Pub Date : 2025-10-30DOI: 10.1016/j.clnu.2025.10.014
Binyu Yang , Wei Wei , Caihong Liu , Yongxiu Huang , Jinglei Ren , Ya Yuan , Ping Fu , Yuliang Zhao
Background & aims
Artificial intelligence (AI) models are increasingly being used to assist in chronic kidney disease (CKD) dietary guidance, but concerns about their accuracy remain. This study aimed to assess the performance of three AI models (ChatGPT, DeepSeek, Gemini) in accordance with the Kidney Disease: Improving Global Outcomes (KDIGO) 2024 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease.
Methods
We compared ChatGPT, DeepSeek, and Gemini with the KDIGO 2024 guidelines through expert and cross-AI assessments. Outputs were scored across five domains: accuracy, clarity, completeness, practicality, and safety.
Results
The AI models were able to generate well-structured dietary advice for CKD patients. DeepSeek received a higher score (7.625) for practicality compared to ChatGPT (6.5) and Gemini (7.0) (p = 0.041). ChatGPT showed numerically higher accuracy scores than the other two models, although there was no statistically significant difference (ChatGPT: 7.25, DeepSeek: 6.875, Gemini: 6.875; p = 0.715). Similarly, scores for clarity (p = 0.489), completeness (p = 0.432) and safety (p = 0.413) were not significantly different. The AI models share several common limitations: they might overlook contraindications (such as recommending a low-protein diet for patients with severe hypoalbuminemia), neglect age-specific needs, and lack real-time knowledge updates.
Conclusions
While AI shows clinical potential, its outputs still require expert validation, real-time updates, and enhanced safety protocols to ensure reliable clinical integration.
{"title":"Using artificial intelligence models to generate dietary recommendations for chronic kidney disease patients: A comparative cross-sectional study","authors":"Binyu Yang , Wei Wei , Caihong Liu , Yongxiu Huang , Jinglei Ren , Ya Yuan , Ping Fu , Yuliang Zhao","doi":"10.1016/j.clnu.2025.10.014","DOIUrl":"10.1016/j.clnu.2025.10.014","url":null,"abstract":"<div><h3>Background & aims</h3><div>Artificial intelligence (AI) models are increasingly being used to assist in chronic kidney disease (CKD) dietary guidance, but concerns about their accuracy remain. This study aimed to assess the performance of three AI models (ChatGPT, DeepSeek, Gemini) in accordance with the Kidney Disease: Improving Global Outcomes (KDIGO) 2024 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease.</div></div><div><h3>Methods</h3><div>We compared ChatGPT, DeepSeek, and Gemini with the KDIGO 2024 guidelines through expert and cross-AI assessments. Outputs were scored across five domains: accuracy, clarity, completeness, practicality, and safety.</div></div><div><h3>Results</h3><div>The AI models were able to generate well-structured dietary advice for CKD patients. DeepSeek received a higher score (7.625) for practicality compared to ChatGPT (6.5) and Gemini (7.0) (p = 0.041). ChatGPT showed numerically higher accuracy scores than the other two models, although there was no statistically significant difference (ChatGPT: 7.25, DeepSeek: 6.875, Gemini: 6.875; p = 0.715). Similarly, scores for clarity (p = 0.489), completeness (p = 0.432) and safety (p = 0.413) were not significantly different. The AI models share several common limitations: they might overlook contraindications (such as recommending a low-protein diet for patients with severe hypoalbuminemia), neglect age-specific needs, and lack real-time knowledge updates.</div></div><div><h3>Conclusions</h3><div>While AI shows clinical potential, its outputs still require expert validation, real-time updates, and enhanced safety protocols to ensure reliable clinical integration.</div></div>","PeriodicalId":10517,"journal":{"name":"Clinical nutrition","volume":"55 ","pages":"Pages 76-80"},"PeriodicalIF":7.4,"publicationDate":"2025-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145457984","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-30DOI: 10.1016/j.clnu.2025.10.003
Clodagh E. Beattie , Borislavova Borislava , Harry A. Smith , Michael T. Ambler , Paul White , Danielle Milne , Aravind V. Ramesh , Alexander Ferriman , Thomas Fisher , Charlotte Horsley , Sherena Jackson , Chloe Jubainville , Kate Lobo , Hannah Maxfield , Javier T. Gonzalez , James A. Betts , Anthony E. Pickering , Matt Thomas
Background and aims
For intensive care unit (ICU) patients fed via a nasogastric (NG) tube, current guidelines recommend continuous feeding through the day and night. Emerging evidence in healthy individuals shows that NG feeding in an intermittent diurnal pattern promotes phasic hormonal, digestive and metabolic responses vital for effective nutrition, though this has not been studied in the critically ill population. This proof-of-concept study aimed to compare the effect of diurnal intermittent versus continuous enteral feeding on hormonal and metabolic outcomes in ICU patients.
Methods
We conducted a single-centre, randomised, open-label trial in the ICU. Adult ICU patients that were anticipated to require NG feeding for >48 h were randomised to an intermittent diurnal regimen (feeds at 8:00, 13:00 and 18:00), or continuous feeding with equivalent nutritional value, for 48 h. The primary outcome was peak plasma insulin within 3 h of delivering the first intermittent feed on the second study day, compared to the same time period in the continuous group. Secondary outcomes included feasibility, tolerability and metabolic profiles.
Results
Thirty patients were randomised to intermittent (n = 13) or continuous (n = 17) feeding. Two patients in the intermittent group were excluded from analysis. Both groups achieved their feed targets. Peak plasma insulin concentrations (mean ± SD) were significantly higher in the intermittent group versus continuous (295.1 ± 167.8 vs. 128.1 ± 57.2 pmol/L, p < 0.001). Plasma glucose concentrations were not significantly different between groups. There were no between-group differences in other plasma metabolites and there were no adverse events such as hyper-/hypo-glycaemia. There was evidence of increased bowel motility in the intermittent group.
Conclusion
Intermittent diurnal feeding, compared to continuous feeding, preserves the physiological insulin response in critically ill adults. Both regimens were well tolerated, supporting the need for a larger trial to assess other clinically important patient-centred outcomes.
Trial registration
This trial was registered prospectively at clinicaltrials.gov (study ID NCT06115044).
