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Nutritional status with tirzepatide in obesity: A post hoc analysis of the SURMOUNT-1-4 randomized clinical trials 替西肽治疗肥胖症的营养状况:一项对SURMOUNT-1-4随机临床试验的事后分析
Pub Date : 2026-03-01 Epub Date: 2026-01-23 DOI: 10.1016/j.obpill.2026.100248
Jaime P. Almandoz , Octavia Pickett-Blakely , Colleen Tewksbury , Adam Stefanski , Sylvia Gonsahn-Bollie , Georgios K. Dimitriadis , Ada Leticia Murro , Dachuang Cao , Qier Meng , Lisa M. Neff

Background

Nutritional deficiencies are common among people with obesity, before and during treatment, such as with very-low-calorie diets and metabolic/bariatric surgery. Obesity management medications (OMMs) can reduce appetite and dietary intake, potentially affecting nutritional status. The impact of OMMs on nutritional outcomes in people with obesity warrants further study.

Methods

We conducted a post hoc analysis of available nutritional status-related data from the randomized, placebo-controlled, phase 3 SURMOUNT-1-4 trials of tirzepatide (N = 4726). Descriptive statistics were utilized to explore available nutritional status-related data from clinical trial reports, including investigator-reported treatment-emergent adverse events (TEAEs) based on 14 MedDRA preferred terms, chosen to identify cases of macronutrient malnutrition; investigator-reported vitamin deficiency-related TEAEs; biomarkers assessed systematically during the trials (albumin; total lymphocyte count [TLC]); reasons for early treatment discontinuation; and participants reaching body mass index (BMI) < 18.5 and < 22 kg/m2.

Results

Investigators reported 3 of 14 TEAEs potentially related to macronutrient malnutrition. TEAE incidence of Abnormal loss of weight, Underweight, and Hypoalbuminemia was 0.03 %, 0.06 %, and 0.03 % with tirzepatide and 0 %, 0 %, and 0.06 % with placebo, respectively. Vitamin deficiency-related TEAEs were reported for 0.99 % and 1.07 % of tirzepatide- and placebo-treated participants, respectively. Albumin <3.3 g/dL occurred in 0.06 % and 0.13 % of tirzepatide- and placebo-treated participants, respectively, while TLC <910/μL occurred in 2.90 % and 1.77 %. Treatment discontinuations potentially related to nutritional status (primarily achievement of desired weight and perceived excessive weight loss) occurred in 0.53 % of participants. Overall, 0.38 % and 0.06 % of tirzepatide- and placebo-treated participants reached BMI <18.5 kg/m2.

Conclusions

TEAEs and treatment discontinuations due to macronutrient malnutrition were uncommon in the SURMOUNT-1-4 trials of tirzepatide for obesity. Lack of routinely collected vitamin and mineral levels during the trials limited assessment of the impact of tirzepatide treatment on micronutrient status. Systematic assessment of nutritional status before and during OMM treatment would enhance future trials.

Clinicaltrials.gov identifiers

NCT04184622 (SURMOUNT-1); NCT04657003 (SURMOUNT-2); NCT04657016 (SURMOUNT-3); and NCT04660643 (SURMOUNT-4).
背景:在治疗前和治疗期间,如极低热量饮食和代谢/减肥手术,营养缺乏在肥胖人群中很常见。肥胖管理药物(OMMs)可以降低食欲和饮食摄入量,潜在地影响营养状况。OMMs对肥胖人群营养结果的影响值得进一步研究。方法:我们对替西肽的随机、安慰剂对照、SURMOUNT-1-4期3期试验(N = 4726)中可用的营养状况相关数据进行了事后分析。描述性统计用于从临床试验报告中探索可用的营养状况相关数据,包括基于14个MedDRA首选术语的研究者报告的治疗紧急不良事件(teae),选择用于确定常量营养素营养不良病例;研究者报告的与维生素缺乏相关的teae;试验期间系统评估的生物标志物(白蛋白、总淋巴细胞计数[TLC]);早期停止治疗的原因;身体质量指数(BMI)分别达到18.5和22 kg/m2。结果14例teae中有3例可能与宏量营养素营养不良有关。替西帕肽组TEAE中体重异常减轻、体重不足和低白蛋白血症的发生率分别为0.03%、0.06%和0.03%,安慰剂组分别为0%、0%和0.06%。在替西肽组和安慰剂组中,维生素缺乏相关teae分别为0.99%和1.07%。在替西肽组和安慰剂组中,白蛋白3.3 g/dL分别为0.06%和0.13%,而TLC 910/μL分别为2.90%和1.77%。有0.53%的参与者因营养状况(主要是达到预期体重和感觉体重减轻过多)而中断治疗。总体而言,接受替西肽和安慰剂治疗的参与者中,分别有0.38%和0.06%的人达到BMI 18.5 kg/m2。结论在替西肽治疗肥胖的SURMOUNT-1-4试验中,因宏量营养素营养不良而导致的糖尿病和停药不常见。试验期间缺乏常规收集的维生素和矿物质水平限制了对替西帕肽治疗对微量营养素状况影响的评估。在OMM治疗前和治疗过程中对营养状况进行系统评估将加强未来的试验。NCT04657003 (SURMOUNT-2);NCT04657016 (SURMOUNT-3);和NCT04660643 (SURMOUNT-4)。
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引用次数: 0
Weight reduction and treatment adherence with tirzepatide using the Individualized Virtual Integrative Medicine (IVIM) protocol 使用个体化虚拟综合医学(IVIM)方案减轻体重和坚持使用替西帕肽治疗
Pub Date : 2026-03-01 Epub Date: 2025-11-29 DOI: 10.1016/j.obpill.2025.100236
Jessica Duncan, Patrick Lee Stevens, Emily Bigby, Courtney Floyd, Josh Malina, Jennifer Nickens, Amber Lambert, Taylor Kantor

