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Effect of COMT Val108/158Met Genotype on Risk for Polydipsia in Chronic Patients with Schizophrenia

Overview of attention for article published in NeuroMolecular Medicine, January 2014
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Title
Effect of COMT Val108/158Met Genotype on Risk for Polydipsia in Chronic Patients with Schizophrenia
Published in
NeuroMolecular Medicine, January 2014
DOI 10.1007/s12017-014-8287-9
Pubmed ID
Authors

Kenji Yamada, Takahiro Shinkai, Hsin-I Chen, Kensuke Utsunomiya, Jun Nakamura

Abstract

Polydipsia is a serious condition often seen among patients with schizophrenia (SCZ). The cause of polydipsia is unknown; hence, it is hard to treat or manage. Animal studies showed that the drinking behavior is regulated by central dopaminergic neurotransmission at the hypothalamus. Meanwhile, the existence of a genetic predisposition to polydipsia in patients with SCZ has been suggested. The purpose of this study was to assess whether a functional polymorphism, Val(108/158)Met in the gene for catechol-O-methyltransferase (COMT), is associated with susceptibility to polydipsia using a Japanese sample of SCZ. Our sample includes 330 chronic patients with SCZ (83 polydipsic patients and 247 non-polydipsic controls). The common COMT Val(108/158)Met polymorphism was genotyped, and the differences in genotype distribution and allele frequency between cases and controls were evaluated using the χ (2) test. A significant association between the COMT Val(108/158)Met polymorphism and polydipsia was found (genotype distribution: χ (2) = 13.0, df = 2, p = 0.001; allele frequency: χ (2) = 7.50, df = 1, p = 0.006). The high-COMT activity group (Val/Val) was more frequent among patients with polydipsia compared with the low-COMT activity group (Val/Met + Met/Met) [odds ratio (OR) = 2.46]. The association survived after controlling for other possible confounding factors, including gender, age, age of onset, current antipsychotic dose, and smoking status. Our results suggest that the COMT Val(108/158)Met genotype may confer susceptibility to polydipsia in SCZ. To our knowledge, this is the first association study between the COMT gene and polydipsia in SCZ. Further studies with larger sample sizes are warranted to confirm present findings.

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Mendeley readers

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The data shown below were compiled from readership statistics for 17 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 17 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 4 24%
Student > Master 3 18%
Other 2 12%
Student > Ph. D. Student 2 12%
Student > Doctoral Student 2 12%
Other 1 6%
Unknown 3 18%
Readers by discipline Count As %
Psychology 4 24%
Medicine and Dentistry 4 24%
Neuroscience 2 12%
Biochemistry, Genetics and Molecular Biology 2 12%
Unknown 5 29%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 06 January 2015.
All research outputs
#23,010,126
of 25,654,806 outputs
Outputs from NeuroMolecular Medicine
#413
of 482 outputs
Outputs of similar age
#282,500
of 321,966 outputs
Outputs of similar age from NeuroMolecular Medicine
#4
of 7 outputs
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