Division of Gastroenterology and Hepatology, Johns Hopkins Medical Institutions, Baltimore, Maryland, USA.
Angioskope Clinic, São José dos Campos, Brazil.
Gastrointest Endosc. 2021 Jun;93(6):1316-1324.e1. doi: 10.1016/j.gie.2020.10.016. Epub 2020 Oct 17.
Endoscopic sleeve gastroplasty (ESG) has been shown to be effective for inducing weight loss. The efficacy of liraglutide, a glucagon-like peptide-1 agonist, to augment weight loss after ESG is unknown. This study aims to evaluate the efficacy of ESG and liraglutide (ESG-L) compared with ESG alone.
This was a retrospective study of prospectively collected data from patients undergoing ESG at 3 outpatient clinics in Brazil between November 2017 and July 2018. Liraglutide was offered to all patients 5 months after ESG. Patients who opted to take liraglutide (ESG-L) were matched 1:1 to patients who declined it (ESG). The primary outcome was percent total body weight loss (%TBWL), and percent excess weight loss (%EWL) 7 months after initiation of liraglutide (12 months after ESG). The secondary outcome was change in percent body fat 12 months after ESG. ESG technique and postprocedure follow-up were identical at all 3 sites.
Propensity score matching yielded 26 matched pairs. Adjusted comparisons between the 2 groups showed that patients who opted to take liraglutide had a superior mean %TBWL 7 months after initiation of liraglutide (ESG-L) compared with those who declined it (ESG) (24.72% ± 2.12% vs 20.51% ± 1.68%, respectively; P < .001). ESG-L had a statistically greater reduction in percent body fat compared with ESG (7.85% ± 1.26% vs 10.54% ± 1.88%, respectively; P < .001) at 12 months.
Addition of liraglutide at 5 months results in superior weight loss and improved efficacy as demonstrated by decreased body fat 12 months after ESG. Further studies are imperative to determine optimal dose, timing, and duration of liraglutide.
内镜下袖状胃成形术(ESG)已被证明可有效减重。胰高血糖素样肽-1 激动剂利拉鲁肽在 ESG 后增加减重效果的疗效尚不清楚。本研究旨在评估 ESG 联合利拉鲁肽(ESG-L)与 ESG 单独治疗的疗效。
这是一项回顾性研究,纳入了 2017 年 11 月至 2018 年 7 月期间巴西 3 家门诊诊所接受 ESG 的患者的前瞻性数据。ESG 后 5 个月为所有患者提供利拉鲁肽。选择服用利拉鲁肽(ESG-L)的患者与拒绝服用的患者(ESG)进行 1:1 匹配。主要结局为总体重减轻百分比(%TBWL)和利拉鲁肽起始后 7 个月(ESG 后 12 个月)的超重体重减轻百分比(%EWL)。次要结局为 ESG 后 12 个月体脂百分比的变化。3 个地点的 ESG 技术和术后随访均相同。
通过倾向评分匹配得到 26 对匹配的患者。两组间调整后的比较显示,与拒绝服用的患者相比,选择服用利拉鲁肽的患者在利拉鲁肽起始后 7 个月的平均 %TBWL 更高(ESG-L:24.72%±2.12%;ESG:20.51%±1.68%;P<0.001)。ESG-L 与 ESG 相比,在 12 个月时体脂百分比的降低更显著(ESG-L:7.85%±1.26%;ESG:10.54%±1.88%;P<0.001)。
ESG 后 5 个月添加利拉鲁肽可获得更好的减重效果,并通过 ESG 后 12 个月时体脂百分比的降低来提高疗效。需要进一步的研究来确定利拉鲁肽的最佳剂量、时机和持续时间。