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Enhanced bioavailability of a krill oil-based milk thistle extract formulation: in vitro and human studies. 提高磷虾油基水飞蓟提取物配方的生物利用度:体外和人体研究。
IF 3.4 4区 医学 Q2 FOOD SCIENCE & TECHNOLOGY Pub Date : 2026-01-07 eCollection Date: 2026-01-01 DOI: 10.29219/fnr.v70.13256
Karin Engelhart-Jentzsch, Ann-Kathrin Gantenbein, Christiane Schön, Manfred Wilhelm, Lena Stadelmayer, Lisa Pross, Tatjana Kaiser-Zimmermann, Gregorio Guerrero, Benjamin Assad Jaghutriz, Claudia Reule

Background/objectives: The milk thistle plant (Silybum marianum) is known for its hepatoprotective properties. However, the poor water solubility of silymarin limits its dissolution in the intestinal tract and restricts its bioavailability following oral administration.

Methods: To improve bioavailability, special formulations, in particular micellar solubilization, are explored. In this study, we examined the transport rate of silymarin in a krill oil-based formulation across a Caco-2 epithelial barrier after upstream digestion simulation in vitro. Furthermore, in a randomized cross-over design study the bioavailability of the krill oil-based formulation was investigated after single dose intake in fasting conditions in healthy participants.

Results: We could demonstrate that the apparent transport coefficient of silybin, measured as lead substance of milk thistle extract, across the epithelium is efficiently boosted by a krill oil formulation, resulting in a 28% increase compared to silymarin powder. Consistent with these findings, a significant enhancement of bioavailability (P < 0.0001) was demonstrated for the krill oil-based formulation in comparison to the milk thistle extract resulting in an 8.59-fold higher AUC0-8h and a 15.08-fold greater Cmax of silybin and faster uptake kinetic after single dose intake.

Discussion and conclusions: These findings suggest that phospholipid-based delivery systems offer a promising strategy for improving the efficacy of lipophilic bioactives. Furthermore, the combination of krill oil with milk thistle extracts efficiently provides silybin, PUFAs, and choline, which are important nutrients contributing to liver and heart health.

背景/目的:水飞蓟植物(Silybum marianum)以其保护肝脏的特性而闻名。然而,水飞蓟素的水溶性差限制了其在肠道中的溶解,并限制了口服给药后的生物利用度。方法:为提高生物利用度,探索特殊配方,特别是胶束增溶。在这项研究中,我们在体外模拟上游消化后,检测了磷虾油基配方中的水飞蓟素通过Caco-2上皮屏障的运输速率。此外,在一项随机交叉设计研究中,研究了健康参与者在禁食条件下单剂量摄入磷虾油后的生物利用度。结果:我们可以证明,水飞蓟素(水飞蓟提取物的铅物质)在磷虾油配方中有效地提高了水飞蓟素在上皮中的表观运输系数,与水飞蓟素粉相比,水飞蓟素粉的表观运输系数提高了28%。与上述结果相一致,磷虾油基制剂与水飞蓟提取物相比,生物利用度显著提高(P < 0.0001),单次给药后水飞蓟宾的AUC0-8h提高8.59倍,Cmax提高15.08倍,吸收动力学加快。讨论和结论:这些发现表明,基于磷脂的递送系统为提高亲脂性生物活性物质的功效提供了一种有希望的策略。此外,磷虾油与水飞蓟提取物的组合有效地提供水飞蓟宾、PUFAs和胆碱,这些都是有助于肝脏和心脏健康的重要营养物质。
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引用次数: 0
Zinc bioaccessibility of foodstuffs after in vitro study in children with illnesses. 儿童疾病体外研究后食品锌的生物可及性。
IF 3.4 4区 医学 Q2 FOOD SCIENCE & TECHNOLOGY Pub Date : 2025-12-26 eCollection Date: 2025-01-01 DOI: 10.29219/fnr.v69.11032
Úrsula García-Conde, Miguel Navarro-Moreno, Beatriz Navajas-Porras, Daniel Hinojosa-Nogueira, Adriana Delgado-Osorio, Sergio Pérez-Burillo, Miguel Navarro-Alarcón, Silvia Pastorizal, Konstantinos Douros, José-Ángel Rufián-Henares

Background: Childhood is a life stage particularly sensitive to malnutrition, including obesity, celiac disease, and food allergies. Zn is an essential element in development, metabolism, and the regulation of inflammatory processes and oxidative stress.

Objective: Zn bioaccessibility (Zn-BA), an indicator of the fraction of Zn available for intestinal absorption, is commonly evaluated through in vitro digestion models. This study applied a novel in vitro digestion-fermentation method to assess Zn-BA in various raw and cooked foods using fecal inocula from children with gluten-related disorders (GRD-CH), obesity (OB-CH), and allergy/intolerance to cow's milk protein (AICM-CH).

Results: The results showed that Zn bioaccessibility in the large intestine (Zn-BALI) values were significantly lower in these clinical groups compared to healthy children (P < 0.001). Mean Zn-BALI values in the large intestine of all foods in GRD-CH are significantly higher (34.7 ± 28.8%) than those determined in OB-CH (29.6 ± 30.1%) and AICM-CH (26.7 ± 30.4%) (P < 0.001). For allergic children, Zn-BALI in animal foods was significantly lower than in plant foods and in both plant and animal foods in the other children's groups (P < 0.05). Zn-BALI in animal foods cooked in liquid media (frying/boiling) was significantly higher than when cooked with hot air (roasting/grilling).

Conclusion: In children, the studied diseases diminished the Zn-BALI, which could negatively affect their appropriate long-term development. In sick children, the higher Zn-BALI in celiac children is probably related to differences in gut microbiota composition, as well as to different metabolites and ligands obtained by the fermentation processes, a fact that should be addressed in future studies.

