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Association of nutrition impact symptoms with dietary intake among patients with advanced cancer referred to palliative care 姑息治疗晚期癌症患者营养影响症状与饮食摄入的关系
IF 2.6 Q3 NUTRITION & DIETETICS Pub Date : 2025-12-31 DOI: 10.1016/j.clnesp.2025.102894
Koji Amano , Vickie E. Baracos , Saori Koshimoto , Tatsuma Sakaguchi , Sayaka Arakawa , Naoharu Mori

Background & aims

Considering that cachexia-related symptoms interfere with dietary intake and compromise nutritional status in advanced cancer patients, these symptoms are classified as nutrition impact symptoms (NISs). However, the extent to which each NIS interferes with dietary intake remains unclear. Therefore, we examined the association between each NIS and dietary intake, considering the impact of an NIS cluster, and investigated the ability of each NIS to predict reduced dietary intake.

Methods

This is a secondary analysis using two datasets obtained from two surveys using a self-reported questionnaire conducted among advanced cancer patients referred to palliative care in multiple cancer hospitals. Participants evaluated 19 NISs (e.g., lack of appetite, early satiety, nausea, abnormal taste, and fatigue) and their dietary intake using a numerical rating scale (NRS) and the Ingesta-Verbal/Visual Analog Scale (IVVAS), respectively. To assess associations between each NIS and dietary intake, multivariate logistic regression analysis was performed adjusting for potential confounders, including four or more NISs with an NRS score of 4 or more as an NIS cluster. Values of the area under the curve (AUC) were also calculated for predicting a median IVVAS score or lower.

Results

Data were obtained from 328 participants in Survey 1 and 220 participants in Survey 2. Lack of appetite, early satiety, nausea, vomiting, abnormal taste, and fatigue were significantly associated with poor dietary intake (odds ratio [OR] 0.73, 95 % confidence interval [CI] 0.66–0.81; OR 0.84, 95 % CI 0.77–0.92; OR 0.80, 95 % CI 0.72–0.89; OR 0.80, 95 % CI 0.71–0.91; OR 0.91, 95 % CI 0.84–1.00; OR 0.90, 95 % CI 0.81–0.99, respectively). However, no significant association was observed for the other 13 NISs. All AUC values were greater than 0.750 for the 19 NISs. The highest AUC values were observed for lack of appetite, early satiety, and nausea (0.831, 95 % CI 0.797–0.866; 0.810, 95 % CI 0.773–0.848; 0.801, 95 % CI 0.764–0.838, respectively).

Conclusions

Lack of appetite, early satiety, nausea, vomiting, abnormal taste, and fatigue were significantly associated with dietary intake independently of the influence of other symptoms and other confounders. Furthermore, lack of appetite, early satiety, and nausea were good predictors for reduced dietary intake.
背景与目的:考虑到恶病质相关症状对晚期癌症患者饮食摄入的干扰和营养状况的损害,这些症状被归类为营养影响症状(NISs)。然而,每种NIS对饮食摄入的干扰程度仍不清楚。因此,考虑到NIS集群的影响,我们研究了每个NIS与饮食摄入量之间的关系,并调查了每个NIS预测饮食摄入量减少的能力。方法:这是一个二次分析,使用两个数据集,从两个调查中获得,使用自我报告的问卷,在多家癌症医院转诊姑息治疗的晚期癌症患者中进行。参与者分别使用数字评定量表(NRS)和摄入-言语/视觉模拟量表(IVVAS)评估19种NISs(如食欲不振、早饱、恶心、味觉异常和疲劳)及其饮食摄入量。为了评估每个NIS与饮食摄入之间的关联,进行了多变量logistic回归分析,调整了潜在的混杂因素,包括4个或更多的NISs, NRS评分为4分或以上作为NIS集群。还计算曲线下面积(AUC)值,以预测IVVAS中位评分或更低。结果:从调查1的328名参与者和调查2的220名参与者中获得数据。食欲不振、早饱、恶心、呕吐、味觉异常和疲劳与不良饮食摄入显著相关(比值比[OR] 0.73, 95%可信区间[CI] 0.66-0.81; OR 0.84, 95% CI 0.77-0.92; OR 0.80, 95% CI 0.72-0.89; OR 0.80, 95% CI 0.71-0.91; OR 0.91, 95% CI 0.84-1.00; OR 0.90, 95% CI 0.81-0.99)。然而,在其他13种NISs中没有观察到显著的关联。19个NISs的AUC值均大于0.750。AUC值最高的是食欲不振、早饱和恶心(分别为0.831,95% CI 0.797-0.866; 0.810, 95% CI 0.773-0.848; 0.801, 95% CI 0.764-0.838)。结论:食欲不振、早饱、恶心、呕吐、味觉异常和疲劳与饮食摄入显著相关,独立于其他症状和其他混杂因素的影响。此外,食欲不振、早饱和恶心是饮食摄入量减少的良好预测指标。
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引用次数: 0
Economic consequences when enteral tube feeding intolerance causes unplanned discontinuation in hospitalized older patients with gastroesophageal reflux disease 住院老年胃食管反流病患者肠内管喂养不耐受导致计划外停药的经济后果。
IF 2.6 Q3 NUTRITION & DIETETICS Pub Date : 2025-12-30 DOI: 10.1016/j.clnesp.2025.102892
Yukikazu Kamada , Kanako Kawano , Akina Iguchi , Noriko Tominaga , Chisato Okamoto , Masatoshi Inoue , Ataru Igarashi , Masafumi Kitakaze

Background & aims

Enteral tube feeding intolerance (ETFI) is a common complication in older patients with gastroesophageal reflux disease (GERD), often leading to unplanned discontinuation of nutritional support. While the clinical consequences of ETFI are well-documented, its economic impact on hospital operations remains unclear. This study aimed to evaluate the financial consequences of ETFI-related discontinuation of enteral nutrition in hospitalized older patients with GERD, focusing on changes in medical resource allocation and hospital revenue under Japan's hybrid reimbursement system.

