No evidence for an association of polymorphisms of the tryptophan hydroxylase gene with affective disorders or attempted suicide among Japanese patients

Citation
H. Kunugi et al., No evidence for an association of polymorphisms of the tryptophan hydroxylase gene with affective disorders or attempted suicide among Japanese patients, AM J PSYCHI, 156(5), 1999, pp. 774-776
Citations number
6
Categorie Soggetti
Psychiatry,"Clinical Psycology & Psychiatry","Neurosciences & Behavoir
Journal title
AMERICAN JOURNAL OF PSYCHIATRY
ISSN journal
0002953X → ACNP
Volume
156
Issue
5
Year of publication
1999
Pages
774 - 776
Database
ISI
SICI code
0002-953X(199905)156:5<774:NEFAAO>2.0.ZU;2-5
Abstract
Objective: Tryptophan hydroxylase is the rate-limiting enzyme in the biosyn thesis of serotonin. The authors examined whether polymorphisms A218C and A 779C in intron 7 of the tryptophan hydroxylase gene are associated with a r isk for affective disorders or suicidal behavior. Method: Subjects were 141 patients with bipolar disorder and 73 patients with unipolar affective dis order, 46 of whom had a history of attempted suicide, and 208 healthy volun teers. All subjects were unrelated to each other, and all were Japanese. Ge notyping was performed by polymerase chain reaction amplification followed by digestion by a restriction enzyme and single-strand conformational polym orphism analysis. Results: There was no significant genotypic or allelic as sociation of the A218C polymorphism with bipolar disorder, unipolar depress ion, or history of attempted suicide. In nearly 100% of the subjects, genot ypes for the A779C were identical to those for the A218C. Conclusions: The authors conclude that the examined polymorphisms are unlikely to have major relevance to the pathogenesis of affective disorders or suicidal behavior.