Type 2 Diabetes Mellitus in Patients with a Prior History of Corticosteroid-induced Hyperglycemia

Jennifer DeZubay, R. Drew, Jennifer Smith, E. Mills, Tara Bell, M. Holland
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Abstract

also been observed in healthy subjects. (3) Prednisone, prednisolone, and methylprednisolone are intermediate-acting corticosteroids with a peak effect four to six hours after administration. (1)(2) After just one dose, postprandial blood glucose may be affected without much effect on fasting blood glucose. (1) However, after repeated doses, these intermediate-acting corticosteroids can cause persistent hyperglycemia. (1) Dexamethasone, a long-acting corticosteroid, is associated with hyperglycemia that may persist for longer than 24 hours. (1) High doses of corticosteroids, defined as more than 30 mg of prednisone equivalent per day, lead to more adverse effects, such as hyperglycemia. (5) Likewise, many adverse effects, including glucose intolerance, are related to the cumulative corticosteroid dose and longer duration of corticosteroid use. A prospective, observational study of 35 patients without pre- existing diabetes, taking high-dose corticosteroids for 6 to 12 weeks, found 40.6% of patients to have elevated fasting or postprandial blood glucose at eight weeks (fasting blood glucose >126 mg/dL). (6) Both higher cumulative corticosteroid doses and continuous corticosteroid administration were associated with a higher incidence of impaired fasting glucose. A case-control study found a slight association between oral glucocorticoid prescriptions and diagnoses of diabetes. (7) The majority of the patients in this study received low daily doses of glucocorticoids. (7) It is presently unknown whether short-term administration of high-dose corticosteroids is associated with the subsequent development of type 2 diabetes, defined as hemoglobin A1c (HbA1c) ≥ 6.5% (48 mmol/mol). (8-9) In addition, no studies have evaluated whether the development of hyperglycemia during the time of short-term, high-dose corticosteroid administration is predictive of type 2 diabetes in the future.
有皮质类固醇诱导的高血糖病史的2型糖尿病患者
也在健康受试者中观察到。(3) 泼尼松、泼尼松和甲基强的松龙是中效皮质类固醇,给药后4-6小时达到峰值。(1) (2)仅服用一剂后,餐后血糖可能会受到影响,而对空腹血糖没有太大影响。(1) 然而,在重复给药后,这些中等作用的皮质类固醇会导致持续的高血糖。(1) 地塞米松是一种长效皮质类固醇,与可能持续24小时以上的高血糖有关。(1) 高剂量的皮质类固醇,定义为每天超过30毫克的泼尼松当量,会导致更多的不良反应,如高血糖。(5) 同样,许多不良反应,包括葡萄糖不耐受,与皮质类固醇的累积剂量和皮质类固醇使用的持续时间较长有关。一项针对35名无糖尿病前期患者的前瞻性观察性研究发现,在服用高剂量皮质类固醇6至12周后,40.6%的患者在8周时空腹或餐后血糖升高(空腹血糖>126 mg/dL)。(6) 较高的累积皮质类固醇剂量和持续皮质类固醇给药均与较高的空腹血糖受损发生率相关。一项病例对照研究发现,口服糖皮质激素处方与糖尿病诊断之间存在轻微关联。(7) 本研究中的大多数患者每天接受低剂量的糖皮质激素治疗。(7) 目前尚不清楚短期服用高剂量皮质类固醇是否与2型糖尿病的后续发展有关,2型糖尿病定义为血红蛋白A1c≥6.5%(48 mmol/mol)。(8-9)此外,没有研究评估短期、高剂量皮质类固醇给药期间高血糖的发展是否可以预测未来的2型糖尿病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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