背景:童年是对营养不良特别敏感的人生阶段,包括肥胖、乳糜泻和食物过敏。锌是发育、代谢、炎症过程和氧化应激调节的必需元素。目的:锌的生物可及性(Zn- ba)是衡量肠道可吸收锌含量的指标,常用体外消化模型来评价。本研究采用一种新的体外消化-发酵方法,通过对患有麸质相关疾病(GRD-CH)、肥胖(OB-CH)和牛奶蛋白过敏/不耐受(AICM-CH)的儿童进行粪便接种,评估各种生熟食品中的锌- ba。结果:与健康儿童相比,临床组锌在大肠中的生物可及性(Zn- bali)值显著降低(P < 0.001)。GRD-CH中各食品大肠Zn-BALI平均值(34.7±28.8%)显著高于OB-CH(29.6±30.1%)和AICM-CH(26.7±30.4%)(P < 0.001)。在过敏儿童中,动物性食品中锌- bali含量显著低于植物性食品,其他各组植物和动物性食品中锌- bali含量均显著低于植物性食品(P < 0.05)。用液体介质(煎炸/煮煮)烹饪的动物性食品中的锌- bali含量明显高于用热空气(烤/烤)烹饪的动物性食品。结论:在儿童中,所研究的疾病降低了Zn-BALI,这可能对其适当的长期发育产生负面影响。在患病儿童中,乳糜泻儿童中较高的锌- bali可能与肠道微生物群组成的差异以及发酵过程中获得的不同代谢物和配体有关,这一事实应在未来的研究中得到解决。
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引用次数: 0
CL22209, a standardized Asparagus racemosus root extract, demonstrates improved ovarian morphology, menstrual regularity, and metabolic parameters in women with polycystic ovary syndrome in a randomized, controlled trial. CL22209是一种标准化的总状芦笋根提取物,在一项随机对照试验中显示,多囊卵巢综合征女性的卵巢形态、月经规律和代谢参数得到改善。
IF 3.4 4区 医学 Q2 FOOD SCIENCE & TECHNOLOGY Pub Date : 2025-12-23 eCollection Date: 2025-01-01 DOI: 10.29219/fnr.v69.13244
Sridevi Kondamudi, Sravanthi Sadu, Sujatha Deva, Aishwarya Yalamanchi, Amulya Yalamanchi

Background and objective: Polycystic ovary syndrome (PCOS) is a leading cause of infertility and metabolic dysfunction in women of reproductive age. Despite its high prevalence, current medical treatments are largely symptom-targeted and often prescribed off-label, highlighting the need for safer, integrative interventions. Botanical formulations with phytoestrogenic and insulin-sensitizing properties may represent a holistic therapeutic approach. The study aims to evaluate the clinical efficacy and safety of a standardized Asparagus racemosus root extract (CL22209) in women diagnosed with PCOS.

Methods: A randomized, double-blind, placebo-controlled clinical trial (registration no: CTRI/2023/11/059457) was conducted in 60 women aged 20-35 years who were diagnosed with PCOS, as determined by the Rotterdam criteria. Participants received either CL22209 (100 mg daily) or a placebo for 84 consecutive days. The primary endpoint was the change in ovarian volume from the baseline. Secondary outcomes included ovarian cyst size and follicle number, menstrual cycle regularity, androgen-related manifestations, anthropometric indices, hormonal parameters, insulin sensitization, and safety.

Results: After 84 days of supplementation, CL22209 significantly (P < 0.0001) reduced mean ovarian volume (20.98%), cyst size (40.97%), and follicle number (20.56%) as compared to placebo. The supplement showed exploratory indications of improved insulin sensitivity and hormonal profiles. Modest changes were also seen in menstrual patterns and anthropometric measures. CL22209 was well-tolerated over the study period.

Conclusion: CL22209 was well-tolerated and demonstrated broad-spectrum efficacy in women diagnosed with PCOS, improving ovarian morphology, metabolic health, and androgen-mediated symptoms. Future studies with larger sample sizes and longer follow-up durations would help to further validate these findings and clarify CL22209's role in the management of PCOS.

