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2019冠状病毒病感染且无糖尿病患者的高血糖:与炎症标志物的关联

Hyperglycemia in COVID-19 infection without diabetes mellitus: Association with inflammatory markers.

作者信息

Geetha Harinivaas Shanmugavel, Singh Garima, Sekar Abinesh, Gogtay Maya, Singh Yuvaraj, Abraham George M, Trivedi Nitin

机构信息

Department of Internal Medicine, Saint Vincent Hospital, Worcester, MA 01608, United States.

Department of Hospice and Palliative Medicine, University of Texas Health, San Antonio, TX 78229, United States.

出版信息

World J Clin Cases. 2023 Feb 26;11(6):1287-1298. doi: 10.12998/wjcc.v11.i6.1287.

Abstract

BACKGROUND

New onset hyperglycemia is common in patients with severe coronavirus disease 2019 (COVID-19) infection. Cytokine storm due to COVID-19 infection is an essential etiology for new-onset hyperglycemia, but factors like direct severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-induced pancreatic β-cell failure have also been postulated to play a role.

AIM

We plan to investigate further the mechanisms underlying SARS-CoV-2 infection-induced hyperglycemia, particularly the rationale of the cytokine-induced hyperglycemia hypothesis, by evaluating the association between inflammatory markers and new onset hyperglycemia in non-diabetic patients with COVID-19 infection.

METHODS

We conducted a retrospective case-control study on adults without diabetes mellitus hospitalized for COVID-19 infection. The serum levels of glucose and inflammatory markers at presentation before initiation of corticosteroid were collected. Hyperglycemia was defined as glucose levels ≥ 140 mg/dL. C-Reactive protein (CRP) ≥ 100 mg/L, ferritin ≥ 530 ng/mL, lactate dehydrogenase (LDH) ≥ 590 U/L, and D-dimer ≥ 0.5 mg/L were considered elevated. We used the test for categorical variables and the Mann-Whitney test for continuous variables and calculated the logistic regression for hyperglycemia.

RESULTS

Of the 520 patients screened, 248 met the inclusion criteria. Baseline demographics were equally distributed between patients with hyperglycemia and those who were normoglycemic. Serum inflammatory markers in patients with or without new-onset hyperglycemia were elevated as follows: CRP (58.1% 65.6%, = 0.29), ferritin (48.4% 34.9%, = 0.14), D-dimer (37.1% 37.1%, = 0.76) and LDH (19.4% 11.8%, = 0.02). Logistic regression analysis showed LDH odds ratio (OR) = 1.623 ( = 0.256). We observed significantly higher mortality (24.2% 9.1%, = 0.001; OR = 2.528, = 0.024) and length of stay (8.89 6.69, = 0.026) in patients with hyperglycemia.

CONCLUSION

Our study showed no association between CRP, ferritin, LDH, D-dimer levels, and new-onset hyperglycemia in non-diabetic patients with COVID-19 infection. It also shows an increased mortality risk and length of stay in patients with hyperglycemia. With new-onset hyperglycemia being closely associated with poor prognostic indices, it becomes pivotal to understand the underlying pathophysiological mechanisms behind the SARS-CoV-2 infection-induced hyperglycemia. We conclude that the stress hyperglycemia hypothesis is not the only mechanism of SARS-CoV-2 infection-induced hyperglycemia but rather a multicausal pathogenesis leading to hyperglycemia that requires further research and understanding. This would help us improve not only the clinical outcomes of COVID-19 disease and inpatient hyperglycemia management but also understand the long-term effects of SARS-CoV-2 infection and further management.

摘要

背景

新型冠状病毒肺炎(COVID-19)重症感染患者中,新发高血糖很常见。COVID-19感染引发的细胞因子风暴是新发高血糖的重要病因,但也有观点认为,严重急性呼吸综合征冠状病毒2(SARS-CoV-2)直接导致胰腺β细胞功能衰竭等因素也发挥了作用。

目的

我们计划通过评估非糖尿病COVID-19感染患者炎症标志物与新发高血糖之间的关联,进一步研究SARS-CoV-2感染导致高血糖的机制,尤其是细胞因子诱导高血糖假说的原理。

方法

我们对因COVID-19感染住院的非糖尿病成年患者进行了一项回顾性病例对照研究。收集了开始使用皮质类固醇之前就诊时的血糖和炎症标志物血清水平。高血糖定义为血糖水平≥140mg/dL。C反应蛋白(CRP)≥100mg/L、铁蛋白≥530ng/mL、乳酸脱氢酶(LDH)≥590U/L和D-二聚体≥0.5mg/L被视为升高。我们对分类变量使用卡方检验,对连续变量使用曼-惠特尼U检验,并计算高血糖的逻辑回归。

结果

在筛查的520例患者中,248例符合纳入标准。高血糖患者和血糖正常患者的基线人口统计学特征分布均衡。有或无新发高血糖患者的血清炎症标志物升高情况如下:CRP(58.1%对65.6%,P=0.29)、铁蛋白(48.4%对34.9%,P=0.14)、D-二聚体(37.1%对37.1%,P=0.76)和LDH(19.4%对11.8%,P=0.02)。逻辑回归分析显示LDH比值比(OR)=1.623(P=0.256)。我们观察到高血糖患者的死亡率(24.2%对9.1%,P=0.001;OR=2.528,P=0.024)和住院时间(8.89对6.69,P=0.026)显著更高。

结论

我们的研究表明,非糖尿病COVID-19感染患者的CRP、铁蛋白、LDH、D-二聚体水平与新发高血糖之间无关联。研究还表明,高血糖患者的死亡风险和住院时间增加。由于新发高血糖与不良预后指标密切相关,了解SARS-CoV-2感染导致高血糖背后的潜在病理生理机制至关重要。我们得出结论,应激性高血糖假说不是SARS-CoV-2感染导致高血糖的唯一机制,而是导致高血糖的多因素发病机制,需要进一步研究和理解。这不仅有助于改善COVID-19疾病的临床结局和住院患者高血糖管理,还有助于了解SARS-CoV-2感染的长期影响及进一步的管理措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39f4/10013116/617e8a3bdb81/WJCC-11-1287-g001.jpg

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