Methods

A retrospective observational study was conducted using patient-level data from a long-term care ward in Japan between April 2018 and March 2021. Patients who initiated enteral tube feeding were categorized based on whether enteral feeding was discontinued due to intolerance. Medical claims data were analyzed to calculate fee-for-service (FFS) and fixed payment system (FPS) charges, unreimbursed medical charges (i.e., revenue loss under FPS), and inpatient living care expenses. Hospital loss simulations were performed based on discontinuation rates and patient characteristics.

Results

Among 149 patients, 23.5 % experienced ETFI-related discontinuation. These patients had significantly lower BMI and shorter feeding durations. Discontinuation was associated with increased unreimbursed medical charges (median JPY +2288/day (USD +15.2/day, USD 1.0 = JPY 150.80) at 1 week post-discontinuation) and decreased living care revenue (median JPY −1179/day (USD −7.82/day)). Multivariate analysis identified ETFI and low BMI (<17.4) as independent predictors of increased hospital revenue losses. Simulations estimated a total loss of JPY 248,000 (USD 1644.56) per 10 hospitalized older patients with GERD over 4 weeks, with greater losses observed in low-BMI patients and those receiving polymeric formulas.

Conclusion

Unplanned discontinuation of enteral tube feeding due to intolerance in older patients with GERD imposes a substantial economic burden on hospitals, primarily through unreimbursed medical charges and reduced living care revenue. Preventive strategies—such as early nutritional intervention and formula selection—may mitigate these losses and support sustainable hospital management.
背景与目的:肠内管喂养不耐受(ETFI)是老年胃食管反流病(GERD)患者的常见并发症,常导致营养支持的计划外中断。虽然ETFI的临床后果有充分的记录,但其对医院业务的经济影响尚不清楚。本研究旨在评估住院老年胃食管反流患者因etfi相关而停止肠内营养的财务后果,重点关注日本混合报销制度下医疗资源分配和医院收入的变化。方法:对2018年4月至2021年3月期间日本一家长期护理病房的患者数据进行回顾性观察性研究。开始肠内管喂养的患者根据肠内喂养是否因不耐受而停止进行分类。对医疗索赔数据进行分析,以计算按服务收费(FFS)和固定支付制度(FPS)收费、未报销的医疗费用(即固定支付制度下的收入损失)和住院生活护理费用。根据停药率和患者特征进行医院损失模拟。结果:149例患者中,23.5%经历了etfi相关停药。这些患者的BMI明显较低,喂养时间也较短。停药后1周,未报销医疗费用增加(中位数为2288日元/天(+15.2美元/天,1.0美元= 150.80日元),生活护理收入减少(中位数为1179日元/天(-7.82美元/天))。多变量分析确定了ETFI和低BMI(结论:老年胃食管反流患者因不耐受而计划外停止肠内管喂养给医院带来了巨大的经济负担,主要是通过未报销的医疗费用和减少的生活护理收入。预防策略,如早期营养干预和配方选择,可以减轻这些损失,并支持可持续的医院管理。
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引用次数: 0
Global leadership initiative on malnutrition-based nutritional phenotype and factors associated with the outcomes of hospitalized patients managed by a nutrition support team: A retrospective study 由营养支持小组管理的住院患者基于营养不良的营养表型和与结果相关因素的全球领导倡议:一项回顾性研究。
IF 2.6 Q3 NUTRITION & DIETETICS Pub Date : 2025-12-30 DOI: 10.1016/j.clnesp.2025.102889
Mathilde Barrallier , Emeric Rageul , Charlotte Nesseler , Quentin Le Cornu , Ronan Thibault
<div><h3>Background and aims</h3><div>What are the Global Leadership Initiative on Malnutrition (GLIM) criteria leading to the diagnosis of malnutrition at hospital, specifically in diabetic patients, is not well known. The factors associated with the clinical outcomes of nutritionally at-risk hospitalized patients have been scarcely investigated.</div></div><div><h3>Aims</h3><div>To characterize the GLIM-based nutritional phenotype of hospitalized patients managed by a Nutrition Support Teams (NST) (primary), and to compare the GLIM malnutrition diagnostic criteria between diabetic and non-diabetic patients (secondary); to identify the factors associated with hospital readmission one month after discharge and one-month mortality (secondary).</div></div><div><h3>Methods</h3><div>We conducted a retrospective observational study including all the consecutive adult patients managed by the NST of a tertiary university hospital. The exclusion criteria were age under 18 yr and absence of assessment of body composition by bioimpedance analysis (BIA). Malnutrition was diagnosed according to the GLIM criteria: the etiologic criterion was the hospitalization for an acute or chronic disease, and three phenotypic criteria were: low body mass index (BMI), weight loss, and/or low fat-free mass index (FFMI) derived from BIA. Food intake was assessed by the Simple Evaluation of Food Intake® (SEFI®). Handgrip strength was measured using a dynamometer. Hospital readmission and death one month after discharge were collected from the electronic medical records (EMR). Multivariable logistic regression analyses using a stepwise top-down selection identified factors associated with one-month hospital readmission and mortality.</div></div><div><h3>Results</h3><div>231 patients were included: 43 % of females, age (mean ± SD), 62.2 ± 15.9 yr, BMI, 23.5 ± 6.4, 73.6 % (170/231) were malnourished, of whom 66.5 % (113/170) had severe malnutrition, and 20.3 % (47/231) had diabetes. Malnutrition was diagnosed according to the three phenotypic criteria in 59/170 patients (34.7 %), two in 56/170 patients (33.1 %), and only one in 54/170 patients (31.8 %). The diabetic patients were less likely to have a low FFMI (29.8 % (14/47) vs 60.9 % (109/179), P < 0.001) or be malnourished (61.7 % (29/47) vs 76.6 % (141/184), P = 0.04), but more likely to have a low handgrip strength (64.3 % (27/42) vs 45.6 % (68/149), P = 0.03) than non-diabetic patients. Multivariable analyses showed that cancer (odds ratio (OR) = 2.51 [1.17–5.37], P = 0.02) and SEFI® score (OR = 0.89 [95 % confidence interval, 0.79–0.99], P = 0.04) were associated with higher risk of hospital readmission, whereas weight loss (OR = 3.20 [1.26–8.17], P = 0.01) and diabetes (OR = 2.76 [1.10–6.91], P = 0.03) were associated with mortality.</div></div><div><h3>Conclusion</h3><div>One third of patients were diagnosed malnutrition with one phenotypic criterion, suggesting that all the GLIM phenotypic criteria should be used t
背景和目的:导致医院营养不良诊断的全球营养不良领导倡议(GLIM)标准是什么,特别是糖尿病患者,尚不清楚。与营养不良住院患者临床结果相关的因素很少被调查。目的:表征由营养支持小组(NST)管理的住院患者的基于GLIM的营养表型(主要),并比较糖尿病和非糖尿病患者的GLIM营养不良诊断标准(次要);为了确定与出院后1个月再入院和1个月死亡率(次要)相关的因素,方法:我们进行了一项回顾性观察研究,包括一家三级大学医院NST管理的所有连续成年患者。排除标准为年龄在18岁以下,没有通过生物阻抗分析(BIA)评估身体成分。根据GLIM标准诊断营养不良:病因标准为急性或慢性疾病住院治疗,表型标准为:低体重指数(BMI)、体重减轻和/或低无脂质量指数(FFMI)。通过食物摄入简单评估®(SEFI®)评估食物摄入。用测力仪测量握力。从电子病历(EMR)中收集出院后1个月的再入院和死亡情况。多变量逻辑回归分析采用逐步自上而下的选择确定了与一个月住院再入院和死亡率相关的因素。结果:纳入231例患者:43%的女性,年龄(mean±SD), 62.2±15.9岁,BMI, 23.5±6.4,73.6%(170/231)营养不良,其中66.5%(113/170)为重度营养不良,20.3%(47/231)为糖尿病。3项表型标准诊断为营养不良者59/170(34.7%),2 / 56/170(33.1%),1 / 54/170(31.8%)。糖尿病患者FFMI较低的发生率较低(29.8% (14/47)vs 60.9%(109/179))。结论:1 / 3的患者采用一种表型标准诊断为营养不良,提示应采用所有GLIM表型标准来保证营养不良的诊断。糖尿病患者的FFMI高于非糖尿病患者,握力低于非糖尿病患者。在NST管理的患者中,低食物摄入和癌症与再入院有关,而糖尿病和体重减轻与早期死亡有关。
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引用次数: 0
Can the 13C-octanoic acid breath test accurately measure gastric emptying after sleeve gastrectomy and Roux-en-Y gastric bypass? A proof-of concept analysis 13c -辛酸呼气试验能准确测量袖式胃切除术和Roux-en-Y胃旁路术后胃排空情况吗?概念验证分析。
IF 2.6 Q3 NUTRITION & DIETETICS Pub Date : 2025-12-29 DOI: 10.1016/j.clnesp.2025.102891
Nele Steenackers , Patrick Augustijns , Wies Deckers , Ellen Deleus , Christophe M. Deroose , Matthias Lannoo , Wei Li , Ann Mertens , Tim Vanuytsel , Greet Vandermeulen , Roman Vangoitsenhoven , Kristin Verbeke , Bart Van der Schueren , Christophe Matthys

