Feier Catalin Vladut Ionut, Vonica Razvan Constantin, Faur Alaviana Monique, Streinu Diana Raluca, Muntean Calin
First Discipline of Surgery, Department X-Surgery, "Victor Babes" University of Medicine and Pharmacy, 2 E. Murgu Sq., 300041 Timisoara, Romania.
First Surgery Clinic, "Pius Brinzeu" Clinical Emergency Hospital, 300723 Timisoara, Romania.
Int J Mol Sci. 2024 Apr 15;25(8):4346. doi: 10.3390/ijms25084346.
The broadening application of glucagon-like peptide (GLP)-1 receptor agonists, specifically semaglutide (Ozempic) for the management of diabetes and obesity brings a critical need to evaluate its safety profile, considering estimates of up to 20 million prescriptions per year in the US until 2035. This systematic review aims to assess the incidence of thyroid cancer and detail the spectrum of adverse events associated with semaglutide, focusing on its implications for patient care. Through a systematic search of PubMed, Scopus, and Embase databases up to December 2023, ten randomized controlled trials (RCTs) involving 14,550 participants, with 7830 receiving semaglutide, were analyzed, with an additional number of 18 studies that were separately discussed because they reported data from the same RCTs. The review focused on thyroid cancer incidence, gastrointestinal symptoms, and other significant adverse events attributed to semaglutide. The incidence of thyroid cancer in semaglutide-treated patients was less than 1%, suggesting no significant risk. Adverse events were predominantly gastrointestinal, including nausea (2.05% to 19.95%) and diarrhea (1.4% to 13%). Nasopharyngitis and vomiting were also notable, with mean prevalences of 8.23% and 5.97%, respectively. Other adverse events included increased lipase levels (mean of 6.5%), headaches (mean prevalence of 7.92%), decreased appetite (reported consistently at 7%), influenza symptoms (mean prevalence of 5.23%), dyspepsia (mean prevalence of 5.18%), and constipation (mean prevalence of 6.91%). Serious adverse events varied from 7% to 25.2%, highlighting the need for vigilant patient monitoring. These findings underscore the gastrointestinal nature of semaglutide's adverse events, which, while prevalent, did not significantly deter from its clinical benefits in the treatment landscape. This systematic review provides a comprehensive assessment of semaglutide's safety profile, with a focus on gastrointestinal adverse events and a low incidence of thyroid cancer. Despite the prevalence of gastrointestinal symptoms, semaglutide remains an efficacious option for managing diabetes and obesity. The detailed characterization of adverse events underscores the importance of monitoring and managing these effects in clinical practice, excluding the hypothesis of carcinogenesis.
胰高血糖素样肽(GLP)-1受体激动剂的应用日益广泛,尤其是司美格鲁肽(Ozempic)用于治疗糖尿病和肥胖症。鉴于预计到2035年美国每年的处方量将高达2000万,因此迫切需要评估其安全性。本系统评价旨在评估甲状腺癌的发病率,并详细阐述与司美格鲁肽相关的不良事件谱,重点关注其对患者护理的影响。通过系统检索截至2023年12月的PubMed、Scopus和Embase数据库,分析了10项随机对照试验(RCT),共涉及14550名参与者,其中7830人接受了司美格鲁肽治疗,另外18项研究因报告了相同RCT的数据而单独讨论。该评价重点关注甲状腺癌发病率、胃肠道症状以及其他归因于司美格鲁肽的重大不良事件。接受司美格鲁肽治疗的患者中甲状腺癌的发病率低于1%,表明风险不显著。不良事件主要为胃肠道反应,包括恶心(2.05%至19.95%)和腹泻(1.4%至13%)。鼻咽炎和呕吐也较为显著,平均患病率分别为8.23%和5.97%。其他不良事件包括脂肪酶水平升高(平均为6.5%)、头痛(平均患病率为7.92%)、食欲减退(一直报告为7%)、流感样症状(平均患病率为5.23%)、消化不良(平均患病率为5.18%)和便秘(平均患病率为6.91%)。严重不良事件的发生率在7%至25.2%之间,凸显了对患者进行密切监测的必要性。这些发现强调了司美格鲁肽不良事件的胃肠道性质,虽然这些不良事件普遍存在,但并未显著影响其在治疗领域的临床益处。本系统评价对司美格鲁肽的安全性进行了全面评估,重点关注胃肠道不良事件和低甲状腺癌发病率。尽管胃肠道症状普遍存在,但司美格鲁肽仍是治疗糖尿病和肥胖症的有效选择。不良事件的详细特征强调了在临床实践中监测和管理这些影响的重要性,排除了致癌作用的假设。