Introduction

Obesity and its downstream effects continue to drive rising rates of chronic disease. Tirzepatide, a dual glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptor agonist, has shown significant potential in supporting weight loss and improving metabolic health. This study examines the use of tirzepatide alongside the Individualized Virtual Integrative Medicine (IVIM) protocol. This is a telehealth-based approach to improving outcomes through consistent access to care and support throughout the weight reduction journey.

Methods

This is a retrospective analysis of 1166 patients who completed at least 52-weeks of the IVIM clinical protocol while on GLP-1 therapy with tirzepatide overseen by a team of board-certified obesity medicine physicians and nurse practitioners. Only patients with a body mass index (BMI) of 30 or greater were included. Due to the branded tirzepatide shortage, patients were provided with the ability to utilize compounded tirzepatide medications, if medically appropriate.

Results

Mean change at 12-weeks for patients both on compounded tirzepatide and branded tirzepatide was −20.12 lbs (−8.80 %), 24-weeks: −35.67 lbs (−15.72 %), 36-weeks: −47.33 lbs (−20.34 %), 52-weeks: −52.28 lbs (−22.74 %). At 72 weeks of therapy, patients had lost an average of −62.79 lbs (−26.54 %). The percentage of patients who lost at least 5 % of their body weight at 52 weeks was: 99.36 %, 10 % or more: 97.12 %, 15 % or more: 84.66 %, 20 % or more: 64.22 %, and 25 % or more: 41.21 %.

Discussion

Patients completing 52-weeks of tirzepatide therapy on the IVIM protocol experienced significant weight loss with a high level of treatment adherence and program utilization. The findings suggest that individualized dose titration and frequent access to support may improve outcomes of patients initiated on weight reduction therapy with GLP-1 medications. These findings support the IVIM protocol as a safe, effective and individualized model for delivering obesity treatment through a curated, patient-centered, virtual approach.
肥胖症及其下游影响继续推动慢性病发病率上升。tizepatide是一种双重葡萄糖依赖性胰岛素性多肽(GIP)和胰高血糖素样肽-1 (GLP-1)受体激动剂,在支持减肥和改善代谢健康方面显示出显著的潜力。本研究考察了替西帕肽与个体化虚拟综合医学(IVIM)方案的使用。这是一种基于远程保健的方法,通过在整个减肥过程中始终如一地获得护理和支持来改善结果。方法回顾性分析1166例患者,这些患者在接受GLP-1和替西帕肽治疗的同时完成了至少52周的IVIM临床方案,并由委员会认证的肥胖医学医生和执业护士团队监督。仅包括身体质量指数(BMI)为30或更高的患者。由于品牌替西肽短缺,如果医学上合适,患者可以使用复方替西肽药物。结果复方替西帕肽和品牌替西帕肽患者12周时的平均变化为- 20.12磅(- 8.80%),24周:- 35.67磅(- 15.72%),36周:- 47.33磅(- 20.34%),52周:- 52.28磅(- 22.74%)。在治疗72周时,患者平均减轻62.79磅(- 26.54%)。52周时体重减轻至少5%的患者比例为:99.36%,10%及以上:97.12%,15%及以上:84.66%,20%及以上:64.22%,25%及以上:41.21%。在IVIM方案下完成52周替西肽治疗的患者体重显著减轻,治疗依从性和方案使用率高。研究结果表明,个体化剂量滴定和频繁获得支持可以改善开始使用GLP-1药物减肥治疗的患者的预后。这些发现支持IVIM方案作为一种安全、有效和个性化的模式,通过精心策划的、以患者为中心的虚拟方法提供肥胖治疗。
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引用次数: 0
Association of Ethiopian Orthodox Tewahedo Christian fasting on appetite hormones and insulin sensitivity in type-II diabetes and healthy subjects in Ethiopia 埃塞俄比亚东正教Tewahedo基督教禁食对埃塞俄比亚ii型糖尿病和健康受试者的食欲激素和胰岛素敏感性的影响
Pub Date : 2026-03-01 Epub Date: 2025-11-15 DOI: 10.1016/j.obpill.2025.100226
Alemayehu Michael , Kaleab Baye