Background

Bariatric surgery alters gastrointestinal anatomy and physiology, complicating functional assessments such as gastric emptying. The 13C-octanoic acid breath test is a simple, non-invasive alternative to scintigraphy, though its validity in bariatric populations requires further validation.

Methods

For this proof-of-concept analysis, gastric emptying data were derived from a cross-sectional study including individuals with obesity, sleeve gastrectomy, and Roux-en-Y gastric bypass (RYGB). Gastric emptying was measured simultaneously using the 13C-octanoic breath test and the reference method, scintigraphy. Gastric emptying half-times (GET1/2) were compared between the two methods using Wilcoxon signed-rank tests in each group. Concordance between both methods was assessed using Kendall's tau correlation coefficients, and Bland–Altman plots.

Results

No significant inter-method differences were observed for GET1/2 in any group. Mean differences were −26.7 min (95 % CI: −72.3; 18.6) for obesity, −3.92 min (95 % CI: −30.8; 23.0) for sleeve gastrectomy, and −8.55 min (95 % CI: −21.3; 4.18) for RYGB. Kendall's tau coefficients indicated positive rank associations within each group, but were non-significant (Obesity: 0.8, P = 0.16; sleeve gastrectomy: 0.90, P = 0.13; RYGB: 0.57, P = 0.33). Bland–Altman plots demonstrated acceptable agreement between the measurements across all groups.

Conclusion

This proof-of-concept analysis suggests that the 13C-octanoic acid breath test has potential as a valid, non-invasive method for assessing gastric emptying in post-bariatric surgery patients. However, larger validation studies are warranted to confirm these preliminary findings.
背景:减肥手术改变了胃肠道解剖和生理,使胃排空等功能评估复杂化。13c -辛酸呼吸测试是一种简单、无创的替代方法,但其在肥胖人群中的有效性需要进一步验证。方法:在这个概念验证分析中,胃排空数据来自一项横断面研究,包括肥胖、袖式胃切除术和Roux-en-Y胃旁路(RYGB)患者。采用13c -辛烷酸呼气试验和参考方法-闪烁图同时测量胃排空。采用Wilcoxon符号秩检验比较两种方法的胃排空半衰期(GET1/2)。使用Kendall's tau相关系数和Bland-Altman图评估两种方法之间的一致性。结果:各组间GET1/2无明显差异。肥胖组的平均差异为-26.7分钟(95% CI: -72.3; 18.6),袖胃切除术组的平均差异为-3.92分钟(95% CI: -30.8; 23.0), RYGB组的平均差异为-8.55分钟(95% CI: -21.3; 4.18)。Kendall's tau系数显示各组间的等级正相关,但不显著(肥胖:0.8,P=0.16;袖胃切除术:0.90,P=0.13; RYGB: 0.57, P=0.33)。Bland-Altman图显示了所有组间测量结果的一致性。结论:这一概念验证分析表明,13c -辛酸呼气试验有潜力作为一种有效的、无创的方法来评估减肥手术后患者的胃排空。然而,需要更大规模的验证研究来证实这些初步发现。
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引用次数: 0
Body composition and functional status in the COVID-19 recovery phase: Prevalence of sarcopenia and sarcopenic obesity COVID-19恢复期的身体成分和功能状态:肌肉减少症和肌肉减少性肥胖的患病率
IF 2.6 Q3 NUTRITION & DIETETICS Pub Date : 2025-12-29 DOI: 10.1016/j.clnesp.2025.102877
Montserrat Montes-Ibarra , Flavio T. Vieira , Maria Cristina Gonzalez , Alan Garcia-Grimaldo , Ivan Armando Osuna-Padilla , Andreia Bauermann-Vieira , Edith Pituskin , Richard B. Thompson , D. Ian Paterson , Carla M. Prado

