KEGG   DISEASE: 強迫性障害
エントリ  
H01450                                                             
名称    
強迫性障害
概要    
Obsessive-compulsive disorder (OCD) is a psychiatric disorder characterized by recurrent, intrusive and disturbing thoughts as well as by repetitive stereotypic behaviors. OCD is a complex disorder and its pathogenesis is most likely influenced by both genetic and environmental factors. Although more than 140 candidate gene studies have been conducted, the findings have been inconclusive due to small sample size and few study replications. Many studies suggest that abnormal serotonergic neurotransmission is one of the most consistent biological findings in OCD. Studies have also reported dopaminergic abnormalities in the basal ganglia and nucleus accumbens, as well as altered glutamate transmission. First line treatments for this disorder are cognitive behavioral therapy (exposure and response prevention) and selective serotonin reuptake inhibitors (SSRIs). In recent years, one of the promising novel treatment strategies developed to improve the efficacy of treatment for patients with OCD is acceptance and commitment therapy (ACT). Recent studies have suggested that age of onset is an important factor in subtyping OCD. Early-onset OCD has been proposed to be associated with greater symptom severity, a higher prevalence of tic-related disorders, a more familial form of the condition, and a greater prevalence of psychiatry disorders in first-degree relatives as compared to late-onset OCD.
カテゴリ  
精神及び行動の障害
階層分類  
ヒト疾患 [BR:jp08402]
 その他の疾患
  精神及び行動の障害
   H01450  強迫性障害
ICD-11 による疾患分類 [BR:jp08403]
 06 精神, 行動, 神経発達の障害
  強迫症または関連症
   6B20  強迫性症
    H01450  強迫性障害
パスウェイ 
hsa04726  Serotonergic synapse
hsa04728  Dopaminergic synapse
hsa04724  Glutamatergic synapse
病因遺伝子 
BDNF (polymorphism) [HSA:627] [KO:K04355]
HTR2A (promoter polymorphism) [HSA:3356] [KO:K04157]
SLC6A4 (polymorphism) [HSA:6532] [KO:K05037]
COMT (polymorphism) [HSA:1312] [KO:K00545]
MAOA (polymorphism) [HSA:4128] [KO:K00274]
SLC1A1 (polymorphism) [HSA:6505] [KO:K05612]
DRD4 (polymorphism) [HSA:1815] [KO:K04147]
治療薬   
クロキサゾラム [DR:D01268]
パロキセチン塩酸塩水和物 [DR:D02260]
フルボキサミンマレイン酸塩 [DR:D00824]
コメント  
For Tourette syndrome, see H00862.
リンク   
ICD-11: 6B20
ICD-10: F42
MeSH: D009771
OMIM: 164230
文献    
  著者
Taylor S
  タイトル
Early versus late onset obsessive-compulsive disorder: evidence for distinct subtypes.
  雑誌
Clin Psychol Rev 31:1083-100 (2011)
DOI:10.1016/j.cpr.2011.06.007
文献    
  著者
Leckman JF, Bloch MH, King RA
  タイトル
Symptom dimensions and subtypes of obsessive-compulsive disorder: a developmental perspective.
  雑誌
Dialogues Clin Neurosci 11:21-33 (2009)
文献    
  著者
Tukel R, Gurvit H, Ozata B, Ozturk N, Ertekin BA, Ertekin E, Baran B, Kalem SA, Buyukgok D, Direskeneli GS
  タイトル
Brain-derived neurotrophic factor gene Val66Met polymorphism and cognitive function in obsessive-compulsive disorder.
  雑誌
Am J Med Genet B Neuropsychiatr Genet 159B:850-8 (2012)
DOI:10.1002/ajmg.b.32092
文献    
  著者
Walitza S, Wewetzer C, Warnke A, Gerlach M, Geller F, Gerber G, Gorg T, Herpertz-Dahlmann B, Schulz E, Remschmidt H, Hebebrand J, Hinney A
  タイトル
5-HT2A promoter polymorphism -1438G/A in children and adolescents with obsessive-compulsive disorders.
  雑誌
Mol Psychiatry 7:1054-7 (2002)
DOI:10.1038/sj.mp.4001105
文献    
  著者
Hu XZ, Lipsky RH, Zhu G, Akhtar LA, Taubman J, Greenberg BD, Xu K, Arnold PD, Richter MA, Kennedy JL, Murphy DL, Goldman D
  タイトル
Serotonin transporter promoter gain-of-function genotypes are linked to obsessive-compulsive disorder.
  雑誌
Am J Hum Genet 78:815-26 (2006)
DOI:10.1086/503850
文献    
  著者
Sampaio AS, Hounie AG, Petribu K, Cappi C, Morais I, Vallada H, do Rosario MC, Stewart SE, Fargeness J, Mathews C, Arnold P, Hanna GL, Richter M, Kennedy J, Fontenelle L, de Braganca Pereira CA, Pauls DL, Miguel EC
  タイトル
COMT and MAO-A polymorphisms and obsessive-compulsive disorder: a family-based association study.
  雑誌
PLoS One 10:e0119592 (2015)
DOI:10.1371/journal.pone.0119592
文献    
  著者
Dickel DE, Veenstra-VanderWeele J, Cox NJ, Wu X, Fischer DJ, Van Etten-Lee M, Himle JA, Leventhal BL, Cook EH Jr, Hanna GL
  タイトル
Association testing of the positional and functional candidate gene SLC1A1/EAAC1 in early-onset obsessive-compulsive disorder.
  雑誌
Arch Gen Psychiatry 63:778-85 (2006)
DOI:10.1001/archpsyc.63.7.778
文献    
  著者
Millet B, Chabane N, Delorme R, Leboyer M, Leroy S, Poirier MF, Bourdel MC, Mouren-Simeoni MC, Rouillon F, Loo H, Krebs MO
  タイトル
Association between the dopamine receptor D4 (DRD4) gene and obsessive-compulsive disorder.
  雑誌
Am J Med Genet B Neuropsychiatr Genet 116B:55-9 (2003)
DOI:10.1002/ajmg.b.10034
文献    
PMID:26288647 (treatment)
  著者
Vakili Y, Gharaee B, Habibi M
  タイトル
Acceptance and Commitment Therapy, Selective Serotonin Reuptake Inhibitors and Their Combination in the Improvement of Obsessive-Compulsive Symptoms and Experiential Avoidance in Patients With Obsessive-Compulsive Disorder.
  雑誌
Iran J Psychiatry Behav Sci 9:e845 (2015)
DOI:10.17795/ijpbs845
文献    
PMID:16585942 (treatment)
  著者
Bloch MH, Landeros-Weisenberger A, Kelmendi B, Coric V, Bracken MB, Leckman JF
  タイトル
A systematic review: antipsychotic augmentation with treatment refractory obsessive-compulsive disorder.
  雑誌
Mol Psychiatry 11:622-32 (2006)
DOI:10.1038/sj.mp.4001823
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