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健康成年人使用糖检测“肠漏”小肠和结肠通透性的试验的开发和验证。

Development and Validation of Test for "Leaky Gut" Small Intestinal and Colonic Permeability Using Sugars in Healthy Adults.

机构信息

Clinical Enteric NeuroscienceTranslational and Epidemiological Research (CENTER), Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.

出版信息

Gastroenterology. 2021 Aug;161(2):463-475.e13. doi: 10.1053/j.gastro.2021.04.020. Epub 2021 Apr 16.

DOI:10.1053/j.gastro.2021.04.020
PMID:33865841
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8328885/
Abstract

BACKGROUND

Oral monosaccharides and disaccharides are used to measure in vivo human gut permeability through urinary excretion.

AIMS

The aims were as follows: (1) to obtain normative data on small intestinal and colonic permeability; (2) to assess variance on standard 16 g fiber diet performed twice; (3) to determine whether dietary fiber influences gut permeability measurements; and (4) to present pilot data using 2 selected probes in patients with diarrhea-predominant irritable bowel syndrome (IBS-D).

METHODS

Sixty healthy female and male adults, age 18-70 years, participated in 3 randomized studies (2 studies on 16.25 g and 1 study on 32.5 g fiber) in otherwise standardized diets. At each test, the following sugars were ingested: C-mannitol, C-mannitol, rhamnose (monosaccharides), sucralose, and lactulose (disaccharides). Standardized meals were administered from 24 hours before and during 24 hours post-sugars with 3 urine collections: 0-2, 2-8, and 8-24 hours. Sugars were measured using high-performance liquid chromatography-tandem mass spectrometry. Eighteen patients with IBS-D underwent 24-hour excretion studies after oral C-mannitol and lactulose.

RESULTS

Baseline sugars (>3-fold above lower limits of quantitation) were identified in the 3 studies: C-mannitol in all participants; sucralose in 4-8, and rhamnose in 1-3. Median excretions/24 h (percentage of administered dose) for C-mannitol, rhamnose, lactulose, and sucralose were ∼30%, ∼15%, 0.32%, and 2.3%, respectively. C-mannitol and rhamnose reflected mainly small intestinal permeability. Intraindividual saccharide excretions were consistent, with minor differences with 16.25 g vs 32.5 g fiber diets. Median interindividual coefficient of variation was 76.5% (10-90 percentile: 34.6-111.0). There were no significant effects of sex, age, or body mass index on permeability measurements in health. C-mannitol measurements are feasible in IBS-D.

CONCLUSIONS

Baseline C-mannitol excretion precludes its use; C-mannitol is the preferred probe for small intestinal permeability.

摘要

背景

口服单糖和二糖被用于通过尿液排泄来测量体内人类肠道通透性。

目的

本研究的目的如下:(1)获得小肠和结肠通透性的正常数据;(2)评估两次标准 16 克纤维饮食的差异;(3)确定膳食纤维是否会影响肠道通透性的测量;(4)在腹泻型肠易激综合征(IBS-D)患者中使用 2 种选定的探针提供初步数据。

方法

60 名年龄在 18-70 岁的健康女性和男性成年人参加了 3 项随机研究(2 项研究使用 16.25 克纤维,1 项研究使用 32.5 克纤维),均在标准饮食下进行。在每次试验中,均摄入以下糖:C-甘露醇、C-甘露醇、鼠李糖(单糖)、蔗糖素和乳果糖(二糖)。在摄入糖前 24 小时至摄入后 24 小时内给予标准化餐,共采集 3 次尿液:0-2、2-8 和 8-24 小时。使用高效液相色谱-串联质谱法测量糖。18 名 IBS-D 患者在口服 C-甘露醇和乳果糖后进行了 24 小时排泄研究。

结果

在 3 项研究中均发现基线糖(高于定量下限的 3 倍以上):所有参与者均有 C-甘露醇;4-8 项有蔗糖素,1-3 项有鼠李糖。C-甘露醇、鼠李糖、乳果糖和蔗糖素的 24 小时排泄量/(给予剂量的百分比)分别约为 30%、15%、0.32%和 2.3%。C-甘露醇和鼠李糖主要反映小肠通透性。个体内糖的排泄是一致的,16.25 克纤维饮食与 32.5 克纤维饮食之间仅有微小差异。个体间变异系数的中位数为 76.5%(10-90%分位数:34.6-111.0)。在健康人群中,性别、年龄或体重指数对通透性测量无显著影响。C-甘露醇测量在 IBS-D 中是可行的。

结论

基线 C-甘露醇排泄排除了其用途;C-甘露醇是测量小肠通透性的首选探针。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4c0/8328885/3f074041e796/nihms-1694702-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4c0/8328885/5b240001e908/nihms-1694702-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4c0/8328885/e4036d7fc2e8/nihms-1694702-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4c0/8328885/28361ad337f3/nihms-1694702-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4c0/8328885/5b31e9e9305f/nihms-1694702-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4c0/8328885/3f074041e796/nihms-1694702-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4c0/8328885/5b240001e908/nihms-1694702-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4c0/8328885/e4036d7fc2e8/nihms-1694702-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4c0/8328885/28361ad337f3/nihms-1694702-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4c0/8328885/5b31e9e9305f/nihms-1694702-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4c0/8328885/3f074041e796/nihms-1694702-f0006.jpg

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