Background & aims

COVID-19 may be associated with unfavourable body composition changes. This includes increased fat mass and decreased muscle mass, which can lead to sarcopenia and sarcopenic obesity (SO), conditions associated with impaired physical performance and reduced quality of life, among other adverse outcomes. This study investigated the prevalence of sarcopenia and SO in individuals who recovered from the first COVID-19 wave and their association with functional outcomes.

Methods

Clinical characteristics, body composition (bioelectrical impedance analysis), functional status (handgrip strength [HGS], 6-min walk test [6MWT]), and lung function (spirometry) were collected.

Results

37 individuals (89.2 % Caucasians, 64.9 % females, median age 48 years [IQR: 40; 60], 10.8 % > 65y) were assessed after a median of 189 days (IQR: 169; 201) post-COVID-19 infection. The combined prevalence of sarcopenia/SO was 40.5 %, was identified in 37.8 %, while a single case (2.7 %) of sarcopenia without obesity was found. The sarcopenia/SO group had lower 6MWT and phase angle, and higher prevalence of hypertension. Sarcopenia/SO was negatively associated with 6MWT performance (β: −115.35, 95 % CI: −161.57 to −69.12), COVID-19 symptoms, disease severity, and duration were not associated with sarcopenia/SO diagnosis.

Conclusion

A high presence of sarcopenia/SO was identified and was negatively associated with health outcomes in individuals post-COVID-19. Thus, it is important to assess and address conditions associated with abnormal body composition after infectious diseases to better inform strategies for improving long-term outcomes.
背景与目的:COVID-19可能与不利的身体组成变化有关。这包括脂肪量增加和肌肉量减少,这可能导致肌肉减少症和肌肉减少性肥胖(SO),以及与身体机能受损和生活质量下降相关的疾病,以及其他不良后果。本研究调查了从第一次COVID-19浪潮中恢复的个体中肌肉减少症和SO的患病率及其与功能结局的关系。方法:收集患者的临床特征、身体组成(生物电阻抗分析)、功能状态(握力[HGS]、6分钟步行试验[6MWT])、肺功能(肺活量测定)。结果:37例患者(89.2%为白种人,64.9%为女性,中位年龄为48岁[IQR: 40; 60], 10.8%为bb0 - 65岁)在感染后189天(IQR: 169; 201)后接受评估。骨骼肌减少症/SO的总患病率为40.5%,其中37.8%被确诊为骨骼肌减少症,而未发现肥胖的骨骼肌减少症单一病例(2.7%)。肌少症/SO组6MWT和相位角较低,高血压患病率较高。肌少症/SO与6MWT表现呈负相关(β: -115.35, 95% CI: -161.57至-69.12),COVID-19症状、疾病严重程度和持续时间与肌少症/SO诊断无关。结论:在covid -19后个体中,肌肉减少症/SO的存在率很高,并且与健康结果呈负相关。因此,重要的是评估和解决传染病后与异常身体成分相关的条件,以更好地为改善长期结果的策略提供信息。
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引用次数: 0
The effect of transcranial direct current stimulation and nutritional counseling therapy on attentional bias to food cues: A randomized clinical trial 经颅直流电刺激和营养咨询治疗对食物线索注意偏倚的影响:一项随机临床试验。
IF 2.6 Q3 NUTRITION & DIETETICS Pub Date : 2025-12-26 DOI: 10.1016/j.clnesp.2025.102886
Jessica Lorenzzi Elkfury , Luciana C. Antunes , Gibson Weydmann , Lizia Nardi Menegassi , Liciane Fernandes Medeiros , Tiago Madeira Cardinal , Betina Franceschini Tocchetto , Iraci L.S. Torres , Felipe Fregni , Lisiane Bizarro , Wolnei Caumo

Background & aims

This study investigated the effects of transcranial direct current stimulation (tDCS) and nutritional counseling therapy (NCT) on attentional bias (AB) in binge eating disorder.

Methods

This study was designed as a pilot randomized, factorial, blind, parallel-controlled clinical trial. Forty women were allocated to one of four groups: active tDCS (a-tDCS), a-tDCS + NCT, s-tDCS (sham tDCS) + NCT, NCT. The 28 home-based tDCS sessions were applied to the DLPFC (anode/right and cathode/left). The outcome was the delta values (pre- and post-treatment AB scores). Each AB score was calculated based on the stimulus onset asynchrony (SOA) at which stimuli were presented (100, 500, and 2000 ms).

Results

Mixed analyses of variance revealed a significant interaction between treatment and SOA (p = 0.035). The a-tDCS with NCT group showed a decrease in AB at an SOA of 500 ms. This decrease significantly differed from the increase observed in the s-tDCS with NCT group for the same SOA (p = 0.027). The a-tDCS with NCT group showed an increase in AB at an SOA of 2000 ms, which differed significantly from the decrease observed at the same SOA in the a-tDCS group (p = 0.032).

Conclusions

The combined therapy (a-tDCS with NCT) decreased AB at the pre-conscious orientation of attention and increased it when conscious orientation was possible.

