Department of Genetics, Genomics and Informatics, University of Tennessee Health Science Center (UTHSC), Memphis, TN, USA.
Laboratory of Integrative Systems Physiology, Interfaculty Institute of Bioengineering, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
Nat Metab. 2021 Sep;3(9):1217-1227. doi: 10.1038/s42255-021-00449-w. Epub 2021 Sep 22.
How lifespan and body weight vary as a function of diet and genetic differences is not well understood. Here we quantify the impact of differences in diet on lifespan in a genetically diverse family of female mice, split into matched isogenic cohorts fed a low-fat chow diet (CD, n = 663) or a high-fat diet (HFD, n = 685). We further generate key metabolic data in a parallel cohort euthanized at four time points. HFD feeding shortens lifespan by 12%: equivalent to a decade in humans. Initial body weight and early weight gains account for longevity differences of roughly 4-6 days per gram. At 500 days, animals on a HFD typically gain four times as much weight as control, but variation in weight gain does not correlate with lifespan. Classic serum metabolites, often regarded as health biomarkers, are not necessarily strong predictors of longevity. Our data indicate that responses to a HFD are substantially modulated by gene-by-environment interactions, highlighting the importance of genetic variation in making accurate individualized dietary recommendations.
寿命和体重如何随饮食和遗传差异而变化尚不清楚。在这里,我们量化了饮食差异对一组遗传多样性雌性小鼠寿命的影响,这些小鼠被分为匹配的同基因队列,分别喂食低脂肪饮食(CD,n=663)或高脂肪饮食(HFD,n=685)。我们进一步在四个时间点处死的平行队列中生成关键代谢数据。HFD 喂养使寿命缩短 12%:相当于人类的十年。初始体重和早期体重增加占寿命差异约 4-6 天/克。在 500 天时,HFD 组动物的体重通常是对照组的四倍,但体重增加的变化与寿命无关。经典的血清代谢物,通常被认为是健康生物标志物,不一定是长寿的强有力预测因素。我们的数据表明,对 HFD 的反应在很大程度上受到基因-环境相互作用的调节,突出了遗传变异在做出准确的个性化饮食建议方面的重要性。