张量值弥散磁共振成像(Tensor-valued diffusion MRI)可检测出患有认知障碍的艾滋病病毒感染者的大脑微观结构变化。

Md Nasir Uddin, Meera V Singh, Abrar Faiyaz, Filip Szczepankiewicz, Markus Nilsson, Zachary D Boodoo, Karli R Sutton, Madalina E Tivarus, Jianhui Zhong, Lu Wang, Xing Qiu, Miriam T Weber, Giovanni Schifitto
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摘要

尽管取得了进步,但艾滋病毒相关神经认知障碍的发病率仍高达约 40%,这主要归因于 cART(联合抗逆转录病毒疗法)前不可逆转的脑损伤等因素。接受联合抗逆转录病毒疗法(cART)治疗的艾滋病病毒感染者(PWH)在相对较短的随访期内不会出现明显的神经认知变化。然而,定量神经成像可能能够检测到正在发生的细微微观结构变化。本研究旨在探讨张量值弥散编码在检测接受 cART 治疗的 PWH 患者大脑微观结构完整性变化方面的灵敏度。此外,研究还探讨了这些指标、神经认知评分以及血浆中神经丝轻链(NFL)和胶质纤维酸性蛋白(GFAP)水平之间的关系。利用 3T 磁共振成像技术,对 24 名重度脑损伤患者和 31 名健康对照者进行了横断面检查。结果显示,各白质区域的 b 张量编码指标存在明显差异,这些指标与认知能力以及神经元和胶质损伤的血液标记物(NFL 和 GFAP)之间存在关联。此外,还观察到艾滋病病毒感染状况与成像指标之间存在明显的交互作用,尤其影响灰质和白质的认知总分。这些研究结果表明,b-张量编码指标在检测艾滋病病毒感染中与轴突损伤相关的细微变化方面具有更高的灵敏度,强调了它们在了解艾滋病病毒感染者神经认知障碍方面的潜在临床意义。
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Tensor-valued diffusion MRI detects brain microstructure changes in HIV infected individuals with cognitive impairment.

Despite advancements, the prevalence of HIV-associated neurocognitive impairment remains at approximately 40%, attributed to factors like pre-cART (combination antiretroviral therapy) irreversible brain injury. People with HIV (PWH) treated with cART do not show significant neurocognitive changes over relatively short follow-up periods. However, quantitative neuroimaging may be able to detect ongoing subtle microstructural changes. This study aimed to investigate the sensitivity of tensor-valued diffusion encoding in detecting such changes in brain microstructural integrity in cART-treated PWH. Additionally, it explored relationships between these metrics, neurocognitive scores, and plasma levels of neurofilament light (NFL) chain and glial fibrillary acidic protein (GFAP). Using MRI at 3T, 24 PWH and 31 healthy controls underwent cross-sectional examination. The results revealed significant variations in b-tensor encoding metrics across white matter regions, with associations observed between these metrics, cognitive performance, and blood markers of neuronal and glial injury (NFL and GFAP). Moreover, a significant interaction between HIV status and imaging metrics was observed, particularly impacting total cognitive scores in both gray and white matter. These findings suggest that b-tensor encoding metrics offer heightened sensitivity in detecting subtle changes associated with axonal injury in HIV infection, underscoring their potential clinical relevance in understanding neurocognitive impairment in PWH.

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