TY - JOUR
T1 - Reduced anti-inflammatory gut microbiota are associated with depression and anhedonia
AU - Mason, Brittany L.
AU - Li, Qiwei
AU - Minhajuddin, Abu
AU - Czysz, Andrew H.
AU - Coughlin, Laura A.
AU - Hussain, Sarah K.
AU - Koh, Andrew Y.
AU - Trivedi, Madhukar H.
N1 - Funding Information:
This work was supported by a NARSAD Young Investigator Award (B.L.M.), the Roberta I. and Norman L. Pollock Fund and the US National Institutes of Health (NIH) grant R01AI123163 (A.Y.K.), and the Center for Depression Research and Clinical Care (director, M.H.T.).
Funding Information:
This work was supported by was supported a NARSAD Young Investigator Award (B.L.M.), the Roberta I. and Norman L. Pollock Fund and the US National Institutes of Health (NIH) grant R01AI123163 (A.Y.K.), and the Center for Depression Research and Clinical Care (director, M.H.T.).
Funding Information:
This work was supported by a NARSAD Young Investigator Award (B.L.M.), the Roberta I. and Norman L. Pollock Fund and the US National Institutes of Health (NIH) grant R01AI123163 (A.Y.K.), and the Center for Depression Research and Clinical Care (director, M.H.T.).
Publisher Copyright:
© 2020
PY - 2020/4/1
Y1 - 2020/4/1
N2 - Introduction: Characterise gut microbiota distributions of participants with co-occurring depression and anxiety, in those with only depression or with anxiety, and determine if gut bacteria differentially correlates with distinct clinical presentations. Methods: Participants (10 healthy controls [mean age: 33, 60% female] and 60 psychiatric subjects; major depressive disorder (comorbid with anxiety), n = 38 [mean age: 39.2, 82% female], anxiety only, n = 8 [mean age: 40.0, 100% female], depression only without anxiety, n = 14 [mean age: 41.9, 79% female]) were characterized by psychiatric assessments. Quantitative PCR and 16S rRNA sequencing were used to characterize the gut microbiota in stool samples. Results: Altered microbiota correlated with pre-defined clinical presentation, with Bacteroides (p = 0.011) and the Clostridium leptum subgroup (p = 0.023) significantly different between clinical categories. Cluster analysis of the total sample using weighted UniFrac β-diversity of the gut microbiota identified two different clusters defined by differences in bacterial distribution. Cluster 2 had higher Bacteroides (p = 0.006), and much reduced presence of Clostridales (p<0.001) compared to Cluster 1. Bifidobacterium (p = 0.0173) was also reduced in Cluster 2 compared to Cluster 1. When evaluated for clinical charateristics, anhedonia scores in Cluster 2 were higher than in Cluster 1. Limitations: The sample is smaller and predominately female. Conclusions: Reduced or absent Clostridia was consistently seen in those with depression, independent of the presence of anxiety. Conversely, reduced Bacteroides may be more associated with the presence of anxiety, independent of the presence of depression. These differences suggest that gut microbiota distribution could help clarify the underlying pathology of comorbid clinical presentation.
AB - Introduction: Characterise gut microbiota distributions of participants with co-occurring depression and anxiety, in those with only depression or with anxiety, and determine if gut bacteria differentially correlates with distinct clinical presentations. Methods: Participants (10 healthy controls [mean age: 33, 60% female] and 60 psychiatric subjects; major depressive disorder (comorbid with anxiety), n = 38 [mean age: 39.2, 82% female], anxiety only, n = 8 [mean age: 40.0, 100% female], depression only without anxiety, n = 14 [mean age: 41.9, 79% female]) were characterized by psychiatric assessments. Quantitative PCR and 16S rRNA sequencing were used to characterize the gut microbiota in stool samples. Results: Altered microbiota correlated with pre-defined clinical presentation, with Bacteroides (p = 0.011) and the Clostridium leptum subgroup (p = 0.023) significantly different between clinical categories. Cluster analysis of the total sample using weighted UniFrac β-diversity of the gut microbiota identified two different clusters defined by differences in bacterial distribution. Cluster 2 had higher Bacteroides (p = 0.006), and much reduced presence of Clostridales (p<0.001) compared to Cluster 1. Bifidobacterium (p = 0.0173) was also reduced in Cluster 2 compared to Cluster 1. When evaluated for clinical charateristics, anhedonia scores in Cluster 2 were higher than in Cluster 1. Limitations: The sample is smaller and predominately female. Conclusions: Reduced or absent Clostridia was consistently seen in those with depression, independent of the presence of anxiety. Conversely, reduced Bacteroides may be more associated with the presence of anxiety, independent of the presence of depression. These differences suggest that gut microbiota distribution could help clarify the underlying pathology of comorbid clinical presentation.
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U2 - 10.1016/j.jad.2020.01.137
DO - 10.1016/j.jad.2020.01.137
M3 - Article
C2 - 32056905
AN - SCOPUS:85078986641
SN - 0165-0327
VL - 266
SP - 394
EP - 401
JO - Journal of affective disorders
JF - Journal of affective disorders
ER -