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School-Provided Meals and the Prevention of Childhood Obesity: A Small part of a Very Important Story. 学校提供的膳食和预防儿童肥胖:一个非常重要的故事的一小部分。
IF 9.5 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Pub Date : 2025-05-15 DOI: 10.1007/s13679-025-00635-x
Danielle Gallegos, Alexandra Manson, Helen Anna Vidgen, Rebecca Byrne, Brittany J Johnson

Purpose of review: To present the evidence base in support of high-income country investment in universal school-provided meals (SPMs) for the purposes of optimising child health and wellbeing, including obesity prevention.

Recent findings: Many countries provide some form of SPMs. Models (universal, free; targeted; subsidised) vary globally, however optimal growth and development of children as a potential outcome is a consistent feature. SPMs can positively impact diet quality, household food and nutrition security and potentially weight status but is dependent on the model. Universal school meals offered as part of whole-of-school approaches appear to be most effective in optimising children's growth and development. Critical elements for successful SPMs include being underpinned by enforceable nutrition and sustainability standards, offered in ways that are stigma-free, being embedded within a whole-school approach and conceptualising SPMS as part of transformative food systems. Weight status is only one of many potential outcomes of SPMs. Implementing universal SPMs is a triple duty action that can address the global syndemic of obesity, undernutrition and climate change. Attention needs to be paid to the model of implementation and key principles for success.

综述目的:提供证据基础,支持高收入国家投资于学校普遍供餐(SPMs),以优化儿童健康和福祉,包括预防肥胖。最近的发现:许多国家提供某种形式的SPMs。型号(通用、免费;目标;补贴)在全球各不相同,但儿童的最佳生长和发展作为潜在结果是一个一致的特征。SPMs可以对饮食质量、家庭食品和营养安全以及潜在的体重状况产生积极影响,但这取决于模型。作为整个学校方法的一部分,提供普遍的学校膳食似乎在优化儿童的生长和发展方面最有效。成功的SPMs的关键要素包括以可执行的营养和可持续性标准为基础,以无污名的方式提供,融入全校的方法,并将SPMs概念化为变革食品系统的一部分。体重状况只是SPMs的许多潜在结果之一。实施普遍的特别措施是一项三重责任行动,可以解决肥胖、营养不良和气候变化等全球问题。需要注意执行模式和成功的关键原则。
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引用次数: 0
Autolysosomal Dysfunction in Obesity-induced Metabolic Inflammation and Related Disorders. 肥胖引起的代谢性炎症及相关疾病的自溶酶体功能障碍。
IF 9.5 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Pub Date : 2025-05-14 DOI: 10.1007/s13679-025-00638-8
Lenny Yi Tong Cheong, Eka Norfaishanty Saipuljumri, Gavin Wen Zhao Loi, Jialiu Zeng, Chih Hung Lo

Purpose of review: Obesity is a global health crisis affecting individuals across all age groups, significantly increasing the risk of metabolic disorders such as type 2 diabetes (T2D), metabolic dysfunction-associated fatty liver disease (MAFLD), and cardiovascular diseases. The World Health Organization reported in 2022 that 2.5 billion adults were overweight, with 890 million classified as obese, emphasizing the urgent need for effective interventions. A critical aspect of obesity's pathophysiology is meta-inflammation-a chronic, systemic low-grade inflammatory state driven by excess adipose tissue, which disrupts metabolic homeostasis. This review examines the role of autolysosomal dysfunction in obesity-related metabolic disorders, exploring its impact across multiple metabolic organs and evaluating potential therapeutic strategies that target autophagy and lysosomal function.

Recent findings: Emerging research highlights the importance of autophagy in maintaining cellular homeostasis and metabolic balance. Obesity-induced lysosomal dysfunction impairs the autophagic degradation process, contributing to the accumulation of damaged organelles and toxic aggregates, exacerbating insulin resistance, lipotoxicity, and chronic inflammation. Studies have identified autophagic defects in key metabolic tissues, including adipose tissue, skeletal muscle, liver, pancreas, kidney, heart, and brain, linking autophagy dysregulation to the progression of metabolic diseases. Preclinical investigations suggest that pharmacological and nutritional interventions-such as AMPK activation, caloric restriction mimetics, and lysosomal-targeting compounds-can restore autophagic function and improve metabolic outcomes in obesity models. Autolysosomal dysfunction is a pivotal contributor to obesity-associated metabolic disorders , influencing systemic inflammation and metabolic dysfunction. Restoring autophagy and lysosomal function holds promise as a therapeutic strategy to mitigate obesity-driven pathologies. Future research should focus on translating these findings into clinical applications, optimizing targeted interventions to improve metabolic health and reduce obesity-associated complications.

