Gut Microbiota Changes in Patients with Bipolar Depression

Shaohua Hu(Chinese Institute for Brain Research), Ang Li(First Affiliated Hospital of Zhengzhou University), Tingting Huang(Zhejiang University), Jianbo Lai(Chinese Institute for Brain Research), Jingjing Li(State Key Laboratory of Diagnosis and Treatment of Infectious Diseases), M. Elizabeth Sublette(Columbia University), Haifeng Lu(State Key Laboratory of Diagnosis and Treatment of Infectious Diseases), Qiaoqiao Lu(Zhejiang University), Yanli Du(Zhejiang University), Zhiying Hu(Hangzhou Red Cross Hospital), Chee H. Ng(The University of Melbourne), Hua Zhang(State Key Laboratory of Diagnosis and Treatment of Infectious Diseases), Jing Lü(Chinese Institute for Brain Research), Tingting Mou(Chinese Institute for Brain Research), Shaojia Lu(Chinese Institute for Brain Research), Dandan Wang(Chinese Institute for Brain Research), Jinfeng Duan(Chinese Institute for Brain Research), Jianbo Hu(Chinese Institute for Brain Research), Manli Huang(Chinese Institute for Brain Research), Ning Wei(Chinese Institute for Brain Research), Weihua Zhou(Chinese Institute for Brain Research), Liemin Ruan(Ningbo First Hospital), Ming D. Li(State Key Laboratory of Diagnosis and Treatment of Infectious Diseases), Yi Xu(Chinese Institute for Brain Research)
Advanced Science
May 15, 2019
Cited by 174Open Access
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Abstract

Abstract This study aims to characterize the gut microbiota in depressed patients with bipolar disorder (BD) compared with healthy controls (HCs), to examine the effects of quetiapine treatment on the microbiota, and to explore the potential of microbiota as a biomarker for BD diagnosis and treatment outcome. Analysis of 16S‐ribosomal RNA gene sequences reveals that gut microbial composition and diversity are significantly different between BD patients and HCs. Phylum Bacteroidetes and Firmicutes are the predominant bacterial communities in BD patients and HCs, respectively. Lower levels of butyrate‐producing bacteria are observed in untreated patients. Microbial composition changes following quetiapine treatment in BD patients. Notably, 30 microbial markers are identified on a random forest model and achieve an area under the curve (AUC) of 0.81 between untreated patients and HCs. Ten microbial markers are identified with the AUC of 0.93 between responder and nonresponder patients. This study characterizes the gut microbiota in BD and is the first to evaluate microbial changes following quetiapine monotherapy. Gut microbiota‐based biomarkers may be helpful in BD diagnosis and predicting treatment outcome, which need further validations.


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