Division of Clinical Pharmacology and Toxicology, Department of Anesthesiology, Pharmacology, Intensive Care and Emergency Medicine, Geneva University Hospitals, Geneva, Switzerland.
School of Pharmaceutical Sciences, University of Geneva, Geneva, Switzerland.
Clin Transl Sci. 2022 Jul;15(7):1796-1804. doi: 10.1111/cts.13297. Epub 2022 Jun 15.
During the latest pandemic, the RECOVERY study showed the benefits of dexamethasone (DEX) use in COVID-19 patients. Obesity has been proven to be an independent risk factor for severe forms of infection, but little information is available in the literature regarding DEX dose adjustment according to body weight. We conducted a prospective, observational, exploratory study at Geneva University Hospitals to assess the impact of weight on DEX pharmacokinetics (PK) in normal-weight versus obese COVID-19 hospitalized patients. Two groups of patients were enrolled: normal-weight and obese (body mass index [BMI] 18.5-25 and >30 kg/m , respectively). All patients received the standard of care therapy of 6 mg DEX orally. Blood samples were collected, and DEX concentrations were measured. The mean DEX AUC and C were lower in the obese compared to the normal-weight group (572.02 ± 258.96 vs. 926.92 ± 552.12 ng h/ml and 138.67 ± 68.03 vs. 203.44 ± 126.30 ng/ml, respectively). A decrease in DEX AUC of 4% per additional BMI unit was observed, defining a significant relationship between weight and DEX AUC (p = 0.004, 95% CI 2-7%). In women, irrespective of the BMI, DEX AUC increased by 214% in comparison to men (p < 0.001, 95% CI 154-298%). Similarly, the mean C increased by 205% in women (p < 0.001, 95% CI 141-297%). Conversely, no significant difference between the obese and normal-weight groups was observed for exploratory treatment outcomes, such as the length of hospitalization. BMI, weight, and gender significantly affected DEX AUC. We conclude that dose adjustment would be needed if the aim is to achieve the same exposures in normal-weight and obese patients.
在最近的一次大流行中,RECOVERY 研究表明了地塞米松(DEX)在 COVID-19 患者中的使用益处。肥胖已被证明是感染严重形式的独立危险因素,但文献中关于根据体重调整 DEX 剂量的信息很少。我们在日内瓦大学附属医院进行了一项前瞻性、观察性、探索性研究,以评估体重对正常体重和肥胖 COVID-19 住院患者 DEX 药代动力学(PK)的影响。招募了两组患者:正常体重组和肥胖组(BMI 分别为 18.5-25 和 >30 kg/m )。所有患者均接受 6mg DEX 口服标准治疗。采集血样并测量 DEX 浓度。与正常体重组相比,肥胖组的 DEX AUC 和 C 均值较低(572.02±258.96 与 926.92±552.12ng·h/ml 和 138.67±68.03 与 203.44±126.30ng/ml 分别)。观察到每增加一个 BMI 单位,DEX AUC 下降 4%,表明体重与 DEX AUC 之间存在显著关系(p=0.004,95%CI 2-7%)。在女性中,无论 BMI 如何,DEX AUC 均比男性增加 214%(p<0.001,95%CI 154-298%)。同样,女性的平均 C 增加 205%(p<0.001,95%CI 141-297%)。相反,肥胖组和正常体重组在住院时间等探索性治疗结果方面没有观察到显著差异。BMI、体重和性别显著影响 DEX AUC。我们得出结论,如果目标是使正常体重和肥胖患者达到相同的暴露量,则需要进行剂量调整。