Table of contents
Microstructure of White Matterโin Bipolar Disorder
The neural mechanism of whiteโmatter change
Closing Remarksโand Future Directions
Futureโdirections for research include:
Introduction
Bipolar disorder (BD) is a complex mental health condition characterized by episodes of debilitating mood swings and cognitive impairment, andโin some cases, psychosis. Having a lifetime prevalence of about 1% globally, BD represents a great burdenโon patients, families, and healthcare systems. With recent advances in neuroimaging and genetics, the neural correlates of BD haveโbegun to be elucidated, with special focus on white matter microstructure. Through these findings, the article assesses the connections between white matter changes, psychotic symptoms, and BD and discusses the implications for personalizedโtreatment and research redirection.
Microstructure of White Matterโin Bipolar Disorder

White matter, which is madeโof myelinated axons, helps in communication between brain regions. Changesโin white matter microstructure have been associated with multiple psychiatric disorders, including BD. Meta-analyses have shown that BD patients have decreased white matter integrity and have consistently reported decreased integrity in the anterior limb of the internal capsule, the anterior cingulate cortex, and the superior longitudinalโfasciculus.
Psychosis and the Widespread Microstructural Impact on WhiteโMatter

Psychosis is one of the keyโfeatures of BD and refers to a detachment from reality, commonly experienced in hallucinations or delusions. Research indicates that psychosis might be linked with more significant changes in whiteโmatter microstructure. A recent study reported a decreased fractional anisotropy (FA) of the corpusโcallosum, anterior cingulate cortex, and superior longitudinal fasciculus in BD patients with psychosis compared to those without psychosis.
The neural mechanism of whiteโmatter change

The preciseโneural basis of white matter changes in BD, however, remains unknown. But there have beenโa few theories that have been suggested:
Neuroinflammation: Long-termโneuroinflammation might lead to the loss of integrity of the white matter and disturbance of neuronal connections.
Oxidative stress: Myelin damage and degeneration secondaryโto oxidative stress can lead to impaired integrity of white matter.
Genetic strengths: Genetic differences, such as myelin-related genetic changes, might play a role in white matter changes in B.
Closing Remarksโand Future Directions
Theโinsights of this study are clinically very relevant:
Early diagnosis: White matterโalterations in BD patients could have been useful in early diagnosis and treatment.
Individualized therapy: Elucidating the neurobiological mechanisms that underlie white matter changes could lead to the inception ofโindividualized therapeutic approaches.
Monitoring disease evolution: Factors measuring white matterโmolecules over time in longitudinal studies may help to understand how the disease evolves and the effectiveness of treatments.
Futureโdirections for research include:
Integration of neuroimaging and genetics: Jointโanalysis of neuroimaging and genetic data may lead toward a better understanding of the neural pathways involved in BD.
Finding new treatments: Some research may target novel treatments thatโfocus on neuroinflammation or oxidative stress.
Bipolar disorder (BD), Psychosis as a potential confounding factor: Further studies are required to clarify the relationship of psychosis and alterations in white matter in BD.
Conclusion
White matter pathways are important, as they mediate communication between brain regions and play an important role in building neural circuitry that is disrupted in bipolarโdisorder. We reviewed the literature reporting on white matter abnormalities in BDโand psychosis and discussed their potential relationships, calling for more precise interpretation of the findings in the context of BD and psychosis, as well as the evolution to studies using more personalized treatment and other exploratory approaches to assess the role of white matter alterations.
References:
Merikangas, K. R., et al. (2011). World Mental Health Survey Initiative: Lifetime Prevalence of Mental Disorders in the World. WorldโPsychiatry 10, 168โ176 (2011).
Benedetti, F., et al. (2011). V.โWhite matter lesions in bipolar disorder. Journal ofโAffective Disorders, 131(1โ2), 155โ162.
Baryshnikov, B. V., et al. (2017). A systematic review and meta-analysis of white matterโmicrostructure in bipolar disorder. Journal of AffectiveโDisorders 209, 101-111.
Wang, Y., et al. (2020). Altered whiteโmatter in patients with and without psychosis in bipolar disorder. Journal of PsychiatricโResearch, 123, 102โ109.
Berk, M., et al. (2011). A meta-analysis of bipolar neuroinflammation:โA systematic review. 31(5), 653-656. {{Cite journal|author=Kipnes|journal=Journal ofโClinical Psychopharmacology|month=October|doi=10.1097/01.jcp.0000230654.03237. Andreazza, A. C., et al. โCerebrospinal FluidโLevels of Glutamate in First Episodes of Psychosis.โ a8|issue=5|pages=653โ656|year=October 2008|pmid=18813142}} (2013). Atherton, K. J., & Niven, H. L. (2013). Oxidative stress andโmitochondrial dysfunction in bipolar disorder. Journal of Psychiatric Research, 47(11), 1723โ1731.
Goes, F. S., et al. (2012). Bipolar disorder (genome-wide asso
Leave a Reply