Innovative approaches to bipolar disorder and its treatment

被引:66
作者
Harrison, Paul J. [1 ,2 ]
Cipriani, Andrea [1 ,2 ]
Harmer, Catherine J. [1 ,2 ]
Nobre, Anna C. [1 ,2 ,3 ]
Saunders, Kate [1 ,2 ]
Goodwin, Guy M. [1 ,2 ]
Geddes, John R. [1 ,2 ]
机构
[1] Univ Oxford, Dept Psychiat, Oxford, England
[2] Oxford Hlth NHS Fdn Trust, Oxford, England
[3] Warneford Hosp, Oxford Ctr Human Brain Act, Oxford, England
来源
SPECIAL ISSUE: THE YEAR IN NEUROLOGY AND PSYCHIATRY | 2016年 / 1366卷
基金
英国医学研究理事会; 英国惠康基金;
关键词
bipolar disorder; clinical; genetics; mood; therapy; GENOME-WIDE ASSOCIATION; PLURIPOTENT STEM-CELLS; COMPARATIVE EFFICACY; LONG-TERM; MOOD STABILIZERS; ADJUNCTIVE ARMODAFINIL; NEURONAL EXCITABILITY; AFFECTIVE INSTABILITY; NETWORK METAANALYSIS; PSYCHIATRIC DISEASE;
D O I
10.1111/nyas.13048
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
All psychiatric disorders have suffered from a dearth of truly novel pharmacological interventions. In bipolar disorder, lithium remains a mainstay of treatment, six decades since its effects were serendipitously discovered. The lack of progress reflects several factors, including ignorance of the disorder's pathophysiology and the complexities of the clinical phenotype. After reviewing the current status, we discuss some ways forward. First, we highlight the need for a richer characterization of the clinical profile, facilitated by novel devices and new forms of data capture and analysis; such data are already promoting a reevaluation of the phenotype, with an emphasis on mood instability rather than on discrete clinical episodes. Second, experimental medicine can provide early indications of target engagement and therapeutic response, reducing the time, cost, and risk involved in evaluating potential mood stabilizers. Third, genomic data can inform target identification and validation, such as the increasing evidence for involvement of calcium channel genes in bipolar disorder. Finally, new methods and models relevant to bipolar disorder, including stem cells and genetically modified mice, are being used to study key pathways and drug effects. A combination of these approaches has real potential to break the impasse and deliver genuinely new treatments.
引用
收藏
页码:76 / 89
页数:14
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