脑源性神经营养因子 (BDNF) 与艾滋病病毒感染者自述的认知功能有关。

Joseph A Belloir, Thomas Myers, Scott Batey, Rebecca Schnall
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摘要

背景:艾滋病病毒感染者(PWH)尽管接受了抗逆转录病毒联合疗法,但仍有罹患艾滋病相关神经认知障碍(HAND)的风险。脑源性神经营养因子(BDNF)与认知功能和神经可塑性有关,但其在 HIV 相关神经炎症中的作用仍未得到充分研究。研究方法本研究分析了 CHAMPS 研究的数据,评估了 140 名成人 HIV 感染者基线时的 BDNF 血清水平和认知功能。认知功能采用 PROMIS 应用认知-能力 8 项问卷进行评估。BDNF水平(pg/ml)采用高灵敏度酶联免疫测定(ELISA)试剂盒进行测定。在对人口统计学变量进行调整后,进行了线性回归分析,以探讨 BDNF 水平、认知功能和艾滋病诊断之间的关联。结果发现发现BDNF水平与PWH的认知功能得分之间存在明显的正相关(p = .03)。此外,有艾滋病诊断史的艾滋病患者的 BDNF 水平明显较低(p = 0.02)。其他人口统计学因素对该人群的认知功能或 BDNF 水平没有明显影响。结论:我们的研究结果凸显了 BDNF 作为 PWH 认知功能下降生物标志物的潜力,并表明其与了解 HAND 病理生理学相关。有必要开展进一步研究,探索影响该人群认知结果的多方面相互作用,并制定有针对性的干预措施,以改善 PWH 的认知健康。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Brain-Derived Neurotrophic Factor (BDNF) is Associated with Self-Reported Cognitive Function in Adults with HIV.

Background: People with HIV (PWH) are at risk of developing HIV-associated neurocognitive disorder (HAND) despite receiving combination antiretroviral therapy. Brain-derived neurotrophic factor (BDNF) has been implicated in cognitive function and neuroplasticity, but its role in HIV-related neuroinflammation remains understudied. Methods: This study analyzed data from the CHAMPS study, assessing BDNF serum levels and cognitive function in 140 adults with HIV at baseline. Cognitive function was evaluated using the PROMIS Applied Cognition-Abilities 8-item questionnaire. BDNF levels (pg/ml) were measured using high sensitivity Enzyme-Linked Immunoassay (ELISA) kits. Linear regression analyses were conducted to explore the associations between BDNF levels, cognitive function, and AIDS diagnosis, adjusting for demographic variables. Results: A significant positive association was found between BDNF levels and cognitive function scores in PWH (p = .03). Additionally, PWH with a history of AIDS diagnosis showed significantly lower BDNF levels (p = .02). Other demographic factors did not significantly impact cognitive function or BDNF levels in this cohort. Conclusions: Our results highlight the potential of BDNF as a biomarker for cognitive decline in PWH and suggest its relevance in understanding HAND pathophysiology. Further research is warranted to explore the multifaceted interactions influencing cognitive outcomes in this population and to develop targeted interventions for improving cognitive health in PWH.

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