背景和目的:对于重症监护病房(ICU)患者通过鼻胃管喂食,目前的指南建议白天和晚上持续喂食。在健康个体中出现的新证据表明,以间歇性的昼夜模式喂养NG可促进对有效营养至关重要的阶段性激素、消化和代谢反应,尽管尚未在危重患者群体中进行研究。这项概念验证性研究旨在比较每日间歇和连续肠内喂养对ICU患者激素和代谢结局的影响。方法:我们在ICU进行了一项单中心、随机、开放标签的试验。预计需要NG喂养48小时的成年ICU患者被随机分配到间歇性日间方案(8:00,13:00和18:00喂养)或具有同等营养价值的连续喂养48小时。主要结局是在第二个研究日首次间歇性喂养后3小时内血浆胰岛素峰值,与连续组的同一时间段相比。次要结局包括可行性、耐受性和代谢特征。结果:30例患者随机分为间歇喂养组(n = 13)和连续喂养组(n = 17)。2例间歇组患者被排除在分析之外。两组都达到了饲料目标。间歇组血浆胰岛素峰值浓度(平均±SD)显著高于连续组(295.1±167.8比128.1±57.2 pmol/L, p < 0.001)。各组间血浆葡萄糖浓度无显著差异。其他血浆代谢物组间无差异,无高血糖/低血糖等不良事件。有证据表明,间歇性组的肠道蠕动有所增加。结论:与连续喂养相比,间歇喂养可保留危重症成人的胰岛素生理反应。两种方案的耐受性都很好,因此需要进行更大规模的试验来评估其他临床重要的以患者为中心的结果。试验注册:本试验在clinicaltrials.gov网站前瞻性注册(研究编号NCT06115044)。
{"title":"Does Intermittent Nutrition Enterally Normalise hormonal and metabolic responses to feeding in critically ill adults? The DINE-normal proof-of-concept study","authors":"Clodagh E. Beattie , Borislavova Borislava , Harry A. Smith , Michael T. Ambler , Paul White , Danielle Milne , Aravind V. Ramesh , Alexander Ferriman , Thomas Fisher , Charlotte Horsley , Sherena Jackson , Chloe Jubainville , Kate Lobo , Hannah Maxfield , Javier T. Gonzalez , James A. Betts , Anthony E. Pickering , Matt Thomas","doi":"10.1016/j.clnu.2025.10.003","DOIUrl":"10.1016/j.clnu.2025.10.003","url":null,"abstract":"<div><h3>Background and aims</h3><div>For intensive care unit (ICU) patients fed via a nasogastric (NG) tube, current guidelines recommend continuous feeding through the day and night. Emerging evidence in healthy individuals shows that NG feeding in an intermittent diurnal pattern promotes phasic hormonal, digestive and metabolic responses vital for effective nutrition, though this has not been studied in the critically ill population. This proof-of-concept study aimed to compare the effect of diurnal intermittent versus continuous enteral feeding on hormonal and metabolic outcomes in ICU patients.</div></div><div><h3>Methods</h3><div>We conducted a single-centre, randomised, open-label trial in the ICU. Adult ICU patients that were anticipated to require NG feeding for >48 h were randomised to an intermittent diurnal regimen (feeds at 8:00, 13:00 and 18:00), or continuous feeding with equivalent nutritional value, for 48 h. The primary outcome was peak plasma insulin within 3 h of delivering the first intermittent feed on the second study day, compared to the same time period in the continuous group. Secondary outcomes included feasibility, tolerability and metabolic profiles.</div></div><div><h3>Results</h3><div>Thirty patients were randomised to intermittent (n = 13) or continuous (n = 17) feeding. Two patients in the intermittent group were excluded from analysis. Both groups achieved their feed targets. Peak plasma insulin concentrations (mean ± SD) were significantly higher in the intermittent group versus continuous (295.1 ± 167.8 vs. 128.1 ± 57.2 pmol/L, p < 0.001). Plasma glucose concentrations were not significantly different between groups. There were no between-group differences in other plasma metabolites and there were no adverse events such as hyper-/hypo-glycaemia. There was evidence of increased bowel motility in the intermittent group.</div></div><div><h3>Conclusion</h3><div>Intermittent diurnal feeding, compared to continuous feeding, preserves the physiological insulin response in critically ill adults. Both regimens were well tolerated, supporting the need for a larger trial to assess other clinically important patient-centred outcomes.</div></div><div><h3>Trial registration</h3><div>This trial was registered prospectively at <span><span>clinicaltrials.gov</span><svg><path></path></svg></span> (study ID NCT06115044).</div></div>","PeriodicalId":10517,"journal":{"name":"Clinical nutrition","volume":"55 ","pages":"Pages 81-89"},"PeriodicalIF":7.4,"publicationDate":"2025-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145457961","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-30DOI: 10.1016/j.clnu.2025.10.013
Michelle Carmen Paulus , Max Melchers , Tim den Ruijter , Marco Reijn , Marcel H. Zwietering , Arthur Raymond Hubert van Zanten
Background & aims
Prolonging the hang time (HT) of administration sets and enteral feeding containers beyond the recommended 24 h may reduce waste, decrease nursing workload and lower hospital costs. The objective of this pilot study was to explore the safety of extending the HT from 24 to 48 h by investigating its impact on the occurrence of diarrhoea and new-onset pneumonia in intensive care unit (ICU) patients.
Methods
This monocenter pilot study had a combined retrospective and prospective cohort (24 and 48-h HT, respectively) design and included ICU patients (≥ 18 years) receiving enteral nutrition for at least 48 h. The primary outcome was diarrhoea, defined as (1) ≥ 3 defecations/day with a Bristol Stool Chart score of 6 or 7, or (2) colostomy/ileostomy output ≥1.5 L/24 h. The secondary outcome was new-onset pneumonia ≥48 h after ICU admission. Associations between HT protocol and the onset of outcomes were assessed by Cox regression analyses. Additionally, retrograde bacterial growth was assessed through microbiological analysis in enteral feeding systems.
Results
A total of 102 ICU patients were included between December 16, 2023 and October 11, 2024, with 51 in each cohort. Actual median HT was 31 [27–45] hours vs. 56 [37–83] hours in the 24 and 48-h groups, respectively (p < 0.001). In multivariable Cox regression, no significant association was found between prolonged HT and diarrhoea-free survival (HR 0.92, 95 % CI 0.55–1.53, p = 0.746) and new-onset pneumonia (HR 1.33, 95 % CI 0.54–3.24, p = 0.537), respectively. Retrograde bacterial growth did not extend beyond the first 30 cm of the administration set and was not correlated to HT.
Conclusion
We observed no association between prolonging the HT of enteral feeding sets from 24 to 48 h and the occurrence of diarrhoea or new-onset pneumonia in ICU patients. However, a substantial, adequately powered, non-inferiority trial must be conducted prior to integrating extended hang times into clinical practice.