Trial registration

ClinicalTrials.gov: NCT 04226794. Registered on July 2, 2019.
背景与目的:本研究探讨经颅直流电刺激(tDCS)和营养咨询治疗(NCT)对暴食症患者注意偏置(AB)的影响。方法:本研究采用随机、盲法、平行对照临床试验。40名女性被分为四组:活动tDCS (a-tDCS)、a-tDCS + NCT、s-tDCS(假tDCS) + NCT、NCT。28个基于家庭的tDCS会话应用于DLPFC(阳极/右和阴极/左)。结果是δ值(治疗前和治疗后的AB评分)。每个AB分数是根据刺激出现时(100ms、500ms和2000ms)的刺激发生异步性(SOA)来计算的。结果:混合方差分析显示治疗与SOA之间有显著的相互作用(p = 0.035)。a- tdcs加NCT组在SOA 500 ms时AB下降。这种下降明显不同于s-tDCS与NCT组在相同SOA下观察到的增加(p = 0.027)。具有NCT的a-tDCS组在SOA为2000 ms时AB增加,这与a-tDCS组在相同SOA下观察到的AB减少有显著差异(p = 0.032)。结论:a-tDCS与NCT联合治疗可降低注意前意识取向时的AB值,并可使注意前意识取向时AB值升高。试验注册:ClinicalTrials.gov: NCT04226794。2019年7月2日注册。
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引用次数: 0
Geriatric nutritional risk and exceptional longevity: Findings from a large-scale population-based study 老年营养风险和超常寿命:一项大规模人群研究的结果。
IF 2.6 Q3 NUTRITION & DIETETICS Pub Date : 2025-12-26 DOI: 10.1016/j.clnesp.2025.102887
Xuhui Liu , Xujie Wang , Rongfei Xie , Qianyue Pan , Biyun Wang , Qiao Zhu , Chunjian Ma

Background

The Geriatric Nutritional Risk Index (GNRI) is a widely used prognostic marker in elderly populations, but its relevance to exceptional longevity remains unclear.

Methods

This study is a cross-sectional analysis using data from 1497 adults aged ≥60 years who participated in the Chinese Healthy Longevity and Mortality Study (CHLMS), a large-scale, population-based study designed to examine the factors influencing exceptional longevity. GNRI was calculated using serum albumin levels and weight-based indices. Multivariable logistic regression models (Models 1–3) were employed to examine the association between GNRI and the probability of reaching age ≥100. Restricted cubic spline and piecewise logistic regression were used to assess nonlinear and threshold effects. Sensitivity analyses included subgroup stratification and categorical transformations of clinical covariates and dietary behaviors.

Results

Among 1497 participants, 736 (49.2 %) were aged ≥100 years, with a higher proportion of females (80.0 % vs 59.1 %; p < 0.001). Centenarians had significantly lower GNRI (92 vs 101), BMI (18.0 vs 20.4 kg/m2), and ADL scores (90 vs 100), all p < 0.001. In fully adjusted models, each unit increase in GNRI was associated with an 11 % decrease in the odds of reaching age ≥100 (Model 3 OR = 0.89; 95 % CI, 0.86–0.91; p < 0.001). Centenarian prevalence declined across GNRI quartiles from 79.8 % (Q1) to 20.2 % (Q4). Restricted cubic spline analysis demonstrated a nonlinear association. Subgroup and sensitivity analyses confirmed the robustness of this association across various demographic and dietary strata.

Conclusions

In centenarians, lower GNRI is associated with greater odds of exceptional longevity. However, as this is a cross-sectional study, causality cannot be inferred. Longitudinal studies are needed to explore this relationship further.
背景:老年营养风险指数(GNRI)是老年人广泛使用的预后指标,但其与超常寿命的相关性尚不清楚。方法:本研究是一项横断面分析,使用1497名年龄≥60岁的成年人的数据,这些成年人参加了中国健康寿命和死亡率研究(CHLMS),这是一项大规模、基于人群的研究,旨在研究影响异常寿命的因素。GNRI采用血清白蛋白水平和体重指标计算。采用多变量logistic回归模型(模型1-3)检验GNRI与达到≥100岁概率之间的关系。使用限制三次样条和分段逻辑回归来评估非线性和阈值效应。敏感性分析包括亚组分层和临床协变量和饮食行为的分类转化。结果:在1497名参与者中,736名(49.2%)年龄≥100岁,女性比例较高(80.0%比59.1%;p2), ADL评分(90比100),均为p结论:在百岁老人中,较低的GNRI与较高的异常长寿几率相关。然而,由于这是一项横断面研究,因果关系无法推断。需要进行纵向研究来进一步探索这种关系。
{"title":"Geriatric nutritional risk and exceptional longevity: Findings from a large-scale population-based study","authors":"Xuhui Liu ,&nbsp;Xujie Wang ,&nbsp;Rongfei Xie ,&nbsp;Qianyue Pan ,&nbsp;Biyun Wang ,&nbsp;Qiao Zhu ,&nbsp;Chunjian Ma","doi":"10.1016/j.clnesp.2025.102887","DOIUrl":"10.1016/j.clnesp.2025.102887","url":null,"abstract":"<div><h3>Background</h3><div>The Geriatric Nutritional Risk Index (GNRI) is a widely used prognostic marker in elderly populations, but its relevance to exceptional longevity remains unclear.</div></div><div><h3>Methods</h3><div>This study is a cross-sectional analysis using data from 1497 adults aged ≥60 years who participated in the Chinese Healthy Longevity and Mortality Study (CHLMS), a large-scale, population-based study designed to examine the factors influencing exceptional longevity. GNRI was calculated using serum albumin levels and weight-based indices. Multivariable logistic regression models (Models 1–3) were employed to examine the association between GNRI and the probability of reaching age ≥100. Restricted cubic spline and piecewise logistic regression were used to assess nonlinear and threshold effects. Sensitivity analyses included subgroup stratification and categorical transformations of clinical covariates and dietary behaviors.</div></div><div><h3>Results</h3><div>Among 1497 participants, 736 (49.2 %) were aged ≥100 years, with a higher proportion of females (80.0 % vs 59.1 %; p &lt; 0.001). Centenarians had significantly lower GNRI (92 vs 101), BMI (18.0 vs 20.4 kg/m<sup>2</sup>), and ADL scores (90 vs 100), all p &lt; 0.001. In fully adjusted models, each unit increase in GNRI was associated with an 11 % decrease in the odds of reaching age ≥100 (Model 3 OR = 0.89; 95 % CI, 0.86–0.91; p &lt; 0.001). Centenarian prevalence declined across GNRI quartiles from 79.8 % (Q1) to 20.2 % (Q4). Restricted cubic spline analysis demonstrated a nonlinear association. Subgroup and sensitivity analyses confirmed the robustness of this association across various demographic and dietary strata.</div></div><div><h3>Conclusions</h3><div>In centenarians, lower GNRI is associated with greater odds of exceptional longevity. However, as this is a cross-sectional study, causality cannot be inferred. Longitudinal studies are needed to explore this relationship further.</div></div>","PeriodicalId":10352,"journal":{"name":"Clinical nutrition ESPEN","volume":"72 ","pages":"Article 102887"},"PeriodicalIF":2.6,"publicationDate":"2025-12-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145849048","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
Konjac mannan oligosaccharides as a sustainer of fasting-associated gut microbiome signature after discontinuation of intermittent fasting in overweight individuals: A protocol for an open-label randomized clinical trial 魔芋甘露寡糖作为超重个体停止间歇性禁食后禁食相关肠道微生物特征的维持者:一项开放标签随机临床试验的方案
IF 2.6 Q3 NUTRITION & DIETETICS Pub Date : 2025-12-24 DOI: 10.1016/j.clnesp.2025.102888
Junhong Su , Guorong Ma , Xianghua Tang , Zhongren Ma , Zhenrong Xie , Maikel P. Peppelenbosch

