Clinica Medica 'A. Murri', Department of Biomedical Sciences and Human Oncology, University of Bari 'Aldo Moro', Bari, Italy.
Department of Medicine II, Saarland University Medical Center, Saarland University, Homburg, Germany.
Eur J Clin Invest. 2020 Oct;50(10):e13338. doi: 10.1111/eci.13338. Epub 2020 Aug 26.
Initial evidence from China suggests that most vulnerable subjects to COVID-19 infection suffer from pre-existing illness, including metabolic abnormalities. The pandemic characteristics and high-lethality rate of COVID-19 infection have raised concerns about interactions between virus pathobiology and components of the metabolic syndrome.
We harmonized the information from the recent existing literature on COVID-19 acute pandemic and mechanisms of damage in non-alcoholic fatty liver disease (NAFLD), as an example of chronic (non-communicable) metabolic pandemic.
COVID-19-infected patients are more fragile with underlying metabolic illness, including hypertension, cardiovascular disease, type 2 diabetes, chronic lung diseases (e.g. asthma, chronic obstructive pulmonary disease and emphysema) and metabolic syndrome. During metabolic abnormalities, expansion of metabolically active fat ('overfat condition') parallels chronic inflammatory changes, development of insulin resistance and accumulation of fat in configuring NAFLD. The deleterious interplay of inflammatory pathways chronically active in NAFLD and acutely in COVID-19-infected patients, can explain liver damage in a subgroup of patients and might condition a worse outcome in metabolically compromised NAFLD patients. In a subgroup of patients with NAFLD, the underlying liver fibrosis might represent an additional and independent risk factor for severe COVID-19 illness, irrespective of metabolic comorbidities.
NAFLD can play a role in the outcome of COVID-19 illness due to frequent association with comorbidities. Initial evidences suggest that increased liver fibrosis in NAFLD might affect COVID-19 outcome. In addition, long-term monitoring of post-COVID-19 NAFLD patients is advisable, to document further deterioration of liver damage. Further studies are required in this field.
来自中国的初步证据表明,COVID-19 感染的大多数易感人群患有先前存在的疾病,包括代谢异常。COVID-19 感染的大流行特征和高致死率引起了人们对病毒病理学和代谢综合征成分之间相互作用的关注。
我们协调了最近关于 COVID-19 急性大流行和非酒精性脂肪性肝病 (NAFLD) 损伤机制的现有文献信息,将其作为慢性(非传染性)代谢大流行的一个例子。
患有潜在代谢疾病的 COVID-19 感染患者更为脆弱,包括高血压、心血管疾病、2 型糖尿病、慢性肺部疾病(如哮喘、慢性阻塞性肺疾病和肺气肿)和代谢综合征。在代谢异常期间,代谢活跃脂肪的扩张(“过度肥胖状态”)与慢性炎症变化、胰岛素抵抗的发展和脂肪在配置 NAFLD 中的积累平行。NAFLD 中慢性活跃和 COVID-19 感染患者中急性活跃的炎症途径的有害相互作用,可以解释一小部分患者的肝损伤,并可能使代谢受损的 NAFLD 患者的预后更差。在一小部分 NAFLD 患者中,潜在的肝纤维化可能是 COVID-19 严重疾病的另一个独立危险因素,而与代谢合并症无关。
由于经常与合并症相关,NAFLD 可能会影响 COVID-19 疾病的结局。初步证据表明,NAFLD 中增加的肝纤维化可能会影响 COVID-19 的结局。此外,建议对 COVID-19 后 NAFLD 患者进行长期监测,以记录肝脏损伤的进一步恶化。在这一领域需要进一步的研究。