Department of Endocrinology, Renmin Hospital of Wuhan University, Wuhan, 430060, China.
Cardiovasc Diabetol. 2022 Sep 19;21(1):188. doi: 10.1186/s12933-022-01625-2.
To determine the risk-assessment role of the immune-inflammatory biomarkers on myocardial damage in COVID-19 patients with diabetes mellitus (DM).
This retrospective study was conducted on 822 COVID-19 inpatients from 1 January to 10 March 2020 at Renmin Hospital of Wuhan University. The demographic data, clinical data, and immune-inflammatory parameters of participants were collected. The predictors of cardiac injury were assessed by Logistics regression analysis.
A total of 246 COVID-19 inpatients were diagnosed with DM (29.9%). The incidence of cardiac injury was higher in patients with DM than in non-DM cases (28.9% vs 9.0%, p < 0.001), even grouped by age, gender, and the level of fasting plasma glucose (FPG). The mortality in diabetic COVID-19 patients with cardiac injury and without cardiac injury was 42.9% and 3.4%, respectively (p < 0.001). COVID-19 patients with DM and cardiac injury presented a decreased number of immunocyte subsets, lower C3 concentration, and a higher level of interleukin-6 (IL-6) and immunoglobulin A (IgA). The independent risk factors for cardiac injury in COVID-19 patients with DM were CD3CD4 T cells counts ≤ 288 cells/μl (adjusted Odds ratio (OR), 2.501; 95% confidence interval (CI) 1.282-4.877; p = 0.007) and IL-6 > 25.68mpg/ml (adjusted OR, 4.345; 95% CI 2.192-10.374; p < 0.001) (all P < 0.05).
For diabetic patients with COVID-19, cardiac injury not only induce severer immune-inflammatory responses, but also increase in-hospital mortality. The decreased number of CD3CD4 T cells and increased IL-6 are recommended to distinguish the people who refer to high risk of cardiac injury and mortality from those persons. However, it remains a testable theory whether decision-making strategies based on the risk status of cardiac injury in COVID-19 patients, especially with DM, would be expected to get better outcomes.
确定免疫炎症生物标志物在合并糖尿病的 COVID-19 患者心肌损伤中的风险评估作用。
本回顾性研究纳入了 2020 年 1 月 1 日至 3 月 10 日期间于武汉大学人民医院住院的 822 例 COVID-19 患者。收集患者的人口统计学资料、临床资料和免疫炎症参数。采用 Logistics 回归分析评估心脏损伤的预测因素。
共纳入 246 例 COVID-19 合并糖尿病患者(29.9%)。与非糖尿病患者相比,糖尿病患者的心脏损伤发生率更高(28.9% vs 9.0%,p<0.001),甚至按年龄、性别和空腹血糖(FPG)水平分组也是如此。糖尿病 COVID-19 合并心脏损伤患者的死亡率为 42.9%,而无心脏损伤患者的死亡率为 3.4%(p<0.001)。合并糖尿病和心脏损伤的 COVID-19 患者的免疫细胞亚群数量减少,C3 浓度降低,白细胞介素-6(IL-6)和免疫球蛋白 A(IgA)水平升高。合并糖尿病的 COVID-19 患者心脏损伤的独立危险因素是 CD3CD4 T 细胞计数≤288 个/μl(校正优势比(OR),2.501;95%置信区间(CI),1.282-4.877;p=0.007)和 IL-6>25.68mpg/ml(校正 OR,4.345;95% CI,2.192-10.374;p<0.001)(均 P<0.05)。
对于 COVID-19 合并糖尿病患者,心脏损伤不仅会引起更严重的免疫炎症反应,而且会增加住院死亡率。建议减少 CD3CD4 T 细胞数量和增加 IL-6 以区分心脏损伤和死亡率高风险人群。然而,基于 COVID-19 患者,特别是合并糖尿病患者心脏损伤风险状况的决策策略是否会带来更好的结果,这仍然是一个有待检验的理论。