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首页> 外文期刊>Psychiatry research >Incremental effect for antisocial personality disorder genetic risk combining 5-HTTLPR and 5-HTTVNTR polymorphisms.
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Incremental effect for antisocial personality disorder genetic risk combining 5-HTTLPR and 5-HTTVNTR polymorphisms.

机译:结合5-HTTLPR和5-HTTVNTR多态性对反社会人格障碍遗传风险的增量效应。

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摘要

As the serotonin transporter gene (SLC6A4 or 5-HTT) is a key regulator of central serotonergic activity, several association studies between Antisocial Personality Disorder (APD) and the SLC6A4 polymorphisms have been conducted in the last decade. In the present study, the role of both 5-HTTLPR and 5-HTTVNTR polymorphisms of the SLC6A4 gene in APD is investigated. A sample of 147 male inmates was analyzed. APD was assessed by Aluja's Antisocial Personality Disorder Scale, a measure that correlates 0.73 with the dimensional score of DSM-IV APD and 0.62 with factor II of the Psychopathy Checklist-Revised. Inmates presenting both 5-HTTLPR S/S+S/L and 5-HTTVNTR 12/12 had a higher risk of being classified in the APD group (Odds ratio=3.48). The results also showed that the genotype and haplotype distribution was more dissimilar when extreme groups were compared with odds ratios up to 6.50. Our results supported that, in addition to the widely investigated 5-HTTLPR polymorphism, the 5-HTTVNTR polymorphism might be an interesting candidate for association studies with APD. Results also suggested that previous failures to replicate the association between serotonin transporter gene polymorphisms and APD, or similar phenotypes, could have been due to an under-representation of extremely high APD subjects in the samples analyzed.
机译:由于5-羟色胺转运蛋白基因(SLC6A4或5-HTT)是中枢5-羟色胺能活动的关键调节剂,因此在过去的十年中,进行了多项反社会人格障碍(APD)与SLC6A4多态性之间的关联研究。在本研究中,研究了SLC6A4基因的5-HTTLPR和5-HTTVNTR多态性在APD中的作用。分析了147名男性囚犯的样本。 APD通过Aluja的“反社会人格障碍量表”进行评估,该量表将0.73与DSM-IV APD的维度得分相关联,并将0.62与修订的《精神病学清单》的II因子相关联。同时患有5-HTTLPR S / S + S / L和5-HTTVNTR 12/12的囚犯被归入APD组的风险更高(几率= 3.48)。结果还显示,当将极端群体进行比较时,基因型和单倍型分布更为相似,优势比高达6.50。我们的结果支持,除了广泛研究的5-HTTLPR多态性之外,5-HTTVNTR多态性可能是与APD关联研究的有趣候选者。结果还表明,先前未能复制5-羟色胺转运蛋白基因多态性与APD或类似表型之间的关联可能是由于所分析样品中APD受试者的代表性不足所致。

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