些时钟与死亡率的相关性;并探索可能解释预测性能差异的因素。治疗(对照、多药物治疗或单药治疗)从 12 个月龄开始。在 21 个月龄时,每个治疗组被进一步分为继续治疗或停止治疗。评估虚弱指数并计算这些时钟。AFRAID、FRIGHT、虚弱指数和死亡率年龄在继续治疗组和对照组之间没有差异。与继续治疗相比,停止某些治疗对某些时钟和死亡率产生了不一致的负面影响。FRIGHT 和虚弱指数,但不是 AFRAID,与死亡率相关。AFRAID 作为死亡率预测指标的偏差和精度在治疗组之间有所不同。停止某些药物治疗对时钟元素的影响,特别是对体重减轻的影响,导致了偏差。总的来说,在这个队列中,FRIGHT 和 AFRAID 测量没有发现治疗效果和有限的停药效果(由于对虚弱或死亡率几乎没有影响,这并不奇怪),对死亡率的预测也存在差异。这些时钟具有实用性,但背景很重要。未来的工作应该对它们进行改进,以便在干预研究中减少来自特定干预效果的偏差。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1dba/9255695/86940adb7c7f/glac067f0001.jpg

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