基于基因检测的量身定制饮食干预对疑似碳水化合物不耐受患者的影响

IF 2.5 4区 医学 Q3 BUSINESS
Alexandra Celi, María Trelis Villanueva, Stephany Lanza, José M Soriano, Juan Francisco Merino Torres
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引用次数: 0

摘要

背景:碳水化合物不耐受是一种复杂的情况,在消耗特定的底物后出现症状,并在从饮食中消除后减轻。乳糖不耐症是最常见的食物不耐症之一。原发性乳糖不耐症与遗传因素、乳糖酶非持续性表型有关,而继发性乳糖不耐症可能是肠道损伤和双糖酶活性丧失引起的暂时症状。果糖的吸收是一个能量独立的过程,导致吸收有限和可变。果糖通过活跃的转运体,特别是在小肠初始段发现的谷氨酸-5和谷氨酸-2,迅速被吸收到血液中。碳水化合物不耐受的管理需要精确的检测方法、准确的诊断和定制的饮食干预。基因检测在确定一个人的基因特征方面起着至关重要的作用,有助于决定是否有必要对特定营养素(如乳糖)进行永久限制。目的:本研究旨在了解可疑碳水化合物不耐受的起源,将基因检测与呼吸测试相结合,以提高治疗方案的有效性,并根据患者的遗传谱和碳水化合物吸收能力定制饮食干预。材料和方法:对乳糖和果糖进行基因检测(乳糖酶不持续性和乳糜泻风险)和呼气测试的组合。推荐低乳糖,低果糖或无麸质饮食;或者根据每个患者的检测结果提供这些方法的组合。结果:营养干预后,除反流和恶心外,所有胃肠道症状和所有肠外症状均有显著改善。结论:根据碳水化合物不耐受的主要和次要原因设计饮食干预措施可以避免不必要的食物限制;通过量身定制的饮食干预改善患者的生活质量和治疗效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of tailored dietary interventions on suspected carbohydrate intolerance patients based on genetic testing.

Background: carbohydrate intolerance presents a complex scenario where symptoms arise following the consumption of specific substrate and alleviate upon their elimination from the diet. Lactose Intolerance is one of the most prevalent types of food intolerance. Primary lactose intolerance is linked to genetic factors, Lactase Non-Persistence phenotype, while secondary lactose intolerance might be a temporary condition resulting from intestinal damage and loss of disaccharidase activity. Fructose absorption is an energy-independent process, leading to limited and variable absorption. Fructose undergoes quick absorption into the bloodstream through active transporters, specifically GLUT-5 and GLUT-2, found in the initial segment of the small intestine. The management of carbohydrate intolerance requires precise testing methods, accurate diagnostics, and customized dietary interventions. Genetic testing plays a crucial role in determining an individual's genetic profile, helping decide whether permanent restrictions on specific nutrients, such as lactose, are necessary.

Objective: this research aims to understand the origin of suspected carbohydrate intolerance, combining genetic testing with breath tests to enhance the efficacy of treatment plans, as customized dietary interventions will be based on the patient's genetic profile and carbohydrate absorption capacity.

Material and methods: a combination of genetic testing (lactase non-persistence and celiac disease risk) and breath test for lactose and fructose were performed. Recommendations such as low lactose, low fructose or gluten-free diets; or a combination of them were provided based on each patient's testing profile results.

Results: after the nutritional intervention, a significant improvement was noted in all gastrointestinal symptoms, except for reflux and nausea, and in all of the extraintestinal symptoms.

Conclusions: designing dietary interventions based on primary and secondary causes for carbohydrate intolerance can avoid unnecessary food restrictions; improving patients' quality of life and treatment effectiveness through tailored dietary interventions.

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来源期刊
Nutricion hospitalaria
Nutricion hospitalaria 医学-营养学
CiteScore
1.90
自引率
8.30%
发文量
181
审稿时长
3-6 weeks
期刊介绍: The journal Nutrición Hospitalaria was born following the SENPE Bulletin (1981-1983) and the SENPE journal (1984-1985). It is the official organ of expression of the Spanish Society of Clinical Nutrition and Metabolism. Throughout its 36 years of existence has been adapting to the rhythms and demands set by the scientific community and the trends of the editorial processes, being its most recent milestone the achievement of Impact Factor (JCR) in 2009. Its content covers the fields of the sciences of nutrition, with special emphasis on nutritional support.
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