Background

Energy restriction, time-restricted feeding, and vegetarian diet intake each have been linked independently to positive health effects. However, little is known about the religious fasts practiced by Ethiopian Orthodox Tewahedo Christians (EOTC) fasting, which combine energy restriction, time-restricted feeding, and vegetarian diet consumption.

Method

This longitudinal study compared the effects of EOTC fasting on appetite hormones, insulin sensitivity, and β-cell function. The fasting cohort comprised both individuals with diabetes and healthy individuals, and was compared against a non-fasting cohort that also included both individuals with diabetes and healthy individuals. We employed pretested structured questionnaire to collect information on fasting patterns, physical activity, and sociodemographic traits. Body weight was measured using an adult digital electronic scale (ASTO), and hormone activity was determined using enzyme-linked immunosorbent assay (ELISA) analyzer.

Results

EOTC fast significantly lower serum level of appetite hormones like glucagon (p < 0.0001, p = 0.001), leptin (p = 0.002, p = 0.046) in both type-II diabetes and healthy subjects respectively compared to non-fasting. Insulin increased significantly (p = 0.002) in people with diabetes while decreased (p = 0.003) in healthy subjects. The concentration of ghrelin (p = 0.030) increased significantly in type-II diabetes but insignificantly (p = 0.135) in healthy subjects when compared to non-fasting. Both fasting people with diabetes and healthy subjects showed significant (p = 0.03, 0.010) improvements in insulin sensitivity and β-cell function respectively.

Conclusion

Concurrent vegetarian diet and energy restriction practiced among EOTC fasting may improve body weight managements. EOTC fasting improves activities of appetite hormones, increase insulin sensitivity and β-cell function (HOMA-IR) in both people with diabetes and healthy subjects. EOTC fasting practice represents a promising, culturally-accepted, non-pharmacological strategy for diabetes prevention and management.
能量限制、限时喂养和素食摄入都与积极的健康影响有独立的联系。然而,人们对埃塞俄比亚东正教特瓦赫多基督徒(EOTC)的宗教禁食知之甚少,这种禁食结合了能量限制、限时进食和素食。方法本研究比较了EOTC禁食对食欲激素、胰岛素敏感性和β细胞功能的影响。禁食队列包括糖尿病患者和健康个体,并与非禁食队列进行比较,非禁食队列也包括糖尿病患者和健康个体。我们采用预先测试的结构化问卷来收集有关禁食模式、身体活动和社会人口特征的信息。采用成人数字电子秤(ASTO)测量体重,采用酶联免疫吸附试验(ELISA)分析仪测定激素活性。结果与非禁食组相比,otc快速组显著降低了2型糖尿病和健康组血清胰高血糖素(p < 0.0001, p = 0.001)和瘦素(p = 0.002, p = 0.046)的食欲激素水平。糖尿病患者胰岛素显著升高(p = 0.002),而健康受试者胰岛素显著降低(p = 0.003)。ii型糖尿病患者的胃饥饿素浓度显著升高(p = 0.030),而健康受试者的胃饥饿素浓度与非禁食受试者相比无显著升高(p = 0.135)。空腹糖尿病患者和健康受试者在胰岛素敏感性和β细胞功能方面分别有显著改善(p = 0.03, 0.010)。结论在EOTC禁食中同时实行素食和能量限制可以改善体重管理。EOTC禁食改善了糖尿病患者和健康受试者的食欲激素活动,增加了胰岛素敏感性和β细胞功能(HOMA-IR)。EOTC禁食实践代表了一种有前途的,文化上接受的,糖尿病预防和管理的非药物策略。
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引用次数: 0
New era in obesity medication access: A commentary 肥胖症药物获取的新时代:评论
Pub Date : 2026-03-01 Epub Date: 2025-12-23 DOI: 10.1016/j.obpill.2025.100244
Harold Edward Bays
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引用次数: 0
Obesity medications and acquired hypothalamic obesity in adults: A two-case experience 成人的减肥药和获得性下丘脑肥胖:两例经验
Pub Date : 2026-03-01 Epub Date: 2026-01-07 DOI: 10.1016/j.obpill.2026.100246
Henry Lang , Madisen F. Dorand , Mahnooor Hassan , Jesse R. Richards

Background

Acquired hypothalamic obesity (HO) lacks well-described adult pharmacotherapy outcomes, creating a unique clinical challenge for providers tasked with the treatment of patients with hypothalamic obesity.

