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No association between bipolar disorder and alleles at a functional polymorphism in the COMT gene

1997; Cambridge University Press; Volume: 170; Issue: 6 Linguagem: Inglês

10.1192/bjp.170.6.526

1472-1465

Nick Craddock, Gillian Spurlock, Peter McGuffin, Michael J. Owen, Marika Nosten‐Bertrand, Frank Bellivier, Rolando Meloni, Marion Leboyer, Jacques Mallet, Lesley Mynett‐Johnson, V. Murphy, Patrick O. McKeon, George Kirov, John Powell, Hiroshi Kunugi, David Collier, Monica Larosa, Benedetta Nacmias, Sandro Sorbi, Sibylle G. Schwab, Manfred Ackenheil, Wolfgang Maier,

Bipolar Disorder and Treatment

Background There is compelling evidence for the existence of susceptibility genes for bipolar disorder. Association studies using functional DNA variations are an important approach for identifying these genes. The enzyme catechol-O-methyltransferase (COMT) plays a key role in the degradation of catecholamine neurotransmitters and is a candidate for involvement in bipolar disorder. Recently a common functional genetic polymorphism that underlies population variation in COM Tactivity has been elucidated and a simple assay developed. Method In a collaboration involving seven European centres, we have undertaken an association study of this functional polymorphism in 412 unrelated West European caucasian DSM - III-R bipolar patients and 368 ethnically matched controls. Results We found no evidence of allelic or genotypic association. Conclusions We can conclude that variation at this functional polymorphism does not make an important contribution to bipolar disorder in the Western European population. Future studies using this powerful experimental approach can be expected to contribute to identification of bipolar susceptibility genes.