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PMID: 9535125 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Association study of a functional catechol-O-methyltransferase gene polymorphism in Japanese schizophrenics.

Neuroscience letters ·Vol. 243 ·No. 1-3 ·1998-02-27 ·Pages 109-12

Ohmori O, Shinkai T, Kojima H, Terao T, Suzuki T, Mita T, Abe K

Abstract

Catechol-O-methyltransferase (COMT) is an enzyme which inactivates catecholamine neurotransmitters by methylation, and is considered a candidate for involvement in schizophrenia. A functional COMT gene polymorphism influencing the enzyme activities, the high activity (val-108) and the low activity allele (met-108), was recently confirmed. We investigated a genetic association between schizophrenia and the COMT gene polymorphism in 150 Japanese schizophrenics and controls. We detected the low activity met-108 allele more frequently in schizophrenics than in the controls, and found that subjects sharing the met-108 allele (val/met and met/met) are significantly more common in the patients than in the controls. The results suggest that the low activity met-108 allele may be involved in susceptibility for schizophrenia.

MeSH Terms
Alleles Catechol O-Methyltransferase/genetics Chromosomes, Human, Pair 22 Dopamine/physiology Female Genetic Linkage Genotype Humans Japan Male Middle Aged Polymorphism, Genetic Schizophrenia/enzymology,genetics
Chemicals
Catechol O-Methyltransferase Dopamine
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Ohmori O
Department of Psychiatry, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan. [email protected]
Shinkai T
Kojima H
Terao T
Suzuki T
Mita T
Abe K
Article Info
Journal
Neuroscience letters
Abbr.
Neurosci Lett
ISSN
0304-3940
Published
1998-02-27
Pages
109-12
Language
English
Region
Ireland
NLM ID
7600130
Subset
IM
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