III Department of Medicine, University Medical Center Hamburg-Eppendorf, Martinistr. 52, 20246, Hamburg, Germany.
Department of General, Visceral and Thoracic Surgery, University Medical Center Hamburg-Eppendorf, 20246, Hamburg, Germany.
Obes Surg. 2022 Oct;32(10):3280-3288. doi: 10.1007/s11695-022-06211-9. Epub 2022 Jul 25.
About 20-25% of patients experience weight regain (WR) or insufficient weight loss (IWL) after bariatric metabolic surgery (BS). Therefore, we aimed to retrospectively assess the effectiveness of adjunct treatment with the GLP-1 receptor agonist semaglutide in non-diabetic patients with WR or IWL after BS.
Post-bariatric patients without type 2 diabetes (T2D) with WR or IWL (n = 44) were included in the analysis. The primary endpoint was weight loss 3 and 6 months after initiation of adjunct treatment. Secondary endpoints included change in BMI, HbA1c, lipid profile, hs-CRP, and liver enzymes.
Patients started semaglutide 64.7 ± 47.6 months (mean ± SD) after BS. At initiation of semaglutide, WR after post-bariatric weight nadir was 12.3 ± 14.4% (mean ± SD). Total weight loss during semaglutide treatment was - 6.0 ± 4.3% (mean ± SD, p < 0.001) after 3 months (3.2 months, IQR 3.0-3.5, n = 38) and - 10.3 ± 5.5% (mean ± SD, p < 0.001) after 6 months (5.8 months, IQR 5.8-6.4, n = 20). At 3 months, categorical weight loss was > 5% in 61% of patients, > 10% in 16% of patients, and > 15% in 2% of patients. Triglycerides (OR = 0.99; p < 0.05), ALT (OR = 0.87; p = 0.05), and AST (OR = 0.89; p < 0.05) at baseline were negatively associated with weight loss of at least 5% at 3 months' follow-up (p < 0.05).
Treatment options to manage post-bariatric excess weight (regain) are scarce. Our results imply a clear benefit of adjunct treatment with semaglutide in post-bariatric patients. However, these results need to be confirmed in a prospective randomized controlled trial to close the gap between lifestyle intervention and revision surgery in patients with IWL or WR after BS.
约 20-25%的患者在接受减重代谢手术后出现体重反弹(WR)或减重不足(IWL)。因此,我们旨在回顾性评估 GLP-1 受体激动剂司美格鲁肽辅助治疗对 BS 后 WR 或 IWL 非糖尿病患者的有效性。
纳入无 2 型糖尿病(T2D)且 WR 或 IWL(n=44)的减重后患者进行分析。主要终点为辅助治疗开始后 3 个月和 6 个月的体重减轻情况。次要终点包括 BMI、HbA1c、血脂谱、hs-CRP 和肝酶的变化。
患者在 BS 后 64.7±47.6 个月(平均±标准差)开始使用司美格鲁肽。在开始使用司美格鲁肽时,WR 是在减重后体重最低点的基础上增加 12.3±14.4%(平均±标准差)。在司美格鲁肽治疗期间,总体重减轻为-6.0±4.3%(平均±标准差,p<0.001),3 个月后(3.2 个月,IQR 3.0-3.5,n=38)和 6 个月后(5.8 个月,IQR 5.8-6.4,n=20)。3 个月时,61%的患者体重减轻>5%,16%的患者体重减轻>10%,2%的患者体重减轻>15%。基线时的甘油三酯(OR=0.99;p<0.05)、ALT(OR=0.87;p=0.05)和 AST(OR=0.89;p<0.05)与 3 个月随访时至少减轻 5%的体重呈负相关(p<0.05)。
管理减重后多余体重(反弹)的治疗选择有限。我们的结果表明,在减重后患者中,司美格鲁肽辅助治疗具有明显益处。然而,这些结果需要在前瞻性随机对照试验中得到证实,以缩小 BS 后 IWL 或 WR 患者生活方式干预与手术修正之间的差距。