中度至重度认知障碍与艾滋病病毒感染者近期和长期酗酒有关:新奥尔良艾滋病患者饮酒(NOAH)研究。

IF 3 Q2 SUBSTANCE ABUSE Alcohol (Hanover, York County, Pa.) Pub Date : 2024-06-02 DOI:10.1111/acer.15378
Taylor Fitzpatrick-Schmidt, Evrim Oral, David A. Welsh, Patricia E. Molina, Tekeda F. Ferguson, Scott Edwards
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摘要

背景:人类免疫缺陷病毒(HIV)会对神经系统产生深远影响,导致神经系统缺陷,包括 HIV 相关神经认知障碍(HAND)。HAND是艾滋病病毒感染者(PWH)中最常见的神经系统合并症,而饮酒可能会加重认知障碍,尤其是在易感人群中。本研究以酒精滥用会加重认知障碍为假设,调查了服务不足的艾滋病病毒感染者队列中饮酒与认知之间的关系:新奥尔良艾滋病患者酒精使用(NOAH)研究的参与者(n = 259;66.7% 为男性;平均年龄为 52 ± 10 岁)的数据被用于横断面分析。认知功能采用蒙特利尔认知评估(MoCA)进行评估,酒精使用情况则采用四项指标进行综合测量:酒精使用障碍识别测试(AUDIT)、30 天时限跟踪(TLFB)、终生饮酒史和磷脂酰乙醇(PEth)水平:参与者的平均 MoCA 得分为(20.7 ± 4.5)分,86.5% 的参与者存在认知障碍(MoCA 结论:我们的研究结果表明,认知障碍的发生率很高:我们的研究结果表明,NOAH 队列中认知功能障碍的发生率很高,并表明酗酒会导致威利斯人的整体认知功能障碍,尤其是在 50 岁及以上的人群中。在进一步探讨饮酒对特定认知领域(包括记忆和语言)的影响时,应纳入更多的认知任务。这些发现强调了将饮酒和 AUD 风险视为可能加剧包括老年残疾人在内的弱势群体认知缺陷的重要因素的重要性。
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Moderate-to-severe cognitive impairment is associated with both recent and chronic alcohol misuse in people with HIV: The New Orleans alcohol use in HIV (NOAH) study

Background

Human immunodeficiency virus (HIV) profoundly impacts the nervous system, leading to neurological deficits including HIV-associated neurocognitive disorder (HAND). HAND represents the most common neurological comorbidity among people with HIV (PWH), and alcohol use may exacerbate cognitive deficits, especially in vulnerable populations. This study investigated relationships between alcohol use and cognition in an underserved cohort of PWH, on the hypothesis that alcohol misuse exacerbates cognitive deficits.

Methods

Data collected from participants (n = 259; 66.7% male; mean age 52 ± 10 years) enrolled in the New Orleans Alcohol Use in HIV (NOAH) study were utilized for cross-sectional analysis. Cognitive function was assessed using the Montreal Cognitive Assessment (MoCA), and alcohol use was comprehensively measured using four metrics: the Alcohol Use Disorders Identification Test (AUDIT), 30-day timeline follow back (TLFB), lifetime drinking history, and phosphatidylethanol (PEth) levels.

Results

The average MoCA score among participants was 20.7 ± 4.5, with 86.5% demonstrating cognitive impairment (MoCA < 26). Individuals with MoCA scores below 18 (moderately or severely cognitively impaired) had a higher frequency of recent severe alcohol misuse and greater lifetime alcohol consumption. Participants at increased risk for AUD (AUDIT ≥ 16) also had worse global cognition and memory task performance than those with lower AUDIT scores; this was particularly true among those aged 50 and older. Analysis of the MoCA sub-score data indicated that participants with increased AUD risk had impairments in the cognitive domains of language and memory.

Conclusions

Our findings demonstrate a high prevalence of cognitive impairment in the NOAH cohort and suggest that alcohol misuse contributes to global cognitive deficits in PWH, especially among individuals aged 50 and older. Further exploration of the impact of alcohol use on specific cognitive domains, including memory and language, should incorporate additional cognitive tasks. These findings highlight the importance of considering alcohol use and AUD risk as significant factors that may exacerbate cognitive deficits in vulnerable populations, including older PWH.

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