Why does COVID-19 disproportionately affect older people?

被引:657
|
作者
Mueller, Amber L. [1 ]
McNamara, Maeve S. [1 ]
Sinclair, David A. [1 ]
机构
[1] Harvard Med Sch, Glenn Ctr Biol Aging Res, Blavatnik Inst, Boston, MA 02115 USA
来源
AGING-US | 2020年 / 12卷 / 10期
关键词
aging; cytokine storm; COVID-19; epigenetic clock; immunity; RESPIRATORY SYNDROME-CORONAVIRUS; ENZYME; 2; ACE2; VITAMIN-D SUPPLEMENTATION; GLYCATION END-PRODUCTS; STRAND BREAK REPAIR; NLRP3; INFLAMMASOME; CYTOKINE STORM; IMMUNE-SYSTEM; GENOMIC STABILITY; ANTIBODY-RESPONSE;
D O I
10.18632/aging.103344
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The severity and outcome of coronavirus disease 2019 (COVID-19) largely depends on a patient's age. Adults over 65 years of age represent 80% of hospitalizations and have a 23-fold greater risk of death than those under 65. In the clinic, COVID-19 patients most commonly present with fever, cough and dyspnea, and from there the disease can progress to acute respiratory distress syndrome, lung consolidation, cytokine release syndrome, endotheliitis, coagulopathy, multiple organ failure and death. Comorbidities such as cardiovascular disease, diabetes and obesity increase the chances of fatal disease, but they alone do not explain why age is an independent risk factor. Here, we present the molecular differences between young, middle-aged and older people that may explain why COVID-19 is a mild illness in some but life-threatening in others. We also discuss several biological age clocks that could be used in conjunction with genetic tests to identify both the mechanisms of the disease and individuals most at risk. Finally, based on these mechanisms, we discuss treatments that could increase the survival of older people, not simply by inhibiting the virus, but by restoring patients' ability to clear the infection and effectively regulate immune responses.
引用
收藏
页码:9959 / 9981
页数:23
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