Meade Christina S, Towe Sheri L, Skalski Linda M, Robertson Kevin R
Duke University School of Medicine, Department of Psychiatry and Behavioral Sciences and Duke Global Health Institute, Box 90519, Durham, NC 27708, USA.
Duke University School of Medicine, Department of Psychiatry and Behavioral Sciences and Duke Global Health Institute, Box 90519, Durham, NC 27708, USA.
Drug Alcohol Depend. 2015 Apr 1;149:128-35. doi: 10.1016/j.drugalcdep.2015.01.034. Epub 2015 Feb 7.
Prior studies have established that methamphetamine and HIV can have additive deleterious effects on neurocognitive functioning, but there has been relatively little research on other stimulants like cocaine. This study investigated the effects of cocaine and HIV on neurocognitive impairment in a large, well-characterized sample.
The sample included 193 adults across four groups: HIV-positive cocaine users (n = 48), HIV-negative cocaine users (n = 53), HIV-positive non-drug users (n = 60), and HIV-negative non-drug users (n = 32). Cocaine users met criteria for lifetime dependence and had past-month cocaine use. A comprehensive battery assessed substance abuse and neurocognitive functioning.
Participants were mostly male (66%) and African-American (85%), with a mean age of 46.09 years. The rate of global impairment was 33%, with no significant main effects across groups on likelihood of impairment. There were main effects for cocaine on processing speed and executive functioning, with cocaine users having greater impairment (F = 9.33 and F = 4.22, respectively), and for HIV on attention, with HIV-infected persons having greater impairment (F = 5.55). There was an interaction effect for executive functioning, with the three patient groups having greater impairment than controls (F = 5.05). Nonparametric analyses revealed significant additive impairment in the presence of both HIV and cocaine for processing speed.
While cocaine does not appear to increase vulnerability to global HIV-associated neurocognitive impairment, it does have independent adverse effects on executive functioning and processing speed. Given prior evidence that domain-specific deficits predict real-world impairments, our results may help explain the poorer behavioral and functional outcomes observed in HIV-infected cocaine users.
先前的研究已证实甲基苯丙胺和艾滋病毒可对神经认知功能产生累加性有害影响,但对于可卡因等其他兴奋剂的研究相对较少。本研究在一个规模大、特征明确的样本中调查了可卡因和艾滋病毒对神经认知损害的影响。
样本包括193名成年人,分为四组:艾滋病毒阳性的可卡因使用者(n = 48)、艾滋病毒阴性的可卡因使用者(n = 53)、艾滋病毒阳性的非吸毒者(n = 60)和艾滋病毒阴性的非吸毒者(n = 32)。可卡因使用者符合终身依赖标准且在过去一个月内使用过可卡因。通过一套综合测试评估药物滥用情况和神经认知功能。
参与者大多为男性(66%)和非裔美国人(85%),平均年龄为46.09岁。整体损害率为33%,各组之间在损害可能性方面无显著的主效应。可卡因对处理速度和执行功能有主效应,可卡因使用者的损害更大(分别为F = 9.33和F = 4.22),艾滋病毒对注意力有主效应,艾滋病毒感染者的损害更大(F = 5.55)。执行功能存在交互效应,三个患者组的损害比对照组更大(F = 5.05)。非参数分析显示,在同时存在艾滋病毒和可卡因的情况下,处理速度存在显著的累加性损害。
虽然可卡因似乎不会增加患全球与艾滋病毒相关的神经认知损害的易感性,但它确实对执行功能和处理速度有独立的不良影响。鉴于先前有证据表明特定领域的缺陷可预测现实世界中的损害,我们的结果可能有助于解释在感染艾滋病毒的可卡因使用者中观察到的更差的行为和功能结果。