Department of Psychiatry, University of Connecticut School of Medicine, Farmington, CT 06030-2103, USA.
Psychiatry Res. 2011 Jan 30;185(1-2):232-7. doi: 10.1016/j.psychres.2009.08.020. Epub 2010 May 23.
In view of the rising prevalence of an overweight body mass among patients living with human immunodeficiency virus/acquired immune deficiency syndrome (HIV/AIDS), clinicians must now be mindful of possible adverse outcomes resulting from the co-occurrence. The present study was designed to examine the additive and interactive effects of HIV/AIDS and an excess body mass, as well as the additional contributions of substance abuse or dependence. The dependent variable was brain function estimated by the measurement of P300 electroencephalographic potentials. P300 potentials were recorded during a task designed to elicit subcomponents with frontal (P300a) and both frontal and non-frontal (P300b) generators. Analyses revealed greater frontal P300a latencies among the 102 HIV-1 seropositive versus the 68 seronegative participants. In addition, frontal P300a latency was further increased by a synergistic interaction of HIV-1 serostatus with a body mass index (BMI)≥25 kg/m². A history of substance abuse/dependence did not alter these changes. However, it did combine with HIV/AIDS to produce a smaller P300a amplitude than was seen in participants with neither disorder. The findings suggest that white matter changes accompanying an excess BMI may exacerbate those that attend HIV/AIDS and thereby slow down frontal brain function. Substance abuse, likewise, interacts with HIV/AIDS but may impair frontal brain function via a different mechanism.
鉴于患有人类免疫缺陷病毒/获得性免疫缺陷综合征(HIV/AIDS)的患者超重的比例不断上升,临床医生现在必须注意到这种共病可能带来的不良后果。本研究旨在检验 HIV/AIDS 和超重这两种情况的累加和交互效应,以及物质滥用或依赖的额外影响。因变量是通过测量 P300 脑电图电位来估计的大脑功能。在设计的一项任务中记录 P300 电位,以引出具有额部(P300a)和额部及非额部(P300b)发生器的子成分。分析显示,102 名 HIV-1 血清阳性者的额部 P300a 潜伏期长于 68 名血清阴性者。此外,HIV-1 血清阳性状态与体重指数(BMI)≥25kg/m²的协同相互作用使额部 P300a 潜伏期进一步延长。物质滥用/依赖的病史并没有改变这些变化。然而,它与 HIV/AIDS 相结合,导致 P300a 振幅比既无障碍的参与者更小。研究结果表明,伴随超重 BMI 的白质变化可能会加重与 HIV/AIDS 相关的变化,从而使额叶脑功能减慢。同样,物质滥用与 HIV/AIDS 相互作用,但可能通过不同的机制损害额叶脑功能。