Bacus Catherine, South Terri-Lynne, Raudszus Sonia, Johansen Odd Erik
Alevia Medical Weight Loss, East Melbourne, Wantirna, Australia.
Lifestyle Metabolic, Brisbane, Australia.
Obes Pillars. 2024 Sep 30;12:100138. doi: 10.1016/j.obpill.2024.100138. eCollection 2024 Dec.
The use of meal replacement products (MRPs) to obtain a caloric deficit while maintaining micro- and macronutrient requirements, has a long tradition in obesity medicine. Limitations include low compliance, variability in efficacy, adverse events (related to acute changes in nutrient intake), and risk of weight regain when discontinued, and their popularity has declined after the emergence of potent GLP-1 receptor analogues (GLP1-RAs). However, GLP-1RAs have limitations, including dose-dependent risk for adverse events (AEs), high cost, as well as weight regain when discontinued. Although concomitant use of MRPs and GLP-1RAs could address some of the limitations, there is a scarcity of data reported on this. Herein we report real world clinical experience of such combined use.
This retrospective case evaluation involved people with obesity that concomitantly used MRPs (Optifast) and a GLP-1RA and were followed at one of three weight management centers in Australia or South Africa. Parameters collected were gender, age, co-morbidities, height, weight, frequency/amount of MRPs used, dose/type of GLP-1RA used, duration of combined use, and occurrence of AEs. Written informed consent for use of data was obtained from each individual, and the data were managed in an anonymized form and summarized descriptively.
A total of seven (5 females) individuals (mean [min, max] age 49 [30,66] years, BMI 44.8 [30.7, 57.9] kg/m) initiated either semaglutide (n=4) or liraglutide (n=3) concomitantly with daily MRPs (starting number of servings/day 2.7 [1,6]) for a duration of 12 [4, 25] months. Change in weight/BMI/% TBW was -32.0 (-9.6, -77.8) kg/-10.3 (-3.4, -24.5) kg/m/-24.2 %. Five individuals experienced ≥1 GLP-1RA related AE (nausea, reflux, burping, diarrhea, constipation). One individual discontinued GLP-1RA, whereas two persons discontinued the use of MRPs.
MRPs can be initiated concomitantly with a GLP-1 RA for weight management. This might enhance weight-loss effectiveness, with potential additional benefits that should be elucidated in further and larger studies.
使用代餐产品(MRP)以在维持微量和常量营养素需求的同时实现热量赤字,在肥胖医学领域有着悠久的传统。其局限性包括依从性低、疗效差异、不良事件(与营养素摄入的急性变化有关)以及停用后体重反弹的风险,并且在强效胰高血糖素样肽-1受体类似物(GLP-1RA)出现后其受欢迎程度有所下降。然而,GLP-1RA也有局限性,包括不良事件(AE)的剂量依赖性风险、成本高以及停用后体重反弹。尽管同时使用MRP和GLP-1RA可以解决一些局限性,但关于这方面的数据报道较少。在此,我们报告这种联合使用的真实世界临床经验。
这项回顾性病例评估涉及同时使用MRP(Optifast)和GLP-1RA的肥胖患者,他们在澳大利亚或南非的三个体重管理中心之一接受随访。收集的参数包括性别、年龄、合并症、身高、体重、MRP的使用频率/量、GLP-1RA的剂量/类型、联合使用的持续时间以及AE 的发生情况。获得了每位个体使用数据的书面知情同意书,数据以匿名形式管理并进行描述性总结。
共有七名(五名女性)个体(平均[最小值,最大值]年龄49[30,66]岁,BMI 44.8[30.7,57.9]kg/m²)开始同时使用司美格鲁肽(n = 4)或利拉鲁肽(n = 3)与每日MRP(开始时每日份数2.7[1,6]),持续12[4,25]个月。体重/BMI/%总体水的变化为-32.0(-9.6,-77.8)kg/-10.3(-3.4,-24.5)kg/m²/-24.2%。五名个体经历了≥1次与GLP-1RA相关的AE(恶心、反流、打嗝、腹泻、便秘)。一名个体停用了GLP-1RA,而两名个体停止使用MRP。
MRP可与GLP-1RA同时开始用于体重管理。这可能会提高减肥效果,潜在的额外益处应在进一步的大型研究中阐明。