Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
319723 | European Neuropsychopharmacology | 2010 | 8 Pages |
Abstract
Bipolar Disorder (BPD) is a complex psychiatric disease with a relevant underlying genetic basis. HTR2A T102C, HTR2C Cys23Ser, SLC6A4 5-HTTLPR and rs25531 polymorphisms were genotyped in 230 BPD patients and inserted as covariates in a mixture regression model of age at onset (AAO). 5-HTTLPR polymorphism associated with early onset component under recessive and additive model. HTR2A T102C, HTR2C Cys23Ser and 5-HTTLPR interaction terms associated with early onset component under dominant, recessive and additive model. These findings suggest a role of genes codifying for elements of the serotonergic system in influencing the AAO in BPD.
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Authors
Mirko Manchia, Clement C. Zai, Alessio Squassina, John B. Vincent, Vincenzo De Luca, James L. Kennedy,