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Dysglycaemia, Inflammation and Psychosis: Findings From the UK ALSPAC Birth Cohort

BACKGROUND: Psychosis is associated with both dysglycaemia and low-grade inflammation, but population-based studies investigating the interplay between these factors are scarce. AIMS: (1) To explore the direction of association between markers of dysglycaemia, inflammation and psychotic experiences...

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Autores principales: Perry, Benjamin Ian, Upthegrove, Rachel, Thompson, Andrew, Marwaha, Steven, Zammit, Stanley, Singh, Swaran Preet, Khandaker, Golam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6403055/
https://www.ncbi.nlm.nih.gov/pubmed/29635418
http://dx.doi.org/10.1093/schbul/sby040
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author Perry, Benjamin Ian
Upthegrove, Rachel
Thompson, Andrew
Marwaha, Steven
Zammit, Stanley
Singh, Swaran Preet
Khandaker, Golam
author_facet Perry, Benjamin Ian
Upthegrove, Rachel
Thompson, Andrew
Marwaha, Steven
Zammit, Stanley
Singh, Swaran Preet
Khandaker, Golam
author_sort Perry, Benjamin Ian
collection PubMed
description BACKGROUND: Psychosis is associated with both dysglycaemia and low-grade inflammation, but population-based studies investigating the interplay between these factors are scarce. AIMS: (1) To explore the direction of association between markers of dysglycaemia, inflammation and psychotic experiences (PEs); and (2) To explore whether dysglycaemia moderates and/or mediates the association between inflammation and PEs. METHOD: Data from the Avon Longitudinal Study of Parents and Children (ALSPAC) birth cohort were modeled using logistic and linear regression to examine cross-sectional and longitudinal associations between markers of dysglycaemia (ages 9 and 18), interleukin-6 (IL-6) (age 9), and PEs (ages 12 and 18). We tested for an interaction between dysglycaemia and IL-6 on risk of PEs at age 18, and tested whether dysglycaemia mediated the relationship between IL-6 and PEs. RESULTS: Based on 2627 participants, at age 18, insulin resistance (IR) was associated with PEs (adjusted OR = 2.32; 95% CI, 1.37–3.97). IR was associated with IL-6 both cross-sectionally and longitudinally. Interaction analyses under a multiplicative model showed that IR moderated the association between IL-6 at age 9 and PEs at age 18 (adjusted OR for interaction term = 2.18; 95% C.I., 1.06–4.49). Mediation analysis did not support a model of IR mediating the relationship between IL-6 and PEs. IMPLICATIONS: IR is associated with PEs in young people even before the onset of clinical psychosis. Metabolic alterations may interact with childhood inflammation to increase risk of PEs. The findings have implications for clinical practice and future research.
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spelling pubmed-64030552019-03-12 Dysglycaemia, Inflammation and Psychosis: Findings From the UK ALSPAC Birth Cohort Perry, Benjamin Ian Upthegrove, Rachel Thompson, Andrew Marwaha, Steven Zammit, Stanley Singh, Swaran Preet Khandaker, Golam Schizophr Bull Regular Articles BACKGROUND: Psychosis is associated with both dysglycaemia and low-grade inflammation, but population-based studies investigating the interplay between these factors are scarce. AIMS: (1) To explore the direction of association between markers of dysglycaemia, inflammation and psychotic experiences (PEs); and (2) To explore whether dysglycaemia moderates and/or mediates the association between inflammation and PEs. METHOD: Data from the Avon Longitudinal Study of Parents and Children (ALSPAC) birth cohort were modeled using logistic and linear regression to examine cross-sectional and longitudinal associations between markers of dysglycaemia (ages 9 and 18), interleukin-6 (IL-6) (age 9), and PEs (ages 12 and 18). We tested for an interaction between dysglycaemia and IL-6 on risk of PEs at age 18, and tested whether dysglycaemia mediated the relationship between IL-6 and PEs. RESULTS: Based on 2627 participants, at age 18, insulin resistance (IR) was associated with PEs (adjusted OR = 2.32; 95% CI, 1.37–3.97). IR was associated with IL-6 both cross-sectionally and longitudinally. Interaction analyses under a multiplicative model showed that IR moderated the association between IL-6 at age 9 and PEs at age 18 (adjusted OR for interaction term = 2.18; 95% C.I., 1.06–4.49). Mediation analysis did not support a model of IR mediating the relationship between IL-6 and PEs. IMPLICATIONS: IR is associated with PEs in young people even before the onset of clinical psychosis. Metabolic alterations may interact with childhood inflammation to increase risk of PEs. The findings have implications for clinical practice and future research. Oxford University Press 2019-03 2018-04-09 /pmc/articles/PMC6403055/ /pubmed/29635418 http://dx.doi.org/10.1093/schbul/sby040 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Regular Articles
Perry, Benjamin Ian
Upthegrove, Rachel
Thompson, Andrew
Marwaha, Steven
Zammit, Stanley
Singh, Swaran Preet
Khandaker, Golam
Dysglycaemia, Inflammation and Psychosis: Findings From the UK ALSPAC Birth Cohort
title Dysglycaemia, Inflammation and Psychosis: Findings From the UK ALSPAC Birth Cohort
title_full Dysglycaemia, Inflammation and Psychosis: Findings From the UK ALSPAC Birth Cohort
title_fullStr Dysglycaemia, Inflammation and Psychosis: Findings From the UK ALSPAC Birth Cohort
title_full_unstemmed Dysglycaemia, Inflammation and Psychosis: Findings From the UK ALSPAC Birth Cohort
title_short Dysglycaemia, Inflammation and Psychosis: Findings From the UK ALSPAC Birth Cohort
title_sort dysglycaemia, inflammation and psychosis: findings from the uk alspac birth cohort
topic Regular Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6403055/
https://www.ncbi.nlm.nih.gov/pubmed/29635418
http://dx.doi.org/10.1093/schbul/sby040
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