Memon Muhammad Y, Ahsan Tasnim, Jabeen Rukhshanda, Latif Saba, Qasim Saeeda F, Imran Paras
Department of Endocrinology, Jinnah Postgraduate Medical Centre (JPMC)/Medicell Institute of Diabetes, Endocrinology and Metabolism (MIDEM), Karachi, Pakistan.
J Family Med Prim Care. 2024 Oct;13(10):4188-4193. doi: 10.4103/jfmpc.jfmpc_159_24. Epub 2024 Oct 18.
To assess the efficacy and safety of Semaglutide (a GLP-1 receptor agonist) in obese patients with and without Type-II Diabetes Mellitus.
This observational analytic cohort study was conducted in a private medical institute in Karachi Pakistan; from August 2022 to January 2023. A total of 65 obese individuals >18 years of age, with or without T2D were included. Semaglutide was started with an initial dose of 0.25 mg with an increase in dose to 0.5 mg, 1 mg and 2 mg with gap of 4 weeks between each dose escalation. Patients were kept on the maximally tolerated dose, not exceeding 2 mg/week. Patients were evaluated on the first and second follow-up at 3 and 6 months respectively, for the same parameters as noted at the initial visit, along with documentation of any adverse effect.
Out of 65 patients, 49.2% were female and 50.8% were male. Mean age was 49.16 ± 14.20 years. 47.7% of the patients had hypertension, 46.2% had diabetes mellitus, 35.4% had dyslipidemia and 13.8% had ischemic heart disease. All patients were using 0.5 mg of semaglutide after three months, however by six months 33.8% were using 1 mg, and 24.6% were on 2 mg, whereas 40% decided to adhere to 0.5 mg and only 1.5% decided to reduce the dose to 0.25 mg due to adverse effects. Patients reported start of the first adverse effect by 3.44 ± 2.27 weeks of starting the drug. By the end of three months, 55.4% of patients in our study reported adverse effect, which declined to 34.5% by the end of six months, and the majority being mild to moderate and the most frequent side effects were gastrointestinal in origin. There was no significant difference in side effect profile in between those with and without diabetes mellitus. The average weight loss was 5.81 ± 2.64 kg and 9.86 ± 3.54 kg after three and six months respectively and the amount of weight loss was almost equal in those with and without T2D. A significant decline was observed in the average HbA1c levels, body mass index ( = <0.001), systolic blood pressure ( = <0.001), diastolic blood pressure ( = <0.001), total cholesterol ( = <0.001), high-density lipoprotein ( = <0.001), low-density lipoprotein ( = <0.001), triglycerides ( = <0.001) and alanine transaminase levels ( = <0.001).
Semaglutide showed substantial weight, HbA1c and cholesterol reductions in those with or without type-II diabetes.
评估司美格鲁肽(一种胰高血糖素样肽-1受体激动剂)在患有和未患有2型糖尿病的肥胖患者中的疗效和安全性。
这项观察性分析队列研究于2022年8月至2023年1月在巴基斯坦卡拉奇的一家私立医疗机构进行。共纳入65名18岁以上的肥胖个体,无论是否患有2型糖尿病。司美格鲁肽起始剂量为0.25mg,每4周剂量递增至0.5mg、1mg和2mg。患者维持在最大耐受剂量,不超过2mg/周。在3个月和6个月的首次和第二次随访中,对患者进行与初诊时相同参数的评估,并记录任何不良反应。
65名患者中,49.2%为女性,50.8%为男性。平均年龄为49.16±14.20岁。47.7%的患者患有高血压,46.2%患有糖尿病,35.4%患有血脂异常,13.8%患有缺血性心脏病。3个月后所有患者均使用0.5mg司美格鲁肽,但6个月时,33.8%的患者使用1mg,24.6%的患者使用2mg,而40%的患者决定维持0.5mg剂量,仅1.5%的患者因不良反应决定将剂量降至0.25mg。患者在开始用药3.44±2.27周后报告出现首次不良反应。到3个月末,本研究中55.4%的患者报告有不良反应,到6个月末降至34.5%,大多数为轻度至中度,最常见的副作用源于胃肠道。患有和未患有糖尿病的患者在副作用方面无显著差异。3个月和6个月后的平均体重减轻分别为5.81±2.64kg和9.86±3.54kg,2型糖尿病患者和非2型糖尿病患者体重减轻量几乎相等。观察到平均糖化血红蛋白水平、体重指数(= <0.001)、收缩压(= <0.001)、舒张压(= <0.001)、总胆固醇(= <0.001)、高密度脂蛋白(= <0.001)、低密度脂蛋白(= <0.001)、甘油三酯(= <0.001)和丙氨酸转氨酶水平(= <0.001)均显著下降。
司美格鲁肽在患有或未患有2型糖尿病的患者中均显示出显著的体重、糖化血红蛋白和胆固醇降低效果。