[Association of D-dimer, inflammatory markers, cytokines abnormality, and disease severity in COVID-19 severe/critical patients in Wuhan]

Zhonghua Xue Ye Xue Za Zhi. 2020 Nov 14;41(11):927-931. doi: 10.3760/cma.j.issn.0253-2727.2020.11.008.
[Article in Chinese]

Abstract

Objective: To analyze the association of D-dimer levels, inflammatory indicators, cytokine abnormality, and disease severity in COVID-19 severe/critical type patients. Methods: The medical records of 41 patients were collected from a single center in Wuhan from February 8, 2020 to March 25, 2020. The patients were divided into severe type group (28 patients) and critical type group (13 patients) . The levels of D-dimer, WBC, ANC, PCT, hsCRP, IL-2R, IL-6, IL-8, and TNF-α were compared among patients with different clinical types of COVID-19 infection. Moreover, the changes in the cytokines were analyzed in patients with different D-dimer levels. And, the levels of D-dimer, IL-2R, IL-6, IL-8, and TNF-α before and after anticoagulant therapy were assessed. Statistical analyses were performed using Student t test, Mann-Whitney U test, and Chi-square test. Results: Among the 41 patients, 23 were men (56.1%) and 18 were women (43.9%) ; the median patient age was 57 y. The age of the critical type patients [ (61.1±10.4) y] was higher than that of severe type patients [ (52.8±11.7) y]; the difference was significant (t=-2.264, P=0.032) . The proportion of critical type patients with chronic diseases, especially hypertension, cardiovascular disease, and cerebrovascular disease, was higher as compared to that in those with severe type patients; the differences were significant (all P<0.05) . The prevalence of dyspnea, sweats, and fatigue symptoms in the critical type patients was higher than that in those with severe type disease; the differences were significant (χ(2)=14.898, 6.972, 7.823; P<0.001, 0.008, 0.005) . The levels of D-dimer, WBC, ANC, PCT, hsCRP, and IL-8 in critical type patients were higher than those in severe type patients; the differences were significant (all P<0.05) . The levels of IL-2R, IL-8, and TNF-α in patients with abnormal D-dimer were higher as compared to those in patients with normal D-dimer levels; the differences were significant (all P<0.05) . Eight patients were treated with prophylactic anticoagulation; the levels of D-dimer, IL-2R, IL-6 and IL-8 after anticoagulant therapy were lower than those before treatment. Conclusions: COVID-19 critical type patients have more serious coagulation-immune dysfunction and dynamic monitoring of D-dimer and cytokines levels helps in identifying critical type patients as early as possible; anticoagulant therapy may improve the patient's condition by correcting coagulation-immune dysfunction.

目的: 分析2019新型冠状病毒肺炎(COVID-19)重型及危重型患者D-二聚体、炎症指标、细胞因子水平与疾病严重程度的关系。 方法: 收集华中科技大学同济医院中法新城院区山西援鄂国家医疗一队2020年2月8日至3月25日收治的41例COVID-19患者病例资料,重型28例,危重型13例,比较不同临床分型COVID-19患者的基本临床特征,入院时D-二聚体、炎症指标[WBC、ANC、降钙素原(PCT)、超敏C-反应蛋白(hsCRP)]、细胞因子(IL-2R、IL-6、IL-8、TNF-α)水平;比较有无D-二聚体异常患者的细胞因子(IL-2R、IL-6、IL-8、TNF-α)水平;并比较抗凝治疗前后患者D-二聚体、细胞因子指标(IL-2R、IL-6、IL-8、TNF-α)水平变化。 结果: 41例患者中,男23例(56.1%),女18例(43.9%),平均年龄(55.4±11.9)岁。危重型患者平均年龄[(61.1±10.4)岁]高于重型患者[(52.8±11.7)岁],差异有统计学意义(t=2.264,P=0.032)。危重型患者合并高血压(χ(2)=10.420,P=0.001)、心血管疾病(χ(2)=6.972,P=0.008)、脑血管疾病(χ(2)=6.972,P=0.008)比例高于重型患者。危重型患者出现呼吸困难、盗汗及乏力症状比例均高于重型患者,差异均有统计学意义(χ(2)分别为14.898、6.972、7.823,P值分别为<0.001、0.008、0.005)。危重型患者D-二聚体、WBC、ANC、PCT、hsCRP、IL-8水平均高于重型患者,差异均有统计学意义(P值均<0.05)。D-二聚体异常患者IL-2R、IL-8、TNF-α水平均较D-二聚体正常者增高,差异均有统计学意义(P值均<0.05)。8例预防性抗凝治疗患者D-二聚体、IL-2R、IL-6、IL-8抗凝治疗后比治疗前水平降低。 结论: COVID-19危重型患者存在更严重的凝血-免疫功能紊乱,动态监测D-二聚体、细胞因子水平有助于早期识别COVID-19危重型患者,抗凝治疗可能通过纠正凝血-免疫功能紊乱促进疾病好转。.

Keywords: COVID-19; Coagulation; Cytokines; D-dimer.

MeSH terms

  • Adult
  • Aged
  • Biomarkers / blood
  • COVID-19 / diagnosis*
  • China
  • Cytokines / blood*
  • Female
  • Fibrin Fibrinogen Degradation Products / analysis*
  • Humans
  • Male
  • Middle Aged
  • Retrospective Studies
  • SARS-CoV-2
  • Severity of Illness Index

Substances

  • Biomarkers
  • Cytokines
  • Fibrin Fibrinogen Degradation Products
  • fibrin fragment D