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双相障碍患者发病年龄的混合回归分析:对 5-羟色胺能基因作用的探讨

Mixture regression analysis on age at onset in bipolar disorder patients: investigation of the role of serotonergic genes.

机构信息

Laboratory of Molecular Genetics, Department of Neurosciences B.B. Brodie, University of Cagliari, Cagliari, Italy.

出版信息

Eur Neuropsychopharmacol. 2010 Sep;20(9):663-70. doi: 10.1016/j.euroneuro.2010.04.001. Epub 2010 May 8.

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.

摘要

双相障碍(BPD)是一种复杂的精神疾病,具有相关的潜在遗传基础。在 230 名 BPD 患者中对 HTR2A T102C、HTR2C Cys23Ser、SLC6A4 5-HTTLPR 和 rs25531 多态性进行了基因分型,并将其作为发病年龄(AAO)混合回归模型的协变量插入。5-HTTLPR 多态性在隐性和加性模型下与早发成分相关。HTR2A T102C、HTR2C Cys23Ser 和 5-HTTLPR 相互作用项在显性、隐性和加性模型下与早发成分相关。这些发现表明编码 5-羟色胺能系统成分的基因在影响 BPD 的 AAO 中起作用。

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