背景与目的:多囊卵巢综合征(PCOS)是育龄妇女不孕和代谢功能障碍的主要原因。尽管其发病率很高,但目前的医疗治疗主要是针对症状的,并且经常在标签外开处方,这突出表明需要更安全的综合干预措施。具有植物雌激素和胰岛素增敏特性的植物制剂可能代表一种整体治疗方法。该研究旨在评估标准总状芦笋根提取物(CL22209)在诊断为PCOS的女性中的临床疗效和安全性。方法:采用随机、双盲、安慰剂对照临床试验(注册号:CTRI/2023/11/059457),对60名年龄在20-35岁、经鹿特丹标准诊断为PCOS的女性进行研究。参与者接受CL22209(每天100毫克)或安慰剂,连续84天。主要终点是卵巢体积较基线的变化。次要结局包括卵巢囊肿大小和卵泡数量、月经周期规律、雄激素相关表现、人体测量指标、激素参数、胰岛素敏感性和安全性。结果:补充84天后,与安慰剂相比,CL22209显著(P < 0.0001)降低了卵巢平均体积(20.98%)、囊肿大小(40.97%)和卵泡数量(20.56%)。补充剂显示出改善胰岛素敏感性和激素谱的探索性迹象。月经模式和人体测量也出现了适度的变化。在整个研究期间,CL22209的耐受性良好。结论:CL22209对诊断为PCOS的女性具有良好的耐受性和广谱疗效,可改善卵巢形态、代谢健康和雄激素介导的症状。未来更大样本量和更长随访时间的研究将有助于进一步验证这些发现,并阐明CL22209在PCOS治疗中的作用。
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引用次数: 0
PRSS22 promotes the immune evasion of gastric cancer via inhibiting ANXA1-mediated degradation of PD-1. PRSS22通过抑制anxa1介导的PD-1降解促进胃癌的免疫逃逸。
IF 3.4 4区 医学 Q2 FOOD SCIENCE & TECHNOLOGY Pub Date : 2025-12-18 eCollection Date: 2025-01-01 DOI: 10.29219/fnr.v69.13155
Jifan Wang, Jing Zhou, Xiaoping Chen
<p><strong>Purpose: </strong>Gastric cancer (GC) ranks as the third most prevalent cause of mortality among malignant tumors globally. This study endeavors to uncover the protective function and underlying mechanism of PRSS22 on the immune evasion of GC.</p><p><strong>Methods: </strong>A total of 24 GC patients and 7 normal volunteer were recruited. The gene chip data GSE291766 in GC was downloaded to analyze the differentially expressed genes (DEGs). DAVID database was used to perform the gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis. TIMER database was used to quantify PRSS22 in different cancers as well as the correlation between the PRSS22 expression and the abundance of immune infiltration by gene module. GEPIA2 was used to analyze the prognostic significance of PRSS22 in GC patients. GC cells (NCI-N87, MKN-45, MKN-28, and AGS) were used to compare the PRSS22 expression with GES-1. Jurkat cells transfected with negative, PRSS22, si-NC, or si-PRSS22 were cultivated with AGS to establish the in vitro coculture system. All mice were inoculated with AGS and injected with negative or sh-PRSS22 lentivirus. qPCR was used to analyze the PRSS22, TP53, Cox2, MYC, TNF-α, CD28, GLUT1, Granzyme B, TCF-1, LAG-3, NR4A, and TIM-3 mRNA levels. Western blotting was used to measure the PRSS22, ANXA1, and PD-1 proteins levels. The commercial kits were used to determine the caspase-3/7/9, LDH, TGF-β, TNF-α, IFNγ, and IL-10 levels. Cell viability, migration, and proliferation were determined using CCK-8, PI fluorescent stain, transwell, and EdU assays. TNFα/CD8 and CD4<sup>+</sup>CD25<sup>+</sup>FoxP3<sup>+</sup> levels were measured by flow analysis. In vivo imaging and immunohistochemical analysis were used to detect the ANXA1 expression. Immunofluorescence analysis was used to determine the PRSS22 and ANXA1 expressions. IP assay was used to analyze the interaction of PRSS22 protein with ANXA1 protein along with PD-1 ubiquitination.</p><p><strong>Results: </strong>PRSS22 was highly expressed in GC patients. The overall survival in GC patients (high-PRSS22) was lower than GC patients (low-PRSS22). PRSS22 mRNA and protein expressions were significantly upregulated in AGS cells. In the GC mouse model, PRSS22 downregulation decreased tumor volume and weight. PRSS22 was manifested in T cells of GC patients. In coculture with AGS and Jurkat cell, PRSS22 could significantly promote cell proliferation, migration, and EdU positivity but reduced LDH activity and PI levels. We discovered that the PRSS22 promoted the immune evasion in T cells of GC. ANXA1 and PD-1 were DEGS in sh-PRSS22 GC samples, and ANXA1/PD-1 pathway might be important for the functions of PRSS22 on immune evasion in the GC model. PRSS22 knockout upregulated ANXA1 but downmodulated PD-1 in <i>in vitro</i> and <i>in vivo</i> experiments. PRSS22 WT protein could interact with the ANXA1 WT protein, and ANXA1 upregulation could promote the ubiquitination of PD-1
目的:胃癌(GC)在全球恶性肿瘤中排名第三。本研究旨在揭示PRSS22对GC免疫逃避的保护作用及其机制。方法:共招募GC患者24例,正常志愿者7例。下载GC中的基因芯片数据GSE291766,分析差异表达基因(DEGs)。使用DAVID数据库进行基因本体(GO)和京都基因与基因组百科全书(KEGG)富集分析。利用TIMER数据库定量分析不同肿瘤组织中PRSS22的表达以及基因模块与免疫浸润丰度的相关性。采用GEPIA2分析PRSS22在GC患者中的预后意义。用GC细胞(NCI-N87、MKN-45、MKN-28和AGS)比较PRSS22与GES-1的表达。用AGS对转染阴性、PRSS22、si-NC和si-PRSS22的Jurkat细胞进行培养,建立体外共培养体系。所有小鼠均接种AGS,并注射阴性或sh-PRSS22慢病毒。采用qPCR方法分析PRSS22、TP53、Cox2、MYC、TNF-α、CD28、GLUT1、颗粒酶B、TCF-1、LAG-3、NR4A、TIM-3 mRNA水平。Western blotting检测PRSS22、ANXA1、PD-1蛋白水平。使用商业试剂盒检测caspase-3/7/9、LDH、TGF-β、TNF-α、IFNγ和IL-10水平。采用CCK-8、PI荧光染色、transwell和EdU测定细胞活力、迁移和增殖。流式分析检测TNFα/CD8和CD4+CD25+FoxP3+水平。采用体内显像和免疫组化分析检测ANXA1的表达。免疫荧光法检测PRSS22和ANXA1的表达。采用IP法分析PRSS22蛋白与ANXA1蛋白的相互作用以及PD-1泛素化。结果:PRSS22在GC患者中高表达。GC患者(高prss22)的总生存率低于GC患者(低prss22)。在AGS细胞中,PRSS22 mRNA和蛋白表达显著上调。在GC小鼠模型中,PRSS22下调使肿瘤体积和重量减小。PRSS22在GC患者的T细胞中有表达。与AGS和Jurkat细胞共培养时,PRSS22能显著促进细胞增殖、迁移和EdU阳性,降低LDH活性和PI水平。我们发现PRSS22促进了GC T细胞的免疫逃逸。sh-PRSS22 GC样品中的ANXA1和PD-1是DEGS, ANXA1/PD-1通路可能对PRSS22在GC模型中的免疫逃避功能起重要作用。在体外和体内实验中,敲除PRSS22可上调ANXA1,下调PD-1。PRSS22 WT蛋白可与ANXA1 WT蛋白相互作用,ANXA1上调可促进PD-1蛋白泛素化。在与AGS和Jurkat细胞共培养时,si-PRSS22处理可以降低肿瘤细胞的生长、迁移、Edu阳性和免疫逃避能力,而抑制ANXA1则可以逆转这种作用。结论:PRSS22抑制anxa1介导的T细胞PD-1降解,促进GC的免疫逃避。因此,靶向PRSS22是一种潜在有效的GC治疗策略。
{"title":"PRSS22 promotes the immune evasion of gastric cancer via inhibiting ANXA1-mediated degradation of PD-1.","authors":"Jifan Wang, Jing Zhou, Xiaoping Chen","doi":"10.29219/fnr.v69.13155","DOIUrl":"10.29219/fnr.v69.13155","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Purpose: &lt;/strong&gt;Gastric cancer (GC) ranks as the third most prevalent cause of mortality among malignant tumors globally. This study endeavors to uncover the protective function and underlying mechanism of PRSS22 on the immune evasion of GC.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;A total of 24 GC patients and 7 normal volunteer were recruited. The gene chip data GSE291766 in GC was downloaded to analyze the differentially expressed genes (DEGs). DAVID database was used to perform the gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis. TIMER database was used to quantify PRSS22 in different cancers as well as the correlation between the PRSS22 expression and the abundance of immune infiltration by gene module. GEPIA2 was used to analyze the prognostic significance of PRSS22 in GC patients. GC cells (NCI-N87, MKN-45, MKN-28, and AGS) were used to compare the PRSS22 expression with GES-1. Jurkat cells transfected with negative, PRSS22, si-NC, or si-PRSS22 were cultivated with AGS to establish the in vitro coculture system. All mice were inoculated with AGS and injected with negative or sh-PRSS22 lentivirus. qPCR was used to analyze the PRSS22, TP53, Cox2, MYC, TNF-α, CD28, GLUT1, Granzyme B, TCF-1, LAG-3, NR4A, and TIM-3 mRNA levels. Western blotting was used to measure the PRSS22, ANXA1, and PD-1 proteins levels. The commercial kits were used to determine the caspase-3/7/9, LDH, TGF-β, TNF-α, IFNγ, and IL-10 levels. Cell viability, migration, and proliferation were determined using CCK-8, PI fluorescent stain, transwell, and EdU assays. TNFα/CD8 and CD4&lt;sup&gt;+&lt;/sup&gt;CD25&lt;sup&gt;+&lt;/sup&gt;FoxP3&lt;sup&gt;+&lt;/sup&gt; levels were measured by flow analysis. In vivo imaging and immunohistochemical analysis were used to detect the ANXA1 expression. Immunofluorescence analysis was used to determine the PRSS22 and ANXA1 expressions. IP assay was used to analyze the interaction of PRSS22 protein with ANXA1 protein along with PD-1 ubiquitination.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;PRSS22 was highly expressed in GC patients. The overall survival in GC patients (high-PRSS22) was lower than GC patients (low-PRSS22). PRSS22 mRNA and protein expressions were significantly upregulated in AGS cells. In the GC mouse model, PRSS22 downregulation decreased tumor volume and weight. PRSS22 was manifested in T cells of GC patients. In coculture with AGS and Jurkat cell, PRSS22 could significantly promote cell proliferation, migration, and EdU positivity but reduced LDH activity and PI levels. We discovered that the PRSS22 promoted the immune evasion in T cells of GC. ANXA1 and PD-1 were DEGS in sh-PRSS22 GC samples, and ANXA1/PD-1 pathway might be important for the functions of PRSS22 on immune evasion in the GC model. PRSS22 knockout upregulated ANXA1 but downmodulated PD-1 in &lt;i&gt;in vitro&lt;/i&gt; and &lt;i&gt;in vivo&lt;/i&gt; experiments. PRSS22 WT protein could interact with the ANXA1 WT protein, and ANXA1 upregulation could promote the ubiquitination of PD-1 ","PeriodicalId":12119,"journal":{"name":"Food & Nutrition Research","volume":"69 ","pages":""},"PeriodicalIF":3.4,"publicationDate":"2025-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12767678/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145911216","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The prevalence and co-occurrence of emulsifiers, thickeners and stabilizers in food products on the Norwegian market. 挪威市场上食品中乳化剂、增稠剂和稳定剂的流行和共存。
IF 3.4 4区 医学 Q2 FOOD SCIENCE & TECHNOLOGY Pub Date : 2025-12-08 eCollection Date: 2025-01-01 DOI: 10.29219/fnr.v69.12986
Åsne Skram Trømborg, Jon Olav Vik, Monica Hauger Carlsen, Harald Carlsen

