Department of Surgery, University of Minnesota, Division of Surgical Oncology, Minneapolis, Minnesota.
Department of Medicine, University of Minnesota, Division of General Internal Medicine, Minneapolis, Minnesota.
Surg Obes Relat Dis. 2021 Oct;17(10):1780-1786. doi: 10.1016/j.soard.2021.05.029. Epub 2021 Jun 29.
SARS-CoV-2 (COVID-19) disease causes significant morbidity and mortality through increased inflammation and thrombosis. Nonalcoholic fatty liver disease (NAFLD) and nonalcoholic steatohepatitis (NASH) are states of chronic inflammation and indicate advanced metabolic disease.
The purpose of this observational study was to characterize the risk of hospitalization for COVID-19 in patients with NAFLD/NASH and evaluate the mitigating effect of various metabolic treatments.
Retrospective analysis of electronic medical record data of 26,896 adults from a 12-hospital Midwest healthcare system with a positive COVID-19 polymerase chain reaction (PCR) test from March 1, 2020, to January 26, 2021.
Variable selection was guided by the least absolute shrinkage and selection operator (LASSO) method, and multiple imputation was used to account for missing data. Multivariable logistic regression and competing risk models were used to assess the odds of being hospitalized within 45 days of a COVID-19 diagnosis. Analysis assessed the risk of hospitalization among patients with a prescription for metformin and statin use within the 3 months prior to the COVID-19 PCR result, history of home glucagon-like peptide 1 receptor agonist (GLP-1 RA) use, and history of metabolic and bariatric surgery (MBS). Interactions were assessed by sex and race.
A history of NAFLD/NASH was associated with increased odds of admission for COVID-19 (odds ratio [OR], 1.88; 95% confidence interval [CI], 1.57-2.26; P < .001) and mortality (OR, 1.96; 95% CI, 1.45-2.67; P < .001). Each additional year of having NAFLD/NASH was associated with a significant increased risk of being hospitalized for COVID-19 (OR, 1.24; 95% CI, 1.14-1.35; P < .001). NAFLD/NASH increased the risk of hospitalization in men, but not women, and increased the risk of hospitalization in all multiracial/multiethnic subgroups. Medication treatments for metabolic syndrome were associated with significantly reduced risk of admission (OR, .81; 95% CI, .67-.99; P < .001 for home metformin use; OR, .71; 95% CI, .65-.83; P < .001 for home statin use). MBS was associated with a significant decreased risk of admission (OR, .48; 95% CI, .33-.69; P < .001).
NAFLD/NASH is a significant risk factor for hospitalization for COVID-19 and appears to account for risk attributed to obesity. Other significant risks include factors associated with socioeconomic status and other co-morbidities, such as history of venous thromboembolism. Treatments for metabolic disease mitigated risks from NAFLD/NASH. More research is needed to confirm the risk associated with visceral adiposity, and patients should be screened for and informed of treatments for metabolic syndrome.
SARS-CoV-2(COVID-19)疾病通过增加炎症和血栓形成导致显著的发病率和死亡率。非酒精性脂肪性肝病(NAFLD)和非酒精性脂肪性肝炎(NASH)是慢性炎症的状态,表明存在进展性代谢疾病。
本观察性研究的目的是描述 NAFLD/NASH 患者因 COVID-19 住院的风险,并评估各种代谢治疗的缓解作用。
对 2020 年 3 月 1 日至 2021 年 1 月 26 日期间来自中西部医疗保健系统的 12 家医院的 26896 名成年人的电子病历数据进行回顾性分析,这些成年人的 COVID-19 聚合酶链反应(PCR)检测结果呈阳性。
变量选择由最小绝对值收缩和选择算子(LASSO)方法指导,使用多重插补来解释缺失数据。多变量逻辑回归和竞争风险模型用于评估 COVID-19 诊断后 45 天内住院的可能性。分析评估了在 COVID-19 PCR 结果前 3 个月内开具二甲双胍和他汀类药物处方、既往家用胰高血糖素样肽 1 受体激动剂(GLP-1 RA)使用史以及代谢和减重手术(MBS)史的患者住院的风险。通过性别和种族评估了交互作用。
NAFLD/NASH 病史与 COVID-19 住院的几率增加相关(比值比[OR],1.88;95%置信区间[CI],1.57-2.26;P<0.001)和死亡率(OR,1.96;95% CI,1.45-2.67;P<0.001)。每增加一年 NAFLD/NASH 与 COVID-19 住院的风险显著增加相关(OR,1.24;95% CI,1.14-1.35;P<0.001)。NAFLD/NASH 增加了男性住院的风险,但不增加女性的住院风险,并且增加了所有多种族/多民族亚组的住院风险。代谢综合征的药物治疗与入院风险显著降低相关(OR,0.81;95% CI,0.67-0.99;P<0.001 用于家用二甲双胍;OR,0.71;95% CI,0.65-0.83;P<0.001 用于家用他汀类药物)。MBS 与入院风险显著降低相关(OR,0.48;95% CI,0.33-0.69;P<0.001)。
NAFLD/NASH 是 COVID-19 住院的一个重要危险因素,似乎与肥胖相关的风险有关。其他重要风险因素包括与社会经济地位和其他合并症相关的因素,例如静脉血栓栓塞史。代谢疾病的治疗减轻了 NAFLD/NASH 的风险。需要进一步研究以确认与内脏肥胖相关的风险,并且应筛查和告知患者代谢综合征的治疗方法。