综述目的:肥胖是影响所有年龄组个体的全球性健康危机,显著增加代谢性疾病的风险,如2型糖尿病(T2D)、代谢功能障碍相关脂肪性肝病(MAFLD)和心血管疾病。世界卫生组织在2022年报告称,有25亿成年人超重,其中8.9亿人被列为肥胖,强调迫切需要采取有效干预措施。肥胖病理生理学的一个关键方面是炎症-一种由过量脂肪组织驱动的慢性、全身性低级别炎症状态,它破坏了代谢稳态。本文综述了自噬酶体功能障碍在肥胖相关代谢疾病中的作用,探讨了其在多个代谢器官中的影响,并评估了针对自噬和溶酶体功能的潜在治疗策略。最新发现:新兴研究强调了自噬在维持细胞稳态和代谢平衡中的重要性。肥胖诱导的溶酶体功能障碍会损害自噬降解过程,导致受损细胞器和毒性聚集体的积累,加剧胰岛素抵抗、脂肪毒性和慢性炎症。研究已经确定了关键代谢组织中的自噬缺陷,包括脂肪组织、骨骼肌、肝脏、胰腺、肾脏、心脏和大脑,将自噬失调与代谢性疾病的进展联系起来。临床前研究表明,药物和营养干预-如AMPK激活,热量限制模拟物和溶酶体靶向化合物-可以恢复肥胖模型的自噬功能并改善代谢结果。自溶酶体功能障碍是肥胖相关代谢障碍的关键因素,影响全身炎症和代谢功能障碍。恢复自噬和溶酶体功能有望作为减轻肥胖驱动病理的治疗策略。未来的研究应侧重于将这些发现转化为临床应用,优化有针对性的干预措施,以改善代谢健康,减少肥胖相关并发症。
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引用次数: 0
Medical Nutrition Therapy in Dermatological Diseases: A Joint Consensus Statement of the Italian Association of Dietetics and Clinical Nutrition (ADI), the Italian Society of Dermatology and Sexually Transmitted Diseases (SIDeMaST), the Italian Society of Nutraceuticals (SINut), Club Ketodiets and Nutraceuticals "KetoNut-SINut" and the Italian Society of Endocrinology (SIE), Club Nutrition, Hormones and Metabolism. 皮肤病的医学营养治疗:意大利营养学和临床营养协会(ADI)、意大利皮肤病和性传播疾病学会(SIDeMaST)、意大利营养保健品学会(SINut)、酮症饮食和营养保健品俱乐部(KetoNut-SINut)、意大利内分泌学会(SIE)、营养、激素和代谢学会(SIE)联合共识声明。
IF 11 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Pub Date : 2025-05-13 DOI: 10.1007/s13679-025-00630-2
Luigi Barrea, Ludovica Verde, Giuseppe Annunziata, Emiliano Antiga, Elisabetta Camajani, Massimiliano Caprio, Maria Grazia Carbonelli, Augusto Carducci, Edda Cava, Giorgia Di Marco, Davide Grassi, Stefania Guida, Barbara Martinelli, Angelo Valerio Marzano, Chiara Moltrasio, Massimiliano Petrelli, Francesca Prignano, Franco Rongioletti, Silvia Savastano, Barbara Paolini, Carmela Bagnato, Giuseppe Argenziano, Arrigo Francesco Giuseppe Cicero, Annamaria Colao, Diego Ferone, Gianluca Aimaretti, Giovanna Muscogiuri

