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Gut permeability and its clinical relevance in schizophrenia

AIM: We aimed to examine the gut permeability in patients with schizophrenia and its relevance to schizophrenia symptoms, medication, cognitive functions, and blood immune markers. METHODS: We selected 22 patients with schizophrenia (mean age: 37.9 ± 10.5 years) comprising 9 men and 13 women. Furthe...

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Autores principales: Ishida, Ikki, Ogura, Jun, Aizawa, Emiko, Ota, Miho, Hidese, Shinsuke, Yomogida, Yukihito, Matsuo, Junko, Yoshida, Sumiko, Kunugi, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8919127/
https://www.ncbi.nlm.nih.gov/pubmed/35080340
http://dx.doi.org/10.1002/npr2.12227
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author Ishida, Ikki
Ogura, Jun
Aizawa, Emiko
Ota, Miho
Hidese, Shinsuke
Yomogida, Yukihito
Matsuo, Junko
Yoshida, Sumiko
Kunugi, Hiroshi
author_facet Ishida, Ikki
Ogura, Jun
Aizawa, Emiko
Ota, Miho
Hidese, Shinsuke
Yomogida, Yukihito
Matsuo, Junko
Yoshida, Sumiko
Kunugi, Hiroshi
author_sort Ishida, Ikki
collection PubMed
description AIM: We aimed to examine the gut permeability in patients with schizophrenia and its relevance to schizophrenia symptoms, medication, cognitive functions, and blood immune markers. METHODS: We selected 22 patients with schizophrenia (mean age: 37.9 ± 10.5 years) comprising 9 men and 13 women. Furthermore, we included 86 healthy controls (mean age: 43.5 ± 11.0 years) comprising 41 men and 45 women. All participants were biologically unrelated and of Japanese descent. We used the Positive and Negative Syndrome Scale (PANSS) and Brief Assessment of Cognition in Schizophrenia (BACS) to measure the severity of schizophrenia symptoms and cognitive functions, respectively. The lactulose‐mannitol loading test was used to measure the permeability of the small intestine. Furthermore, we used the lactulose to mannitol ratio (LMR) as an index of gut permeability. We measured the C‐reactive protein and natural killer (NK) cell activity in the blood as highly sensitive immune markers. RESULTS: The patients had a significantly higher rate of “leaky gut” (defined as LMR ≥ 0.1) compared to the control group (22.7% vs. 5.8%, odds ratio: 4.8 [95% confidence interval, 1.2‐18.3], Fisher's exact test, P = 0.03). There was no significant correlation between the LMR and PANSS scores or in the daily antipsychotic dose. In addition, the LMR was negatively correlated with the total Z‐score of the BACS and NK cell activity in the patients. CONCLUSIONS: Our results suggest a higher rate of abnormally increased gut permeability in patients with schizophrenia than in controls. Moreover, gut permeability may be related to the cognitive and cellular immunity function of patients with schizophrenia.
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spelling pubmed-89191272022-03-18 Gut permeability and its clinical relevance in schizophrenia Ishida, Ikki Ogura, Jun Aizawa, Emiko Ota, Miho Hidese, Shinsuke Yomogida, Yukihito Matsuo, Junko Yoshida, Sumiko Kunugi, Hiroshi Neuropsychopharmacol Rep Original Articles AIM: We aimed to examine the gut permeability in patients with schizophrenia and its relevance to schizophrenia symptoms, medication, cognitive functions, and blood immune markers. METHODS: We selected 22 patients with schizophrenia (mean age: 37.9 ± 10.5 years) comprising 9 men and 13 women. Furthermore, we included 86 healthy controls (mean age: 43.5 ± 11.0 years) comprising 41 men and 45 women. All participants were biologically unrelated and of Japanese descent. We used the Positive and Negative Syndrome Scale (PANSS) and Brief Assessment of Cognition in Schizophrenia (BACS) to measure the severity of schizophrenia symptoms and cognitive functions, respectively. The lactulose‐mannitol loading test was used to measure the permeability of the small intestine. Furthermore, we used the lactulose to mannitol ratio (LMR) as an index of gut permeability. We measured the C‐reactive protein and natural killer (NK) cell activity in the blood as highly sensitive immune markers. RESULTS: The patients had a significantly higher rate of “leaky gut” (defined as LMR ≥ 0.1) compared to the control group (22.7% vs. 5.8%, odds ratio: 4.8 [95% confidence interval, 1.2‐18.3], Fisher's exact test, P = 0.03). There was no significant correlation between the LMR and PANSS scores or in the daily antipsychotic dose. In addition, the LMR was negatively correlated with the total Z‐score of the BACS and NK cell activity in the patients. CONCLUSIONS: Our results suggest a higher rate of abnormally increased gut permeability in patients with schizophrenia than in controls. Moreover, gut permeability may be related to the cognitive and cellular immunity function of patients with schizophrenia. John Wiley and Sons Inc. 2022-01-25 /pmc/articles/PMC8919127/ /pubmed/35080340 http://dx.doi.org/10.1002/npr2.12227 Text en © 2022 The Authors. Neuropsychopharmacology Reports published by John Wiley & Sons Australia, Ltd on behalf of the Japanese Society of Neuropsychopharmacology https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Ishida, Ikki
Ogura, Jun
Aizawa, Emiko
Ota, Miho
Hidese, Shinsuke
Yomogida, Yukihito
Matsuo, Junko
Yoshida, Sumiko
Kunugi, Hiroshi
Gut permeability and its clinical relevance in schizophrenia
title Gut permeability and its clinical relevance in schizophrenia
title_full Gut permeability and its clinical relevance in schizophrenia
title_fullStr Gut permeability and its clinical relevance in schizophrenia
title_full_unstemmed Gut permeability and its clinical relevance in schizophrenia
title_short Gut permeability and its clinical relevance in schizophrenia
title_sort gut permeability and its clinical relevance in schizophrenia
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8919127/
https://www.ncbi.nlm.nih.gov/pubmed/35080340
http://dx.doi.org/10.1002/npr2.12227
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