Department of Cardiology, The Third Affiliated Hospital of Soochow University, Changzhou, China.
Department of Endocrinology, The Third Affiliated Hospital of Soochow University, Changzhou, China.
Front Endocrinol (Lausanne). 2024 Feb 15;15:1287795. doi: 10.3389/fendo.2024.1287795. eCollection 2024.
Inflammation is a predictor of severe complications in patients with COVID-19 infection under a variety of clinical settings. A few studies suggested that COVID-19 infection was a trigger of hyperglycemic crises including diabetic ketoacidosis (DKA) and/or hyperglycemic hyperosmolar state (HHS). However, the association between inflammation and hyperglycemic crises in diabetic patients with COVID-19 infection is unclear.
One hundred and twenty-four patients with type 2 diabetes mellitus (T2DM) and COVID-19 infection from January 2023 to March 2023 were retrospectively analyzed. Demographic, clinical, and laboratory data, especially inflammatory markers including white blood cell (WBC), neutrophils, neutrophil-to-lymphocyte ratio (NLR), c-reactive protein (CRP) and procalcitonin (PCT) were collected and compared between patients with or without DKA and/or HHS. Multivariable logistic regression analysis was conducted to explore the association between inflammatory biomarkers and the prevalence of hyperglycemic crises. Patients were followed up 6 months for outcomes.
Among 124 diabetic patients with COVID-19, 9 were diagnosed with DKA or HHS. Comparing COVID-19 without acute diabetic complications (ADC), patients with DKA or HHS showed elevated levels of c-reactive protein (CRP, =0.0312) and procalcitonin (PCT, =0.0270). The power of CRP and PCT to discriminate DKA or HHS with the area under the receiver operating characteristics curve (AUROC) were 0.723 and 0.794, respectively. Multivariate logistic regression indicated 1.95-fold and 1.97-fold increased risk of DKA or HHS with 1-unit increment of CRP and PCT, respectively. However, neither CRP nor PCT could predict poor outcomes in diabetic patients with COVID-19.
In this small sample size study, we firstly found that elevated serum CRP and PCT levels increased the risk of hyperglycemic crises in T2DM patients with COVID-19 infection. More study is needed to confirm our findings.
在各种临床环境下,炎症是 COVID-19 感染患者发生严重并发症的预测指标。一些研究表明,COVID-19 感染是包括糖尿病酮症酸中毒(DKA)和/或高血糖高渗状态(HHS)在内的高血糖危象的触发因素。然而,COVID-19 感染的糖尿病患者中炎症与高血糖危象之间的关系尚不清楚。
回顾性分析了 2023 年 1 月至 3 月期间 124 例 2 型糖尿病(T2DM)合并 COVID-19 感染的患者。收集并比较了患者的人口统计学、临床和实验室数据,特别是炎症标志物,包括白细胞(WBC)、中性粒细胞、中性粒细胞与淋巴细胞比值(NLR)、C 反应蛋白(CRP)和降钙素原(PCT),以比较有无 DKA 和/或 HHS 的患者。采用多变量逻辑回归分析探讨炎症标志物与高血糖危象发生率的相关性。对患者进行了 6 个月的随访,以观察结局。
在 124 例合并 COVID-19 的糖尿病患者中,有 9 例被诊断为 DKA 或 HHS。与无急性糖尿病并发症(ADC)的 COVID-19 患者相比,DKA 或 HHS 患者的 CRP(=0.0312)和 PCT(=0.0270)水平升高。CRP 和 PCT 鉴别 DKA 或 HHS 的受试者工作特征曲线(AUROC)下面积分别为 0.723 和 0.794。多变量逻辑回归表明,CRP 和 PCT 每增加 1 个单位,DKA 或 HHS 的风险分别增加 1.95 倍和 1.97 倍。然而,CRP 和 PCT 均不能预测 COVID-19 合并糖尿病患者的不良结局。
在这项小样本量研究中,我们首次发现血清 CRP 和 PCT 水平升高增加了 COVID-19 感染的 T2DM 患者发生高血糖危象的风险。需要进一步的研究来证实我们的发现。