Levy Shauna, Attia Abdallah, Elshazli Rami M, Abdelmaksoud Ahmed, Tatum Danielle, Aiash Hani, Toraih Eman A
Department of Surgery, Tulane University School of Medicine, New Orleans, LA 70112, USA.
Department of Biochemistry and Molecular Genetics, Faculty of Physical Therapy, Horus University-Egypt, New Damietta 34517, Egypt.
Cancers (Basel). 2024 Dec 30;17(1):78. doi: 10.3390/cancers17010078.
: Glucagon-like peptide-1 receptor agonists (GLP-1RAs) have demonstrated significant efficacy in obesity treatment beyond their original development for type-2 diabetes management. This comprehensive study investigated the relationship between GLP-1RA use and cancer incidence in individuals with obesity across a 5-year follow-up period. : We conducted a large-scale cohort study using the TriNetX US Collaborative Network database (2013-2023) examining adult patients with obesity. The study utilized propensity score matching to pair GLP-1RA-treated patients with controls (1:1) using the nearest neighbor method. Cancer incidence served as the primary outcome measure over the 5-year follow-up, with subgroup analyses considering individual GLP-1RA agents, patient sex, and BMI categories. : Analysis revealed significant cancer-risk reductions associated with GLP-1RA use across multiple cancer types compared to matched controls. Notable risk reductions were observed in gastrointestinal (HR 0.67, 95% CI 0.59-0.75), skin (HR 0.62, 95% CI 0.55-0.70), breast (HR 0.72, 95% CI 0.64-0.82), female genital (HR 0.61, 95% CI 0.53-0.71), prostate (HR 0.68, 95% CI 0.58-0.80), and lymphoid/hematopoietic cancers (HR 0.69, 95% CI 0.60-0.80). Semaglutide demonstrated superior protective effects, particularly in gastrointestinal cancers (HR 0.45, 95% CI 0.37-0.53). Conversely, liraglutide showed increased risks for thyroid (HR 1.70, 95% CI 1.03-2.82) and respiratory cancers (HR 1.62, 95% CI 1.13-2.32). : This research provides compelling evidence for GLP-1RA's potential role in cancer-risk reduction, with semaglutide showing particularly promising results. The differential effects observed among GLP-1RA agents emphasize the importance of personalized medicine approaches. These findings suggest significant implications for clinical practice and future research in both obesity management and cancer prevention.
胰高血糖素样肽-1受体激动剂(GLP-1RAs)在肥胖治疗中已显示出显著疗效,其最初并非用于治疗2型糖尿病。这项全面的研究调查了在5年随访期内,使用GLP-1RAs与肥胖个体癌症发病率之间的关系。
我们使用TriNetX美国协作网络数据库(2013 - 2023年)进行了一项大规模队列研究,研究对象为成年肥胖患者。该研究利用倾向得分匹配法,采用最近邻法将接受GLP-1RA治疗的患者与对照组(1:1)配对。癌症发病率作为5年随访期间的主要结局指标,并进行亚组分析,考虑个体GLP-1RA药物、患者性别和BMI类别。
分析显示,与匹配的对照组相比,使用GLP-1RAs与多种癌症类型的癌症风险显著降低相关。在胃肠道(风险比[HR] 0.67,95%置信区间[CI] 0.59 - 0.75)、皮肤(HR 0.62,95% CI 0.55 - 0.70)、乳腺(HR 0.72,95% CI 0.64 - 0.82)、女性生殖系统(HR 0.61,95% CI 0.53 - 0.71)、前列腺(HR 0.68,95% CI 0.58 - 0.80)以及淋巴/造血系统癌症(HR 0.69,95% CI 0.60 - 0.80)方面观察到显著的风险降低。司美格鲁肽显示出更好的保护作用,尤其是在胃肠道癌症方面(HR 0.45,95% CI 0.37 - 0.53)。相反,利拉鲁肽显示甲状腺癌(HR 1.70,95% CI 1.03 - 2.82)和呼吸道癌症(HR 1.62,95% CI 1.13 - 2.32)的风险增加。
这项研究为GLP-1RAs在降低癌症风险方面的潜在作用提供了有力证据,司美格鲁肽显示出特别有前景的结果。在GLP-1RA药物中观察到的不同效果强调了个性化医疗方法的重要性。这些发现对肥胖管理和癌症预防的临床实践及未来研究具有重要意义。