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

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...

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Published in:Journal of psychiatric research 2023-06, Vol.162, p.140-149
Main Authors: Gokulakrishnan, Kuppan, Nikhil, Joyappa, Viswanath, Biju, Thirumoorthy, Chinnasamy, Narasimhan, Sandhya, Devarajan, Bharanidharan, Joseph, Ebin, David, Arul Kevin Daniel, Sharma, Sapna, Vasudevan, Kavitha, Sreeraj, Vanteemar S., Holla, Bharath, Shivakumar, Venkataram, Debnath, Monojit, Venkatasubramanian, Ganesan, Varambally, Shivarama
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creator Gokulakrishnan, Kuppan
Nikhil, Joyappa
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Narasimhan, Sandhya
Devarajan, Bharanidharan
Joseph, Ebin
David, Arul Kevin Daniel
Sharma, Sapna
Vasudevan, Kavitha
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Debnath, Monojit
Venkatasubramanian, Ganesan
Varambally, Shivarama
description 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-naïve (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 between the study groups. A specific genus-level microbial panel of Ruminococcus, UCG005, Clostridium_sensu_stricto_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. [Display omitted]
doi_str_mv 10.1016/j.jpsychires.2023.05.021
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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-naïve (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 between the study groups. 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subjects 16s rRNA
Biomarkers
Cross-Sectional Studies
Diagnostic marker
Feces - microbiology
Gastrointestinal Microbiome - genetics
Gut microbiome
Humans
Risperidone
RNA, Ribosomal, 16S - genetics
Schizophrenia
Schizophrenia - microbiology
title Comparison of gut microbiome profile in patients with schizophrenia and healthy controls - A plausible non-invasive biomarker?
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