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Advances toward precision medicine for bipolar disorder: mechanisms & molecules

Journal

MOLECULAR PSYCHIATRY
Volume 26, Issue 1, Pages 168-185

Publisher

SPRINGERNATURE
DOI: 10.1038/s41380-020-0831-4

Keywords

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Funding

  1. Stuart & Suzanne Steele MGH Research Scholars Program, NIH [R01MH120227, R01AT009144, R01MH113858]

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Bipolar disorder presents a significant unmet medical need, with challenges in effective treatment and prevention. Despite more than 50 years since the introduction of lithium, understanding of its mechanisms and the pathophysiology of bipolar disorder remains limited, hindering the development of new treatments. Progress has been made in understanding the genetic complexity of bipolar disorder, but effective treatments for acute bipolar depression are still lacking. New therapeutic strategies based on defined molecular mechanisms and neural circuits may offer promise for improving the treatment of bipolar disorder.
Given its chronicity, contribution to disability and morbidity, and prevalence of more than 2%, the effective treatment, and prevention of bipolar disorder represents an area of significant unmet medical need. While more than half a century has passed since the introduction of lithium into widespread use at the birth of modern psychopharmacology, that medication remains a mainstay for the acute treatment and prevention of recurrent mania/hypomania and depression that characterize bipolar disorder. However, the continued limited understanding of how lithium modulates affective behavior and lack of validated cellular and animal models have resulted in obstacles to discovering more effective mood stabilizers with fewer adverse side effects. In particular, while there has been progress in developing new pharmacotherapy for mania, developing effective treatments for acute bipolar depression remain inadequate. Recent large-scale human genetic studies have confirmed the complex, polygenic nature of the risk architecture of bipolar disorder, and its overlap with other major neuropsychiatric disorders. Such discoveries have begun to shed light on the pathophysiology of bipolar disorder. Coupled with broader advances in human neurobiology, neuropharmacology, noninvasive neuromodulation, and clinical trial design, we can envision novel therapeutic strategies informed by defined molecular mechanisms and neural circuits and targeted to the root cause of the pathophysiology. Here, we review recent advances toward the goal of better treatments for bipolar disorder, and we outline major challenges for the field of translational neuroscience that necessitate continued focus on fundamental research and discovery.

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