背景与目的:延长给药盒和肠内喂养容器的悬挂时间(HT)超过推荐的24小时,可以减少浪费,减少护理工作量,降低医院成本。本初步研究的目的是通过研究HT对重症监护病房(ICU)患者腹泻和新发肺炎发生的影响,探讨将HT从24小时延长至48小时的安全性。方法:本单中心先导研究采用回顾性和前瞻性队列(分别为24小时和48小时)设计,纳入接受肠内营养至少48小时的ICU患者(≥18岁)。主要结局为腹泻,定义为(1)≥3次排便/天,布里斯托尔大便表评分为6或7,或(2)结肠造口/回肠造口输出量≥1.5 L/24小时。次要结局为ICU入院后≥48小时新发肺炎。通过Cox回归分析评估HT方案与结局发生之间的关系。此外,通过肠道喂养系统的微生物分析评估逆行细菌生长。结果:2023年12月16日至2024年10月11日共纳入102例ICU患者,每组51例。24和48 h组的实际中位HT分别为31[27-45]小时和56[37-83]小时(p < 0.001)。在多变量Cox回归中,HT延长与无腹泻生存(HR 0.92, 95% CI 0.55-1.53, p = 0.746)和新发肺炎(HR 1.33, 95% CI 0.54-3.24, p = 0.537)之间未发现显著关联。细菌逆行生长没有超出给药组的前30厘米,与HT无关。结论:我们观察到延长24 ~ 48 h肠内喂养组HT与ICU患者腹泻或新发肺炎的发生无相关性。然而,在将延长的悬挂时间纳入临床实践之前,必须进行实质性的、充分的、非劣效性的试验。
{"title":"Exploring the safety of prolonging the hang time of enteral feeding systems in the intensive care unit","authors":"Michelle Carmen Paulus , Max Melchers , Tim den Ruijter , Marco Reijn , Marcel H. Zwietering , Arthur Raymond Hubert van Zanten","doi":"10.1016/j.clnu.2025.10.013","DOIUrl":"10.1016/j.clnu.2025.10.013","url":null,"abstract":"<div><h3>Background & aims</h3><div>Prolonging the hang time (HT) of administration sets and enteral feeding containers beyond the recommended 24 h may reduce waste, decrease nursing workload and lower hospital costs. The objective of this pilot study was to explore the safety of extending the HT from 24 to 48 h by investigating its impact on the occurrence of diarrhoea and new-onset pneumonia in intensive care unit (ICU) patients.</div></div><div><h3>Methods</h3><div>This monocenter pilot study had a combined retrospective and prospective cohort (24 and 48-h HT, respectively) design and included ICU patients (≥ 18 years) receiving enteral nutrition for at least 48 h. The primary outcome was diarrhoea, defined as (1) ≥ 3 defecations/day with a Bristol Stool Chart score of 6 or 7, or (2) colostomy/ileostomy output ≥1.5 L/24 h. The secondary outcome was new-onset pneumonia ≥48 h after ICU admission. Associations between HT protocol and the onset of outcomes were assessed by Cox regression analyses. Additionally, retrograde bacterial growth was assessed through microbiological analysis in enteral feeding systems.</div></div><div><h3>Results</h3><div>A total of 102 ICU patients were included between December 16, 2023 and October 11, 2024, with 51 in each cohort. Actual median HT was 31 [27–45] hours vs. 56 [37–83] hours in the 24 and 48-h groups, respectively (p < 0.001). In multivariable Cox regression, no significant association was found between prolonged HT and diarrhoea-free survival (HR 0.92, 95 % CI 0.55–1.53, p = 0.746) and new-onset pneumonia (HR 1.33, 95 % CI 0.54–3.24, p = 0.537), respectively. Retrograde bacterial growth did not extend beyond the first 30 cm of the administration set and was not correlated to HT.</div></div><div><h3>Conclusion</h3><div>We observed no association between prolonging the HT of enteral feeding sets from 24 to 48 h and the occurrence of diarrhoea or new-onset pneumonia in ICU patients. However, a substantial, adequately powered, non-inferiority trial must be conducted prior to integrating extended hang times into clinical practice.</div></div>","PeriodicalId":10517,"journal":{"name":"Clinical nutrition","volume":"55 ","pages":"Pages 57-65"},"PeriodicalIF":7.4,"publicationDate":"2025-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145451163","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-29DOI: 10.1016/j.clnu.2025.10.010
Saba Vaezi , Jessica L. Freeling , Bruna O. de Vargas , Lee Weidauer , Marni E. Shoemaker , Wade M. Sanders , Moul Dey
Background and aims
The aging population in the U.S. faces increased cardiometabolic risk, reducing healthspan and increasing public health burden. These vulnerabilities may be compounded by ultra-processed food (UPF). No feeding trial has evaluated UPF reduction in older adults within the framework of Dietary Guidelines for Americans (DGA). This study addressed the gap using representative omnivorous and lacto-ovo vegetarian patterns.
Methods
The secondary outcomes of the Protein-Distinct Macronutrient-Equivalent Diet 2 (PRODMED2) trial compared two DGA-aligned, low-UPF diets with each other and with a high-UPF habitual baseline (BSL) diet in 36 community-dwelling older adults. The diets featured minimally processed pork (MPP) and lentils (MPL) as representative animal- and plant-based primary proteins, each provided for 8 weeks without calorie restriction and separated by a 2-week washout. Diet compositions and intakes, body composition, cardiometabolic biomarkers, and hormones linked to nutrient sensing and energy balance were measured before and after interventions, with a subset of measures repeated at ∼1-year post-intervention follow-up (FUP). Data were primarily analyzed using robust linear mixed-effects models adjusted for covariates.
Results
Switching from a high-UPF BSL (∼50%E) to either low-UPF diets (∼13%E), unintentionally lowered energy intake (Δ-333 vs Δ-437 kcal/d, MPP vs MPL), resulting in reductions in body weight (Δ-3.8 vs Δ-4.4 kg), and fat mass (Δ-2.6 vs Δ-2.9 kg). Both diets improved HOMA-IR, insulin, C-peptide, total cholesterol, LDL, apolipoprotein B, non-HDL, and CRP relative to BSL (all, p < 0.038 BSL vs post-diet, no significance between diets). Fasting leptin declined (Δ-1.9 vs Δ-2.5 ng/mL MPP vs MPL) and FGF21 increased (Δ+65 vs Δ+88 pg/mL MPP vs MPL) in both diet phases (all, p < 0.026 BSL vs post-diet, no significance between diets). At FUP, as UPF exposure increased to 44 %, dietary intakes, weight, adiposity, and biomarkers returned toward BSL.
