Department of Psychiatry and Behavioral Sciences, Duke University School of Medicine, Durham, North Carolina, 27710, USA.
Brain Imaging and Analysis Center, Duke University Medical Center, Durham, North Carolina, 27710, USA.
Ann Clin Transl Neurol. 2023 Sep;10(9):1633-1646. doi: 10.1002/acn3.51854. Epub 2023 Jul 20.
White matter hyperintensities (WMH), a marker of cerebral small vessel disease and predictor of cognitive decline, are observed at higher rates in persons with HIV (PWH). The use of cocaine, a potent central nervous system stimulant, is disproportionately common in PWH and may contribute to WMH.
The sample included of 110 PWH on antiretroviral therapy. Fluid-attenuated inversion recovery (FLAIR) and T1-weighted anatomical MRI scans were collected, along with neuropsychological testing. FLAIR images were processed using the Lesion Segmentation Toolbox. A hierarchical regression model was run to investigate predictors of WMH burden [block 1: demographics; block 2: cerebrovascular disease (CVD) risk; block 3: lesion burden].
The sample was 20% female and 79% African American with a mean age of 45.37. All participants had persistent HIV viral suppression, and the median CD4 T-cell count was 750. Nearly a third (29%) currently used cocaine regularly, with an average of 23.75 (SD = 20.95) days in the past 90. In the hierarchical linear regression model, cocaine use was a significant predictor of WMH burden (β = .28). WMH burden was significantly correlated with poorer cognitive function (r = -0.27). Finally, higher WMH burden was significantly associated with increased serum concentrations of interferon-γ-inducible protein 10 (IP-10) but lower concentrations of myeloperoxidase (MPO); however, these markers did not differ by COC status.
WMH burden is associated with poorer cognitive performance in PWH. Cocaine use and CVD risk independently contribute to WMH, and addressing these conditions as part of HIV care may mitigate brain injury underlying neurocognitive impairment.
脑白质高信号(WMH)是脑小血管病的标志物和认知能力下降的预测因子,在 HIV 感染者(PWH)中更为常见。可卡因是一种强效的中枢神经系统兴奋剂,在 PWH 中使用比例过高,可能导致 WMH。
该样本包括 110 名接受抗逆转录病毒治疗的 PWH。采集了液体衰减反转恢复(FLAIR)和 T1 加权解剖 MRI 扫描以及神经心理学测试。使用病变分割工具箱处理 FLAIR 图像。运行了一个分层回归模型,以研究 WMH 负担的预测因素[第 1 块:人口统计学;第 2 块:脑血管疾病(CVD)风险;第 3 块:病变负担]。
样本中 20%为女性,79%为非裔美国人,平均年龄为 45.37 岁。所有参与者均持续抑制 HIV 病毒,中位 CD4 T 细胞计数为 750。近三分之一(29%)的人经常使用可卡因,过去 90 天中有 23.75 天(SD=20.95)。在分层线性回归模型中,可卡因使用是 WMH 负担的一个重要预测因子(β=0.28)。WMH 负担与认知功能较差显著相关(r=-0.27)。最后,WMH 负担越高与干扰素-γ诱导蛋白 10(IP-10)的血清浓度升高显著相关,但与髓过氧化物酶(MPO)的浓度降低显著相关;然而,COC 状态对这些标志物没有影响。
WMH 负担与 PWH 的认知功能较差相关。可卡因使用和 CVD 风险独立导致 WMH,将这些情况作为 HIV 护理的一部分可能会减轻神经认知障碍的脑损伤。