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Changes in the gut microbiome associated with infliximab in patients with bipolar disorder

OBJECTIVES: Available information exists supporting the gut–brain axis, but additional information is needed to explore how the gut microbiome changes when exposed to mood disorder treatments. We sought to explore the effects of a novel treatment for bipolar disorder (BD), infliximab, on the gut mic...

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Autores principales: Bharwani, Aadil, Szamosi, Jake C., Taylor, Valerie H., Lee, Yena, Bala, Asem, Mansur, Rodrigo, Subramaniapillai, Mehala, Surette, Michael, McIntyre, Roger S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413825/
https://www.ncbi.nlm.nih.gov/pubmed/34152099
http://dx.doi.org/10.1002/brb3.2259
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author Bharwani, Aadil
Szamosi, Jake C.
Taylor, Valerie H.
Lee, Yena
Bala, Asem
Mansur, Rodrigo
Subramaniapillai, Mehala
Surette, Michael
McIntyre, Roger S.
author_facet Bharwani, Aadil
Szamosi, Jake C.
Taylor, Valerie H.
Lee, Yena
Bala, Asem
Mansur, Rodrigo
Subramaniapillai, Mehala
Surette, Michael
McIntyre, Roger S.
author_sort Bharwani, Aadil
collection PubMed
description OBJECTIVES: Available information exists supporting the gut–brain axis, but additional information is needed to explore how the gut microbiome changes when exposed to mood disorder treatments. We sought to explore the effects of a novel treatment for bipolar disorder (BD), infliximab, on the gut microbiome. METHODS: Participants with a primary diagnosis of BD (n = 15) who participated in a 12‐week, randomized placebo‐controlled trial evaluating the efficacy of adjunctive infliximab in the treatment of BD were recruited and followed. Stool samples were collected prior to randomization and at 12 weeks. 16S rRNA sequencing was employed in order to analyze the gut microbial community profile. RESULTS: A total of 17 participants were randomized to infliximab (n = 9; mean [SD] age, 47.6 [10.3] years; 8 female) or to placebo (n = 8; mean [SD] age, 45.9 [10.7] years; 7 female) but two participants from the infliximab group were lost to follow‐up post randomization. Across all time points, there were no differences in the diversity on either Shannon or Simpson's Diversity indices. Comparison of Aitchison distances revealed a lack of clustering of the microbiota by time point, but did reveal a small overall effect of treatment that was not significantly different at individual time points. There were also no effects of either time or treatment on differential abundance at either the amplicon sequence variant or genus level. CONCLUSIONS: These observations indicate that no community‐wide changes in the microbiota diversity and profile were detected after the use of infliximab treatment.
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spelling pubmed-84138252021-09-07 Changes in the gut microbiome associated with infliximab in patients with bipolar disorder Bharwani, Aadil Szamosi, Jake C. Taylor, Valerie H. Lee, Yena Bala, Asem Mansur, Rodrigo Subramaniapillai, Mehala Surette, Michael McIntyre, Roger S. Brain Behav Original Research OBJECTIVES: Available information exists supporting the gut–brain axis, but additional information is needed to explore how the gut microbiome changes when exposed to mood disorder treatments. We sought to explore the effects of a novel treatment for bipolar disorder (BD), infliximab, on the gut microbiome. METHODS: Participants with a primary diagnosis of BD (n = 15) who participated in a 12‐week, randomized placebo‐controlled trial evaluating the efficacy of adjunctive infliximab in the treatment of BD were recruited and followed. Stool samples were collected prior to randomization and at 12 weeks. 16S rRNA sequencing was employed in order to analyze the gut microbial community profile. RESULTS: A total of 17 participants were randomized to infliximab (n = 9; mean [SD] age, 47.6 [10.3] years; 8 female) or to placebo (n = 8; mean [SD] age, 45.9 [10.7] years; 7 female) but two participants from the infliximab group were lost to follow‐up post randomization. Across all time points, there were no differences in the diversity on either Shannon or Simpson's Diversity indices. Comparison of Aitchison distances revealed a lack of clustering of the microbiota by time point, but did reveal a small overall effect of treatment that was not significantly different at individual time points. There were also no effects of either time or treatment on differential abundance at either the amplicon sequence variant or genus level. CONCLUSIONS: These observations indicate that no community‐wide changes in the microbiota diversity and profile were detected after the use of infliximab treatment. John Wiley and Sons Inc. 2021-06-21 /pmc/articles/PMC8413825/ /pubmed/34152099 http://dx.doi.org/10.1002/brb3.2259 Text en © 2021 The Authors. Brain and Behavior published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Bharwani, Aadil
Szamosi, Jake C.
Taylor, Valerie H.
Lee, Yena
Bala, Asem
Mansur, Rodrigo
Subramaniapillai, Mehala
Surette, Michael
McIntyre, Roger S.
Changes in the gut microbiome associated with infliximab in patients with bipolar disorder
title Changes in the gut microbiome associated with infliximab in patients with bipolar disorder
title_full Changes in the gut microbiome associated with infliximab in patients with bipolar disorder
title_fullStr Changes in the gut microbiome associated with infliximab in patients with bipolar disorder
title_full_unstemmed Changes in the gut microbiome associated with infliximab in patients with bipolar disorder
title_short Changes in the gut microbiome associated with infliximab in patients with bipolar disorder
title_sort changes in the gut microbiome associated with infliximab in patients with bipolar disorder
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413825/
https://www.ncbi.nlm.nih.gov/pubmed/34152099
http://dx.doi.org/10.1002/brb3.2259
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