Introduction

Microstructure of White Matterโ€‚in Bipolar Disorder

The neural mechanism of whiteโ€‚matter change

Closing Remarksโ€‚and Future Directions

Futureโ€‚directions for research include:

Conclusion

References:

Introduction

Bipolar disorder (BD) is a complex mental health condition characterized by episodes of debilitating mood swings and cognitive impairment, andโ€‚in some cases, psychosis. Having a lifetime prevalence of about 1% globally, BD represents a great burdenโ€‚on patients, families, and healthcare systems. With recent advances in neuroimaging and genetics, the neural correlates of BD haveโ€‚begun 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 personalizedโ€‚treatment and research redirection.

Microstructure of White Matterโ€‚in Bipolar Disorder

White matter, which is madeโ€‚of myelinated axons, helps in communication between brain regions. Changesโ€‚in 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 longitudinalโ€‚fasciculus.

Psychosis and the Widespread Microstructural Impact on Whiteโ€‚Matter

Psychosis is one of the keyโ€‚features 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 whiteโ€‚matter microstructure. A recent study reported a decreased fractional anisotropy (FA) of the corpusโ€‚callosum, anterior cingulate cortex, and superior longitudinal fasciculus in BD patients with psychosis compared to those without psychosis.

The neural mechanism of whiteโ€‚matter change

The preciseโ€‚neural basis of white matter changes in BD, however, remains unknown. But there have beenโ€‚a few theories that have been suggested:

Neuroinflammation: Long-termโ€‚neuroinflammation might lead to the loss of integrity of the white matter and disturbance of neuronal connections.

Oxidative stress: Myelin damage and degeneration secondaryโ€‚to 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 Remarksโ€‚and Future Directions

Theโ€‚insights of this study are clinically very relevant:

Early diagnosis: White matterโ€‚alterations 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 ofโ€‚individualized therapeutic approaches.

Monitoring disease evolution: Factors measuring white matterโ€‚molecules over time in longitudinal studies may help to understand how the disease evolves and the effectiveness of treatments.

Futureโ€‚directions for research include:

Integration of neuroimaging and genetics: Jointโ€‚analysis 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 thatโ€‚focus 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 bipolarโ€‚disorder. We reviewed the literature reporting on white matter abnormalities in BDโ€‚and 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. Worldโ€‚Psychiatry 10, 168โ€“176 (2011).

Benedetti, F., et al. (2011). V.โ€‚White matter lesions in bipolar disorder. Journal ofโ€‚Affective Disorders, 131(1โ€“2), 155โ€“162.

Baryshnikov, B. V., et al. (2017). A systematic review and meta-analysis of white matterโ€‚microstructure in bipolar disorder. Journal of Affectiveโ€‚Disorders 209, 101-111.

Wang, Y., et al. (2020). Altered whiteโ€‚matter in patients with and without psychosis in bipolar disorder. Journal of Psychiatricโ€‚Research, 123, 102โ€“109.

Berk, M., et al. (2011). A meta-analysis of bipolar neuroinflammation:โ€‚A systematic review. 31(5), 653-656. {{Cite journal|author=Kipnes|journal=Journal ofโ€‚Clinical Psychopharmacology|month=October|doi=10.1097/01.jcp.0000230654.03237. Andreazza, A. C., et al. โ€œCerebrospinal Fluidโ€‚Levels of Glutamate in First Episodes of Psychosis.โ€ a8|issue=5|pages=653โ€“656|year=October 2008|pmid=18813142}} (2013). Atherton, K. J., & Niven, H. L. (2013). Oxidative stress andโ€‚mitochondrial dysfunction in bipolar disorder. Journal of Psychiatric Research, 47(11), 1723โ€“1731.

Goes, F. S., et al. (2012). Bipolar disorder (genome-wide asso


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