Dermatological diseases such as acne, hidradenitis suppurativa (HS), and psoriasis are driven by chronic inflammation and oxidative stress. Emerging evidence highlights the role of nutrition in modulating these conditions, particularly through dietary patterns rich in antioxidants, polyphenols, and unsaturated fatty acids. RECENT FINDINGS: The Mediterranean diet (MedDiet) has demonstrated potential benefits due to its anti-inflammatory and immunomodulatory effects, while very low-energy ketogenic therapy (VLEKT) has shown promise in rapidly improving disease severity. Specific nutrients, including omega-3 fatty acids, probiotics, and micronutrients, may further contribute to disease management. However, the current literature is limited by small-scale studies and the lack of standardized dietary guidelines. PURPOSE OF REVIEW: This Consensus Statement, developed collaboratively by the Italian Association of Dietetics and Clinical Nutrition (ADI), the Italian Society of Dermatology and Sexually Transmitted Diseases (SIDeMaST), the Italian Society of Nutraceuticals (SINut), Club Ketodiets and Nutraceuticals "KetoNut-SINut" and the Italian Society of Endocrinology (SIE), Club Nutrition, Hormones and Metabolism, aimed to establish an evidence-based framework for medical nutrition therapy (MNT) of the most common inflammatory skin diseases, including acne, HS and psoriasis.

痤疮、化脓性汗腺炎(HS)和牛皮癣等皮肤病是由慢性炎症和氧化应激引起的。新出现的证据强调了营养在调节这些疾病中的作用,特别是通过富含抗氧化剂、多酚和不饱和脂肪酸的饮食模式。最近的研究发现:地中海饮食(MedDiet)由于其抗炎和免疫调节作用而显示出潜在的益处,而极低能量生酮疗法(VLEKT)在快速改善疾病严重程度方面显示出希望。特定营养素,包括omega-3脂肪酸、益生菌和微量营养素,可能进一步有助于疾病管理。然而,目前的文献受到小规模研究和缺乏标准化饮食指南的限制。审核目的:本共识声明由意大利营养与临床营养协会(ADI)、意大利皮肤病与性传播疾病学会(SIDeMaST)、意大利营养保健品学会(SINut)、意大利酮饮食与营养保健品学会(KetoNut-SINut)、意大利内分泌学会(SIE)、营养、激素与代谢学会(Club Nutrition, hormone and Metabolism)共同制定。旨在为最常见的炎症性皮肤病(包括痤疮、HS和牛皮癣)的医学营养治疗(MNT)建立循证框架。
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引用次数: 0
Acceptance and Commitment Therapy for Obesity. 肥胖的接受与承诺疗法。
IF 9.5 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Pub Date : 2025-05-10 DOI: 10.1007/s13679-025-00634-y
Leah M Schumacher, Nicole Miller, Emma L Jennings, Reena Chabria, Meghan L Butryn

Purpose of review: To describe the recent literature on acceptance and commitment therapy (ACT) interventions for individuals with obesity. The review begins with a brief overview of the ACT model, describes seminal work in this area, and examines more recent literature on the use of ACT to improve outcomes among individuals with obesity.

Recent findings: Early trials established ACT's efficacy for weight loss among adults with obesity. More recent research has focused on testing efficacy among adolescents, measuring effects in "real world" settings, refining interventions to optimize outcomes and enhance scalability, and examining outcomes beyond weight (e.g., internalized weight stigma, eating regulation). Current data indicate that ACT-based interventions produce comparable, or, in some cases, superior weight loss compared to standard behavioral interventions. ACT has also shown promise for improving other outcomes of interest. ACT may improve a variety of obesity-related outcomes, although additional research is needed.

回顾的目的:描述最近关于接受和承诺治疗(ACT)干预肥胖个体的文献。本文首先简要概述了ACT模型,描述了该领域的开创性工作,并检查了最近关于使用ACT改善肥胖个体预后的文献。近期发现:早期试验证实ACT对肥胖成人减肥有效。最近的研究集中在测试青少年的有效性,测量“现实世界”环境中的效果,改进干预措施以优化结果并增强可扩展性,以及检查体重以外的结果(例如,内化的体重耻辱,饮食调节)。目前的数据表明,与标准行为干预相比,基于act的干预产生了相当的体重减轻,或者在某些情况下,效果更好。ACT也显示出改善其他相关结果的希望。ACT可以改善多种与肥胖相关的结果,尽管还需要进一步的研究。
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引用次数: 0
Cannabis, Weight, and Weight-Related Behaviors. 大麻、体重和与体重相关的行为。
IF 9.5 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Pub Date : 2025-05-08 DOI: 10.1007/s13679-025-00633-z
Kasey P S Goodpaster

Purpose of review: Review recent research regarding the relationship between cannabis use, weight, eating behaviors, eating disorders, and physical activity.

