Section of Endocrinology, Department of Medicine, Aga Khan University Hospital, Karachi, Pakistan.
Aster Sanad Hospital, Riyadh, Saudi Arabia.
Endocrine. 2023 Apr;80(1):64-70. doi: 10.1007/s12020-022-03290-7. Epub 2022 Dec 29.
Primary aim was to assess the safety of SGLT2-i in patients with Type 2 Diabetes Mellitus (T2D) in a real-life scenario during Ramadan by finding the frequency and severity of hypoglycemic/hyperglycemic events, dehydration, and Diabetic ketoacidosis (DKA). Secondary aim was to assess changes in glycated hemoglobin (HbA1c), weight and creatinine levels.
This prospective, observational, controlled cohort study was conducted at Aga Khan University Hospital, Karachi, Pakistan from March 15 to June 30, 2021. Participants were over 21 years of age, on stable doses of SGLT2-I, which was started at least 2 months before Ramadan. Endpoint assessments were done 1 month before and within 6 weeks after Ramadan.
Of 102 participants enrolled, 82 completed the study. Most (52%) were males, with mean age 52.2 ± 9.5 years and average duration of T2D 11.2 ± 6.5 years. 63% were on Empagliflozin (mean dose; 14.8 ± 7.2 mg/day) whereas 37% were on Dapagliflozin (mean dose; 8.2 ± 2.7 mg/day). Six (7.3%) documented symptoms of hypoglycemia. However, no episode of severe hypoglycemia, hyperglycemia, dehydration, DKA, hospitalization or discontinuation of SGLT2i was reported. HbA1c changes were (7.7 ± 1.2% from 7.9 ± 2.3%, p 0.34), weight (78.4 ± 12.9 kgs from 78.9 ± 13.3, p 0.23) and eGFR (87.8 ± 27.9 from 94.3 ± 37.6, p < 0.001). The reasons of study participants drop outs were: six did not keep any fasts; four discontinued study participation for personal reasons; three were out of city and missed post Ramadan follow-up, two protocol violation and five could not be contacted for post-Ramadan follow up during the third wave of COVID-19.
Results showed the safety of SGLT2i agents during Ramadan in the Pakistani population recommending it as a treatment option in adults with T2D, without any additional adverse events.
本研究旨在评估在斋月期间,2 型糖尿病(T2D)患者使用 SGLT2-i 的安全性,方法是发现低血糖/高血糖事件、脱水和糖尿病酮症酸中毒(DKA)的频率和严重程度。次要目的是评估糖化血红蛋白(HbA1c)、体重和肌酐水平的变化。
这是一项前瞻性、观察性、对照队列研究,于 2021 年 3 月 15 日至 6 月 30 日在巴基斯坦卡拉奇的 Aga Khan 大学医院进行。参与者年龄在 21 岁以上,稳定剂量的 SGLT2-I,在斋月前至少 2 个月开始使用。在斋月前 1 个月和斋月后 6 周内进行终点评估。
在纳入的 102 名参与者中,82 名完成了研究。大多数(52%)为男性,平均年龄为 52.2±9.5 岁,平均 T2D 病程为 11.2±6.5 年。63%服用恩格列净(平均剂量为 14.8±7.2mg/天),37%服用达格列净(平均剂量为 8.2±2.7mg/天)。有 6 人(7.3%)记录有低血糖症状。然而,没有严重低血糖、高血糖、脱水、DKA、住院或停止使用 SGLT2i 的报告。HbA1c 变化为(从 7.9±2.3%降至 7.7±1.2%,p=0.34),体重(从 78.9±13.3kg 降至 78.4±12.9kg,p=0.23)和 eGFR(从 94.3±37.6ml/min/1.73m2 降至 87.8±27.9ml/min/1.73m2,p<0.001)。研究参与者退出的原因是:6 人没有进行任何斋戒;4 人因个人原因停止参与研究;3 人不在城市,错过了斋月后的随访;2 人违反了方案;5 人在第三波 COVID-19 期间无法联系到进行斋月后的随访。
结果表明,SGLT2i 药物在斋月期间在巴基斯坦人群中的安全性,推荐将其作为 T2D 成人的治疗选择,没有任何额外的不良事件。