Laboratory of Epidemiology and Population Science, National Institute on Aging, National Institutes of Health, 251 Bayview Boulevard, Baltimore, MD 21224, USA.
Laboratory of Epidemiology and Population Science, National Institute on Aging, National Institutes of Health, 251 Bayview Boulevard, Baltimore, MD 21224, USA.
Ageing Res Rev. 2022 Jan;73:101536. doi: 10.1016/j.arr.2021.101536. Epub 2021 Dec 6.
The pursuit to discover the fundamental biology and mechanisms of aging within the context of the physical and social environment is critical to designing interventions to prevent and treat its complex phenotypes. Aging research is critically linked to understanding health disparities because these inequities shape minority aging, which may proceed on a different trajectory than the overall population. Health disparities are characteristically seen in commonly occurring age-associated diseases such as cardiovascular and cerebrovascular disease as well as diabetes mellitus and cancer. The early appearance and increased severity of age-associated disease among African American and low socioeconomic status (SES) individuals suggests that the factors contributing to the emergence of health disparities may also induce a phenotype of 'premature aging' or 'accelerated aging' or 'weathering'. In marginalized and low SES populations with high rates of early onset age-associated disease the interaction of biologic, psychosocial, socioeconomic and environmental factors may result in a phenotype of accelerated aging biologically similar to premature aging syndromes with increased susceptibility to oxidative stress, premature accumulation of oxidative DNA damage, defects in DNA repair and higher levels of biomarkers of oxidative stress and inflammation. Health disparities, therefore, may be the end product of this complex interaction in populations at high risk. This review will examine the factors that drive both health disparities and the accelerated aging phenotype that ultimately contributes to premature mortality.
在物理和社会环境的背景下,探索衰老的基本生物学和机制对于设计预防和治疗其复杂表型的干预措施至关重要。衰老研究与理解健康差异密切相关,因为这些不平等现象塑造了少数族裔的衰老,而少数族裔的衰老可能与整个人群的衰老轨迹不同。健康差异在常见的与年龄相关的疾病中表现明显,如心血管和脑血管疾病以及糖尿病和癌症。非裔美国人和社会经济地位(SES)较低的个体中与年龄相关的疾病出现较早且严重程度增加,这表明导致健康差异的因素也可能导致“过早衰老”或“加速衰老”或“老化”的表型。在发病年龄较早的边缘化和 SES 较低的人群中,生物、心理社会、社会经济和环境因素的相互作用可能导致与过早衰老综合征相似的加速衰老表型,表现为氧化应激易感性增加、氧化 DNA 损伤过早积累、DNA 修复缺陷以及氧化应激和炎症生物标志物水平升高。因此,健康差异可能是高风险人群中这种复杂相互作用的最终产物。这篇综述将探讨导致健康差异和加速衰老表型的因素,这些因素最终导致过早死亡。