Department of Physiology and The Eisdell Moore Centre, Faculty of Medical and Health Sciences, The University of Auckland, Private Bag, Auckland 1142, New Zealand.
Int J Mol Sci. 2022 Jul 1;23(13):7348. doi: 10.3390/ijms23137348.
This article provides a theoretical overview of the association between age-related hearing loss (ARHL), immune system ageing (immunosenescence), and chronic inflammation. ARHL, or presbyacusis, is the most common sensory disability that significantly reduces the quality of life and has a high economic impact. This disorder is linked to genetic risk factors but is also influenced by a lifelong cumulative effect of environmental stressors, such as noise, otological diseases, or ototoxic drugs. Age-related hearing loss and other age-related disorders share common mechanisms which often converge on low-grade chronic inflammation known as "inflammaging". Various stimuli can sustain inflammaging, including pathogens, cell debris, nutrients, and gut microbiota. As a result of ageing, the immune system can become defective, leading to the accumulation of unresolved inflammatory processes in the body. Gut microbiota plays a central role in inflammaging because it can release inflammatory mediators and crosstalk with other organ systems. A proinflammatory gut environment associated with ageing could result in a leaky gut and the translocation of bacterial metabolites and inflammatory mediators to distant organs via the systemic circulation. Here, we postulate that inflammaging, as a result of immunosenescence and gut dysbiosis, accelerates age-related cochlear degeneration, contributing to the development of ARHL. Age-dependent gut dysbiosis was included as a hypothetical link that should receive more attention in future studies.
本文提供了年龄相关性听力损失(ARHL)、免疫系统衰老(免疫衰老)和慢性炎症之间关联的理论概述。ARHL 或老年性聋是最常见的感觉障碍,它大大降低了生活质量,并具有很高的经济影响。这种疾病与遗传风险因素有关,但也受到环境应激因素(如噪声、耳科疾病或耳毒性药物)终身累积效应的影响。年龄相关性听力损失和其他年龄相关性疾病具有共同的机制,这些机制通常集中在称为“炎症老化”的低水平慢性炎症上。各种刺激可以维持炎症老化,包括病原体、细胞碎片、营养物质和肠道微生物群。随着年龄的增长,免疫系统可能会出现缺陷,导致体内未解决的炎症过程积累。肠道微生物群在炎症老化中起着核心作用,因为它可以释放炎症介质,并与其他器官系统相互作用。与衰老相关的促炎肠道环境可能导致肠道通透性增加,细菌代谢物和炎症介质通过全身循环转移到远处器官。在这里,我们假设炎症老化是由于免疫衰老和肠道菌群失调引起的,加速了与年龄相关的耳蜗退化,导致 ARHL 的发展。年龄依赖性肠道菌群失调被作为一个假设的联系包含在内,这在未来的研究中应该得到更多的关注。