Background

Our previous studies show that the improvement in cardiometabolic traits by intermittent fasting is associated with remodeling the gut microbiome, with short-chain fatty acids (SCFA) producing bacteria being evident. These effects, however, are largely lost when intermittent fasting is discontinued. Konjac mannan oligosaccharides (KMOS) are a commercial nature-deprived prebiotic, which has been reported to increase the levels of intestinal SCFA-producing bacteria. However, the capacity of continued KMOS consumption to maintain intermittent fasting-provoked levels of SCFA-producing bacteria, remains unknown.

Methods

This study aims to test whether a KMOS supplement positively affects fasting-provoked SCFA-producing bacteria levels during, and in particularly, after discontinuation of intermittent fasting. This prospective, randomized, controlled trial will be conducted in overweight volunteers aged 18–65. All participants will perform one month of intermittent fasting followed by one month of an ad libitum diet. Participants will be randomly assigned to receive KMOS (1.5 g/d) during fasting, both during fasting and the subsequent ad libitum period, or neither. Primary outcomes will be relative abundance of SCFA-producing bacteria in fecal samples, as determined by 16s rRNA sequencing. Secondary outcomes will be changes in body weight, blood pressure, and serum lipid levels.

Conclusions

Findings from this trial will answer the question whether KMOS can maintain fasting-associated SCFA producer level and metabolic benefits when fasting is discontinued.

