Jakimovski Dejan, Bergsland Niels, Dwyer Michael G, Traversone John, Hagemeier Jesper, Fuchs Tom A, Ramasamy Deepa P, Weinstock-Guttman Bianca, Benedict Ralph H B, Zivadinov Robert
Department of Neurology, Buffalo Neuroimaging Analysis Center, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, State University of New York, Buffalo, NY, United States.
IRCCS, Fondazione Don Carlo Gnocchi, Milan, Italy.
Front Neurol. 2020 Jul 17;11:700. doi: 10.3389/fneur.2020.00700. eCollection 2020.
Reports suggest presence of cerebral hypoperfusion in multiple sclerosis (MS). Currently there are no studies that examine if the cerebral MS perfusion is affected by presence of cardiovascular comorbidities. To investigate associations between cerebral perfusion and disease outcomes in MS patients with and without comorbid cardiovascular diseases (CVD). One hundred three MS patients (75.7% female) with average age of 54.4 years and 21.1 years of disease duration underwent 3T MRI dynamic susceptibility contrast (DSC) imaging and were tested with Expanded Disability Status Scale, Multiple Sclerosis Severity Score (MSSS), Timed 25-Foot Walk (T25FW), 9-Hole Peg Test (9HPT) and Symbol Digit Modalities Test (SDMT). Structural and perfusion-based normalized measures of cerebral blood flow (nCBF), cerebral blood volume (nCBV) and mean transit time (MTT) of global, tissue-specific and deep gray matter (DGM) areas were derived. CBV and CBF were normalized by the normal-appearing white matter counterpart. In linear step-wise regression analysis, age- and sex-adjusted, MSSS ( = 0.186) was associated with whole brain volume (WBV) (β = -0.244, = 0.046) and gray matter (GM) nCBF (β = -0.22, = 0.035). T25FW ( = 0.278) was associated with WBV (β = -0.289, = 0.012) and hippocampus nCBV (β = -0.225, = 0.03). 9HPT ( = 0.401) was associated with WBV (β = 0.195, = 0.049) and thalamus MTT (β = -0.198, =0.032). After adjustment for years of education, SDMT ( = 0.412) was explained by T2-lesion volume (β = -0.305, = 0.001), and GM nCBV (β = 0.236, = 0.013). No differences in MTT, nCBF nor nCBV measures between patients with ( = 42) and without CVD ( = 61) were found. Perfusion-measures were also not able to distinguish CVD status in a logistic regression model. Decreased GM and deep GM perfusion is associated with poorer MS outcomes, but not with presence of CVD.
报告显示多发性硬化症(MS)存在脑灌注不足。目前尚无研究探讨脑MS灌注是否受心血管合并症的影响。旨在调查合并和未合并心血管疾病(CVD)的MS患者脑灌注与疾病预后之间的关联。103例MS患者(女性占75.7%),平均年龄54.4岁,病程21.1年,接受了3T磁共振成像动态磁敏感对比(DSC)成像,并采用扩展残疾状态量表、多发性硬化症严重程度评分(MSSS)、25英尺步行时间(T25FW)、9孔插钉试验(9HPT)和符号数字模态试验(SDMT)进行测试。得出了全脑、组织特异性和深部灰质(DGM)区域基于结构和灌注的脑血流量(nCBF)、脑血容量(nCBV)和平均通过时间(MTT)的标准化测量值。CBV和CBF通过外观正常的白质对应物进行标准化。在线性逐步回归分析中,经年龄和性别调整后,MSSS(=0.186)与全脑体积(WBV)(β=-0.244,=0.046)和灰质(GM)nCBF(β=-0.22,=0.035)相关。T25FW(=0.278)与WBV(β=-0.289,=0.012)和海马nCBV(β=-0.225,=0.03)相关。9HPT(=0.401)与WBV(β=0.195,=0.049)和丘脑MTT(β=-0.198,=0.032)相关。在调整教育年限后,SDMT(=0.412)可由T2病变体积(β=-0.305,=0.001)和GM nCBV(β=0.236,=0.013)解释。未发现合并CVD(=42)和未合并CVD(=61)的患者在MTT、nCBF或nCBV测量值上存在差异。在逻辑回归模型中,灌注测量值也无法区分CVD状态。GM和深部GM灌注降低与较差的MS预后相关,但与CVD的存在无关。