Department of Psychiatry (8231), University of California, San Diego, 220 Dickinson St., Suite B, San Diego, CA, 92103, USA.
J Neurovirol. 2014 Feb;20(1):85-98. doi: 10.1007/s13365-014-0233-y. Epub 2014 Jan 28.
Prior studies examining the combined adverse effects of HIV and methamphetamine (MA) on the central nervous system (CNS) have focused on younger to middle-aged adults with recent MA use diagnoses. Aging, HIV, and MA all converge on prefrontal and temporolimbic neural systems and confer independent risk for neurocognitive and functional decline. Thus, this study sought to determine the residual impact of a remote history of MA dependence on neurocognitive and real-world outcomes in older people living with HIV (PLWH). Participants included 116 older (≥50 years) and 94 younger (<40 years) adults classified into one of six study groups based on HIV serostatus (HIV+/HIV-) and lifetime histories of MA dependence (MA+/MA-): older HIV-MA- (n = 36), older HIV+MA- (n = 49), older HIV+MA+ (n = 31), younger HIV-MA- (n = 27), younger HIV+MA- (n = 33), and younger HIV+MA+ (n = 34). No participant-met criteria for current MA use disorders and histories of MA dependence were remote in both the older (average of nearly 9 years prior to evaluation) and younger (average of over 2 years prior to evaluation) HIV+MA+ groups. Findings revealed that a remote history of MA dependence exerts a significant detrimental impact on specific aspects of neurocognitive performance (e.g., memory) and a broad range of real-world functioning outcomes (e.g., employment) among older, but not younger PLWH. These results suggest that MA-associated neurotoxicity may have significant "legacy" effects on both neurocognitive and functional outcomes to which older PLWH are particularly vulnerable.
先前研究检查了 HIV 和冰毒(MA)对中枢神经系统(CNS)的联合不良影响,这些研究主要集中在近期 MA 使用诊断的年轻到中年成年人身上。衰老、HIV 和 MA 都集中在前额叶和颞边缘神经系统,并独立增加神经认知和功能下降的风险。因此,本研究旨在确定过去 MA 依赖对老年 HIV 感染者(PLWH)的神经认知和现实世界结果的残余影响。参与者包括 116 名老年人(≥50 岁)和 94 名年轻人(<40 岁),根据 HIV 血清状况(HIV+/HIV-)和 MA 依赖的终生史,分为六个研究组之一:老年 HIV-MA-(n=36)、老年 HIV+MA-(n=49)、老年 HIV+MA+(n=31)、年轻 HIV-MA-(n=27)、年轻 HIV+MA-(n=33)和年轻 HIV+MA+(n=34)。没有参与者符合当前 MA 使用障碍和 MA 依赖史的标准,且在老年(评估前近 9 年)和年轻(评估前超过 2 年)HIV+MA+组中,MA 依赖史均为既往史。研究结果表明,过去 MA 依赖史对老年 PLWH 的神经认知表现(例如记忆)和广泛的现实世界功能结果(例如就业)的特定方面产生了显著的不利影响,但对年轻 PLWH 没有影响。这些结果表明,MA 相关的神经毒性可能对老年 PLWH 特别容易受到影响的神经认知和功能结果产生重大“遗留”影响。