Conclusion
Results demonstrate that low-UPF eating aligns with DGA pattern and is feasible across both plant- and animal-based diets. Both omnivorous and lacto-ovo vegetarian interventions promoted caloric reduction, weight and visceral fat loss, improved insulin sensitivity and lipid metabolism, and reduced inflammatory markers. These effects may involve nutrient sensing via FGF21 and leptin. Low-UPF diets may provide a practical approach to support healthy aging.
Registration of the clinical trial
The trial is registered at www.clinicaltrials.gov as NCT05581953 on October 12, 2022.
背景与目的:美国老龄化人口面临心脏代谢风险增加、健康寿命缩短和公共卫生负担增加的问题。超加工食品(UPF)可能会加剧这些脆弱性。在美国膳食指南(DGA)的框架内,没有喂养试验评估老年人UPF的减少。本研究使用具有代表性的杂食和乳蛋素食模式来解决这一差距。方法:蛋白质不同常量营养素当量饮食2 (PRODMED2)试验的次要结果比较了36名社区居住老年人的两种与dga一致的低upf饮食和高upf习惯基线(BSL)饮食。饮食以最低限度加工猪肉(MPP)和扁豆(MPL)为代表的动物和植物基础初级蛋白质,每种饮食都提供8周的无热量限制,并通过2周的洗脱期分开。在干预前后测量饮食组成和摄入量、身体组成、心脏代谢生物标志物以及与营养感知和能量平衡相关的激素,并在干预后随访(FUP) 1年重复测量一部分。数据主要使用校正协变量的鲁棒线性混合效应模型进行分析。结果:从高upf BSL (~ 50%E)切换到低upf饮食(~ 13%E),无意中降低了能量摄入(Δ-333 vs Δ-437 kcal/d, MPP vs MPL),导致体重(Δ-3.8 vs Δ-4.4 kg)和脂肪量(Δ-2.6 vs Δ-2.9 kg)的减少。与BSL相比,两种饮食均改善了HOMA-IR、胰岛素、c肽、总胆固醇、LDL、载脂蛋白B、非高密度脂蛋白和CRP (BSL与饮食后相比均p < 0.038,饮食之间无显著性差异)。在两个饮食阶段,空腹瘦素下降(Δ-1.9 vs Δ-2.5 ng/mL MPP vs MPL), FGF21增加(Δ+65 vs Δ+88 pg/mL MPP vs MPL)(所有,BSL与饮食后p < 0.026,饮食之间无统计学意义)。在FUP时,当UPF暴露增加到44%时,饮食摄入量、体重、肥胖和生物标志物都恢复到BSL。结论:结果表明,低upf饮食与DGA模式一致,并且在植物性和动物性饮食中都是可行的。杂食和乳蛋素食干预都促进了热量的减少,体重和内脏脂肪的减少,改善了胰岛素敏感性和脂质代谢,并减少了炎症标志物。这些影响可能涉及通过FGF21和瘦素感知营养。低upf饮食可能是一种支持健康老龄化的实用方法。临床试验注册:该试验于2022年10月12日在www.Clinicaltrials: gov注册为NCT05581953。
{"title":"Impacts of minimally-processed omnivorous vs lacto-ovo-vegetarian diets on insulin sensitivity, lipid profile, and adiposity in older adults: Secondary findings from a randomized crossover feeding trial","authors":"Saba Vaezi , Jessica L. Freeling , Bruna O. de Vargas , Lee Weidauer , Marni E. Shoemaker , Wade M. Sanders , Moul Dey","doi":"10.1016/j.clnu.2025.10.010","DOIUrl":"10.1016/j.clnu.2025.10.010","url":null,"abstract":"<div><h3>Background and aims</h3><div>The aging population in the U.S. faces increased cardiometabolic risk, reducing healthspan and increasing public health burden. These vulnerabilities may be compounded by ultra-processed food (UPF). No feeding trial has evaluated UPF reduction in older adults within the framework of Dietary Guidelines for Americans (DGA). This study addressed the gap using representative omnivorous and lacto-ovo vegetarian patterns.</div></div><div><h3>Methods</h3><div>The secondary outcomes of the Protein-Distinct Macronutrient-Equivalent Diet 2 (PRODMED2) trial compared two DGA-aligned, low-UPF diets with each other and with a high-UPF habitual baseline (BSL) diet in 36 community-dwelling older adults. The diets featured minimally processed pork (MPP) and lentils (MPL) as representative animal- and plant-based primary proteins, each provided for 8 weeks without calorie restriction and separated by a 2-week washout. Diet compositions and intakes, body composition, cardiometabolic biomarkers, and hormones linked to nutrient sensing and energy balance were measured before and after interventions, with a subset of measures repeated at ∼1-year post-intervention follow-up (FUP). Data were primarily analyzed using robust linear mixed-effects models adjusted for covariates.</div></div><div><h3>Results</h3><div>Switching from a high-UPF BSL (∼50%E) to either low-UPF diets (∼13%E), unintentionally lowered energy intake (Δ-333 vs Δ-437 kcal/d, MPP vs MPL), resulting in reductions in body weight (Δ-3.8 vs Δ-4.4 kg), and fat mass (Δ-2.6 vs Δ-2.9 kg). Both diets improved HOMA-IR, insulin, C-peptide, total cholesterol, LDL, apolipoprotein B, non-HDL, and CRP relative to BSL (all, <em>p</em> < 0.038 BSL vs post-diet, no significance between diets). Fasting leptin declined (Δ-1.9 vs Δ-2.5 ng/mL MPP vs MPL) and FGF21 increased (Δ+65 vs Δ+88 pg/mL MPP vs MPL) in both diet phases (all, <em>p</em> < 0.026 BSL vs post-diet, no significance between diets). At FUP, as UPF exposure increased to 44 %, dietary intakes, weight, adiposity, and biomarkers returned toward BSL.</div></div><div><h3>Conclusion</h3><div>Results demonstrate that low-UPF eating aligns with DGA pattern and is feasible across both plant- and animal-based diets. Both omnivorous and lacto-ovo vegetarian interventions promoted caloric reduction, weight and visceral fat loss, improved insulin sensitivity and lipid metabolism, and reduced inflammatory markers. These effects may involve nutrient sensing via FGF21 and leptin. Low-UPF diets may provide a practical approach to support healthy aging.</div></div><div><h3>Registration of the clinical trial</h3><div>The trial is registered at <span><span>www.clinicaltrials.gov</span><svg><path></path></svg></span> as NCT05581953 on October 12, 2022.</div></div>","PeriodicalId":10517,"journal":{"name":"Clinical nutrition","volume":"55 ","pages":"Pages 90-103"},"PeriodicalIF":7.4,"publicationDate":"2025-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145470718","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-29DOI: 10.1016/j.clnu.2025.10.011
Yixi Sun , Ruiyuan Zhang , Ling Tian , Tingting Liu , Yang Pan , Xiao Sun , Zhijie Huang , Jia Fan , Jing Chen , Kai Zhang , Shengxu Li , Wei Chen , Lydia A. Bazzano , Jiang He , Joshua D. Bundy , Tanika N. Kelly , Changwei Li
Background
Inosine has been investigated as a dietary supplement for athlete performance, inflammation, and neurological disease. A recent study in a hypercholesterolemic rat model has shown its potential for treating atherosclerosis.
