Comparison of gut microbiome profile in patients with schizophrenia and healthy controls- A plausible non-invasive biomarker?

被引:11
作者
Gokulakrishnan, Kuppan [1 ,8 ]
Nikhil, Joyappa [1 ]
Viswanath, Biju [2 ]
Thirumoorthy, Chinnasamy [1 ]
Narasimhan, Sandhya [1 ]
Devarajan, Bharanidharan [6 ]
Joseph, Ebin [2 ]
David, Arul Kevin Daniel [2 ]
Sharma, Sapna [5 ]
Vasudevan, Kavitha [7 ]
Sreeraj, Vanteemar S. [2 ]
Holla, Bharath [3 ]
Shivakumar, Venkataram [3 ]
Debnath, Monojit [4 ]
Venkatasubramanian, Ganesan [2 ]
Varambally, Shivarama [2 ,3 ]
机构
[1] Natl Inst Mental Hlth & Neuro Sci NIMHANS, Dept Neurochem, Hosur Rd, Bengaluru 560029, Karnataka, India
[2] Natl Inst Mental Hlth & Neuro Sci NIMHANS, Dept Psychiat, Hosur Rd, Bengaluru 560029, Karnataka, India
[3] Natl Inst Mental Hlth & Neuro Sci NIMHANS, Dept Integrat Med, Hosur Rd, Bengaluru 560029, Karnataka, India
[4] Natl Inst Mental Hlth & Neuro Sci NIMHANS, Dept Human Genet, Hosur Rd, Bengaluru 560029, Karnataka, India
[5] Tech Univ Munich, Chair Food Chem & Mol Sensory Sci, Lise Meitner Str 34, D-85354 Freising Weihenstephan, Germany
[6] Aravind Med Res Fdn, Dept Bioinformat, Madurai, Tamil Nadu, India
[7] Madras Diabet Res Fdn, Dept Foods Nutr & Dietet Res, Chennai, Tamil Nadu, India
[8] Natl Inst Mental Hlth & Neuro Sci NIMHANS, Dept Neurochem, DBT Wellcome Trust India Alliance, Bengaluru 560029, India
基金
英国惠康基金;
关键词
Gut microbiome; 16s rRNA; Risperidone; Schizophrenia; Diagnostic marker; ANTIPSYCHOTICS; BRAIN; RISK;
D O I
10.1016/j.jpsychires.2023.05.021
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
The human gut microbiome regulates brain function through the microbiome-gut-brain axis and is implicated in several neuropsychiatric disorders. However, the relationship between the gut microbiome and the pathogenesis of schizophrenia (SCZ) is poorly defined, and very few studies have examined the effect of antipsychotic treatment response. We aim to study the differences in the gut microbiota among drug-naive (DN SCZ) and risperidone-treated SCZ patients (RISP SCZ), compared to healthy controls (HCs). We recruited a total of 60 participants, from the clinical services of a large neuropsychiatric hospital, which included DN SCZ, RISP SCZ and HCs (n = 20 each). Fecal samples were analyzed using 16s rRNA sequencing in this cross-sectional study. No significant differences were found in taxa richness (alpha diversity) but microbial composition differed between SCZ patients (both DN and RISP) and HCs (PERMANOVA, p = 0.02). Linear Discriminant Analysis Effect Size (LEfSe) and Random Forest model identified the top six genera, which significantly differed in abundance be-tween the study groups. A specific genus-level microbial panel of Ruminococcus, UCG005, Clostridium_sensu_s-tricto_1 and Bifidobacterium could discriminate SCZ patients from HCs with an area under the curve (AUC) of 0.79, HCs vs DN SCZ (AUC: 0.68), HCs vs RISP SCZ (AUC: 0.93) and DN SCZ vs RISP SCZ (AUC: 0.87). Our study identified distinct microbial signatures that could aid in the differentiation of DN SCZ, RISP SCZ, and HCs. Our findings contribute to a better understanding of the role of the gut microbiome in SCZ pathophysiology and suggest potential targeted interventions.
引用
收藏
页码:140 / 149
页数:10
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