Abstract
Biological aging is characterized by a chronic low-grade inflammation level. This chronic phenomenon has been named “inflamm-aging” and is a highly significant risk factor for morbidity and mortality in the older persons. The most common theories of inflamm-aging include redox stress, mitochondrial dysfunction, glycation, deregulation of the immune system, hormonal changes, epigenetic modifications, and dysfunction telomere attrition. Inflamm-aging plays a role in the initiation and progression of age-related diseases such as type II diabetes, Alzheimer’s disease, cardiovascular disease, frailty, sarcopenia, osteoporosis, and cancer. This review will cover the identification of pathways that control age-related inflammation across multiple systems and its potential causal role in contributing to adverse health outcomes. AC.
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CITATION STYLE
Fougère, B., Boulanger, E., Nourhashémi, F., Guyonnet, S., & Cesari, M. (2017, September 1). Retraction:Chronic inflammation: Accelerator of biological aging. Journals of Gerontology - Series A Biological Sciences and Medical Sciences. Oxford University Press. https://doi.org/10.1093/gerona/glw240
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