Background: As the intake of food that has undergone substantial processing increases, the intake of common additives like Emulsifiers, Thickeners, and Stabilizers (ETSs) also increases. Several ETSs have drawn attention due to potential negative health effects.

Objective: This study aimed to map the prevalence and co-occurrence patterns of ETSs across food products on the Norwegian market, examining their distribution across different food groups and products with varying nutritional profiles, including those classified as hyper-palatable.

Design: Food product information, including ingredient lists and nutritional information, was obtained from two online databases used by major grocery chains, thus representative of the Norwegian market and analyzed for presence or absence of ETSs.

Results: Thirty-two percent of food products contained at least one ETS, 60% of these contained more than one ETS, and many ETSs were found more frequently in combinations with others than individually. ETSs were present in a broad range of food products, with the highest percentage seen in the food groups Bakery, Cakes & Pastries, and Desserts & Ice cream. Mono- and diglycerides of fatty acids (E471) and diphosphates (E450) were the most used food additives. Fifty-eight percent of the food products analyzed were classified as hyper-palatable, though relationships with ETSs were variable across food groups.

Conclusion: This is the first comprehensive analysis of its kind, providing a basemap for future research on the potential health effects of modern food products, particularly considering the limited understanding of how multiple ETSs may interact within biological systems.

背景:随着大量加工食品摄入量的增加,乳化剂、增稠剂和稳定剂(ets)等常见添加剂的摄入量也在增加。由于潜在的负面健康影响,一些碳排放交易体系引起了人们的注意。目的:本研究旨在绘制挪威市场上食品中碳排放交易体系的患病率和共存模式,研究其在不同食品组和具有不同营养概况的产品中的分布,包括那些被归类为超级美味的产品。设计:食品信息,包括成分表和营养信息,从两个主要杂货连锁店使用的在线数据库中获得,因此具有挪威市场的代表性,并分析是否存在碳排放交易体系。结果:32%的食品含有至少一种ETS,其中60%含有不止一种ETS,许多ETS与其他ETS的组合比单独发现的频率更高。碳排放交易体系存在于广泛的食品产品中,在烘焙食品、蛋糕和糕点以及甜点和冰淇淋中所占比例最高。脂肪酸的单甘油酯和双甘油酯(E471)和二磷酸盐(E450)是使用最多的食品添加剂。所分析的58%的食品被归类为超级美味,尽管与碳排放交易体系的关系在不同的食品组中有所不同。结论:这是此类研究的首次全面分析,为未来研究现代食品的潜在健康影响提供了基础,特别是考虑到对生物系统中多种ets如何相互作用的了解有限。
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引用次数: 0
Diet and nutrition key factors for oral microbiota composition: a systematic review. 饮食和营养对口腔微生物群组成的关键因素:系统综述。
IF 3.4 4区 医学 Q2 FOOD SCIENCE & TECHNOLOGY Pub Date : 2025-11-24 eCollection Date: 2025-01-01 DOI: 10.29219/fnr.v69.11956
Heriberto Castro García, Vania Urias Orona, Luis Fernando Méndez, Andrea Arreguin Coronado, Marcela Alejandra Gloria Garza

Background: Diet and nutrition are essential in preserving oral health as they influence the microbiota balance and modulate inflammatory responses. The relationship between dietary patterns (DPs) and oral diseases such as caries and periodontitis has garnered significant scientific attention. Objective. This review aims to analyze the impact of various DPs, nutrients, and supplementation with probiotics and prebiotics on oral health and microbiota modulation.

