San Diego State University/UC San Diego Joint Doctoral Program in Clinical Psychology, San Diego, CA, USA.
UC San Diego, Department of Psychiatry, San Diego, CA, USA.
J Int Neuropsychol Soc. 2022 Jul;28(6):600-610. doi: 10.1017/S1355617721000783. Epub 2021 Jul 26.
Given the aging population of people with HIV (PWH), along with increasing rates of binge drinking among both PWH and the general older adult population, this study examined the independent and interactive effects of HIV, binge drinking, and age on neurocognition.
Participants were 146 drinkers stratified by HIV and binge drinking status (i.e., ≥4 drinks for women and ≥5 drinks for men within approximately 2 h): HIV+/Binge+ ( = 30), HIV-/Binge+ ( = 23), HIV+/Binge- ( = 55), HIV-/Binge- ( = 38). All participants completed a comprehensive neuropsychological battery measuring demographically-corrected global and domain-specific neurocognitive T scores. ANCOVA models examined independent and interactive effects of HIV and binge drinking on neurocognitive outcomes, adjusting for overall alcohol consumption, lifetime substance use, sex, and age. Subsequent multiple linear regressions examined whether HIV/Binge group moderated the relationship between age and neurocognition.
HIV+/Binge+ participants had worse global neurocognition, processing speed, delayed recall, and working memory than HIV-/Binge- participants (s < .05). While there were significant main effects of HIV and binge drinking, their interaction did not predict any of those neurocognitive outcomes (s > .05). Significant interactions between age and HIV/Binge group showed that HIV+/Binge+ participants demonstrated steeper negative relationships between age and neurocognitive outcomes of learning, delayed recall, and motor skills compared to HIV-/Binge- participants (s < .05).
Results showed adverse additive effects of HIV and binge drinking on neurocognitive functioning, with older adults demonstrating the most vulnerability to these effects. Findings support the need for interventions to reduce binge drinking, especially among older PWH.
鉴于艾滋病毒感染者(PWH)人口老龄化,以及 PWH 和一般老年人群体中 binge drinking 的发生率不断上升,本研究考察了 HIV、 binge drinking 和年龄对神经认知的独立和交互作用。
参与者根据 HIV 和 binge drinking 状态分层为 146 名饮酒者(即:女性≥4 杯,男性≥5 杯,在大约 2 小时内):HIV+/Binge+(n = 30)、HIV-/Binge+(n = 23)、HIV+/Binge-(n = 55)、HIV-/Binge-(n = 38)。所有参与者都完成了一项全面的神经心理学测试,该测试衡量了经人口统计学校正的全球和特定领域的神经认知 T 分数。ANCOVA 模型考察了 HIV 和 binge drinking 对神经认知结果的独立和交互作用,调整了总饮酒量、终生物质使用、性别和年龄。随后的多元线性回归检验了 HIV/Binge 组是否调节了年龄与神经认知之间的关系。
HIV+/Binge+ 参与者的全球认知、处理速度、延迟回忆和工作记忆比 HIV-/Binge- 参与者差(s <.05)。虽然 HIV 和 binge drinking 有显著的主效应,但它们的交互作用并没有预测任何这些神经认知结果(s >.05)。年龄与 HIV/Binge 组之间的显著交互作用表明,与 HIV-/Binge- 参与者相比,HIV+/Binge+ 参与者在学习、延迟回忆和运动技能等神经认知结果与年龄之间表现出更陡峭的负相关关系(s <.05)。
结果显示 HIV 和 binge drinking 对神经认知功能有不利的累加效应,而老年人对此类效应最脆弱。研究结果支持需要采取干预措施来减少 binge drinking,尤其是在老年 PWH 中。