Objective
This study aimed to investigate the associations between plasma inosine and lipid parameters, and to discover potential mediating pathways.
Methods
We profiled inosine and 886 known metabolites in plasma samples from 1,121 participants of a biracial cohort. Linear regression models assessed inosine's association with total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), log transformed triglycerides (log-TG), and TC to HDL-C ratio (TC/HDL-C), adjusting for relevant covariates. Significant findings were replicated in 78 adults from the Protein and Blood Pressure (ProBP) study, a cross-over randomized control trial by testing longitudinal associations between inosine changes and lipid changes after dietary supplementation of soy protein, milk protein, and carbohydrates. For a replicated association, we employed two complementary approaches to identify potential mediators for enrichment analysis.
Results
In the discovery cohort, inosine was positively associated with HDL-C (β = 1.77, 95 % confidence interval [CI]: 0.003 to 3.54) and negatively associated with TC/HDL-C (β = −0.24, 95 % CI: −0.41 to −0.08) and log-TG (β = −0.08, 95 % CI: −0.15 to −0.02). These results were replicated in ProBP after soy protein intervention with inosine changes leading to increase of HDL-C (β = 1.82, 95 % CI: 0.36 to 3.27) and decrease of TC/HDL-C (β = −0.14, 95 % CI:-0.28 to −0.002) and TG (β = −12.79, 95 % CI: −21.00 to −4.58). Sex-stratified analyses revealed a more pronounced association in women than men, particularly for HDL-C. Six metabolites and 29 enriched pathways of high confidence were identified.
Conclusion
In humans, inosine is associated with better profiles of HDL-C, TC/HDL-C, and log-TG, with more pronounced effects in women for HDL-C.
The ProBP trial was registered at ClinicalTrials.gov as NCT00107744.
{"title":"Associations of plasma inosine with lipid parameters in a biracial community cohort","authors":"Yixi Sun , Ruiyuan Zhang , Ling Tian , Tingting Liu , Yang Pan , Xiao Sun , Zhijie Huang , Jia Fan , Jing Chen , Kai Zhang , Shengxu Li , Wei Chen , Lydia A. Bazzano , Jiang He , Joshua D. Bundy , Tanika N. Kelly , Changwei Li","doi":"10.1016/j.clnu.2025.10.011","DOIUrl":"10.1016/j.clnu.2025.10.011","url":null,"abstract":"<div><h3>Background</h3><div>Inosine has been investigated as a dietary supplement for athlete performance, inflammation, and neurological disease. A recent study in a hypercholesterolemic rat model has shown its potential for treating atherosclerosis.</div></div><div><h3>Objective</h3><div>This study aimed to investigate the associations between plasma inosine and lipid parameters, and to discover potential mediating pathways.</div></div><div><h3>Methods</h3><div>We profiled inosine and 886 known metabolites in plasma samples from 1,121 participants of a biracial cohort. Linear regression models assessed inosine's association with total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), log transformed triglycerides (log-TG), and TC to HDL-C ratio (TC/HDL-C), adjusting for relevant covariates. Significant findings were replicated in 78 adults from the Protein and Blood Pressure (ProBP) study, a cross-over randomized control trial by testing longitudinal associations between inosine changes and lipid changes after dietary supplementation of soy protein, milk protein, and carbohydrates. For a replicated association, we employed two complementary approaches to identify potential mediators for enrichment analysis.</div></div><div><h3>Results</h3><div>In the discovery cohort, inosine was positively associated with HDL-C (β = 1.77, 95 % confidence interval [CI]: 0.003 to 3.54) and negatively associated with TC/HDL-C (β = −0.24, 95 % CI: −0.41 to −0.08) and log-TG (β = −0.08, 95 % CI: −0.15 to −0.02). These results were replicated in ProBP after soy protein intervention with inosine changes leading to increase of HDL-C (β = 1.82, 95 % CI: 0.36 to 3.27) and decrease of TC/HDL-C (β = −0.14, 95 % CI:-0.28 to −0.002) and TG (β = −12.79, 95 % CI: −21.00 to −4.58). Sex-stratified analyses revealed a more pronounced association in women than men, particularly for HDL-C. Six metabolites and 29 enriched pathways of high confidence were identified.</div></div><div><h3>Conclusion</h3><div>In humans, inosine is associated with better profiles of HDL-C, TC/HDL-C, and log-TG, with more pronounced effects in women for HDL-C.</div><div>The ProBP trial was registered at ClinicalTrials.gov as NCT00107744.</div></div>","PeriodicalId":10517,"journal":{"name":"Clinical nutrition","volume":"55 ","pages":"Pages 113-123"},"PeriodicalIF":7.4,"publicationDate":"2025-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145470611","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-28DOI: 10.1016/j.clnu.2025.10.009
Ruixin Zhu , Yu Dong , Jie Guo , Jingjing He , Huiyu Chen , Ran Wang , Fazheng Ren , Anne Raben , J. Alfredo Martinez
Recent advances in artificial intelligence, wearable biosensors, and multi-omics technologies, combined with interdisciplinary translational collaborations, are transforming the landscape of nutrition, particularly by enabling precision nutrition. We propose computational nutrition as an emerging interdisciplinary field that aims to address complex challenges in nutrition and health and drive paradigm shifts in nutrition research through computational methods in statistics and computer science (e.g., statistical modeling, simulation, causal inference, machine learning, and deep learning) and multi-modal data. Computational nutrition employs epidemiology and data science as its methodologies and integrates expertise from nutrition, food science, computer science, statistics, systems biology, and public health. The main research directions of computational nutrition are: 1) prediction of personalized metabolic responses to foods and establishment of individualized dietary reference intakes; 2) causal inference in nutrition and diseases and evaluation of individualized treatment effects of nutritional interventions; 3) precise and dynamic assessment and monitoring of diet-related disease risks; 4) simulation and evaluation of public health nutrition policies and sustainability assessment of dietary patterns. Critical challenges such as the reliability of wearable biosensors, trade-offs in feature selection, ethics of algorithms and health equity, and interpretability of algorithms are raised, which must be addressed to ensure human well-being and rights.
