在艾滋病毒和甲基苯丙胺的情况下,COMT Val158Met对执行功能的影响

Chad A Bousman, Mariana Cherner, Stephen J Glatt, J Hampton Atkinson, Igor Grant, Ming T Tsuang, Ian P Everall
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引用次数: 16

摘要

在健康个体中,儿茶酚- o -甲基转移酶(COMT) Val等位基因与执行功能障碍有关。在艾滋病毒感染和/或甲基苯丙胺依赖的情况下,这种关系的性质尚不清楚,这两种情况可以改变多巴胺能系统的功能。我们试图确定COMT和执行功能障碍之间的假定关系是否可以在hiv感染和/或冰毒依赖的个体中观察到,并通过检查其他认知领域来探索这种关系的特异性。利用现有的229名有或没有HIV感染和/或冰毒依赖的男性队列,我们发现,与Val/Val和Val/Met携带者相比,HIV组和对照组中的Met/Met携带者表现出更好的执行功能。然而,这种效应在纯冰毒组和合并症组(即HIV+/冰毒+)中减弱。其他神经认知领域的检查与执行功能的影响不一致。结果支持Met/Met基因型对hiv感染者和对照组执行功能的神经保护作用。在纯冰毒组和共病组中,Met/Met基因型导致的多巴胺清除率较慢可能会增加冰毒不良反应的风险,导致与Val等位基因携带者相当的执行功能障碍。
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Impact of COMT Val158Met on executive functioning in the context of HIV and methamphetamine.

The catechol-O-methyltransferease (COMT) Val allele has been linked to executive dysfunction among healthy individuals. The nature of this relationship is unknown in the context of HIV infection and/or methamphetamine (METH) dependence, two conditions that can alter dopaminergic system functioning. We sought to determine if the putative relationship between COMT and executive dysfunction could be observed among individuals with and without HIV-infection and/or METH dependence, and to explore the specificity of this relationship by examining other cognitive domains. Utilizing an existing cohort of 229 men with and without HIV infection and/or METH dependence we found that Met/Met carriers within the HIV-only and control groups, displayed better executive functioning compared to Val/Val and Val/Met carriers. However, this effect was attenuated in the METH-only and comorbid (ie, HIV+/METH+) groups. Examination of other neurocognitive domains were not consistent with effects found for executive functioning. Results support the presumed neuroprotective effect of Met/Met genotype on executive functioning among HIV-only and control groups. Among METH-only and comorbid groups, the slower rate of dopamine clearance conferred by the Met/Met genotype may increase the risk of adverse effects of METH, resulting in comparable executive dysfunction to that of Val allele carriers.

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