Clinical trial registration

ChiCTR2200058139.
背景:我们之前的研究表明,间歇性禁食对心脏代谢特性的改善与肠道微生物群的重塑有关,其中产生短链脂肪酸(SCFA)的细菌很明显。然而,当停止间歇性禁食时,这些效果基本上消失了。魔芋甘露寡糖(KMOS)是一种商业化的天然益生元,据报道,它可以增加肠道中产生scfa的细菌的水平。然而,持续消耗KMOS以维持间歇性禁食引起的scfa产生细菌水平的能力仍然未知。方法:本研究旨在测试KMOS补充剂是否会在间歇性禁食期间,特别是在停止禁食后,对禁食引起的scfa产生细菌水平产生积极影响。这项前瞻性、随机、对照试验将在18-65岁的超重志愿者中进行。所有参与者将进行一个月的间歇性禁食,然后是一个月的随意饮食。参与者将被随机分配在禁食期间接受KMOS (1.5 g/d),在禁食期间和随后的自由活动期间,或两者都不接受。主要结果将是粪便样本中产生scfa的细菌的相对丰度,由16s rRNA测序确定。次要结果是体重、血压和血脂水平的变化。结论:该试验的结果将回答KMOS是否可以在禁食停止时维持与禁食相关的SCFA生成水平和代谢益处。临床试验注册:ChiCTR2200058139。
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引用次数: 0
The impact of olive oil polyphenol supplementation on metabolic syndrome parameters The OleoMetS study: A randomized, controlled clinical trial 补充橄榄油多酚对代谢综合征参数的影响OleoMetS研究:一项随机对照临床试验
IF 2.6 Q3 NUTRITION & DIETETICS Pub Date : 2025-12-20 DOI: 10.1016/j.clnesp.2025.102883
George Samoutis , Tassos C. Kyriakides , Nicholas Demetriou , Evdoxia Poulianiti , Gregoria Samouti , Sophronia Samouti , Panagiotis Diamantakos , Eleni Melliou , Prokopios Magiatis
<div><h3>Background & aims</h3><div>Olive oil aldehydic phenols (OOPs), including oleocanthal, oleacein, oleuropein aglycone, and ligstroside aglycone, are highly bioactive secoiridoids with unique health-protective properties. Preclinical investigations have demonstrated that OOPs possess anti-inflammatory and antioxidant attributes. The aim of the study was to assess the direct health properties of OOPs as a food supplement in humans diagnosed with metabolic syndrome. Fasting Blood Glucose (FBG) and Hemoglobin A1c (HbA1c) were chosen as primary endpoints because they are key indicators of glucose control, a core aspect of metabolic syndrome. Their combined assessment offers a comprehensive view of both short-term and long-term glucose regulation, making them highly relevant for evaluating interventions.</div></div><div><h3>Methods</h3><div>This double-blind, randomized, controlled clinical trial screened 110 individuals for eligibility between September 16, 2024, and January 27, 2025. Eight did not meet the inclusion criteria for metabolic syndrome, and 102 eligible participants were randomly assigned to the OOPs supplement or placebo group using a computer-generated randomization sequence to receive either the OOPs supplement or placebo. The 12-week intervention provided either a 10 mg/day polyphenol-rich olive oil extract food supplement (80 % oleocanthal/oleacein, 18 % oleuropein aglycon/ligstroside aglycon) or a placebo. No changes to lifestyle were recommended, and diet and physical activity were assessed at week 6. Fasting blood glucose (FBG) and hemoglobin A1C (HbA1c) were the primary outcomes. Secondary outcomes included lipid profile, C-reactive protein (CRP), body mass index (BMI), blood pressure, waist circumference, liver function tests (LFTs), estimated glomerular filtration rate (eGFR), uric acid, and fatigue scores. Repeated measures ANOVA/Linear Mixed Models were used to compare the mean changes (12 weeks-baseline) in fasting blood glucose levels between the intervention group and the placebo arm. Similar analysis (changes since baseline) was conducted for the continuous secondary outcomes. For categorical outcomes, changes since baseline were compared using chi-square methods. Bonferroni adjustments were made for multiple comparisons as appropriate.</div></div><div><h3>Results</h3><div>All 102 randomized participants completed the 12-week intervention and were included in the final analysis. The intervention group demonstrated significant improvements across various metabolic and physiological markers compared to the placebo group. Notable reductions were observed in FBG (mean difference: −7.06 mg/dL, p < 0.0001) and HbA1c (−0.29 %, p < 0.0001). Additionally, the intervention led to significant decreases in BMI (−1.15, p < 0.0001), systolic blood pressure (−7.66 mmHg, p = 0.004), triglycerides (−8.57, p = 0.0003), oxidized LDL (−5.01, p < 0.0001), uric acid (−1.04, p < 0.0001), ALT (−4.92, p = 0.0002), and fa
背景与目的:橄榄油醛类酚(OOPs)是一种具有高生物活性的环烯醚萜类化合物,具有独特的保健作用,包括油酸苷、油酸苷、油酸苷苷元和油酸苷元。临床前研究表明,OOPs具有抗炎和抗氧化特性。该研究的目的是评估OOPs作为一种食物补充剂对诊断为代谢综合征的人的直接健康特性。选择空腹血糖(FBG)和血红蛋白A1c (HbA1c)作为主要终点,因为它们是血糖控制的关键指标,是代谢综合征的核心方面。他们的综合评估提供了短期和长期血糖调节的全面观点,使其与评估干预措施高度相关。方法:这项双盲、随机、对照临床试验在2024年9月16日至2025年1月27日期间筛选了110名符合条件的患者。8人不符合代谢综合征的纳入标准,102名符合条件的参与者使用计算机生成的随机化序列随机分配到OOPs补充剂组或安慰剂组,接受OOPs补充剂或安慰剂。为期12周的干预提供了10mg/天的富含多酚的橄榄油提取物食品补充剂(80%油橄榄醇/油橄榄醇,18%油橄榄醇苷/油橄榄苷)或安慰剂。不建议改变生活方式,并在第6周评估饮食和身体活动。空腹血糖(FBG)和血红蛋白A1C (HbA1c)是主要结局。次要结局包括血脂、c反应蛋白(CRP)、体重指数(BMI)、血压、腰围、肝功能测试(LFTs)、肾小球滤过率(eGFR)、尿酸和疲劳评分。使用重复测量方差分析/线性混合模型比较干预组和安慰剂组之间空腹血糖水平的平均变化(12周基线)。对连续次要结局进行了类似的分析(自基线以来的变化)。对于分类结果,使用卡方方法比较自基线以来的变化。在适当的情况下对多重比较进行Bonferroni调整。结果:所有102名随机受试者完成了为期12周的干预并纳入最终分析。与安慰剂组相比,干预组在各种代谢和生理指标上表现出显著的改善。FBG显著降低(平均差值:-7.06 mg/dL)。结论:补充OOPs有望改善MetS患者的关键代谢指标。该干预措施耐受性良好,无严重不良事件报告。需要进行更长的干预期、随访和更高的OOPs剂量的进一步研究,以评估影响的长期持久性和程度。试验注册:ClinicalTrials.gov标识符:NCT07144488。
{"title":"The impact of olive oil polyphenol supplementation on metabolic syndrome parameters The OleoMetS study: A randomized, controlled clinical trial","authors":"George Samoutis ,&nbsp;Tassos C. Kyriakides ,&nbsp;Nicholas Demetriou ,&nbsp;Evdoxia Poulianiti ,&nbsp;Gregoria Samouti ,&nbsp;Sophronia Samouti ,&nbsp;Panagiotis Diamantakos ,&nbsp;Eleni Melliou ,&nbsp;Prokopios Magiatis","doi":"10.1016/j.clnesp.2025.102883","DOIUrl":"10.1016/j.clnesp.2025.102883","url":null,"abstract":"&lt;div&gt;&lt;h3&gt;Background &amp; aims&lt;/h3&gt;&lt;div&gt;Olive oil aldehydic phenols (OOPs), including oleocanthal, oleacein, oleuropein aglycone, and ligstroside aglycone, are highly bioactive secoiridoids with unique health-protective properties. Preclinical investigations have demonstrated that OOPs possess anti-inflammatory and antioxidant attributes. The aim of the study was to assess the direct health properties of OOPs as a food supplement in humans diagnosed with metabolic syndrome. Fasting Blood Glucose (FBG) and Hemoglobin A1c (HbA1c) were chosen as primary endpoints because they are key indicators of glucose control, a core aspect of metabolic syndrome. Their combined assessment offers a comprehensive view of both short-term and long-term glucose regulation, making them highly relevant for evaluating interventions.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Methods&lt;/h3&gt;&lt;div&gt;This double-blind, randomized, controlled clinical trial screened 110 individuals for eligibility between September 16, 2024, and January 27, 2025. Eight did not meet the inclusion criteria for metabolic syndrome, and 102 eligible participants were randomly assigned to the OOPs supplement or placebo group using a computer-generated randomization sequence to receive either the OOPs supplement or placebo. The 12-week intervention provided either a 10 mg/day polyphenol-rich olive oil extract food supplement (80 % oleocanthal/oleacein, 18 % oleuropein aglycon/ligstroside aglycon) or a placebo. No changes to lifestyle were recommended, and diet and physical activity were assessed at week 6. Fasting blood glucose (FBG) and hemoglobin A1C (HbA1c) were the primary outcomes. Secondary outcomes included lipid profile, C-reactive protein (CRP), body mass index (BMI), blood pressure, waist circumference, liver function tests (LFTs), estimated glomerular filtration rate (eGFR), uric acid, and fatigue scores. Repeated measures ANOVA/Linear Mixed Models were used to compare the mean changes (12 weeks-baseline) in fasting blood glucose levels between the intervention group and the placebo arm. Similar analysis (changes since baseline) was conducted for the continuous secondary outcomes. For categorical outcomes, changes since baseline were compared using chi-square methods. Bonferroni adjustments were made for multiple comparisons as appropriate.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Results&lt;/h3&gt;&lt;div&gt;All 102 randomized participants completed the 12-week intervention and were included in the final analysis. The intervention group demonstrated significant improvements across various metabolic and physiological markers compared to the placebo group. Notable reductions were observed in FBG (mean difference: −7.06 mg/dL, p &lt; 0.0001) and HbA1c (−0.29 %, p &lt; 0.0001). Additionally, the intervention led to significant decreases in BMI (−1.15, p &lt; 0.0001), systolic blood pressure (−7.66 mmHg, p = 0.004), triglycerides (−8.57, p = 0.0003), oxidized LDL (−5.01, p &lt; 0.0001), uric acid (−1.04, p &lt; 0.0001), ALT (−4.92, p = 0.0002), and fa","PeriodicalId":10352,"journal":{"name":"Clinical nutrition ESPEN","volume":"71 ","pages":"Article 102883"},"PeriodicalIF":2.6,"publicationDate":"2025-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145809600","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
GLP-2 analogues in short bowel syndrome: A systematic review and meta-analysis of randomized controlled trials 短肠综合征的GLP-2类似物:随机对照试验的系统回顾和荟萃分析。
IF 2.6 Q3 NUTRITION & DIETETICS Pub Date : 2025-12-18 DOI: 10.1016/j.clnesp.2025.102881
Pedro Batista Castro , Heitor Soares Brandão , Glauco Martins de Araujo , Gustavo Procópio Silva , Luísa Gonçalves Carvalho , Palle Bekker Jeppesen , Samuel I. dos Santos Pereira