Design: A systematic search was conducted in PubMed, Scopus, and Web of Science databases for clinical studies published between 2010 and 2024. A total of 514 articles were retrieved, 78 were evaluated at the full-text level, and 22 original clinical studies were included based on eligibility criteria. These studies were grouped into three categories: dietary interventions without supplementation, probiotic/prebiotic supplementation, and combined strategies.

Results: Healthy DPs, such as the Mediterranean and vegetarian diets, showed anti-inflammatory effects and positively modulated oral microbiota by reducing pathogenic species linked to oral diseases. In contrast, high sugar consumption was associated with increased acidogenic bacterial species and dental caries. Probiotics, particularly strains of Lactobacillus and Bifidobacterium, demonstrated therapeutic benefits in managing gingivitis, halitosis, and caries, while prebiotics supported the growth of beneficial bacteria, complementing probiotic efficacy.

Discussion: Nutritional interventions modulate oral microbiota by shifting microbial profiles toward eubiosis and attenuating inflammatory responses. The effectiveness of probiotics appears to be strain-dependent and may vary with host conditions, while prebiotics support their colonization and metabolic activity.

Conclusion: Dietary interventions directly influence oral health by modulating microbiota composition and inflammatory responses. Probiotics show clinical promise, though their long-term, strain-specific effects need further study. Prebiotics may enhance these benefits by supporting probiotic activity. A diet rich in plant-based foods and bioactive compounds, combined with targeted supplementation, represents a viable strategy to promote oral health and microbiota balance.

背景:饮食和营养对保持口腔健康至关重要,因为它们影响微生物群平衡并调节炎症反应。饮食模式与龋齿和牙周炎等口腔疾病之间的关系已经引起了重大的科学关注。目标。本文旨在分析各种DPs、营养素以及补充益生菌和益生元对口腔健康和微生物群调节的影响。设计:系统检索PubMed、Scopus和Web of Science数据库,检索2010年至2024年间发表的临床研究。共检索到514篇文章,78篇在全文水平上进行评估,22篇原始临床研究根据入选标准被纳入。这些研究被分为三类:饮食干预不补充,益生菌/益生元补充,和联合策略。结果:健康的DPs,如地中海和素食饮食,显示出抗炎作用,并通过减少与口腔疾病相关的致病物种积极调节口腔微生物群。相反,高糖摄入与致酸细菌种类增加和龋齿有关。益生菌,特别是乳酸菌和双歧杆菌菌株,在治疗牙龈炎、口臭和龋齿方面具有治疗作用,而益生元支持有益菌的生长,补充了益生菌的功效。讨论:营养干预通过将微生物谱转向益生菌和减轻炎症反应来调节口腔微生物群。益生菌的有效性似乎是菌株依赖的,可能随宿主条件而变化,而益生元支持它们的定植和代谢活性。结论:饮食干预通过调节微生物群组成和炎症反应直接影响口腔健康。益生菌显示出临床前景,尽管它们的长期、菌株特异性效果需要进一步研究。益生元可以通过支持益生菌活性来增强这些益处。富含植物性食物和生物活性化合物的饮食,结合有针对性的补充,是促进口腔健康和微生物群平衡的可行策略。
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引用次数: 0
Causal relationships between 25-hydroxyvitamin D levels and laryngeal cancer risk: A two-sample Mendelian randomization study. 25-羟基维生素D水平与喉癌风险之间的因果关系:一项双样本孟德尔随机研究。
IF 3.4 4区 医学 Q2 FOOD SCIENCE & TECHNOLOGY Pub Date : 2025-11-17 eCollection Date: 2025-01-01 DOI: 10.29219/fnr.v69.11489
Dapeng Wang, Li Zhang, Yanfen Cui, Ruyuan Guo, Fuli Zhang, Junjie Zhang, Xiaotang Yang

Background: The relationship between 25-hydroxyvitamin D (25(OH)D) levels and the risk of laryngeal cancer (LC) is unclear. This study aimed to explore the causal association between 25(OH)D levels and LC risk using the two-sample Mendelian randomization (MR) analysis.

Methods: Single-nucleotide polymorphisms for 25(OH)D levels and LC were extracted from published genome-wide association studies (GWAS) or the Medical Research Council Integrative Epidemiology Unit (MRC-IEU) Open GWAS project. Univariable MR and multivariable MR analyses were performed. Five MR methods including MR-Egger, weighted-median, inverse-variance weighted (IVW), simple mode, and weighted mode were applied.

Results: Univariable MR analysis identified the fact that genetically predicted higher levels of 25(OH)D were associated with lower odds of LC [IVW: (odds ratio (OR) = 0.9993, 95% confidence interval (CI), 0.9987-0.9999; P = 0.019)]. Multivariable MR analyses suggested that genetically predicted higher levels of 25(OH)D were correlated with lower risk of LC after adjusting for pack-years of cigarette smoking (CS) [IVW: (OR = 0.9993, 95% CI, 0.9987-0.9998; P = 0.006)] or both pack-years of CS and weekly alcoholic drinks [IVW: (OR = 0.9993, 95% CI, 0.9988-0.9998; P = 0.011)], but this was not significant after adjusting only for weekly alcoholic drinks [IVW: (OR = 0.9995, 95% CI, 0.9989-1.0001; P = 0.077)].

Conclusions: This MR analyses supported a slight protective effect of higher levels of 25(OH)D on the risk of LC.

