Department of Physics and Astronomy, University of Rochester, Rochester, NY, United States.
Department of Neurology, University of Rochester, Rochester, NY, United States.
Neuroimage Clin. 2021;32:102786. doi: 10.1016/j.nicl.2021.102786. Epub 2021 Aug 28.
The aim of this study was to assess, in the context of cerebral small vessel disease (CSVD), whether cardiovascular risk factors and white matter hyperintensities (WMHs) were associated with brain tissue susceptibility as measured by quantitative susceptibility mapping (QSM). Given that CSVD is diagnosed by the presence of lacunar strokes, periventricular and deep WMHs, increased perivascular spaces, and microbleeds, we expected that QSM could capture changes in brain tissue due to underlying CSVD pathology. We compared a cohort of 101 HIV-infected individuals (mean age ± SD = 53.2 ± 10.9 years) with mild to moderate cardiovascular risk scores, as measured by the Reynolds risk score, to 102 age-matched controls (mean age (SD) = 50.3 (15.7) years) with similar Reynolds scores. We performed brain MRI to assess CSVD burden by acquiring 3D T1-MPRAGE, 3D FLAIR, 2D T2-TSE, and mGRE for QSM. We found that signs of CSVD are significantly higher in individuals with HIV-infection compared to controls and that WMH volumes are significantly correlated with age and cardiovascular risk scores. Regional QSM was associated with cardiovascular risk factors, age, sex, and WMH volumes but not HIV status. These results suggest that QSM may be an early imaging marker reflective of alterations in brain microcirculation.
本研究旨在评估在脑小血管病(CSVD)背景下,心血管危险因素和脑白质高信号(WMHs)与定量磁化率映射(QSM)测量的脑组织磁化率之间的关系。鉴于 CSVD 的诊断依据是腔隙性脑梗死、脑室周围和深部 WMH、血管周围间隙增大和微出血的存在,我们预计 QSM 可以捕捉到由于潜在 CSVD 病理引起的脑组织变化。我们比较了一组 101 名 HIV 感染个体(平均年龄 ± 标准差=53.2 ± 10.9 岁)和 102 名年龄匹配的对照组(平均年龄(标准差)=50.3(15.7)岁),这些对照组的心血管风险评分均较低(通过 Reynolds 风险评分评估)。我们进行了脑部 MRI 检查,通过获取 3D T1-MPRAGE、3D FLAIR、2D T2-TSE 和 mGRE 来评估 QSM 的 CSVD 负担。结果发现,与对照组相比,HIV 感染者的 CSVD 征象明显更高,WMH 体积与年龄和心血管风险评分显著相关。局部 QSM 与心血管危险因素、年龄、性别和 WMH 体积有关,但与 HIV 状态无关。这些结果表明,QSM 可能是一种反映脑微循环改变的早期影像学标志物。