Methods

We conducted a retrospective chart review to evaluate clinical outcomes in two patients who developed hypothalamic obesity following treatment for tumors of the central nervous system. Medical records from the research center were systematically examined to identify individuals meeting criteria for acquired hypothalamic obesity, defined by significant weight gain associated with hypothalamic injury secondary to tumor therapy.

Results

Two individuals with acquired hypothalamic obesity were identified, both of whom achieved clinically significant weight loss taking tirzepatide with phentermine, and tirzepatide with phentermine/topiramate combination therapy. In case 1, the patient presented with cirrhosis, dyslipidemia, and transaminitis. Tirzepatide was initiated and escalated to 7.5 mg weekly, without weight response, prompting the addition of phentermine 8 mg daily. Dual therapy yielded 12.26 % weight loss over 7 months. In case 2, the patient presented with hypertension and obstructive sleep apnea (OSA). Tirzepatide 2.5 mg weekly combined with phentermine/topiramate was initiated. Tirzepatide was escalated to 5 mg, with phentermine/topiramate subsequently increased to 37.5/50 mg daily, producing 35.10 % weight loss over 11 months.

Conclusion

Tirzepatide-based combination therapy was associated with clinically meaningful weight loss and comorbidity improvement in adults with HO. These cases support further study of targeted, multimodal regimens in patients with acquired HO.
背景:获得性下丘脑肥胖(HO)缺乏明确的成人药物治疗结果,这给下丘脑肥胖患者的治疗工作带来了独特的临床挑战。方法回顾性分析2例中枢神经系统肿瘤治疗后出现下丘脑肥胖的患者的临床结果。研究中心的医疗记录被系统地检查,以确定符合获得性下丘脑肥胖标准的个体,下丘脑肥胖的定义是与肿瘤治疗继发的下丘脑损伤相关的显著体重增加。结果2例获得性下丘脑肥胖患者,均通过替西帕肽联合芬特明、替西帕肽联合芬特明/托吡酯治疗取得临床显著的体重减轻效果。在病例1中,患者表现为肝硬化、血脂异常和转氨炎。开始使用替西帕肽,并逐渐增加到每周7.5 mg,体重无反应,促使每天添加8 mg芬特明。双重治疗在7个月内体重减轻了12.26%。病例2患者表现为高血压和阻塞性睡眠呼吸暂停(OSA)。开始使用替西帕肽2.5 mg /周联合芬特明/托吡酯。替西帕肽增加到5mg,芬特明/托吡酯随后增加到37.5/ 50mg,在11个月内体重减轻35.10%。结论以替西帕肽为基础的联合治疗与成人HO患者临床意义的体重减轻和合并症改善相关。这些病例支持对获得性HO患者进行靶向、多模式治疗方案的进一步研究。
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引用次数: 0
Reporting the effectiveness of dietary intervention on weight loss outcomes in patients with obesity and overweight: a retrospective chart review at a Center of Excellence in UAE 报告饮食干预对肥胖和超重患者减肥结果的有效性:阿联酋卓越中心的回顾性图表回顾
Pub Date : 2026-03-01 Epub Date: 2025-12-05 DOI: 10.1016/j.obpill.2025.100241
Mona Joumaa , Madeeha Kalsekar , Momina Malik , Fatemeh Akbarpoor , Dana Abdelrahim , Sara El Ghandour

Background

A modest weight loss of ≥5 % among patients with obesity is associated with a reduced risk of type 2 diabetes, hypertension, and other obesity-related complications. Dietary interventions play a central role in obesity management and improving metabolic health, yet region-specific data from the United Arab Emirates (UAE) remains limited.

Methods

This retrospective chart review aims to assess effectiveness of dietary intervention on weight loss outcomes in patients with overweight and obesity attending a Center of Excellence for Weight Reduction and Obesity Management in UAE. This study included adult patients with BMI ≥25 kg/m2 who received individualized dietary counseling between September 2018 and September 2021. Patients who had undergone bariatric procedures or on obesity medications were excluded. Anthropometric and body composition data were collected before and after intervention. Outcomes included changes in weight, BMI, fat mass, visceral fat, and other metabolic parameters. Statistical analyses included paired t-tests, correlation coefficients, and multivariate regression to assess associations between intervention frequency, duration, and weight-related outcomes.

Results

A total of 266 patients (mean age 44.46 ± 8.18 years; 63.9 % female) were included. Following the intervention, participants achieved significant mean weight loss of 5.12 % (p < 0.001), with corresponding reductions in BMI (4.93 %, p < 0.001), fat mass (10.11 %, p < 0.001), and visceral fat (34.34 %, p = 0.014). More frequent sessions and longer follow-up durations were significantly associated with greater improvements in BMI, fat mass, and fat percentage. Gender-based analysis revealed that males experienced greater reductions in fat mass and resting energy expenditure compared to females.