背景:25-羟基维生素D (25(OH)D)水平与喉癌(LC)风险之间的关系尚不清楚。本研究旨在通过双样本孟德尔随机化(MR)分析探讨25(OH)D水平与LC风险之间的因果关系。方法:从已发表的全基因组关联研究(GWAS)或医学研究委员会综合流行病学单位(MRC-IEU)开放GWAS项目中提取25(OH)D水平和LC的单核苷酸多态性。进行单变量MR和多变量MR分析。采用MR- egger、加权中位数、反方差加权(IVW)、简单模式和加权模式5种MR方法。结果:单变量MR分析发现,基因预测较高水平的25(OH)D与较低的LC几率相关[IVW:(优势比(OR) = 0.9993, 95%可信区间(CI), 0.9987-0.9999;P = 0.019)]。先生多变量分析表明基因预测高25 (OH) D水平较低的相关信用证的风险调整后的久吸烟(CS) [IVW: (OR = 0.9993, 95% CI, 0.9987 - -0.9998; P = 0.006))或两个久CS和每周的酒精饮料(IVW: (OR = 0.9993, 95% CI, 0.9988 - -0.9998; P = 0.011)),但这不是重要的调整后只有每周的酒精饮料(IVW: (OR = 0.9995, 95% CI, 0.9989 - -1.0001; P = 0.077)]。结论:MR分析支持高水平的25(OH)D对LC风险有轻微的保护作用。
{"title":"Causal relationships between 25-hydroxyvitamin D levels and laryngeal cancer risk: A two-sample Mendelian randomization study.","authors":"Dapeng Wang, Li Zhang, Yanfen Cui, Ruyuan Guo, Fuli Zhang, Junjie Zhang, Xiaotang Yang","doi":"10.29219/fnr.v69.11489","DOIUrl":"10.29219/fnr.v69.11489","url":null,"abstract":"<p><strong>Background: </strong>The relationship between 25-hydroxyvitamin D (25(OH)D) levels and the risk of laryngeal cancer (LC) is unclear. This study aimed to explore the causal association between 25(OH)D levels and LC risk using the two-sample Mendelian randomization (MR) analysis.</p><p><strong>Methods: </strong>Single-nucleotide polymorphisms for 25(OH)D levels and LC were extracted from published genome-wide association studies (GWAS) or the Medical Research Council Integrative Epidemiology Unit (MRC-IEU) Open GWAS project. Univariable MR and multivariable MR analyses were performed. Five MR methods including MR-Egger, weighted-median, inverse-variance weighted (IVW), simple mode, and weighted mode were applied.</p><p><strong>Results: </strong>Univariable MR analysis identified the fact that genetically predicted higher levels of 25(OH)D were associated with lower odds of LC [IVW: (odds ratio (OR) = 0.9993, 95% confidence interval (CI), 0.9987-0.9999; <i>P</i> = 0.019)]. Multivariable MR analyses suggested that genetically predicted higher levels of 25(OH)D were correlated with lower risk of LC after adjusting for pack-years of cigarette smoking (CS) [IVW: (OR = 0.9993, 95% CI, 0.9987-0.9998; <i>P</i> = 0.006)] or both pack-years of CS and weekly alcoholic drinks [IVW: (OR = 0.9993, 95% CI, 0.9988-0.9998; <i>P</i> = 0.011)], but this was not significant after adjusting only for weekly alcoholic drinks [IVW: (OR = 0.9995, 95% CI, 0.9989-1.0001; <i>P</i> = 0.077)].</p><p><strong>Conclusions: </strong>This MR analyses supported a slight protective effect of higher levels of 25(OH)D on the risk of LC.</p>","PeriodicalId":12119,"journal":{"name":"Food & Nutrition Research","volume":"69 ","pages":""},"PeriodicalIF":3.4,"publicationDate":"2025-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12664297/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145647835","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Fructose-containing sugars and metabolic risk: a systematic review and meta-analysis. 含果糖糖与代谢风险:一项系统综述和荟萃分析。
IF 3.4 4区 医学 Q2 FOOD SCIENCE & TECHNOLOGY Pub Date : 2025-11-11 eCollection Date: 2025-01-01 DOI: 10.29219/fnr.v69.11062
Prasetya Guntari, Astina Junaida, Palupi Eny, Namkieat Pichamon, Jiamjarasrangsi Wiroj, Sapwarobol Suwimol

Background: Fructose-containing sugars are widely consumed, yet their metabolic effects remain debated.

Objective: This meta-analysis aimed to evaluate the impact of different fructose-containing sugars on glycaemic control, lipid profiles, and uric acid levels in adults.

Methods: A total of 17 study codes from seven clinical trials were included, with intervention durations ranging from 7 h to 49 days. Interventions were classified as fructose, fructose-glucose mixtures (F/G), honey, or sucrose. Comparators varied and included unsweetened beverages, artificial sweeteners, and habitual diets. Meta-analyses using random-effects models assessed outcomes including fasting blood glucose (FBG), serum insulin, total cholesterol (TC), low-density lipoprotein cholesterol (LDL-c), very low-density lipoprotein cholesterol (VLDL-c), and uric acid. Effect sizes were reported as Hedges' g.

Results: Fructose-glucose mixtures intake significantly increased FBG (Hedges' g = 0.474, P = 0.002) and serum insulin (Hedges' g = 0.592, P < 0.001), while fructose, honey, and sucrose showed no significant effects. Monosaccharide intake modestly increased insulin (P = 0.006). Fructose and sucrose alone did not affect TC, but their combined intake resulted in a significant increase (Hedges' g = 0.412, P = 0.009). No significant changes were observed in LDL-c, VLDL-c, or pooled metabolic outcomes. Fructose intake was strongly associated with increased uric acid (Hedges' g = 1.628, P < 0.001), and pooled analysis of fructose, F/G, and honey also showed a significant increase (Hedges' g = 0.550, P = 0.028).

Conclusion: The short-term consumption of added sugars - fructose, sucrose, and F/G mixtures - had minimal effects on FBG, insulin, triglycerides (TG), non-esterified fatty acids (NEFAs), high-density lipoprotein cholesterol (HDL-c), and VLDL-c. However, significant increases in TC and LDL-c were observed, particularly with fructose and sucrose, indicating adverse effects on lipid metabolism. Some fructose interventions, especially those using high-fructose corn syrup, also showed marked increases in uric acid. While acute metabolic changes were limited, these findings suggest that regular intake of added sugars may elevate cardiometabolic risk. Long-term studies are warranted to clarify chronic effects and inform dietary guidelines.

