The Intestinal Microbiota in Acute Anorexia Nervosa and During Renourishment: Relationship to Depression, Anxiety, and Eating Disorder Psychopathology

被引:228
作者
Kleiman, Susan C. [1 ]
Watson, Hunna J. [2 ,4 ,5 ]
Bulik-Sullivan, Emily C. [6 ]
Huh, Eun Young [3 ]
Tarantino, Lisa M. [2 ]
Bulik, Cynthia M. [1 ,2 ,7 ]
Carroll, Ian M. [3 ]
机构
[1] Univ N Carolina, Dept Nutr, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Psychiat, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Dept Med, Chapel Hill, NC 27599 USA
[4] Curtin Univ, Sch Psychol & Speech Pathol, Bentley, WA, Australia
[5] Univ Western Australia, Sch Paediat & Child Hlth, Nedlands, WA 6009, Australia
[6] Kenyon Coll, Gambier, OH USA
[7] Karolinska Inst, Dept Med Epidemiol & Biostat, Stockholm, Sweden
来源
PSYCHOSOMATIC MEDICINE | 2015年 / 77卷 / 09期
基金
瑞典研究理事会;
关键词
eating disorders; anorexia nervosa; intestinal microbiota; gut-brain axis; depression; anxiety; PITUITARY-ADRENAL-SYSTEM; GUT MICROBIOTA; BIOCHEMICAL-ABNORMALITIES; CARDIAC ABNORMALITIES; MOLECULAR ANALYSIS; BOWEL; MORTALITY; COMMUNITY; LACTOBACILLUS; COMORBIDITY;
D O I
10.1097/PSY.0000000000000247
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective The relevance of the microbe-gut-brain axis to psychopathology is of interest in anorexia nervosa (AN), as the intestinal microbiota plays a critical role in metabolic function and weight regulation. Methods We characterized the composition and diversity of the intestinal microbiota in AN, using stool samples collected at inpatient admission (T1; n = 16) and discharge (T2; n = 10). At T1, participants completed the Beck Depression and Anxiety Inventories and the Eating Disorder Examination-Questionnaire. Patients with AN were compared with healthy individuals who participated in a previous study (healthy comparison group; HCG). Genomic DNA was isolated from stool samples, and bacterial composition was characterized by 454 pyrosequencing of the 16S rRNA gene. Sequencing results were processed by the Quantitative Insights Into Microbial Ecology pipeline. We compared T1 versus T2 samples, samples from both points were compared with HCG (n = 12), and associations between psychopathology and T1 samples were explored. Results In patients with AN, significant changes emerged between T1 and T2 in taxa abundance and beta (between-sample) diversity. Patients with AN had significantly lower alpha (within-sample) diversity than did HCG at both T1 (p = .0001) and T2 (p = .016), and differences in taxa abundance were found between AN patients and HCG. Levels of depression, anxiety, and eating disorder psychopathology at T1 were associated with composition and diversity of the intestinal microbiota. Conclusions We provide evidence of an intestinal dysbiosis in AN and an association between mood and the enteric microbiota in this patient population. Future directions include mechanistic investigations of the microbe-gut-brain axis in animal models and association of microbial measures with metabolic changes and recovery indices.
引用
收藏
页码:969 / 981
页数:13
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