Colonic Microbiota Encroachment Correlates With Dysglycemia in Humans

被引:110
作者
Chassaing, Benoit [1 ]
Raja, Shreya M. [2 ,3 ]
Lewis, James D. [4 ]
Srinivasan, Shanthi [2 ,3 ]
Gewirtz, Andrew T. [1 ,2 ]
机构
[1] Georgia State Univ, Ctr Inflammat Immun & Infect, Inst Biomed Sci, Atlanta, GA 30303 USA
[2] Emory Univ, Sch Med, Dept Med, Digest Dis Div, Atlanta, GA 30322 USA
[3] Atlanta VA Med Ctr, Decatur, GA USA
[4] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA
来源
CELLULAR AND MOLECULAR GASTROENTEROLOGY AND HEPATOLOGY | 2017年 / 4卷 / 02期
基金
美国国家卫生研究院;
关键词
Metabolic Syndrome; Mucus Layer; Microbiota; LOW-GRADE INFLAMMATION; GUT MICROBIOTA; METABOLIC SYNDROME; PATHOGENESIS; COLITIS; MUCUS; MICE;
D O I
10.1016/j.jcmgh.2017.04.001
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
BACKGROUND AND AIMS: Mucoid structures that coat the epithelium play an essential role in keeping the intestinal microbiota at a safe distance from host cells. Encroachment of bacteria into the normally almost-sterile inner mucus layer has been observed in inflammatory bowel disease and in mouse models of colitis. Moreover, such microbiota encroachment has also been observed in mouse models of metabolic syndrome, which are associated low-grade intestinal inflammation. Hence, we investigated if microbiota encroachment might correlate with indices of metabolic syndrome in humans. METHODS: Confocal microscopy was used to measure bacterial-epithelial distance of the closest bacteria per highpowered field in colonic biopsies of all willing participants undergoing cancer screening colonoscopies. RESULTS: We observed that, among all subjects, bacterialepithelial distance was inversely correlated with body mass index, fasting glucose levels, and hemoglobin A(1C). However, this correlation was driven by dysglycemic subjects, irrespective of body mass index, whereas the difference in bacterial-epithelial distance between obese and nonobese subjects was eliminated by removal of dysglycemic subjects. CONCLUSIONS: We conclude that microbiota encroachment is a feature of insulin resistance-associated dysglycemia in humans.
引用
收藏
页码:205 / 221
页数:17
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