Drucker Daniel J
Department of Medicine, Lunenfeld-Tanenbaum Research Institute, Mt. Sinai Hospital, University of Toronto, 600 University Avenue, Toronto, ON M5G 1X5, Canada.
Cell Metab. 2021 Mar 2;33(3):479-498. doi: 10.1016/j.cmet.2021.01.016. Epub 2021 Jan 21.
The increased prevalence of obesity, diabetes, and cardiovascular risk factors in people hospitalized with severe COVID-19 illness has engendered considerable interest in the metabolic aspects of SARS-CoV-2-induced pathophysiology. Here, I update concepts informing how metabolic disorders and their co-morbidities modify the susceptibility to, natural history, and potential treatment of SARS-CoV-2 infection, with a focus on human biology. New data informing genetic predisposition, epidemiology, immune responses, disease severity, and therapy of COVID-19 in people with obesity and diabetes are highlighted. The emerging relationships of metabolic disorders to viral-induced immune responses and viral persistence, and the putative importance of adipose and islet ACE2 expression, glycemic control, cholesterol metabolism, and glucose- and lipid-lowering drugs is reviewed, with attention to controversies and unresolved questions. Rapid progress in these areas informs our growing understanding of SARS-CoV-2 infection in people with diabetes and obesity, while refining the therapeutic strategies and research priorities in this vulnerable population.
在因重症 COVID-19 疾病住院的患者中,肥胖、糖尿病和心血管危险因素的患病率增加,这引发了人们对 SARS-CoV-2 诱导的病理生理学代谢方面的极大兴趣。在此,我更新了一些概念,这些概念说明了代谢紊乱及其合并症如何改变对 SARS-CoV-2 感染的易感性、自然病程和潜在治疗方法,重点关注人类生物学。突出了有关肥胖和糖尿病患者中 COVID-19 的遗传易感性、流行病学、免疫反应、疾病严重程度和治疗的新数据。回顾了代谢紊乱与病毒诱导的免疫反应和病毒持续存在之间新出现的关系,以及脂肪和胰岛 ACE2 表达、血糖控制、胆固醇代谢以及降糖和降脂药物的假定重要性,并关注了争议和未解决的问题。这些领域的快速进展使我们对糖尿病和肥胖患者的 SARS-CoV-2 感染有了越来越多的了解,同时也完善了这一弱势群体的治疗策略和研究重点。