Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/119015
Title: Evidence of activation of the Toll-like receptor-4 proinflammatory pathway in patients with schizophrenia
Author: García Bueno, Borja
Gassó Astorga, Patricia
MacDowell, Karina S.
Callado, Luis F.
Mas Herrero, Sergi
Bernardo Arroyo, Miquel
Lafuente, Amàlia, 1952-
Meana, J.Javier
Leza, Juan C.
Keywords: Esquizofrènia
Inflamació
Malalties mentals
Schizophrenia
Inflammation
Mental illness
Issue Date: 12-Apr-2016
Publisher: Canadian Medical Association
Abstract: BACKGROUND: Alterations in the innate immune/inflammatory system may underlie the pathophysiology of schizophrenia, but we do not understand the mechanisms involved. The main agents of innate immunity are the Toll-like receptors (TLRs), which detect molecular patterns associated with damage and pathogens. The TLR first reported was TLR4, and it is still the most studied one. METHODS: We aimed to describe putative modifications to the TLR4 proinflammatory pathway using 2 different strategies in 2 cohorts of patients with schizophrenia and matched controls: 1) quantification of protein and mRNA expression in postmortem prefrontal cortex samples from 30 patients with schizophrenia and 30 controls, and 2) identification of single nucleotide polymorphisms associated with the risk of schizophrenia using whole blood samples from 214 patients with schizophrenia and 216 controls. RESULTS: We found evidence of alterations in the expression of the initial elements of the TLR4 signalling pathway (TLR4, Myeloid differentiation primary response gene 88 [MyD88] and nuclear factor-κ B [NF-κB]) in the PFC of patients with schizophrenia. These alterations seem to depend on the presence/absence of antipsychotic treatment at death. Moreover, a polymorphism within the MyD88 gene was significantly associated with schizophrenia risk. LIMITATIONS: The use of 2 different approaches in 2 different cohorts, the lack of a complementary neuropsychiatric group, the possible confounding effects of antipsychotic treatment and suicide are the main limitations of our study. CONCLUSION: The evidence from this dual approach suggests there is an altered innate immune response in patients with chronic schizophrenia in which the TLR4 proinflammatory pathway could be affected. Improved understanding of the stimuli and mechanisms responsible for this response could lead to improved schizophrenia treatment and better control of the side effects of current antipsychotics.
Note: Reproducció del document publicat a: https://doi.org/10.1503/jpn.150195
It is part of: Journal of Psychiatry & Neuroscience, 2015, vol. 41, num. 3, p. E46-E55
Related resource: https://doi.org/10.1503/jpn.150195
URI: http://hdl.handle.net/2445/119015
ISSN: 1180-4882
Appears in Collections:Articles publicats en revistes (Fonaments Clínics)
Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)

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