{"title":"From prediction of personalized metabolic responses to foods to computational nutrition: Concepts of an emerging interdisciplinary field","authors":"Ruixin Zhu , Yu Dong , Jie Guo , Jingjing He , Huiyu Chen , Ran Wang , Fazheng Ren , Anne Raben , J. Alfredo Martinez","doi":"10.1016/j.clnu.2025.10.009","DOIUrl":"10.1016/j.clnu.2025.10.009","url":null,"abstract":"<div><div>Recent advances in artificial intelligence, wearable biosensors, and multi-omics technologies, combined with interdisciplinary translational collaborations, are transforming the landscape of nutrition, particularly by enabling precision nutrition. We propose computational nutrition as an emerging interdisciplinary field that aims to address complex challenges in nutrition and health and drive paradigm shifts in nutrition research through computational methods in statistics and computer science (e.g., statistical modeling, simulation, causal inference, machine learning, and deep learning) and multi-modal data. Computational nutrition employs epidemiology and data science as its methodologies and integrates expertise from nutrition, food science, computer science, statistics, systems biology, and public health. The main research directions of computational nutrition are: 1) prediction of personalized metabolic responses to foods and establishment of individualized dietary reference intakes; 2) causal inference in nutrition and diseases and evaluation of individualized treatment effects of nutritional interventions; 3) precise and dynamic assessment and monitoring of diet-related disease risks; 4) simulation and evaluation of public health nutrition policies and sustainability assessment of dietary patterns. Critical challenges such as the reliability of wearable biosensors, trade-offs in feature selection, ethics of algorithms and health equity, and interpretability of algorithms are raised, which must be addressed to ensure human well-being and rights.</div></div>","PeriodicalId":10517,"journal":{"name":"Clinical nutrition","volume":"55 ","pages":"Pages 11-23"},"PeriodicalIF":7.4,"publicationDate":"2025-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145430521","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Reply – letter to the editor: The JOHAS (Judgement of Objective Hypersteatosis and Atrophy in Sarcopenia) index; an index for sarcopenia or low muscle mass?","authors":"Yuzo Yamamoto , Kyosuke Agawa, Masahide Awazu, Noriko Omura, Shunji Nakayama, Hiromi Maeda","doi":"10.1016/j.clnu.2025.10.008","DOIUrl":"10.1016/j.clnu.2025.10.008","url":null,"abstract":"","PeriodicalId":10517,"journal":{"name":"Clinical nutrition","volume":"55 ","pages":"Pages 1-2"},"PeriodicalIF":7.4,"publicationDate":"2025-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145415510","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-27DOI: 10.1016/j.clnu.2025.09.020
Ting Gao , Yan Li , Li Niu , Zihan Wang , Shenjun Li , Yunmeng Niu , Ye Li , Yuhan Meng , Xiaohui Gao , Xinyi Xu
Background & aims
Emerging evidence suggests a possible association between dairy product intake and cognitive function in older adults; however, previous findings remain inconsistent. This study aimed to systematically evaluate the association between dairy intake and cognitive outcomes in older adults, and explore potential dose-response relationships and regional differences.
Methods
We searched PubMed, MEDLINE, Embase, Cochrane Library, Scopus, and CINAHL from their inception to 31 December 2024. Dose–response analysis was performed for cohort studies to assess the impact of different types and quantities of dairy intake on cognitive subdomains. Meta-regression was used to explore sources of heterogeneity. The results were presented as relative risks (RRs), odds ratios (ORs), and mean differences (MDs) with 95 % confidence intervals (CIs). The methodology followed the PRISMA guidelines for systematic reviews and meta-analyses.
Results
A total of 38 studies were included, comprising 21 cohort studies, 15 cross-sectional studies, and 2 randomized controlled trials. We stratified dairy products intake levels, and higher total dairy intake was associated with a reduced risk of cognitive decline and improved global cognitive function (Cohort: medium vs low, RR: 0.92, 95 % CI: 0.85, 0.99; high vs low, RR: 0.85, 95 % CI: 0.73, 0.98; Cross-sectional: high vs low, OR: 0.64, 95 % CI: 0.49, 0.82). Fermented dairy products were associated with improved verbal memory and executive function, whereas higher milk intake showed a potential association with poorer verbal memory in certain instances (medium vs low, MD: −0.04; 95 % CI: −0.09, 0.01; high vs low, MD: −0.05; 95 % CI: −0.09, −0.01). Evidence showed nonlinear associations, with the lowest risk of cognitive decline associated with a daily intake of 150 g of dairy products (p-nonlinear = 0.009, RR: 0.86, 95 % CI: 0.78, 0.95), and 30 g/day of whole-fat dairy (p-nonlinear = 0.007, RR: 0.83, 95 % CI: 0.74, 0.94). Regional differences were observed, with cognitive outcomes varying between European and Asian populations, possibly reflecting dietary habits and cultural contexts.
Conclusions
Dairy intake, especially fermented products and moderate total intake, may support cognitive health in older adults, though associations vary by region and dairy type. More high-quality studies are needed to clarify these relationships and guide dietary recommendations.