Recent findings: Cannabis, particularly the cannabinoid Δ9-tegrahydrocannabinol (THC), is associated with increased appetite, food cravings, overconsumption, and decreased physical activity. Cannabidiol (CBD) appears to be associated with decreased appetite. While cannabis use is not correlated with binge eating, cannabis use disorder is associated with loss of control eating. Despite cannabis' association with unhealthy eating and sedentary behavior, most studies suggest that cannabis use is not associated with weight gain, or may even facilitate weight loss. The state of the literature regarding the relationship between cannabis, weight, and weight-related behaviors is complex. Most studies do not differentiate between cannabinoid profiles, routes of administration, or whether cannabis use is problematic. Patients presenting for weight management should be cautioned about cannabis, particularly THC, potentially increasing risk of unhealthy eating and activity patterns.

综述目的:综述最近关于大麻使用、体重、饮食行为、饮食失调和身体活动之间关系的研究。最近的研究发现:大麻,特别是大麻素Δ9-tegrahydrocannabinol (THC),与食欲增加、对食物的渴望、过度消费和身体活动减少有关。大麻二酚(CBD)似乎与食欲下降有关。虽然大麻使用与暴饮暴食无关,但大麻使用障碍与饮食失控有关。尽管大麻与不健康的饮食和久坐不动的行为有关,但大多数研究表明,使用大麻与体重增加无关,甚至可能有助于减肥。关于大麻、体重和体重相关行为之间关系的文献状况是复杂的。大多数研究没有区分大麻素概况,给药途径,或者大麻使用是否有问题。要求控制体重的患者应谨慎使用大麻,特别是四氢大麻酚,这可能会增加不健康饮食和活动模式的风险。
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引用次数: 0
What is the Role of Primary Prevention of Obesity in an Age of Effective Pharmaceuticals? 在一个有效药物的时代,初级预防肥胖的作用是什么?
IF 9.5 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Pub Date : 2025-05-07 DOI: 10.1007/s13679-025-00632-0
María Gómez-Martín, Oliver J Canfell, Li Kheng Chai, Anna K Jansson, Robyn Littlewood, Clair Sullivan, Dawn Power, Erin D Clarke, Louisa Ells, Nienke De Vlieger, Tracy L Burrows, Clare E Collins

Purpose of review: To examine the evidence and continuing role of strategies for the primary prevention and treatment of obesity in the context of effective obesity pharmacotherapies, through a narrative review.

Recent findings: Global policies to improve nutritional labelling and reduce sugar-sweetened beverages consumption have been implemented worldwide (> 45 countries) with some success which varies by population and environment. Tailored behavioural interventions are effective and essential to reduce individual risk of progression from preclinical to clinical obesity. Pharmacotherapies are powerful treatment agents for clinical obesity but must consider nutritional and metabolic risks of use and discontinuation. The obesogenic environment continues to undermine individual agency to adopt healthier dietary and physical activity patterns. Population health informatics tools could inform tailored interventions based on real-time risk and contribute to obesity prevention and treatment. Efforts to rebalance investment towards obesity prevention must continue to improve population health and reduce healthcare burden.

综述目的:通过一篇叙述性综述,探讨在有效的肥胖药物治疗背景下,肥胖症初级预防和治疗策略的证据和持续作用。最近的发现:改善营养标签和减少含糖饮料消费的全球政策已在世界范围内实施(bbbb45个国家),并取得了一些成功,但因人口和环境而异。量身定制的行为干预对于降低个体从临床前肥胖发展到临床肥胖的风险是有效和必要的。药物治疗是临床肥胖的有力治疗手段,但必须考虑使用和停药的营养和代谢风险。致肥环境继续破坏个体机构采取更健康的饮食和体育活动模式。人口健康信息学工具可以根据实时风险为量身定制的干预措施提供信息,并有助于预防和治疗肥胖。重新平衡投资以预防肥胖的努力必须继续改善人口健康并减轻医疗保健负担。
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引用次数: 0
The Interplay of UCP3 and PCSK1 Variants in Severe Obesity. UCP3和PCSK1变异在重度肥胖中的相互作用
IF 9.5 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Pub Date : 2025-04-26 DOI: 10.1007/s13679-025-00631-1
Ludovica Verde, Martina Galasso, Dawn K Coletta, Silvia Savastano, Lawrence J Mandarino, Annamaria Colao, Luigi Barrea, Giovanna Muscogiuri

