KEGG   DISEASE: 双極性障害
エントリ  
H01653                                                             
名称    
双極性障害;
躁うつ病
  下位グループ
大感情障害 (MAFD)
概要    
Bipolar disorder, previously known as manic depressive illness, is a severe chronic mood disorder, characterized by the recurrence of mania (hypomania), depression, or mixed episodes. It is one of the main causes of disability among young people, leading to cognitive and functional impairment and raised mortality, particularly death by suicide. Mania is the most characteristic phase of bipolar disorder. While mood elevation and euphoria are commonly described phenotypic descriptors of mania, irritability and anger may dominate. At the present time, there is solid evidence supporting the use of lithium, the anticonvulsants valproate and carbamazepine, and some antipsychotics in mania. Manic or hypomanic episodes differ in severity and length. In a hypomanic episode, a disturbance in functioning can be seen by others but does not typically cause severe impairment or require admission to hospital. At onset, most patients with bipolar disorder present with a depressive episode that differs subtly from unipolar depression. The first step in the management of bipolar disorder is to confirm the diagnosis of mania or hypomania and define the patient's mood state, because the therapeutic approach differs considerably for hypomania, mania, depression, and euthymia. While effective pharmacological treatments exist for bipolar disorder, the pathophysiology of the condition essentially remains unknown. Although bipolar disorder is one of the most heritable psychiatric disorders, a multifactorial model in which gene and environment interact is currently thought to best fit this disorder. Many risk alleles of small effect which are described in genome-wide association studies, contribute to the polygenic risk of bipolar disorder. It is suggested that the dopaminergic system may play a central role in bipolar disorder, although no singular dysfunction of neurotransmitter systems has been identified.
カテゴリ  
精神及び行動の障害
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 06 精神, 行動, 神経発達の障害
  気分症
   双極症または関連症
    6A60  双極症I型
     H01653  双極性障害
    6A61  双極症II型
     H01653  双極性障害
病因遺伝子 
(MAFD7) XBP1 [HSA:7494] [KO:K09027]
治療薬   
カルバマゼピン [DR:D00252]
バルプロ酸ナトリウム [DR:D00710]
ラモトリギン [DR:D00354]
クロルプロマジン塩酸塩 [DR:D00789]
クロルプロマジンフェノールフタリン酸塩 [DR:D04034]
レボメプロマジン塩酸塩 [DR:D01520]
レボメプロマジンマレイン酸塩 [DR:D02248]
ハロペリドール [DR:D00136]
ルラシドン塩酸塩 [DR:D04820]
オランザピン [DR:D00454]
クエチアピンフマル酸塩 [DR:D00458]
スルトプリド塩酸塩 [DR:D02208]
炭酸リチウム [DR:D00801]
アリピプラゾール [DR:D01164]
チミペロン [DR:D02035]
コメント  
Bipolar I disorder: At least one manic episode must be presented, although major depressive episodes are typical but not needed for diagnosis.
Bipolar II disorder: At least one hypomanic episode and one major depressive episode are needed for diagnosis.
See also H01646 Major depressive disorder.
リンク   
ICD-11: 6A60 6A61
ICD-10: F31
MeSH: D001714
OMIM: 125480 309200 612371
文献    
  著者
Grande I, Berk M, Birmaher B, Vieta E
  タイトル
Bipolar disorder.
  雑誌
Lancet 387:1561-72 (2016)
DOI:10.1016/S0140-6736(15)00241-X
文献    
  著者
Graham RK, Parker GB, Breakspear M, Mitchell PB
  タイトル
Clinical characteristics and temperament influences on 'happy' euphoric and 'snappy' irritable bipolar hypo/manic mood states.
  雑誌
J Affect Disord 174:144-9 (2015)
DOI:10.1016/j.jad.2014.11.042
文献    
  著者
Cousins DA, Butts K, Young AH
  タイトル
The role of dopamine in bipolar disorder.
  雑誌
Bipolar Disord 11:787-806 (2009)
DOI:10.1111/j.1399-5618.2009.00760.x
文献    
  著者
Citrome L
  タイトル
Cariprazine in bipolar disorder: clinical efficacy, tolerability, and place in therapy.
  雑誌
Adv Ther 30:102-13 (2013)
DOI:10.1007/s12325-013-0004-9
文献    
  著者
Vieta E, Sanchez-Moreno J
  タイトル
Acute and long-term treatment of mania.
  雑誌
Dialogues Clin Neurosci 10:165-79 (2008)
文献    
  著者
Kakiuchi C, Iwamoto K, Ishiwata M, Bundo M, Kasahara T, Kusumi I, Tsujita T, Okazaki Y, Nanko S, Kunugi H, Sasaki T, Kato T
  タイトル
Impaired feedback regulation of XBP1 as a genetic risk factor for bipolar disorder.
  雑誌
Nat Genet 35:171-5 (2003)
DOI:10.1038/ng1235
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