{"title":"Dairy products intake and its association with cognitive function in older adults: A systematic review and dose–response meta-analysis","authors":"Ting Gao , Yan Li , Li Niu , Zihan Wang , Shenjun Li , Yunmeng Niu , Ye Li , Yuhan Meng , Xiaohui Gao , Xinyi Xu","doi":"10.1016/j.clnu.2025.09.020","DOIUrl":"10.1016/j.clnu.2025.09.020","url":null,"abstract":"<div><h3>Background & aims</h3><div>Emerging evidence suggests a possible association between dairy product intake and cognitive function in older adults; however, previous findings remain inconsistent. This study aimed to systematically evaluate the association between dairy intake and cognitive outcomes in older adults, and explore potential dose-response relationships and regional differences.</div></div><div><h3>Methods</h3><div>We searched PubMed, MEDLINE, Embase, Cochrane Library, Scopus, and CINAHL from their inception to 31 December 2024. Dose–response analysis was performed for cohort studies to assess the impact of different types and quantities of dairy intake on cognitive subdomains. Meta-regression was used to explore sources of heterogeneity. The results were presented as relative risks (RRs), odds ratios (ORs), and mean differences (MDs) with 95 % confidence intervals (CIs). The methodology followed the PRISMA guidelines for systematic reviews and meta-analyses.</div></div><div><h3>Results</h3><div>A total of 38 studies were included, comprising 21 cohort studies, 15 cross-sectional studies, and 2 randomized controlled trials. We stratified dairy products intake levels, and higher total dairy intake was associated with a reduced risk of cognitive decline and improved global cognitive function (Cohort: medium vs low, RR: 0.92, 95 % CI: 0.85, 0.99; high vs low, RR: 0.85, 95 % CI: 0.73, 0.98; Cross-sectional: high vs low, OR: 0.64, 95 % CI: 0.49, 0.82). Fermented dairy products were associated with improved verbal memory and executive function, whereas higher milk intake showed a potential association with poorer verbal memory in certain instances (medium vs low, MD: −0.04; 95 % CI: −0.09, 0.01; high vs low, MD: −0.05; 95 % CI: −0.09, −0.01). Evidence showed nonlinear associations, with the lowest risk of cognitive decline associated with a daily intake of 150 g of dairy products (<em>p</em>-nonlinear = 0.009, RR: 0.86, 95 % CI: 0.78, 0.95), and 30 g/day of whole-fat dairy (<em>p</em>-nonlinear = 0.007, RR: 0.83, 95 % CI: 0.74, 0.94). Regional differences were observed, with cognitive outcomes varying between European and Asian populations, possibly reflecting dietary habits and cultural contexts.</div></div><div><h3>Conclusions</h3><div>Dairy intake, especially fermented products and moderate total intake, may support cognitive health in older adults, though associations vary by region and dairy type. More high-quality studies are needed to clarify these relationships and guide dietary recommendations.</div></div>","PeriodicalId":10517,"journal":{"name":"Clinical nutrition","volume":"55 ","pages":"Pages 24-41"},"PeriodicalIF":7.4,"publicationDate":"2025-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145444098","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-25DOI: 10.1016/j.clnu.2025.10.006
Wenjie Chen , Hongzhuo Qin , Zhaokai Zhou , Yun Chen , Xiaowei Xu , Yajun Chen , Jieyu He , Ran Xu , Hua Gao , Qiong Lu
Aims
GLP-1 receptor agonists (GLP-1RAs) are first-line therapies for type 2 diabetes (T2DM) due to their additional weight-lowering and cardiovascular benefits. However, their impact on muscle mass is debated, posing a concern for sarcopenia in older adults with T2DM. This systematic review and meta-analysis aimed to evaluate the effects of GLP-1RAs on body composition and sarcopenia-related markers in diabetic patients and relevant preclinical models, and to explore the underlying mechanisms.
Methods
We systematically searched PubMed, Web of Science, MEDLINE, Cochrane Library, and EMBASE to identify relevant randomized controlled trials and animal studies on the impact of GLP-1 RAs on muscle in diabetic participants. Standardized Mean Difference (SMD) or Mean Difference (MD) with 95 % confidence intervals (CI) were calculated using random-effects or fixed-effect models to synthesize the effects on anthropometric, functional, and molecular endpoints.
Results
A total of 254 articles were retrieved, yielding 18 eligible studies after screening against the inclusion criteria. These comprised six human studies measuring lean mass, four clinical trials assessing Skeletal Muscle Mass Index (SMI), and eight animal studies. The animal studies investigated parameters including muscle mass, muscle fiber cross-sectional area, grip strength, lean mass percentage, myogenin, MyoD, Atrogin-1, MuRF-1, myostatin, GLUT4, SIRT1, and inflammatory cytokines (IL-1β, IL-6, TNF-α).
Conclusions
GLP-1 RAs were found to increase the percentage of lean body mass in animal models, improve body composition, enhance skeletal muscle strength, elevate concentrations of muscle growth factors, and reduce muscle growth inhibitory factors and inflammatory factors. These effects promote muscle cell proliferation and differentiation, accelerate muscle protein synthesis, leading to better overall muscle function. Confirming these promising preclinical findings requires large-scale randomized controlled trials in humans.
目的:GLP-1受体激动剂(GLP-1RAs)由于其额外的减肥和心血管益处而成为2型糖尿病(T2DM)的一线治疗药物。然而,它们对肌肉质量的影响存在争议,引起了老年2型糖尿病患者肌肉减少症的关注。本系统综述和荟萃分析旨在评估GLP-1RAs对糖尿病患者和相关临床前模型的体成分和肌肉减少相关标志物的影响,并探讨其潜在机制。方法:我们系统地检索PubMed、Web of Science、MEDLINE、Cochrane Library和EMBASE,以确定GLP-1 RAs对糖尿病参与者肌肉影响的相关随机对照试验和动物研究。使用随机效应或固定效应模型计算95%置信区间(CI)的标准化平均差(SMD)或平均差(MD),以综合对人体测量、功能和分子终点的影响。结果:共检索到254篇文献,根据纳入标准筛选后获得18项符合条件的研究。其中包括6项测量瘦质量的人体研究,4项评估骨骼肌质量指数(SMI)的临床试验,以及8项动物研究。动物实验研究的参数包括肌肉质量、肌纤维横截面积、握力、瘦质量百分比、肌生成素、MyoD、Atrogin-1、MuRF-1、肌生长抑制素、GLUT4、SIRT1和炎症因子(IL-1β、IL-6、TNF-α)。结论:GLP-1 RAs可提高动物模型的瘦体质量百分比,改善体成分,增强骨骼肌力量,提高肌肉生长因子浓度,降低肌肉生长抑制因子和炎症因子。这些作用促进肌肉细胞的增殖和分化,加速肌肉蛋白质的合成,导致更好的整体肌肉功能。确认这些有希望的临床前发现需要大规模的人体随机对照试验。
