社论:炎症性肠病和膳食乳化剂——一个继续存在的难题

IF 6.6 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Stephanie Gold, Natasha Haskey, Maitreyi Raman
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引用次数: 0

摘要

超加工食品(upf)对炎症性肠病(IBD)发病机制的影响越来越被认识[1-3]。临床和临床前研究将upf(包括膳食乳化剂)与生态失调、粘膜层破坏和免疫激活联系起来[1,2]。由于加工食品消费的增加与包括IBD在内的慢性疾病发病率和流行率的增加有关,因此UPF消费对IBD相关结果的影响引起了人们的极大兴趣[10]。Fitzpatrick等人于2010年在活动性回肠克罗恩病患者中进行了一项双盲随机对照试验。19名参与者接受高乳化剂饮食(HED)或低乳化剂饮食(LED) 4周。两组患者在临床疾病活动度、肠道超声检查结果或生活质量改善方面无显著差异。作者的结论是,研究结果不支持目前建议患者避免食用乳化剂的建议。对照喂养研究,如本研究,为分离和评估特定食物成分的影响提供了机会。该研究的显著优势包括其盲法、随机设计;精心制定的饮食干预措施;整合临床生物标志物和患者报告的结果来评估有效性。这项研究也有一些局限性。小样本和高退出率(20%,10名患者使用HED, 9名患者使用LED)限制了得出乳化剂与其他饮食成分或疾病活动对胃肠道症状的影响的明确结论的能力。此外,短期的饮食干预期可能还不够长,不足以看到乳化剂的全部影响,特别是在这个小队列中。此外,该研究缺乏对饮食质量和其他潜在的混淆性饮食成分的正式评估。虽然饮食遵循“健康饮食指南”,但标准化的饮食评估工具,如健康饮食指数或地中海饮食评分,可以识别乳化剂含量以外的差异[5-9]。乳化剂的定量也受到限制,没有区分天然乳化剂和合成乳化剂(例如,聚山梨酸酯80与蛋黄),尽管它们对微生物组的潜在影响不同。此外,NOVA对实际食物摄入量的分类,而不是推荐的食物摄入量,将提供更准确的饮食评估。尽管据报道,基于饮食日记的饮食依从性很高,但仍不清楚有多少患者在干预期间完全依从。评估饮食依从性至关重要,尤其是在一项参与者如此之少的研究中。此外,虽然饮食设计是为了满足能量需求,但所有患者都经历了体重减轻,这可能是由于饮食少报,也可能导致乳化剂消耗减少。为了更好地了解乳化剂和炎症之间的联系,需要更大规模的前瞻性研究,包括客观结果,如微生物多样性、肠道通透性和内镜下愈合,以及有效的饮食依从性措施。区分天然乳化剂和合成乳化剂也将指导临床建议。在此之前,应告知患者文献中的可变性,并建议尽可能避免使用含有乳化剂的upf。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Editorial: Inflammatory Bowel Disease and Dietary Emulsifiers—A Conundrum That Continues

The impact of ultra-processed foods (UPFs) on inflammatory bowel disease (IBD) pathogenesis is increasingly recognised [1-3]. Clinical and preclinical studies link UPFs, including dietary emulsifiers, to dysbiosis, mucous layer disruption and immune activation [1, 2]. Since the increasing consumption of processed foods has been linked to increased incidence and prevalence of chronic disease, including IBD, the influence of UPF consumption on IBD-related outcomes is of major interest [1].

Fitzpatrick et al. [4] conducted a double-blinded randomised controlled trial in patients with active ileal Crohn's disease. Nineteen participants received either a high emulsifier diet (HED) or low emulsifier diet (LED) for 4 weeks. There were no significant differences in improvement in clinical disease activity, intestinal ultrasound findings or quality of life between the two groups. The authors concluded that the findings did not support the current recommendations for patients to avoid dietary emulsifiers.

Controlled feeding studies, such as this [4], provide an opportunity to isolate and assess the impact of specific food components. Notable strengths of this study included its blinded, randomised design; carefully formulated dietary interventions; and integration of clinical biomarkers and patient-reported outcomes to evaluate effectiveness.

The study also had several limitations. The small sample and high dropout rate (> 20%, with 10 patients on HED and nine on LED) limit the ability to draw definitive conclusions about the impact of emulsifiers versus other dietary components, or disease activity on gastrointestinal symptoms. Moreover, the short dietary intervention period may not have been long enough to see the full impact of the emulsifiers, especially in this small cohort.

Moreover, the study lacked formal assessment of dietary quality and other potential confounding dietary components. While the diets followed ‘healthy eating guidelines’, standardised dietary assessment tools such as the Healthy Eating Index or the Mediterranean Diet Score could have identified differences beyond emulsifier content [5-9]. Emulsifier quantification was also limited with no distinction between naturally occurring and synthetic emulsifiers (e.g., polysorbate 80 vs. egg yolks), despite their potential for differing effects on the microbiome [10]. Furthermore, NOVA classification of the actual rather than recommended food intake would have provided a more accurate diet assessment.

Despite the reported high adherence to the diets based on food diaries, it remains unclear how many patients were fully compliant during the intervention. Assessing dietary compliance is crucial, particularly in a study with so few participants. Additionally, while the diets were designed to meet energy requirements, all patients experienced weight loss, which may be secondary to dietary underreporting and may have led to a reduction in emulsifier consumption as well.

Larger, prospective studies with objective outcomes, such as microbial diversity, intestinal permeability and endoscopic healing, and with validated measures of dietary adherence are needed to better understand the link between emulsifiers and inflammation. Distinguishing between natural and synthetic emulsifiers will also guide clinical recommendations. Until then, patients should be counselled on the variability in the literature and advised to avoid UPFs with emulsifiers when possible.

Stephanie Gold: conceptualization, methodology, writing – original draft, writing – review and editing. Natasha Haskey: conceptualization, writing – review and editing. Maitreyi Raman: conceptualization, methodology, writing – review and editing.

S.G.: Nestle Nutrition Institute Fellow 2023, supported by a Crohn's and Colitis Foundation Career Development Award, Medical Board Member of Nutritional Therapy for IBD. M.R.: Speaker Fees: Fresenius Kabi, AbbVie. Grant Support: Pfizer, AbbVie, Johnson & Johnson. LyfeMD—Cofounder, CMO. N.H.: Medical Board Member of Nutritional Therapy for IBD.

This article is linked to Fitzpatrick et al papers. To view these articles, visit https://doi.org/10.1111/apt.70041 and https://doi.org/10.1111/apt.70148.

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来源期刊
CiteScore
15.60
自引率
7.90%
发文量
527
审稿时长
3-6 weeks
期刊介绍: Alimentary Pharmacology & Therapeutics is a global pharmacology journal focused on the impact of drugs on the human gastrointestinal and hepato-biliary systems. It covers a diverse range of topics, often with immediate clinical relevance to its readership.
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