背景:含果糖的糖被广泛食用,但其代谢作用仍有争议。目的:本荟萃分析旨在评估不同含果糖糖对成人血糖控制、血脂和尿酸水平的影响。方法:纳入7项临床试验共17项研究代码,干预时间为7 h ~ 49天。干预措施分为果糖、果糖-葡萄糖混合物(F/G)、蜂蜜或蔗糖。比较对象多种多样,包括无糖饮料、人工甜味剂和习惯性饮食。meta分析采用随机效应模型评估结果,包括空腹血糖(FBG)、血清胰岛素、总胆固醇(TC)、低密度脂蛋白胆固醇(LDL-c)、极低密度脂蛋白胆固醇(VLDL-c)和尿酸。结果:果糖-葡萄糖混合物摄入显著增加空腹血糖(Hedges' g = 0.474, P = 0.002)和血清胰岛素(Hedges' g = 0.592, P < 0.001),而果糖、蜂蜜和蔗糖无显著影响。单糖摄入适度增加胰岛素(P = 0.006)。单独摄入果糖和蔗糖对TC没有影响,但它们的联合摄入导致TC显著增加(Hedges’g = 0.412, P = 0.009)。LDL-c、VLDL-c或汇总代谢结果未观察到显著变化。果糖摄入与尿酸升高密切相关(Hedges' g = 1.628, P < 0.001),合并分析果糖、F/ g和蜂蜜也显示显著升高(Hedges' g = 0.550, P = 0.028)。结论:短期摄入添加糖——果糖、蔗糖和F/G混合物——对FBG、胰岛素、甘油三酯(TG)、非酯化脂肪酸(NEFAs)、高密度脂蛋白胆固醇(HDL-c)和VLDL-c的影响很小。然而,观察到TC和LDL-c显著增加,特别是果糖和蔗糖,表明对脂质代谢有不利影响。一些果糖干预,尤其是那些使用高果糖玉米糖浆的干预,也显示出尿酸的显著增加。虽然急性代谢变化有限,但这些发现表明,定期摄入添加糖可能会增加心脏代谢风险。有必要进行长期研究,以阐明慢性影响并为饮食指南提供信息。
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引用次数: 0
Food procurement in upper secondary schools in a Norwegian county: nutritional quality and environmental impacts. 挪威某县高中的食品采购:营养质量和环境影响。
IF 3.4 4区 医学 Q2 FOOD SCIENCE & TECHNOLOGY Pub Date : 2025-11-11 eCollection Date: 2025-01-01 DOI: 10.29219/fnr.v69.12600
Marie M Bjøntegaard, Mari Mohn Paulsen, Bob van Oort, Lene Frost Andersen

Background: Public food procurement has the potential to play a significant role in transforming the food system.

Objective: This study aimed to investigate the nutritional quality and environmental impacts of food procurement in public upper secondary schools within a large county in Norway.

Design: A cross-sectional study with food procurement data from 35 upper secondary school canteens, analysed using a food-and-nutrient calculation system at the University of Oslo, which also includes a life cycle assessment (LCA) food database.

Results: Food procurement amongst school canteens did not align with guidelines for food and meals in upper secondary schools and recommendations for nutritional considerations in public food procurement. There was considerable variability between the schools' food procurement regarding nutritional quality and environmental impacts. However, on average, high levels of saturated fat and added sugar, as well as inadequate levels of folate, vitamin D, iron and iodine, were observed. Red meat and dairy products exhibited the most significant environmental impacts between the food groups.

Discussion: Few studies have utilised food procurement data to evaluate nutritional quality and environmental impacts of school meals. Using food procurement instead of actual consumption data introduces some uncertainties, including limited knowledge about the amount of food waste, quantities actually consumed and demographics of the canteen users. Identifying key nutrients of concern can be invaluable in guiding meal planning and food procurement, especially in a school setting. Our environmental analysis supported current literature by illustrating the high impact of animal-based foods relative to plant-based foods.

Conclusions: The present study found both nutritional and environmental limitations in food procurement in public upper secondary schools in a large Norwegian county. Encouraging procurement of plant-based proteins and sustainably sourced fish whilst reducing purchases of full-fat dairy products would better align with the guidelines for food and meals in schools and reduce the environmental impact. Moreover, significant variability in procurement practices that do not comply with the guidelines suggests a need for clearer guidance and follow-up.

背景:公共食品采购有可能在粮食系统转型中发挥重要作用。目的:本研究旨在调查挪威一个大县公立高中食品采购的营养质量和环境影响。设计:对来自35所高中食堂的食品采购数据进行横断面研究,使用奥斯陆大学的食品和营养计算系统进行分析,该系统还包括生命周期评估(LCA)食品数据库。结果:学校食堂的食品采购与高中食品和膳食指南以及公共食品采购中营养考虑的建议不一致。学校的食品采购在营养质量和环境影响方面存在相当大的差异。然而,平均而言,饱和脂肪和添加糖含量较高,叶酸、维生素D、铁和碘含量不足。红肉和奶制品对环境的影响最大。讨论:很少有研究利用食品采购数据来评估学校膳食的营养质量和环境影响。使用食品采购数据而不是实际消费数据会带来一些不确定性,包括对食物浪费量、实际消费数量和食堂用户人口统计数据的了解有限。确定关注的关键营养素对于指导膳食计划和食品采购,特别是在学校环境中,是非常宝贵的。我们的环境分析通过说明动物性食品相对于植物性食品的高影响来支持当前的文献。结论:本研究发现挪威一个大县的公立高中食品采购存在营养和环境限制。鼓励采购植物蛋白和可持续来源的鱼类,同时减少全脂乳制品的购买,将更好地符合学校食品和膳食指南,并减少对环境的影响。此外,不符合准则的采购做法有很大差异,这表明需要更明确的指导和后续行动。
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引用次数: 0
Causal relationships of serum iron metabolites with sepsis and cardiomyopathy: a Mendelian randomization analysis. 血清铁代谢产物与败血症和心肌病的因果关系:孟德尔随机分析。
IF 3.4 4区 医学 Q2 FOOD SCIENCE & TECHNOLOGY Pub Date : 2025-11-03 eCollection Date: 2025-01-01 DOI: 10.29219/fnr.v69.12623
Jian Zhang, Jing Cui, Quanrui Li, Geng Tian

Objective: The study aims to investigate the causal relationships of serum iron (SI) metabolites with sepsis and cardiomyopathy as two distinct outcomes.