Obesity is a heterogeneous and multifactorial disease with a strong genetic component. While polygenic obesity accounts for most common cases, rare monogenic variants contribute, particularly in severe, early-onset obesity. Among the lesser-studied candidates are UCP3 and PCSK1, genes involved in key metabolic pathways. RECENT FINDINGS: The UCP3 p.Val192Ile (c.574G > A) and PCSK1 p.Asn221Asp (c.661 A > G) variants have been independently associated with metabolic pathways, including fatty acid oxidation and hormone processing, as well as a modestly increased risk of obesity. Clinical and genetic characterization of two patients with severe early-onset obesity revealed the co-occurrence of these variants, which were associated with metabolic disturbances such as insulin resistance. PURPOSE OF THE REVIEW: This narrative review examined the functional and clinical significance of UCP3 and PCSK1 variants in severe obesity, presenting two case reports to illustrate their potential impact. Our findings support a potential model in which rare variants in distinct metabolic genes may interact synergistically to exacerbate disease severity. Further studies are needed to elucidate their combined functional effects and contributions to obesity pathogenesis.

肥胖是一种异质性和多因素的疾病,具有很强的遗传成分。虽然多基因肥胖是最常见的病例,但罕见的单基因变异也是原因之一,尤其是在严重的早发性肥胖中。研究较少的候选基因包括UCP3和PCSK1,它们参与关键的代谢途径。最近的研究发现:UCP3 p.v all192ile (c.574G > A)和PCSK1 p.v asn221asp (c.661 A)A > G)变异与代谢途径独立相关,包括脂肪酸氧化和激素加工,以及适度增加肥胖风险。两名严重早发性肥胖患者的临床和遗传特征揭示了这些变异的共同发生,这些变异与胰岛素抵抗等代谢紊乱有关。综述的目的:这篇叙述性综述研究了UCP3和PCSK1变异在严重肥胖中的功能和临床意义,并提出了两个病例报告来说明它们的潜在影响。我们的发现支持了一种潜在的模型,即不同代谢基因的罕见变异可能协同作用,加剧疾病的严重程度。需要进一步的研究来阐明它们的综合功能作用和在肥胖发病中的作用。
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引用次数: 0
When Weight Matters: How Obesity Impacts Reproductive Health and Pregnancy-A Systematic Review. 当体重问题:肥胖如何影响生殖健康和怀孕-系统综述。
IF 11 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Pub Date : 2025-04-16 DOI: 10.1007/s13679-025-00629-9
Konstantina Barbouni, Vaidas Jotautis, Dimitra Metallinou, Athina Diamanti, Eirini Orovou, Alina Liepinaitienė, Petros Nikolaidis, Grigorios Karampas, Antigoni Sarantaki

Purpose of review: This systematic review evaluates the impact of obesity on both male and female reproductive health, assisted reproductive technology (ART) outcomes, and pregnancy-related complications, providing a comprehensive synthesis of the evidence.

