A genetic variant in CAMKK2 gene is possibly associated with increased risk of bipolar disorder.

Atakhorrami, Minoo and Rahimi-Aliabadi, Simin and Jamshidi, Javad and Moslemi, Elham and Movafagh, Abolfazl and Ohadi, Mina and Mirabzadeh, Arash and Emamalizadeh, Babak and Ghaedi, Hamid and Gholipour, Fatemeh and Fazeli, Atena and Motallebi, Marzieh and Taghavi, Shaghayegh and Ahmadifard, Azadeh and Mohammadihosseinabad, Saeed and Shafiei Zarneh, Amir Ehtesham and Shahmohammadibeni, Neda and Madadi, Faranak and Andarva, Monavvar and Darvish, Hossein (2016) A genetic variant in CAMKK2 gene is possibly associated with increased risk of bipolar disorder. Journal of neural transmission (Vienna, Austria : 1996), 123 (3). pp. 323-8. ISSN 1435-1463

Full text not available from this repository.

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.

Item Type: Article
Divisions: School of Medicine
Depositing User: Unnamed user with email eprints@fums.ac.ir
Date Deposited: 09 Mar 2017 19:01
Last Modified: 09 Mar 2017 19:01
URI: http://eprints.fums.ac.ir/id/eprint/427

Actions (login required)

View Item View Item