Inflamm-aging as a diverse and context-dependent process: from species and population differences to individual trajectories.

IF 12.4
Maximilien Franck, Camille Daunizeau, Jacob E Aronoff, Kamaryn Tanner, Benjamin C Trumble, Claudio Franceschi, Johannes Hertel, Tamás Fülöp, Maël Lemoine, Michael Gurven, Alan A Cohen
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Abstract

Inflamm-aging is widely considered a hallmark of aging, yet emerging evidence challenges its universality. Here, we re-examine inflamm-aging through an eco-evolutionary lens, underlining its context dependence across biological scales. Combining mechanistic, evolutionary, comparative, anthropological, genetic, and environmental evidence, we show how fundamental inflammatory mechanisms are integrated and regulated in diverse biological contexts, representing a suite of flexible stress responses. Drawing on studies from non-industrialized populations, which suggest that inflamm-aging reflects mismatches between evolved human biology and industrialized exposomes, we explore how population-specific evolutionary histories and environmental exposures shape differential predispositions and trajectories of inflamm-aging. We propose that, to the extent that inflammation represents this broad suite of stress responses, increases in at least some dimensions of inflammation with age should be nearly universal, as other physiological processes break down and internal stresses mount. However, the particular set of internal stressors that is triggered in a given species, environmental context, or individual is likely more specific, implying that there is unlikely to be any universal signature of inflamm-aging. The question of whether inflamm-aging is universal thus hinges on whether it is defined broadly as any increase in activation of any inflammatory systems, or more narrowly as a particular suite, such as those activated in industrialized populations with high levels of sedentary behavior and cardiometabolic diseases. Inflamm-aging is ultimately a norm of reaction - an aging-related inflammatory profile whose phenotypic expression varies with genotype and environment - and research should therefore focus on understanding how ecological, evolutionary, and environmental factors modulate inflammation and its age-related trajectory.

炎症老化作为一个多样化和环境依赖的过程:从物种和种群差异到个体轨迹。
炎症老化被广泛认为是衰老的标志,但新出现的证据对其普遍性提出了挑战。在这里,我们通过生态进化的视角重新审视炎症老化,强调其在生物尺度上的环境依赖性。结合机械、进化、比较、人类学、遗传学和环境证据,我们展示了基本的炎症机制如何在不同的生物环境中被整合和调节,代表了一套灵活的应激反应。非工业化人群的研究表明,炎症老化反映了进化的人类生物学与工业化暴露体之间的不匹配,我们探索了特定人群的进化历史和环境暴露如何塑造炎症老化的差异倾向和轨迹。我们认为,在某种程度上,炎症代表了这种广泛的应激反应,随着其他生理过程的崩溃和内部压力的增加,炎症至少在某些方面随着年龄的增长应该是几乎普遍的。然而,在特定物种、环境背景或个体中触发的特定内应激源可能更具有特异性,这意味着不太可能存在任何普遍的炎症老化特征。因此,炎症老化是否具有普遍性的问题取决于它是被广义地定义为任何炎症系统激活的增加,还是更狭义地定义为一组特定的系统,比如那些在久坐不动和患有心脏代谢疾病的工业化人群中激活的系统。炎症老化最终是一种反应规范——一种与衰老相关的炎症谱,其表型表达随基因型和环境而变化——因此,研究应侧重于了解生态、进化和环境因素如何调节炎症及其与年龄相关的轨迹。
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