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The blood-brain barrier in bipolar disorders: A systematic review.
Wakonigg Alonso, Clara; McElhatton, Frances; O'Mahony, Brian; Campbell, Matthew; Pollak, Thomas A; Stokes, Paul R A.
Afiliação
  • Wakonigg Alonso C; Institute of Psychiatry & Psychology and Neuroscience, King's College London,United Kingdom. Electronic address: clarawako@gmail.com.
  • McElhatton F; Institute of Psychiatry & Psychology and Neuroscience, King's College London,United Kingdom.
  • O'Mahony B; Institute of Psychiatry & Psychology and Neuroscience, King's College London,United Kingdom.
  • Campbell M; Smurfit Institute of Genetics, Trinity College Dublin, Lincoln Place Gate, Dublin 2, Ireland.
  • Pollak TA; Dept of Psychosis Studies, Institute of Psychiatry & Psychology and Neuroscience, King's College London, United Kingdom; South London and Maudsley NHS Foundation Trust,Bethlem Royal Hospital, Monks Orchard Road, Beckenham, Kent, BR3 3BX, United Kingdom.
  • Stokes PRA; South London and Maudsley NHS Foundation Trust,Bethlem Royal Hospital, Monks Orchard Road, Beckenham, Kent, BR3 3BX, United Kingdom; Centre for Affective Disorders, Department of Psychological Medicine, Institute of Psychiatry & Psychology and Neuroscience, King's College London,United Kingdom.
J Affect Disord ; 361: 434-444, 2024 Sep 15.
Article em En | MEDLINE | ID: mdl-38897301
ABSTRACT

BACKGROUND:

Bipolar disorders (BD) are chronic, debilitating disorders. The blood-brain barrier (BBB) has been increasingly investigated in BD. This systematic review aimed to assess the available evidence on the relationship between BD and markers of BBB dysfunction.

METHODS:

A systematic search in PubMed, Embase, PsycINFO, CINAHL and Web of Science was run where the primary outcomes were BBB markers such as S100B, albumin ratio, matrix metalloproteinase (MMP), cell adhesion molecule (CAM), and tight junction proteins. Techniques included blood, cerebrospinal fluid (CSF), post-mortem, genetic and imaging methods in BD compared to healthy controls.

RESULTS:

55 studies were identified, 38 of which found an association between BD and markers of BBB dysfunction. 16/29 studies found increased blood/CSF albumin ratio, S100B, CAMs or MMP levels in BD participants compared to controls. 5/19 post-mortem studies found increased levels of chondroitin sulphate proteoglycans, intercellular CAM, neurexin or claudin-5 mRNA in distinct locations throughout the brain in BD compared to controls. One imaging study identified extensive BBB leakage in 30 % of BD participants, compared to 0 % in controls.

LIMITATIONS:

The diversity in methodologies used in the included studies makes direct comparison of results challenging. Furthermore, imaging methods are the gold standard, but only one study used them. Other markers are only indicative of BBB permeability.

CONCLUSIONS:

This review suggests an association between BD and BBB dysfunction. Further research is needed to provide definite answers considering the existing literature's limitations, and to clarify whether this association provides a pathogenic mechanism, or is an epiphenomenon of BD.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno Bipolar / Barreira Hematoencefálica / Subunidade beta da Proteína Ligante de Cálcio S100 Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno Bipolar / Barreira Hematoencefálica / Subunidade beta da Proteína Ligante de Cálcio S100 Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article