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Associations between gut microbiota and Alzheimer’s disease, major depressive disorder, and schizophrenia
by
Qi, Lu
, Wang, Wenxiu
, Yang, Ruotong
, Huang, Tao
, Zhuang, Zhenhuang
in
Alzheimer's disease
/ Arginine
/ Bacilli
/ Bias
/ Biomedical and Life Sciences
/ Biomedicine
/ Causality
/ Complications and side effects
/ Development and progression
/ Digestive system
/ Dysbiosis
/ Genetic analysis
/ Genetic association
/ Genetic diversity
/ Genome-wide association studies
/ Genomes
/ Genomics
/ Gut microbiota
/ Health aspects
/ Immunology
/ Intestinal microflora
/ Major depressive disorder
/ Mendelian randomization
/ Mental depression
/ Mental disorders
/ Metabolites
/ Microbiomes
/ Microbiota
/ Microbiota (Symbiotic organisms)
/ Neurobiology
/ Neurodegenerative diseases
/ Neurology
/ Neuropsychiatric disorder
/ Neurosciences
/ Physiological aspects
/ Risk factors
/ Schizophrenia
/ Serotonin
/ γ-Aminobutyric acid
2020
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Associations between gut microbiota and Alzheimer’s disease, major depressive disorder, and schizophrenia
by
Qi, Lu
, Wang, Wenxiu
, Yang, Ruotong
, Huang, Tao
, Zhuang, Zhenhuang
in
Alzheimer's disease
/ Arginine
/ Bacilli
/ Bias
/ Biomedical and Life Sciences
/ Biomedicine
/ Causality
/ Complications and side effects
/ Development and progression
/ Digestive system
/ Dysbiosis
/ Genetic analysis
/ Genetic association
/ Genetic diversity
/ Genome-wide association studies
/ Genomes
/ Genomics
/ Gut microbiota
/ Health aspects
/ Immunology
/ Intestinal microflora
/ Major depressive disorder
/ Mendelian randomization
/ Mental depression
/ Mental disorders
/ Metabolites
/ Microbiomes
/ Microbiota
/ Microbiota (Symbiotic organisms)
/ Neurobiology
/ Neurodegenerative diseases
/ Neurology
/ Neuropsychiatric disorder
/ Neurosciences
/ Physiological aspects
/ Risk factors
/ Schizophrenia
/ Serotonin
/ γ-Aminobutyric acid
2020
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Associations between gut microbiota and Alzheimer’s disease, major depressive disorder, and schizophrenia
by
Qi, Lu
, Wang, Wenxiu
, Yang, Ruotong
, Huang, Tao
, Zhuang, Zhenhuang
in
Alzheimer's disease
/ Arginine
/ Bacilli
/ Bias
/ Biomedical and Life Sciences
/ Biomedicine
/ Causality
/ Complications and side effects
/ Development and progression
/ Digestive system
/ Dysbiosis
/ Genetic analysis
/ Genetic association
/ Genetic diversity
/ Genome-wide association studies
/ Genomes
/ Genomics
/ Gut microbiota
/ Health aspects
/ Immunology
/ Intestinal microflora
/ Major depressive disorder
/ Mendelian randomization
/ Mental depression
/ Mental disorders
/ Metabolites
/ Microbiomes
/ Microbiota
/ Microbiota (Symbiotic organisms)
/ Neurobiology
/ Neurodegenerative diseases
/ Neurology
/ Neuropsychiatric disorder
/ Neurosciences
/ Physiological aspects
/ Risk factors
/ Schizophrenia
/ Serotonin
/ γ-Aminobutyric acid
2020
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Associations between gut microbiota and Alzheimer’s disease, major depressive disorder, and schizophrenia
Journal Article
Associations between gut microbiota and Alzheimer’s disease, major depressive disorder, and schizophrenia
2020
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Overview
Background
Growing evidence has shown that alterations in the gut microbiota composition were associated with a variety of neuropsychiatric conditions. However, whether such associations reflect causality remains unknown. We aimed to reveal the causal relationships among gut microbiota, metabolites, and neuropsychiatric disorders including Alzheimer’s disease (AD), major depressive disorder (MDD), and schizophrenia (SCZ).
Methods
A two-sample bi-directional Mendelian randomization analysis was performed by using genetic variants from genome-wide association studies as instrumental variables for gut microbiota, metabolites, AD, MDD, and SCZ, respectively.
Results
We found suggestive associations of host-genetic-driven increase in
Blautia
(OR, 0.88; 95%CI, 0.79–0.99;
P
= 0.028) and elevated γ-aminobutyric acid (GABA) (0.96; 0.92–1.00;
P
= 0.034), a downstream product of
Blautia
-dependent arginine metabolism, with a lower risk of AD. Genetically increased
Enterobacteriaceae family
and
Enterobacteriales order
were potentially associated with a higher risk of SCZ (1.09; 1.00–1.18;
P
= 0.048), while
Gammaproteobacteria class
(0.90; 0.83–0.98;
P
= 0.011) was related to a lower risk for SCZ. Gut production of serotonin was potentially associated with an increased risk of SCZ (1.07; 1.00–1.15;
P
= 0.047). Furthermore, genetically increased
Bacilli class
was related to a higher risk of MDD (1.07; 1.02–1.12;
P
= 0.010). In the other direction, neuropsychiatric disorders altered gut microbiota composition.
Conclusions
These data for the first time provide evidence of potential causal links between gut microbiome and AD, MDD, and SCZ. GABA and serotonin may play an important role in gut microbiota-host crosstalk in AD and SCZ, respectively. Further investigations in understanding the underlying mechanisms of associations between gut microbiota and AD, MDD, and SCZ are required.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
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