Recent findings: Obesity is a critical factor adversely affecting reproductive health, ART success rates, and pregnancy outcomes. Recent studies indicate hormonal disruptions, metabolic syndrome, and epigenetic modifications as central mechanisms linking obesity to infertility and adverse pregnancy results. A systematic search adhering to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines included 35 studies, focusing on obesity-related reproductive outcomes. The review highlights that obesity disrupts hormonal balance, including reductions in sex hormone-binding globulin (SHBG) and testosterone levels, alongside increased insulin resistance and chronic inflammation. These mechanisms impair ovarian function, endometrial receptivity, and sperm quality, resulting in prolonged time-to-pregnancy (TTP), reduced ART success rates, and increased miscarriage risk. During pregnancy, maternal obesity elevates risks of gestational diabetes mellitus (GDM), preeclampsia, and cesarean delivery while contributing to neonatal complications, such as macrosomia and neonatal intensive care unit (NICU) admissions. The findings emphasize the dual impact of maternal and paternal obesity on offspring health, particularly through epigenetic modifications leading to intergenerational metabolic dysfunction. This review underscores the necessity of preconception weight management, individualized ART protocols, and tailored antenatal care to mitigate obesity's adverse effects on reproductive outcomes. Future research should focus on understanding male infertility mechanisms, optimizing ART interventions for individuals with obesity, and conducting longitudinal studies on the intergenerational impacts of obesity on reproductive health. This synthesis provides actionable insights to guide clinical practices and future investigations.

综述目的:本系统综述评估了肥胖对男性和女性生殖健康、辅助生殖技术(ART)结局和妊娠相关并发症的影响,提供了一个全面的综合证据。最近的研究发现:肥胖是影响生殖健康、抗逆转录病毒治疗成功率和妊娠结局的关键因素。最近的研究表明,激素紊乱、代谢综合征和表观遗传修饰是肥胖与不孕症和不良妊娠结果相关的主要机制。根据系统评价和荟萃分析(PRISMA)指南的首选报告项目进行系统搜索,包括35项研究,重点关注肥胖相关的生殖结果。该综述强调,肥胖会破坏荷尔蒙平衡,包括性激素结合球蛋白(SHBG)和睾丸激素水平的降低,以及胰岛素抵抗和慢性炎症的增加。这些机制损害卵巢功能、子宫内膜容受性和精子质量,导致妊娠时间延长、ART成功率降低和流产风险增加。在怀孕期间,孕妇肥胖会增加妊娠期糖尿病(GDM)、先兆子痫和剖宫产的风险,同时会导致新生儿并发症,如巨大儿和新生儿重症监护病房(NICU)入院。研究结果强调了母亲和父亲的肥胖对后代健康的双重影响,特别是通过表观遗传修饰导致代际代谢功能障碍。这篇综述强调了孕前体重管理、个性化抗逆转录病毒治疗方案和量身定制的产前护理的必要性,以减轻肥胖对生殖结果的不利影响。未来的研究应侧重于了解男性不育的机制,优化针对肥胖个体的ART干预措施,并对肥胖对生殖健康的代际影响进行纵向研究。这种综合为指导临床实践和未来的研究提供了可行的见解。
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引用次数: 0
Assessing Weight Stigma Interventions: A Systematic Review of Randomized Controlled Trials. 评估体重病耻感干预:随机对照试验的系统回顾。
IF 9.5 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Pub Date : 2025-04-14 DOI: 10.1007/s13679-025-00628-w
Christy Wang, William D Murley, Sameeksha Panda, Caroline A Stiver, Cambria L Garell, Tannaz Moin, Amanda K Crandall, A Janet Tomiyama

Purpose of review: The primary goals of this pre-registered systematic review were to critically evaluate the existing randomized controlled trials targeting weight stigma/bias and identify promising avenues for future research.

Recent findings: Prior systematic reviews have highlighted intervention strategies such as shifting causal attributions of obesity, evoking empathy, deploying weight-inclusive approaches, increasing education, and combining these strategies. Here, we provide an updated systematic review of weight stigma interventions. A systematic search was conducted following the PRISMA guidelines and performed in PubMed/Medline, PubMed, PsycINFO, and Google Scholar until October 2024, yielding a final sample of 56 articles. In addition to previously established strategies, we identified several novel strategies, such as cognitive dissonance and connection building. Interventions can largely shift attitudinal outcomes, but future research should extend beyond attitude measures, assess weight bias over a longer term, and across more diverse populations.

