Center for Health Sciences, SRI International, Menlo Park, California; Department of Psychiatry & Behavioral Sciences, Stanford University School of Medicine, Stanford, California.
Department of Psychiatry & Behavioral Sciences, Stanford University School of Medicine, Stanford, California.
Biol Psychiatry. 2024 Feb 1;95(3):231-244. doi: 10.1016/j.biopsych.2023.07.023. Epub 2023 Aug 18.
Antiretroviral treatment has enabled people living with HIV infection to have a near-normal life span. With longevity comes opportunities for engaging in risky behavior, including initiation of excessive drinking. Given that both HIV infection and alcohol use disorder (AUD) can disrupt brain white matter integrity, we questioned whether HIV infection, even if successfully treated, or AUD alone results in signs of accelerated white matter aging and whether HIV+AUD comorbidity further accelerates brain aging.
Longitudinal magnetic resonance imaging-FLAIR data were acquired over a 15-year period from 179 control individuals, 204 participants with AUD, 70 participants with HIV, and 75 participants with comorbid HIV+AUD. White matter hyperintensity (WMH) volumes were quantified and localized, and their functional relevance was examined with cognitive and motor testing.
The 3 diagnostic groups each had larger WMH volumes than the control group. Although all 4 groups exhibited accelerating volume increases with aging, only the HIV groups showed faster WMH enlargement than control individuals; the comorbid group showed faster acceleration than the HIV-only group. Sex and HIV infection length, but not viral suppression status, moderated acceleration. Correlations emerged between WMH volumes and attention/working memory and executive function scores of the AUD and HIV groups and between WMH volumes and motor skills in the 3 diagnostic groups.
Even treated HIV can show accelerated aging, possibly from treatment sequelae or legacy effects, and notably from AUD comorbidity. WMH volumes may be especially relevant for tracking HIV and AUD brain health because each condition is associated with liability for hypertensive processes, for which WMHs are considered a marker.
抗逆转录病毒治疗使感染艾滋病毒的人能够拥有接近正常的寿命。随着寿命的延长,人们有机会从事危险行为,包括开始过度饮酒。鉴于艾滋病毒感染和酒精使用障碍(AUD)都可能破坏大脑白质的完整性,我们想知道,即使成功治疗了 HIV 感染,或者仅仅是 AUD 是否会导致大脑白质老化加速的迹象,以及 HIV+AUD 合并症是否会进一步加速大脑老化。
在 15 年的时间里,从 179 名对照个体、204 名 AUD 参与者、70 名 HIV 参与者和 75 名合并 HIV+AUD 的参与者中获得了纵向磁共振成像-FLAIR 数据。定量和定位了脑白质高信号(WMH)体积,并通过认知和运动测试检查了其功能相关性。
3 个诊断组的 WMH 体积均大于对照组。尽管所有 4 个组都表现出与年龄相关的体积增加加速,但只有 HIV 组显示出比对照组更快的 WMH 增大;合并组比仅 HIV 组的加速更快。性别和 HIV 感染时间,但不是病毒抑制状态,调节了加速。AUD 和 HIV 组的 WMH 体积与注意力/工作记忆和执行功能评分之间,以及 3 个诊断组的 WMH 体积与运动技能之间存在相关性。
即使经过治疗的 HIV 也可能表现出加速老化,可能是由于治疗的后遗症或遗留效应,特别是由于 AUD 合并症。WMH 体积可能特别适合追踪 HIV 和 AUD 的大脑健康,因为每种情况都与高血压过程的易感性有关,而 WMH 被认为是高血压过程的标志物。