Conclusion

The dietary intervention resulted in significant improvements in anthropometric and body composition indices. These findings support the efficacy of individualized, dietitian-led interventions in managing obesity. The observed gender differences highlight the importance of tailored approaches in obesity care. This study contributes to the limited body of evidence on effective, non-pharmacological obesity management strategies in UAE.
背景:肥胖患者适度体重减轻≥5%与2型糖尿病、高血压和其他肥胖相关并发症的风险降低相关。饮食干预在肥胖管理和改善代谢健康方面发挥着核心作用,但来自阿拉伯联合酋长国(UAE)的特定区域数据仍然有限。方法本回顾性图表综述旨在评估饮食干预对阿联酋减肥和肥胖管理卓越中心超重和肥胖患者减肥结果的有效性。该研究纳入了2018年9月至2021年9月期间接受个性化饮食咨询的BMI≥25 kg/m2的成年患者。接受过减肥手术或服用过减肥药物的患者被排除在外。在干预前后收集人体测量和身体成分数据。结果包括体重、BMI、脂肪量、内脏脂肪和其他代谢参数的变化。统计分析包括配对t检验、相关系数和多变量回归,以评估干预频率、持续时间和体重相关结果之间的关联。结果共纳入266例患者,平均年龄44.46±8.18岁,女性占63.9%。干预后,参与者平均体重显著减轻5.12% (p < 0.001), BMI (4.93%, p < 0.001)、脂肪量(10.11%,p < 0.001)和内脏脂肪(34.34%,p = 0.014)也相应减少。更频繁的治疗和更长的随访时间与BMI、脂肪量和脂肪百分比的改善显著相关。基于性别的分析显示,与女性相比,男性在脂肪量和静息能量消耗方面的减少幅度更大。结论饮食干预可显著改善患者的人体测量指标和体成分指标。这些发现支持了个性化、营养师主导的干预措施在控制肥胖方面的有效性。观察到的性别差异突出了肥胖治疗中量身定制方法的重要性。这项研究为阿联酋有效的非药物肥胖管理策略提供了有限的证据。
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引用次数: 0
Clinical review of how glucagon-like peptide-1 agonist obesity medications decrease sexual desire, and a biopsychosocial model for why we don’t ‘see’ it 胰高血糖素样肽-1激动剂减肥药物如何降低性欲的临床回顾,以及为什么我们没有“看到”它的生物心理社会模型
Pub Date : 2026-03-01 Epub Date: 2025-11-20 DOI: 10.1016/j.obpill.2025.100233
Sonya T. Gelfand , Meghan C. Tveit , James A. Simon

Background

While prevailing assumptions suggest that improved body image and erectile function, even in people with diabetes, associated with glucagon-like peptide-1 (GLP-1) agonist medications would correlate with heightened sexual function, there is limited literature on the effects of GLP-1 agonists on hedonistic pleasures such as sexual activity. In this paper, we aim to elucidate the potential implications of GLP-1 agonists on sexual desire by proposing a serotonergic mechanism by which GLP-1 agonists theoretically decrease sexual desire, and a biopsychosocial perspective on why this effect may be camouflaged by competing influences.

Methods

This was a narrative review analysis with target literature search. A PubMed search was conducted to identify systematic reviews or meta-analyses investigating the effects of GLP-1 agonists on physiological and lifestyle factors. We used the same methodology to investigate the connection between GLP-1 agonism and the brain’s reward pathways to elucidate whether a connection exists between GLP-1 agonism and sexual desire.

Results

We established a theoretical model for how GLP-1 agonist modulation via increased serotonergic activity at the 5-HT2C receptor may result in diminished sexual desire. We then applied a biopsychosocial framework to highlight why this effect may be overlooked by GLP-1-treated patients and clinicians. Although the serotonergic pathway may create a physiological decrease in sexual desire for patients taking GLP-1 agonists, we postulate that this diminishing influence of GLP-1 agonism is both compounded by factors such as undesirable side effects and increased SHBG and offset by the enhancing influences on sexual desire such as increased total testosterone, and improved vascular reactivity and mood.

