Carrageenan and insulin resistance in humans: a randomised double-blind cross-over trial.

IF 7 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL BMC Medicine Pub Date : 2024-11-26 DOI:10.1186/s12916-024-03771-8
Robert Wagner, Janine Buettner, Martin Heni, Louise Fritsche, Stephanie Kullmann, Moritz Wagmüller, Andreas Peter, Hubert Preissl, Jürgen Machann, Reiner Jumpertz von Schwartzenberg, Andreas L Birkenfeld, Ulrich-Frank Pape, Gerrit van Hall, Peter Plomgaard, Hans-Ulrich Häring, Andreas Fritsche, Kelsey N Thompson, Reinhild Klein, Norbert Stefan
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Abstract

Background: The potential impact of specific food additives, common in Western diets, on the risk of developing type 2 diabetes is not well understood. This study focuses on carrageenan, a widely used food additive known to induce insulin resistance and gut inflammation in animal models, and its effects on human health.

Methods: In a randomised, double-blind, placebo-controlled, cross-over trial conducted at a university hospital metabolic study centre, 20 males (age 27.4 ± 4.3 years, BMI 24.5 ± 2.5 kg/m2) participated. The intervention involved oral intake of carrageenan (250 mg) or placebo in the morning and in the evening and each intervention lasted 2 weeks. The primary outcome measured was insulin sensitivity (using oral glucose tolerance test [OGTT] and hyperinsulinaemic-euglycaemic clamp). Additional end-points included whole body and hepatic insulin sensitivity, MRI-measured brain inflammation and insulin resistance, intestinal permeability (via lactulose-mannitol test and plasma zonulin levels), and gut microbiome composition. Immune-cell activation and pro-inflammatory cytokine release from peripheral blood mononuclear cells were measured.

Results: Overall insulin sensitivity did not show significant differences between the treatments. However, interactions between BMI and treatment were observed (OGTT-based insulin sensitivity index: p=0.04, fasting insulin resistance: p=0.01, hepatic insulin sensitivity index: p=0.04). In overweight participants, carrageenan exposure resulted in lower whole body and hepatic insulin sensitivity, a trend towards increased brain inflammation, and elevated C-reactive protein (CRP) and IL-6 levels compared to placebo. Additionally, carrageenan was associated with increased intestinal permeability. In vitro natural killer (NK-)cell activation and increased pro-inflammatory cytokine release were found after carrageenan exposure in the participant's peripheral blood mononuclear cells.

Conclusions: These findings suggest that carrageenan, a common food additive, may contribute to insulin resistance and subclinical inflammation in overweight individuals through pro-inflammatory mechanisms in the gut. Further investigation into the long-term health impacts of carrageenan and other food additives is warranted.

Trial registration: NCT02629705.

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卡拉胶与人体胰岛素抵抗:随机双盲交叉试验。
背景:西方饮食中常见的特定食品添加剂对罹患 2 型糖尿病风险的潜在影响尚不十分清楚。卡拉胶是一种广泛使用的食品添加剂,已知可在动物模型中诱发胰岛素抵抗和肠道炎症,本研究重点关注卡拉胶及其对人体健康的影响:在大学医院代谢研究中心进行的一项随机、双盲、安慰剂对照、交叉试验中,20 名男性(年龄为 27.4 ± 4.3 岁,体重指数为 24.5 ± 2.5 kg/m2)参加了试验。干预措施包括早晚口服卡拉胶(250 毫克)或安慰剂,每次干预持续 2 周。测量的主要结果是胰岛素敏感性(采用口服葡萄糖耐量试验[OGTT]和高胰岛素血症-高血糖钳夹)。其他终点包括全身和肝脏胰岛素敏感性、核磁共振成像测量的脑部炎症和胰岛素抵抗、肠道通透性(通过乳糖-甘露醇试验和血浆zonulin水平)以及肠道微生物组组成。对免疫细胞活化和外周血单核细胞释放的促炎细胞因子进行了测量:结果:总体胰岛素敏感性在不同治疗之间没有显著差异。然而,观察到体重指数与治疗之间存在相互作用(基于 OGTT 的胰岛素敏感性指数:P=0.04;空腹胰岛素抵抗:P=0.01;肝脏胰岛素敏感性指数:P=0.04)。在超重参与者中,与安慰剂相比,接触卡拉胶会导致全身和肝脏胰岛素敏感性降低,脑部炎症呈增加趋势,C反应蛋白(CRP)和IL-6水平升高。此外,卡拉胶还与肠道渗透性增加有关。体外自然杀伤(NK)细胞活化和促炎细胞因子释放增加是在接触卡拉胶后在参与者外周血单核细胞中发现的:这些研究结果表明,卡拉胶这种常见的食品添加剂可能会通过肠道内的促炎机制,导致超重人群的胰岛素抵抗和亚临床炎症。有必要进一步调查卡拉胶和其他食品添加剂对健康的长期影响:NCT02629705.
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来源期刊
BMC Medicine
BMC Medicine 医学-医学:内科
CiteScore
13.10
自引率
1.10%
发文量
435
审稿时长
4-8 weeks
期刊介绍: BMC Medicine is an open access, transparent peer-reviewed general medical journal. It is the flagship journal of the BMC series and publishes outstanding and influential research in various areas including clinical practice, translational medicine, medical and health advances, public health, global health, policy, and general topics of interest to the biomedical and sociomedical professional communities. In addition to research articles, the journal also publishes stimulating debates, reviews, unique forum articles, and concise tutorials. All articles published in BMC Medicine are included in various databases such as Biological Abstracts, BIOSIS, CAS, Citebase, Current contents, DOAJ, Embase, MEDLINE, PubMed, Science Citation Index Expanded, OAIster, SCImago, Scopus, SOCOLAR, and Zetoc.
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