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A genetic variant in CAMKK2 gene is possibly associated with increased risk of bipolar disorder.
Atakhorrami, Minoo; Rahimi-Aliabadi, Simin; Jamshidi, Javad; Moslemi, Elham; Movafagh, Abolfazl; Ohadi, Mina; Mirabzadeh, Arash; Emamalizadeh, Babak; Ghaedi, Hamid; Gholipour, Fatemeh; Fazeli, Atena; Motallebi, Marzieh; Taghavi, Shaghayegh; Ahmadifard, Azadeh; Mohammadihosseinabad, Saeed; Shafiei Zarneh, Amir Ehtesham; Shahmohammadibeni, Neda; Madadi, Faranak; Andarva, Monavvar; Darvish, Hossein.
Afiliação
  • Atakhorrami M; Department of Biology, Faculty of Basic Sciences, Islamic Azad University, East Tehran Branch (Ghiamdasht), Tehran, Iran.
  • Rahimi-Aliabadi S; Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Jamshidi J; Noncommunicable Diseases Research Center, Fasa University of Medical Sciences, Fasa, Iran.
  • Moslemi E; Department of Biology, Faculty of Basic Sciences, Islamic Azad University, East Tehran Branch (Ghiamdasht), Tehran, Iran.
  • Movafagh A; Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Ohadi M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Mirabzadeh A; Department of Psychiatry, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Emamalizadeh B; Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Ghaedi H; Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Gholipour F; Department of Psychiatry, Emam Hossien Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Fazeli A; Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Motallebi M; Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Taghavi S; Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Ahmadifard A; Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Mohammadihosseinabad S; Department of Genetics, School of Medicine, Unit of Medical Sciences, Islamic Azad University, Tehran, Iran.
  • Shafiei Zarneh AE; Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Shahmohammadibeni N; Cellular and Molecular Biology Research Center, Babol University of Medical Sciences, Babol, Iran.
  • Madadi F; Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Andarva M; Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Darvish H; Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran. darvish_mg@sbmu.ac.ir.
J Neural Transm (Vienna) ; 123(3): 323-8, 2016 Mar.
Article em En | MEDLINE | ID: mdl-26354101
ABSTRACT
A recent large-scale study have reported that rs1063843, a single nucleotide polymorphism located in the CAMKK2 gene is highly associated with schizophrenia in European and Han Chinese populations. Increasing evidences show that schizophrenia and bipolar disorder have some common genetic variance. Here, we evaluated the association of this variant with schizophrenia and bipolar disorder in Iranian population. Genomic DNA was extracted from peripheral blood of 500 schizophrenic patients, 500 bipolar patients and 500 normal controls and all were genotyped for the rs1063843 using a PCR-RFLP method. The allele frequency of rs1063843 was significantly different in both schizophrenia and bipolar patients comparing to control group. For the first time, we showed that rs1063843 is highly associated with bipolar disorder, although more replication studies are needed to confirm our findings. Our results also support the findings of previous studies suggesting a significant association between rs1063843 and schizophrenia.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtorno Bipolar / Predisposição Genética para Doença / Quinase da Proteína Quinase Dependente de Cálcio-Calmodulina Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: J Neural Transm (Vienna) Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Irã

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtorno Bipolar / Predisposição Genética para Doença / Quinase da Proteína Quinase Dependente de Cálcio-Calmodulina Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: J Neural Transm (Vienna) Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Irã