综述目的:本预注册系统综述的主要目的是批判性地评估现有针对体重病耻感/偏见的随机对照试验,并为未来的研究确定有希望的途径。最近的发现:先前的系统综述强调了干预策略,如改变肥胖的因果归因,唤起同理心,采用体重包容方法,增加教育,并将这些策略结合起来。在这里,我们提供了体重病耻感干预的最新系统综述。按照PRISMA指南进行系统检索,并在PubMed/Medline、PubMed、PsycINFO和谷歌Scholar中进行检索,直到2024年10月,最终样本为56篇文章。除了先前建立的策略外,我们还确定了一些新的策略,如认知失调和连接建立。干预措施可以在很大程度上改变态度结果,但未来的研究应该超越态度测量,在更长期和更多样化的人群中评估体重偏差。
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引用次数: 0
Understanding the Link Between Sterol Regulatory Element Binding Protein (SREBPs) and Metabolic Dysfunction Associated Steatotic Liver Disease (MASLD). 了解甾醇调节元件结合蛋白(SREBPs)与代谢功能障碍相关的脂肪变性肝病(MASLD)之间的联系。
IF 9.5 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Pub Date : 2025-04-14 DOI: 10.1007/s13679-025-00626-y
Pervej Alom Barbhuiya, Ren Yoshitomi, Manash Pratim Pathak

Purpose of the review: This review aims to summarize the current scientific understanding on the complex interplay between sterol regulatory element-binding proteins (SREBPs) and metabolic dysfunction associated steatotic liver disease (MASLD) by critically examining a few significant molecular pathways. Additionally, the review explores the potential of both natural and synthetic SREBP inhibitors as promising therapeutic candidates for MASLD.

Recent findings: SREBPs are central regulators of lipid homeostasis, with SREBP-1c primarily controlling fatty acid synthesis and SREBP-2 regulating cholesterol metabolism. Dysregulation of SREBP activity, often triggered by excessive caloric intake, insulin resistance, or endoplasmic reticulum (ER) stress, contributes to the development of metabolic syndrome and MASLD. SREBP-1c overexpression leads to increased de novo lipogenesis (DNL), hepatic lipid accumulation, and insulin resistance, while SREBP-2 modulates cholesterol metabolism via miRNA-33 and ABCA1 regulation leading to the pathogenesis of MASLD. The PI3K-Akt-mTORC1 pathway plays a critical role in SREBP activation, linking nutrient availability to lipid synthesis. Synthetic SREBP inhibitors, such as fatostatin and 25-hydroxycholesterol, and natural compounds, including kaempferol and resveratrol, show promise in modulating SREBP activity in vivo.

Conclusion: While targeting SREBP pathways presents a promising avenue for mitigating MASLD, further scientific investigation is imperative to identify and validate potential molecular targets. Although current studies on synthetic and natural SREBP inhibitors demonstrate encouraging results, rigorous pre-clinical and clinical research is warranted to translate these findings into effective MASLD treatments.

综述目的:本综述旨在通过严格检查几个重要的分子途径,总结目前对固醇调节元件结合蛋白(SREBPs)与代谢功能障碍相关的脂肪变性肝病(MASLD)之间复杂相互作用的科学认识。此外,该综述还探讨了天然和合成SREBP抑制剂作为MASLD治疗候选药物的潜力。最近的研究发现:srebp是脂质稳态的中心调节因子,SREBP-1c主要控制脂肪酸合成,SREBP-2调节胆固醇代谢。SREBP活性的失调通常由过多的热量摄入、胰岛素抵抗或内质网(ER)应激引发,有助于代谢综合征和MASLD的发展。SREBP-1c过表达导致新生脂肪生成(DNL)增加、肝脏脂质积累和胰岛素抵抗,而SREBP-2通过miRNA-33和ABCA1调节胆固醇代谢,导致MASLD的发病机制。PI3K-Akt-mTORC1通路在SREBP激活中起关键作用,将营养物质可用性与脂质合成联系起来。合成的SREBP抑制剂,如脂肪抑制素和25-羟基胆固醇,以及天然化合物,包括山奈酚和白藜芦醇,在体内显示出调节SREBP活性的希望。结论:虽然靶向SREBP通路是缓解MASLD的有希望的途径,但需要进一步的科学研究来确定和验证潜在的分子靶点。尽管目前对合成和天然SREBP抑制剂的研究显示出令人鼓舞的结果,但需要严格的临床前和临床研究来将这些发现转化为有效的MASLD治疗。
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Current Obesity Reports
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