Methods: Genome-wide association studies (GWAS) data for SI, serum ferritin (SF), serum transferrin (STF), transferrin receptor (TFRC), sepsis, and cardiomyopathy were obtained from the EBI website. Transferrin saturation percentage (TSP) data were from the Genetics of Iron Status Consortium. Due to lack of GWAS for acute sepsis-induced cardiomyopathy (SIC), cardiomyopathy GWAS was used as a genetic proxy. Causal relationships were analysed using inverse-variance weighting, MR-Egger, weighted median, simple mode, and weighted mode methods. Power calculations, Cochran's Q test, MR-PRESSO, and Steiger directionality test were performed for quality control.

Results: In the analysis of iron metabolites and cardiomyopathy, there were 2 single nucleotide polymorphisms (SNPs) in SI (mean F-statistic = 12.3), 69 SNPs in SF (mean F-statistic = 28.7), 3 SNPs in STF (mean F-statistic = 15.2), 2 SNPs in TFRC (mean F-statistic = 11.8), and 24 SNPs in TSP (mean F-statistic = 22.4); and SF was a risk factor for cardiomyopathy (OR = 1.750, 95%CI: 1.152~2.657, P = 0.009). Furthermore, in the analysis of iron metabolites and sepsis, there were 2 SNPs in SI, 86 SNPs in SF, 4 SNPs in STF, 4 SNPs in TFRC, and 29 SNPs in TSP; and SF was a risk factor of sepsis (OR = 3.079, 95%CI: 1.420~6.679, P = 0.004). The Steiger directionality test confirmed that the causal direction was from ferritin to both outcomes. The results of quality control revealed no heterogeneity or horizontal pleiotropy among SNPs. In addition, there was no significant change in the MR analysis results after the removal of single SNP.

Conclusion: SF may increase the risk of both sepsis and cardiomyopathy, potentially through inflammation-iron metabolism pathways rather than direct iron toxicity.

目的:本研究旨在探讨血清铁(SI)代谢物与败血症和心肌病这两种不同结局的因果关系。方法:从EBI网站获得SI、血清铁蛋白(SF)、血清转铁蛋白(STF)、转铁蛋白受体(TFRC)、败血症和心肌病的全基因组关联研究(GWAS)数据。转铁蛋白饱和百分比(TSP)数据来自遗传学铁状态联合会。由于急性败血症性心肌病(SIC)缺乏GWAS,因此心肌病GWAS被用作遗传代理。采用反方差加权法、MR-Egger法、加权中位数法、简单模式法和加权模式法分析因果关系。采用功率计算、Cochran’s Q检验、MR-PRESSO、Steiger方向性检验进行质量控制。结果:在铁代谢产物与心肌病分析中,SI组有2个单核苷酸多态性(SNPs)(平均F-statistic = 12.3), SF组有69个SNPs(平均F-statistic = 28.7), STF组有3个SNPs(平均F-statistic = 15.2), TFRC组有2个SNPs(平均F-statistic = 11.8), TSP组有24个SNPs(平均F-statistic = 22.4);SF是心肌病的危险因素(OR = 1.750, 95%CI: 1.152~2.657, P = 0.009)。此外,在铁代谢产物与败血症的分析中,SI有2个snp, SF有86个snp, STF有4个snp, TFRC有4个snp, TSP有29个snp;SF是脓毒症的危险因素(OR = 3.079, 95%CI: 1.420~6.679, P = 0.004)。Steiger方向性检验证实因果方向是从铁蛋白到两种结果。质量控制结果显示snp之间没有异质性或水平多效性。此外,去除单个SNP后MR分析结果无明显变化。结论:SF可能增加败血症和心肌病的风险,可能是通过炎症-铁代谢途径而不是直接的铁毒性。
{"title":"Causal relationships of serum iron metabolites with sepsis and cardiomyopathy: a Mendelian randomization analysis.","authors":"Jian Zhang, Jing Cui, Quanrui Li, Geng Tian","doi":"10.29219/fnr.v69.12623","DOIUrl":"10.29219/fnr.v69.12623","url":null,"abstract":"<p><strong>Objective: </strong>The study aims to investigate the causal relationships of serum iron (SI) metabolites with sepsis and cardiomyopathy as two distinct outcomes.</p><p><strong>Methods: </strong>Genome-wide association studies (GWAS) data for SI, serum ferritin (SF), serum transferrin (STF), transferrin receptor (TFRC), sepsis, and cardiomyopathy were obtained from the EBI website. Transferrin saturation percentage (TSP) data were from the Genetics of Iron Status Consortium. Due to lack of GWAS for acute sepsis-induced cardiomyopathy (SIC), cardiomyopathy GWAS was used as a genetic proxy. Causal relationships were analysed using inverse-variance weighting, MR-Egger, weighted median, simple mode, and weighted mode methods. Power calculations, Cochran's Q test, MR-PRESSO, and Steiger directionality test were performed for quality control.</p><p><strong>Results: </strong>In the analysis of iron metabolites and cardiomyopathy, there were 2 single nucleotide polymorphisms (SNPs) in SI (mean <i>F</i>-statistic = 12.3), 69 SNPs in SF (mean <i>F</i>-statistic = 28.7), 3 SNPs in STF (mean F-statistic = 15.2), 2 SNPs in TFRC (mean <i>F</i>-statistic = 11.8), and 24 SNPs in TSP (mean <i>F</i>-statistic = 22.4); and SF was a risk factor for cardiomyopathy (OR = 1.750, 95%CI: 1.152~2.657, <i>P</i> = 0.009). Furthermore, in the analysis of iron metabolites and sepsis, there were 2 SNPs in SI, 86 SNPs in SF, 4 SNPs in STF, 4 SNPs in TFRC, and 29 SNPs in TSP; and SF was a risk factor of sepsis (OR = 3.079, 95%CI: 1.420~6.679, <i>P</i> = 0.004). The Steiger directionality test confirmed that the causal direction was from ferritin to both outcomes. The results of quality control revealed no heterogeneity or horizontal pleiotropy among SNPs. In addition, there was no significant change in the MR analysis results after the removal of single SNP.</p><p><strong>Conclusion: </strong>SF may increase the risk of both sepsis and cardiomyopathy, potentially through inflammation-iron metabolism pathways rather than direct iron toxicity.</p>","PeriodicalId":12119,"journal":{"name":"Food & Nutrition Research","volume":"69 ","pages":""},"PeriodicalIF":3.4,"publicationDate":"2025-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12664298/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145647844","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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Food & Nutrition Research
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