{"title":"Glucagon-like peptide-1 receptor agonists and sarcopenia-related markers in diabetes: A systematic review and meta-analysis","authors":"Wenjie Chen , Hongzhuo Qin , Zhaokai Zhou , Yun Chen , Xiaowei Xu , Yajun Chen , Jieyu He , Ran Xu , Hua Gao , Qiong Lu","doi":"10.1016/j.clnu.2025.10.006","DOIUrl":"10.1016/j.clnu.2025.10.006","url":null,"abstract":"<div><h3>Aims</h3><div>GLP-1 receptor agonists (GLP-1RAs) are first-line therapies for type 2 diabetes (T2DM) due to their additional weight-lowering and cardiovascular benefits. However, their impact on muscle mass is debated, posing a concern for sarcopenia in older adults with T2DM. This systematic review and meta-analysis aimed to evaluate the effects of GLP-1RAs on body composition and sarcopenia-related markers in diabetic patients and relevant preclinical models, and to explore the underlying mechanisms.</div></div><div><h3>Methods</h3><div>We systematically searched PubMed, Web of Science, MEDLINE, Cochrane Library, and EMBASE to identify relevant randomized controlled trials and animal studies on the impact of GLP-1 RAs on muscle in diabetic participants. Standardized Mean Difference (SMD) or Mean Difference (MD) with 95 % confidence intervals (CI) were calculated using random-effects or fixed-effect models to synthesize the effects on anthropometric, functional, and molecular endpoints.</div></div><div><h3>Results</h3><div>A total of 254 articles were retrieved, yielding 18 eligible studies after screening against the inclusion criteria. These comprised six human studies measuring lean mass, four clinical trials assessing Skeletal Muscle Mass Index (SMI), and eight animal studies. The animal studies investigated parameters including muscle mass, muscle fiber cross-sectional area, grip strength, lean mass percentage, myogenin, MyoD, Atrogin-1, MuRF-1, myostatin, GLUT4, SIRT1, and inflammatory cytokines (IL-1β, IL-6, TNF-α).</div></div><div><h3>Conclusions</h3><div>GLP-1 RAs were found to increase the percentage of lean body mass in animal models, improve body composition, enhance skeletal muscle strength, elevate concentrations of muscle growth factors, and reduce muscle growth inhibitory factors and inflammatory factors. These effects promote muscle cell proliferation and differentiation, accelerate muscle protein synthesis, leading to better overall muscle function. Confirming these promising preclinical findings requires large-scale randomized controlled trials in humans.</div></div>","PeriodicalId":10517,"journal":{"name":"Clinical nutrition","volume":"55 ","pages":"Pages 42-56"},"PeriodicalIF":7.4,"publicationDate":"2025-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145444106","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-25DOI: 10.1016/j.clnu.2025.10.007
Rocco Barazzoni , John L. Sievenpiper , Laurence Genton , Cyril WC. Kendall , Maria D. Ballesteros-Pomar , Annalisa Giosuè , Yves Boirie , Laura Chiavaroli , Tommy Cederholm , Anne-Marie Aas , Cristina Cuerda , Charilaos Dimosthenopoulos , Nicolaas E. Deutz , Hana Kahleova , Lorenzo M. Donini , Ursula Schwab , Stephane M. Schneider , Gabriele Riccardi , Stanislaw Klek , Jordi Salas-Salvadó , Jeffrey I. Mechanick
Diabetes mellitus is a systemic chronic disease with growing prevalence and potential multiorgan complications leading to clinical, social, and economic burdens. Nutritional and metabolic derangements are important components of both type 1 (T1DM) and type 2 diabetes (T2DM), but assessment of nutritional state, body composition and muscle function is commonly neglected. Likely reasons include high prevalence of overweight, obesity, or excess visceral fat in highly-prevalent T2DM, potentially diverting attention from undernutrition risk. Diabetes and adiposity are mechanistically related to sarcopenia, defined as reduction of skeletal muscle strength and mass, through complex muscle-catabolic derangements, conferring additional risk for negative outcomes. Awareness of diabetes-induced muscle abnormalities remains low among healthcare professionals, patients and policymakers, contributing to research, knowledge and practice gaps. Lifestyle recommendations and treatments centered on nutritional care and physical activity to preserve and improve muscle mass and function remain poorly implemented. The European Society for Clinical Nutrition and Metabolism (ESPEN) and the Diabetes Nutrition Study Group (DNSG), reference group for the European Association for the Study of Diabetes, recognize sarcopenic diabetes as a distinct clinical condition and priority for research and education, and call for action to enhance awareness, stimulate research and promote consensus on sarcopenic diabetes diagnostic criteria, prevention and management.
{"title":"Sarcopenic diabetes is an under-recognized and unmet clinical priority. A call for action from the European Society for Clinical Nutrition and Metabolism and the Diabetes Nutrition Study Group","authors":"Rocco Barazzoni , John L. Sievenpiper , Laurence Genton , Cyril WC. Kendall , Maria D. Ballesteros-Pomar , Annalisa Giosuè , Yves Boirie , Laura Chiavaroli , Tommy Cederholm , Anne-Marie Aas , Cristina Cuerda , Charilaos Dimosthenopoulos , Nicolaas E. Deutz , Hana Kahleova , Lorenzo M. Donini , Ursula Schwab , Stephane M. Schneider , Gabriele Riccardi , Stanislaw Klek , Jordi Salas-Salvadó , Jeffrey I. Mechanick","doi":"10.1016/j.clnu.2025.10.007","DOIUrl":"10.1016/j.clnu.2025.10.007","url":null,"abstract":"<div><div>Diabetes mellitus is a systemic chronic disease with growing prevalence and potential multiorgan complications leading to clinical, social, and economic burdens. Nutritional and metabolic derangements are important components of both type 1 (T1DM) and type 2 diabetes (T2DM), but assessment of nutritional state, body composition and muscle function is commonly neglected. Likely reasons include high prevalence of overweight, obesity, or excess visceral fat in highly-prevalent T2DM, potentially diverting attention from undernutrition risk. Diabetes and adiposity are mechanistically related to sarcopenia, defined as reduction of skeletal muscle strength and mass, through complex muscle-catabolic derangements, conferring additional risk for negative outcomes. Awareness of diabetes-induced muscle abnormalities remains low among healthcare professionals, patients and policymakers, contributing to research, knowledge and practice gaps. Lifestyle recommendations and treatments centered on nutritional care and physical activity to preserve and improve muscle mass and function remain poorly implemented. The European Society for Clinical Nutrition and Metabolism (ESPEN) and the Diabetes Nutrition Study Group (DNSG), reference group for the European Association for the Study of Diabetes, recognize sarcopenic diabetes as a distinct clinical condition and priority for research and education, and call for action to enhance awareness, stimulate research and promote consensus on sarcopenic diabetes diagnostic criteria, prevention and management.</div></div>","PeriodicalId":10517,"journal":{"name":"Clinical nutrition","volume":"55 ","pages":"Pages 208-218"},"PeriodicalIF":7.4,"publicationDate":"2025-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145562793","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}