Sharma Angelica, Lazarus Katharine, Papadopoulou Deborah, Prabhudev Hemanth, Tan Tricia, Meeran Karim, Choudhury Sirazum
Division of Diabetes, Endocrinology and Metabolism, Department of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
Department of Endocrinology, Imperial College Healthcare NHS Trust, London, UK.
Endocr Connect. 2023 Jul 26;12(8):e230097. doi: 10.1530/EC-23-0097.
Patients with adrenal insufficiency (AI) have a higher mortality than the general population, possibly because of excess glucocorticoid exposure at inappropriate times. The cortisol circadian rhythm is difficult to mimic with twice- or thrice-daily hydrocortisone. Prednisolone is a once-daily alternative which may improve patient compliance through its convenience.
Prednisolone day curves can be used to accurately downtitrate patients to the minimum effective dose. This study aimed to review prednisolone day curves and determine therapeutic ranges at different time points after administration.
Between August 2013 and May 2021, 108 prednisolone day curves from 76 individuals receiving prednisolone replacement were analysed. Prednisolone concentrations were determined by ultra-high-performance liquid chromatography-tandem mass spectrometry. Spearman's correlation coefficient was used to determine the relationship between 2-, 4-, and 6-h prednisolone levels compared to the previously validated standard 8-h prednisolone level (15-25 μg/L).
The median dose was 4 mg of prednisolone once daily. There was a strong correlation between the 4- and 8-h (R = 0.8829, P ≤ 0.0001) and 6- and 8-h prednisolone levels (R = 0.9530, P ≤ 0.0001). Target ranges for prednisolone were 37-62 μg/L at 4 h, 24-39 μg/L at 6 h, and 15-25 μg/L at 8 h. Prednisolone doses were successfully reduced in 21 individuals, and of these, 3 were reduced to 2 mg once daily. All patients were well upon follow-up.
This is the largest evaluation of oral prednisolone pharmacokinetics in humans. Low-dose prednisolone of 2-4 mg is safe and effective in most patients with AI. Doses can be titrated with either 4-, 6-, or 8-h single time point drug levels.
肾上腺功能不全(AI)患者的死亡率高于普通人群,这可能是由于在不适当的时间过量暴露于糖皮质激素。氢化可的松每日两次或三次给药难以模拟皮质醇的昼夜节律。泼尼松龙是一种每日一次的替代药物,因其便利性可能会提高患者的依从性。
泼尼松龙日曲线可用于准确地将患者的药物剂量下调至最低有效剂量。本研究旨在回顾泼尼松龙日曲线,并确定给药后不同时间点的治疗范围。
在2013年8月至2021年5月期间,分析了76例接受泼尼松龙替代治疗的个体的108条泼尼松龙日曲线。通过超高效液相色谱-串联质谱法测定泼尼松龙浓度。使用Spearman相关系数来确定泼尼松龙在2小时、4小时和6小时时的水平与先前验证的标准8小时泼尼松龙水平(15-25μg/L)之间的关系。
泼尼松龙的中位剂量为每日一次4mg。泼尼松龙在4小时和8小时时的水平之间(R = 0.8829,P≤0.0001)以及在6小时和8小时时的水平之间存在强相关性(R = 0.9530,P≤0.0001)。泼尼松龙在4小时时的目标范围为37-62μg/L,在6小时时为24-39μg/L,在8小时时为15-25μg/L。21例个体的泼尼松龙剂量成功降低,其中3例降至每日一次2mg。所有患者在随访时情况良好。
这是对口服泼尼松龙在人体药代动力学的最大规模评估。低剂量2-4mg的泼尼松龙对大多数AI患者是安全有效的。剂量可根据4小时、6小时或8小时的单一时间点药物水平进行滴定。