Background & aims

The efficacy of glucagon-like peptide-2 (GLP-2) analogues in patients with short bowel syndrome (SBS) with intestinal failure (IF) is not well established. We aimed to compare the efficacy of GLP-2 analogues relative to placebo in patients with SBS dependent on parenteral support (PS).

Methods

PubMed, Embase, and Cochrane Central were searched from inception to April 15, 2025 for randomized controlled trials (RCTs) comparing GLP-2 analogues with placebo in patients with SBS. Endpoints included change in weekly PS volume, clinical response, enteral autonomy, and ≥1-day/week PS reduction. Pooled risk ratios (RRs) and standardized mean differences (SMDs) with 95% confidence intervals (CIs) were calculated using random-effects models. SMD was used due to differences in reporting units (mL/day vs. L/week).

Results

We included 283 patients from 4 RCTs, including one crossover trial; 188 (66.4%) received GLP-2 analogues. Weekly absolute PS volume reduction was significantly greater with GLP-2 analogues than with placebo (SMD −0.54; 95% CI −0.71 to −0.36; p = 0.0022; I2 = 0%), with consistent results in a sensitivity analysis restricted to week 24. There were no significant differences in clinical response (RR 1.94; 95% CI 0.57 to 6.56; p = 0.1453; I2 = 23.7%) and enteral autonomy (RR 4.21; 95% CI 0.00 to 280351.17; p = 0.3479; I2 = 0%) between groups. Clinical response was defined as achieving a ≥20% reduction in weekly PS volume from baseline sustained through weeks 20 and 24. Reduction in PS by ≥ 1 day/week was more frequent with GLP-2 analogues (RR 2.27; 95% CI 1.59 to 3.26; p = 0.0219; I2 = 0%).

Conclusion

This meta-analysis of 4 RCTs including 283 patients showed that GLP-2 analogues significantly reduced weekly PS volume and more often achieved ≥1-day/week reductions in PS compared with placebo, with no significant differences in enteral autonomy or clinical response.
背景与目的:胰高血糖素样肽-2 (GLP-2)类似物对短肠综合征(SBS)合并肠衰竭(IF)患者的疗效尚不明确。我们的目的是比较GLP-2类似物相对于安慰剂对依赖肠外支持(PS)的SBS患者的疗效。方法:检索PubMed, Embase和Cochrane Central从成立到2025年4月15日的随机对照试验(rct),比较GLP-2类似物与安慰剂在SBS患者中的作用。终点包括每周PS量的变化、临床反应、肠内自主性和≥1天/周PS减少。采用随机效应模型计算合并风险比(rr)和95%置信区间(ci)的标准化平均差(SMDs)。由于报告单位(mL/天vs. L/周)的差异,使用了SMD。结果:我们纳入了来自4项随机对照试验的283例患者,包括1项交叉试验;188例(66.4%)接受GLP-2类似物治疗。GLP-2类似物的每周绝对PS体积减少明显大于安慰剂(SMD -0.54; 95% CI -0.71至-0.36;p=0.0022; I2=0%),在仅限于第24周的敏感性分析中结果一致。两组患者临床反应(RR 1.94; 95% CI 0.57 ~ 6.56; p=0.1453; I2=23.7%)和肠内自主性(RR 4.21; 95% CI 0.00 ~ 280351.17; p=0.3479; I2=0%)差异无统计学意义。临床缓解的定义是在第20周和第24周内,每周PS量比基线减少≥20%。GLP-2类似物降低PS≥1天/周的频率更高(RR 2.27; 95% CI 1.59至3.26;p=0.0219; I2=0%)。结论:这项包含283例患者的4项随机对照试验的荟萃分析显示,与安慰剂相比,GLP-2类似物显著降低了每周PS量,并且更经常达到≥1天/周的PS减少,在肠内自主性或临床反应方面没有显著差异。
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引用次数: 0
期刊
Clinical nutrition ESPEN
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