Weight and cardiometabolic effects of a novel oral shape-shifting superabsorbent hydrogel capsule: Prespecified and exploratory analysis of the Epitomee capsule RESET study

H.E. Bays , J.D. Ard , P.M. O'Neil , T.A. Wadden , R.F. Kushner , J.M. Jakicic , H.R. Wyatt , F.L. Greenway , M. Kamar , E. Ganon-Elazar , L. Cohen Asaraf , D.H. Ryan
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Abstract

Background

Management of obesity potentially improves cardiometabolic risk factors in patients with metabolic syndrome (MetS). The Epitomee capsule is a non-pharmacological, biodegradable device treatment for weight reduction in patients with overweight and obesity.

Methods

This secondary analysis of the Randomized Evaluation of Safety and Efficacy of the Epitomee capsule Trial (RESET) (a randomized, 24-week, multicenter, placebo-controlled, double-blind trial that enrolled 279 adults aged ≥18 years with a BMI of 27–40 kg/m2) evaluated changes in cardiometabolic parameters in participants treated with Epitomee or placebo combined with lifestyle counseling among (a) the entire RESET study population, and (b) participants meeting diagnostic criteria for prediabetes. Predefined and exploratory endpoints included changes in waist circumference, glycemic parameters, blood pressure, and lipid blood levels; this analysis also assessed percent weight loss in participants with MetS.

Results

Waist circumference, systolic and diastolic blood pressure and some measures of glycemia and lipids, improved with both Epitomee and placebo with no significant differences. Participants with prediabetes treated with Epitomee showed significantly greater reductions in HOMA-IR (p < 0.007) and insulin levels (p < 0.003) than the placebo group. Participants with MetS at baseline experienced significantly greater percent change in initial weight when treated with the Epitomee capsule (n = 27) compared to placebo (n = 31), −8.3% vs −5.2 %, respectively (p < 0.0004). Similar percentages of participants with MetS in both groups achieved ≥5 % weight reduction (59.3 % and 54.8 %, in Epitomee and placebo groups respectively). Significantly more participants with MetS treated with Epitomee achieved ≥10 % weight reduction compared with those treated with placebo (40.7 % vs. 6.5 %, respectively, p < 0.002).

Conclusion

Treatment with either Epitomee and placebo combined with lifestyle improve cardiometabolic risk factors. Compared to placebo, Epitomee significantly reduced HOMA-IR and insulin levels in participants with prediabetes. Among participants with MetS, Epitomee significantly reduced body weight [ClinicalTrials.gov ID NCT04222322].

Abstract Image

一种新型口服变形高吸收水凝胶胶囊对体重和心脏代谢的影响:对Epitomee胶囊RESET研究的预先指定和探索性分析
背景:肥胖管理可能改善代谢综合征(MetS)患者的心脏代谢危险因素。Epitomee胶囊是一种非药物、可生物降解的装置,用于超重和肥胖患者的减肥治疗。方法:对Epitomee胶囊试验(RESET)(一项随机、24周、多中心、安慰剂对照、双盲试验,招募279名年龄≥18岁、BMI为27-40 kg/m2的成年人)的安全性和有效性的随机评估,评估了在(a)整个RESET研究人群中,接受Epitomee或安慰剂联合生活方式咨询治疗的参与者心脏代谢参数的变化。(b)符合糖尿病前期诊断标准的参与者。预定终点和探索性终点包括腰围、血糖参数、血压和血脂水平的变化;该分析还评估了met患者体重减轻的百分比。结果患者的腰围、收缩压、舒张压及部分血糖、血脂指标均有改善,与安慰剂组比较差异无统计学意义。接受Epitomee治疗的糖尿病前期患者HOMA-IR显著降低(p <;0.007)和胰岛素水平(p <;0.003)。与安慰剂(n = 31)相比,接受Epitomee胶囊(n = 27)治疗的基线met患者的初始体重变化百分比显著更高,分别为- 8.3%和- 5.2% (p <;0.0004)。两组met患者体重减轻≥5%的比例相似(Epitomee组和安慰剂组分别为59.3%和54.8%)。与安慰剂治疗组相比,接受Epitomee治疗的met患者体重减轻≥10%的显著增加(分别为40.7%对6.5%,p <;0.002)。结论表组蛋白或安慰剂联合生活方式治疗可改善心脏代谢危险因素。与安慰剂相比,Epitomee显著降低了糖尿病前期患者的HOMA-IR和胰岛素水平。在met患者中,Epitomee显著降低了体重[ClinicalTrials.gov ID NCT04222322]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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