Conclusion

Failing to systematically measure and report on sexual desire as a potential adverse outcome of GLP-1 agonist use overlooks an essential aspect of patient well-being. Future research should prioritize longitudinal studies to assess changes in sexual desire among individuals prescribed GLP-1 agonists.
虽然普遍的假设认为,改善身体形象和勃起功能,甚至在糖尿病患者中,与胰高血糖素样肽-1 (GLP-1)激动剂药物可能与提高性功能有关,但关于GLP-1激动剂对性活动等享乐主义快感的影响的文献有限。在本文中,我们旨在阐明GLP-1激动剂对性欲的潜在影响,提出GLP-1激动剂理论上降低性欲的5 -羟色胺能机制,并从生物心理社会角度解释为什么这种作用可能被竞争影响掩盖。方法采用目标文献检索的叙事回顾分析法。PubMed检索进行了系统评价或荟萃分析,调查GLP-1激动剂对生理和生活方式因素的影响。我们使用相同的方法来研究GLP-1激动作用与大脑奖赏通路之间的联系,以阐明GLP-1激动作用与性欲之间是否存在联系。结果我们建立了GLP-1激动剂如何通过增加5-HT2C受体的血清素能活性来调节可能导致性欲减退的理论模型。然后,我们应用生物心理社会框架来强调为什么glp -1治疗的患者和临床医生可能会忽视这种影响。尽管5 -羟色胺能途径可能会使服用GLP-1激动剂的患者产生生理上的性欲下降,但我们假设GLP-1激动剂的这种减弱影响既会因不良副作用和SHBG增加等因素而加剧,也会因总睾酮增加、血管反应性和情绪改善等对性欲的增强影响而抵消。未能系统地测量和报告作为GLP-1激动剂使用的潜在不良后果的性欲,忽视了患者健康的一个重要方面。未来的研究应优先考虑纵向研究,以评估服用GLP-1激动剂的个体的性欲变化。
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引用次数: 0
Nutritional and lifestyle supportive care recommendations for management of obesity with GLP-1 - based therapies: An expert consensus statement using a modified Delphi approach 以GLP-1为基础的治疗方法管理肥胖的营养和生活方式支持护理建议:使用改进的德尔菲方法的专家共识声明
Pub Date : 2026-03-01 Epub Date: 2025-11-11 DOI: 10.1016/j.obpill.2025.100228
J.L. Sievenpiper , J. Ard , M. Blüher , W. Chen , J.B. Dixon , A. Fitch , L. Gigliotti , K. Khunti , A. Lecube , M.E.J. Lean , B. Mittendorfer , A.F.H. Pfeiffer , D.H. Ryan , T. Vilsbøll , L.F. Van Gaal

Background

Liraglutide, semaglutide and tirzepatide have transformed the management of obesity. However, dose-related gastrointestinal effects, obesity-associated nutritional insufficiencies, and poor long-term adherence may limit their long-term health benefits. Despite a recent joint advisory summarizing nutritional and lifestyle supportive care priorities with these therapies, there is still a significant lack of direct evidence to guide clinical practice, making consensus-based recommendations necessary.

Methods

The consensus statement development was based on an initial scoping review that included searching PubMed, Embase, Web of Science, Cochrane, and Medline for relevant scientific publications from January 1, 2021 through June 30, 2025. An international multidisciplinary panel consisting of physicians, clinical researchers, and dietitians employed a modified Delphi process to develop clinical practice recommendations for nutritional and lifestyle strategies that may assist people on glucagon-like peptide 1 based therapies (GBT) in optimizing treatment experience and improving health outcomes.

Results

A total of 52 consensus statements were developed, outlining key considerations for the practical management of obesity and associated complications with GBTs, with a focus on nutritional factors in relation to obesity, body composition, physical activity, and the management of common gastrointestinal symptoms such as nausea, vomiting, diarrhoea, and constipation. The consensus statements include practical strategies supporting the weight loss journey, from before starting a GBT, during the weight loss and weight maintenance phases, and in case of GBT discontinuation. The statements were primarily derived from indirect evidence, including from existing evidence and established guidelines for nutrition therapy in bariatric medicine and relevant clinical experience.

