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Missense mutation of the cholecystokinin B receptor gene: lack of association with panic disorder.
Kato, T; Wang, Z W; Zoega, T; Crowe, R R.
Afiliação
  • Kato T; Department of Psychiatry, University of Iowa College of Medicine, Iowa City 52242-1000, USA.
Am J Med Genet ; 67(4): 401-5, 1996 Jul 26.
Article em En | MEDLINE | ID: mdl-8837709
Cholecystokinin tetrapeptide (CCK4) is known to induce panic attacks in patients with panic disorder at a lower dose than in normal controls. Therefore, the cholecystokinin B (CCKB) receptor gene is a candidate gene for panic disorder. We searched for mutations in the CCKB gene in 22 probands of panic disorder pedigrees, using single-strand conformation polymorphism (SSCP) analysis. Two polymorphisms were detected. A polymorphism in an intron (2491 C-->A) between exons 4 and 5 was observed in 10 of 22 probands. A missense mutation in the extracellular loop of exon 2 (1550 G-->A, Val125-->Ile) was found in only one proband. This mutation was also examined in additional 34 unrelated patients with panic disorder and 112 controls. The prevalence rate of this mutation was 8.8% in patients with panic disorder (3/34) and 4.4% in controls (5/112). The mutation did not segregate with panic disorder in two families where this could be tested. These results suggest no pathophysiological significance of this mutation in panic disorder.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores da Colecistocinina / Transtorno de Pânico / Polimorfismo Conformacional de Fita Simples Tipo de estudo: Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Am J Med Genet Ano de publicação: 1996 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores da Colecistocinina / Transtorno de Pânico / Polimorfismo Conformacional de Fita Simples Tipo de estudo: Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Am J Med Genet Ano de publicação: 1996 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos