Pharmacology Research Center, Zahedan University of Medical Sciences, Zahedan, 9816743463, Iran.
Department of Infectious Disease, School of Medicine, Zahedan University of Medical Sciences, Zahedan, 9816743463, Iran.
Inflammopharmacology. 2022 Oct;30(5):1645-1657. doi: 10.1007/s10787-022-01029-4. Epub 2022 Jul 14.
It is known that severe acute respiratory coronavirus 2 (SARS-CoV-2) is the viral strain responsible for the recent coronavirus disease 2019 (COVID-19) pandemic. Current documents have demonstrated that the virus causes a PGE2 storm in a substantial proportion of patients via upregulating cyclooxygenase-2 (COX-2) and downregulating prostaglandin E2 (PGE2)-degrading enzymes within the host cell.
Herein, we aimed to study how short-term treatment with celecoxib (Celebrex), a selective COX-2 inhibitor, affects demographic features, early symptoms, O saturation, and hematological indices of cases with COVID-19.
A total of 67 confirmed COVID-19 cases with a mild or moderate disease, who had been referred to an institutional hospital in south-eastern Iran from October 2020 to September 2021, were enrolled. Demographic characteristics, symptoms, and hematological indices of the patients were recorded within different time periods. One-way ANOVA or Kruskal-Wallis tests were used to determine differences between data sets based on normal data distribution.
O saturation was statistically different between the control group and patients receiving celecoxib (p = 0.039). There was no marked difference between the groups in terms of the symptoms they experienced (p > 0.05). On the first days following Celebrex therapy, analysis of complete blood counts showed that white blood cell (WBC) counts were markedly lower in patients treated with a high dose of celecoxib (0.4 g/day) than in controls (p = 0.026). However, mean lymphocyte levels in patients receiving a high dose of celecoxib (0.4 g/day) were markedly higher than in patients receiving celecoxib with half of the dose (0.2 g/day) for one week or the untreated subjects (p = 0.004). Changes in platelet count also followed the WBC alteration pattern.
Celecoxib is a relatively safe, inexpensive, and widely available drug with non-steroidal anti-inflammatory properties. The therapeutic efficacy of celecoxib depends on the administrated dose. Celecoxib might improve disease-free survival in patients with COVID-19.
众所周知,严重急性呼吸冠状病毒 2(SARS-CoV-2)是导致最近的 2019 年冠状病毒病(COVID-19)大流行的病毒株。目前的文献表明,该病毒通过上调宿主细胞中环氧化酶-2(COX-2)和下调前列腺素 E2(PGE2)降解酶,在很大比例的患者中引发 PGE2 风暴。
本文旨在研究短期使用塞来昔布(Celebrex),一种选择性 COX-2 抑制剂,对 COVID-19 患者的人口统计学特征、早期症状、血氧饱和度和血液学指标的影响。
共纳入 2020 年 10 月至 2021 年 9 月期间从伊朗东南部一家机构医院转诊的 67 例确诊为 COVID-19 的轻症或中度患者。记录患者在不同时期的人口统计学特征、症状和血液学指标。基于正态数据分布,使用单因素方差分析或 Kruskal-Wallis 检验来确定数据集之间的差异。
血氧饱和度在对照组和接受塞来昔布治疗的患者之间存在统计学差异(p=0.039)。两组患者的症状无明显差异(p>0.05)。在塞来昔布治疗的最初几天,全血细胞计数分析显示,高剂量塞来昔布(0.4g/天)治疗组的白细胞(WBC)计数明显低于对照组(p=0.026)。然而,高剂量塞来昔布(0.4g/天)治疗组的平均淋巴细胞水平明显高于接受半剂量塞来昔布(0.2g/天)治疗一周或未接受治疗的患者(p=0.004)。血小板计数的变化也遵循白细胞的变化模式。
塞来昔布是一种相对安全、廉价且广泛可用的具有非甾体抗炎特性的药物。塞来昔布的治疗效果取决于给药剂量。塞来昔布可能改善 COVID-19 患者的无病生存率。