Conclusions

These expert consensus recommendations offer healthcare professionals practical guidance on nutritional and lifestyle interventions for patients undergoing GBT-related weight management, complementing current recommendations. Further direct evidence is urgently required to inform and enhance optimal clinical care.
利拉鲁肽、西马鲁肽和替西帕肽已经改变了肥胖的治疗方法。然而,剂量相关的胃肠道效应、肥胖相关的营养不足和长期依从性差可能会限制它们的长期健康益处。尽管最近的一项联合咨询总结了这些疗法的营养和生活方式支持护理的优先事项,但仍然明显缺乏指导临床实践的直接证据,因此有必要提出基于共识的建议。方法共识声明的制定是基于初步的范围审查,包括检索PubMed、Embase、Web of Science、Cochrane和Medline从2021年1月1日至2025年6月30日的相关科学出版物。一个由医生、临床研究人员和营养师组成的国际多学科小组采用改进的德尔菲过程来制定营养和生活方式策略的临床实践建议,这些建议可能有助于胰高血糖素样肽1基础疗法(GBT)患者优化治疗体验和改善健康结果。结果共制定了52项共识声明,概述了肥胖及GBTs相关并发症实际管理的关键考虑因素,重点关注与肥胖、身体组成、身体活动相关的营养因素,以及恶心、呕吐、腹泻和便秘等常见胃肠道症状的管理。共识声明包括支持减肥之旅的实用策略,从开始GBT之前,在减肥和体重维持阶段,以及在GBT停止的情况下。这些陈述主要来自间接证据,包括现有证据和减肥医学中营养治疗的既定指南以及相关的临床经验。结论这些专家共识建议为gbbt相关体重管理患者的营养和生活方式干预提供了实用指导,是对现有建议的补充。迫切需要进一步的直接证据来告知和加强最佳临床护理。
{"title":"Nutritional and lifestyle supportive care recommendations for management of obesity with GLP-1 - based therapies: An expert consensus statement using a modified Delphi approach","authors":"J.L. Sievenpiper ,&nbsp;J. Ard ,&nbsp;M. Blüher ,&nbsp;W. Chen ,&nbsp;J.B. Dixon ,&nbsp;A. Fitch ,&nbsp;L. Gigliotti ,&nbsp;K. Khunti ,&nbsp;A. Lecube ,&nbsp;M.E.J. Lean ,&nbsp;B. Mittendorfer ,&nbsp;A.F.H. Pfeiffer ,&nbsp;D.H. Ryan ,&nbsp;T. Vilsbøll ,&nbsp;L.F. Van Gaal","doi":"10.1016/j.obpill.2025.100228","DOIUrl":"10.1016/j.obpill.2025.100228","url":null,"abstract":"<div><h3>Background</h3><div>Liraglutide, semaglutide and tirzepatide have transformed the management of obesity. However, dose-related gastrointestinal effects, obesity-associated nutritional insufficiencies, and poor long-term adherence may limit their long-term health benefits. Despite a recent joint advisory summarizing nutritional and lifestyle supportive care priorities with these therapies, there is still a significant lack of direct evidence to guide clinical practice, making consensus-based recommendations necessary.</div></div><div><h3>Methods</h3><div>The consensus statement development was based on an initial scoping review that included searching PubMed, Embase, Web of Science, Cochrane, and Medline for relevant scientific publications from January 1, 2021 through June 30, 2025. An international multidisciplinary panel consisting of physicians, clinical researchers, and dietitians employed a modified Delphi process to develop clinical practice recommendations for nutritional and lifestyle strategies that may assist people on glucagon-like peptide 1 based therapies (GBT) in optimizing treatment experience and improving health outcomes.</div></div><div><h3>Results</h3><div>A total of 52 consensus statements were developed, outlining key considerations for the practical management of obesity and associated complications with GBTs, with a focus on nutritional factors in relation to obesity, body composition, physical activity, and the management of common gastrointestinal symptoms such as nausea, vomiting, diarrhoea, and constipation. The consensus statements include practical strategies supporting the weight loss journey, from before starting a GBT, during the weight loss and weight maintenance phases, and in case of GBT discontinuation. The statements were primarily derived from indirect evidence, including from existing evidence and established guidelines for nutrition therapy in bariatric medicine and relevant clinical experience.</div></div><div><h3>Conclusions</h3><div>These expert consensus recommendations offer healthcare professionals practical guidance on nutritional and lifestyle interventions for patients undergoing GBT-related weight management, complementing current recommendations. Further direct evidence is urgently required to inform and enhance optimal clinical care.</div></div>","PeriodicalId":100977,"journal":{"name":"Obesity Pillars","volume":"17 ","pages":"Article 100228"},"PeriodicalIF":0.0,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145799725","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Logistics, effectiveness, safety, and accessibility: Factors determining obesity medication patient preferences from a photovoice analysis 物流,有效性,安全性和可及性:从光声分析中决定肥胖药物患者偏好的因素
Pub Date : 2026-03-01 Epub Date: 2025-11-27 DOI: 10.1016/j.obpill.2025.100238
Alvin Mondoh , Francisca Contreras , Hilary Craig , Michael Crotty , Carel W. le Roux

Background

Obesity is a chronic, relapsing, and multifactorial disease that necessitates sustained, patient-centred management. Although pharmacotherapy is now an integral component of obesity care, there is limited evidence regarding the factors influencing patients’ choices among specific medications. As part of the Innovative Medicines Initiative 2 (IMI2) programme. Stratification of Obesity Phenotypes to Optimize Future Obesity Therapy (SOPHIA) and the second phase of a three-part qualitative doctoral programme, the present study is built upon previous interview findings that examined how patients conceptualize and interpret the factors shaping their pharmacotherapy preferences.

Methods

A qualitative Photovoice methodology was employed with treatment naive adults attending a specialist weight management clinic. Participants captured photographs reflecting factors shaping their medication choices and they also engaged in facilitated reflective interviews. Data was analysed using the MAXQDA 2024 software and the Braun and Clarke's framework for reflexive thematic analysis.

Results

The photovoice analysis revealed 4 themes around patient preferences for obesity medications including a) Logistics around Lifestyle, b) Effectiveness, c) Safety, risk and tolerability and d) Accessibility.

Conclusion

Patient preferences for obesity pharmacotherapy arise from the interaction of efficacy expectations with logistical challenged, while concerns regarding safety and accessibility also contribute to decision making. Clinicians should include explanations how the medications can fit into the lifestyle of patients, while also addressing structural barriers that may affect access to treatment, but ultimately allowing patients to understand the balance between efficacy and safety will allow optimal shared decision-making to support sustainable pharmacotherapy pathways.
背景:肥胖是一种慢性、复发性和多因素疾病,需要持续的、以患者为中心的管理。虽然药物治疗现在是肥胖治疗的一个组成部分,但关于影响患者选择特定药物的因素的证据有限。作为创新药物倡议2 (IMI2)规划的一部分。肥胖表型分层以优化未来肥胖治疗(SOPHIA)和一个由三部分组成的定性博士课程的第二阶段,本研究建立在之前的访谈结果的基础上,调查了患者如何概念化和解释影响其药物治疗偏好的因素。方法采用定性光声法对在某体重管理专科诊所就诊的初诊成人进行治疗。参与者拍摄的照片反映了影响他们药物选择的因素,他们还参与了便利的反思性访谈。数据分析使用MAXQDA 2024软件和Braun和Clarke的反思性主题分析框架。结果光声分析揭示了患者对减肥药偏好的4个主题,包括a)围绕生活方式的物流,b)有效性,c)安全性,风险和耐受性以及d)可及性。结论患者对肥胖药物治疗的偏好源于对疗效的期望与后勤挑战的相互作用,而对安全性和可及性的关注也有助于决策。临床医生应该解释药物如何适应患者的生活方式,同时也要解决可能影响治疗的结构性障碍,但最终让患者了解疗效和安全性之间的平衡,从而实现最佳的共同决策,以支持可持续的药物治疗途径。
{"title":"Logistics, effectiveness, safety, and accessibility: Factors determining obesity medication patient preferences from a photovoice analysis","authors":"Alvin Mondoh ,&nbsp;Francisca Contreras ,&nbsp;Hilary Craig ,&nbsp;Michael Crotty ,&nbsp;Carel W. le Roux","doi":"10.1016/j.obpill.2025.100238","DOIUrl":"10.1016/j.obpill.2025.100238","url":null,"abstract":"<div><h3>Background</h3><div>Obesity is a chronic, relapsing, and multifactorial disease that necessitates sustained, patient-centred management. Although pharmacotherapy is now an integral component of obesity care, there is limited evidence regarding the factors influencing patients’ choices among specific medications. As part of the Innovative Medicines Initiative 2 (IMI2) programme. Stratification of Obesity Phenotypes to Optimize Future Obesity Therapy (SOPHIA) and the second phase of a three-part qualitative doctoral programme, the present study is built upon previous interview findings that examined how patients conceptualize and interpret the factors shaping their pharmacotherapy preferences.</div></div><div><h3>Methods</h3><div>A qualitative Photovoice methodology was employed with treatment naive adults attending a specialist weight management clinic. Participants captured photographs reflecting factors shaping their medication choices and they also engaged in facilitated reflective interviews. Data was analysed using the MAXQDA 2024 software and the Braun and Clarke's framework for reflexive thematic analysis.</div></div><div><h3>Results</h3><div>The photovoice analysis revealed 4 themes around patient preferences for obesity medications including a) Logistics around Lifestyle, b) Effectiveness, c) Safety, risk and tolerability and d) Accessibility.</div></div><div><h3>Conclusion</h3><div>Patient preferences for obesity pharmacotherapy arise from the interaction of efficacy expectations with logistical challenged, while concerns regarding safety and accessibility also contribute to decision making. Clinicians should include explanations how the medications can fit into the lifestyle of patients, while also addressing structural barriers that may affect access to treatment, but ultimately allowing patients to understand the balance between efficacy and safety will allow optimal shared decision-making to support sustainable pharmacotherapy pathways.</div></div>","PeriodicalId":100977,"journal":{"name":"Obesity Pillars","volume":"17 ","pages":"Article 100238"},"PeriodicalIF":0.0,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145694478","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Improving nutritional assessment in GLP-1RA therapy: Beyond self-reports to equitable interventions 改善GLP-1RA治疗中的营养评估:超越自我报告到公平干预
Pub Date : 2025-12-01 Epub Date: 2025-09-30 DOI: 10.1016/j.obpill.2025.100213
Parth Aphale, Himanshu Shekhar, Shashank Dokania
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引用次数: 0
期刊
Obesity Pillars
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