Buffalo Neuroimaging Analysis Center, Department of Neurology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, State University of New York, Buffalo, NY.
Translational Imaging Center at Clinical Translational Research Center, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, State University of New York, Buffalo, NY.
J Neuroimaging. 2020 May;30(3):342-350. doi: 10.1111/jon.12709. Epub 2020 May 11.
Numerous sex-specific differences in multiple sclerosis (MS) susceptibility, disease manifestation, disability progression, inflammation, and neurodegeneration have been previously reported. Previous magnetic resonance imaging (MRI) studies have shown structural differences between female and male MS brain volumes. To determine sex-specific global and tissue-specific brain volume throughout the MS life span in a real-world large MRI database.
A total of 2,199 MS patients (female/male ratio of 1,651/548) underwent structural MRI imaging on either a 1.5-T or 3-T scanner. Global and tissue-specific volumes of whole brain (WBV), white matter, and gray matter (GMV) were determined by utilizing Structural Image Evaluation using Normalisation of Atrophy Cross-sectional (SIENAX). Lateral ventricular volume (LVV) was determined with the Neurological Software Tool for REliable Atrophy Measurement (NeuroSTREAM). General linear models investigated sex and age interactions, and post hoc comparative sex analyses were performed.
Despite being age-matched with female MS patents, a greater proportion of male MS patients were diagnosed with progressive MS and had lower normalized WBV (P < .001), GMV (P < .001), and greater LVV (P < .001). In addition to significant stand-alone main effects, an interaction between sex and age had an additional effect on the LVV (F-statistics = 4.53, P = .033) and GMV (F-statistics = 4.59, P = .032). The sex and age interaction was retained in both models of LVV (F-statistics = 3.31, P = .069) and GMV (F-statistics = 6.1, P = .003) when disease subtype and disease-modifying treatment (DMT) were also included. Although male MS patients presented with significantly greater LVV and lower GMV during the early and midlife period when compared to their female counterparts (P < .001 for LVV and P < .019 for GMV), these differences were nullified in 60+ years old patients. Similar findings were seen within a subanalysis of MS patients that were not on any DMT at the time of enrollment.
There are sex-specific differences in the LVV and GMV over the MS life span.
多发性硬化症(MS)易感性、疾病表现、残疾进展、炎症和神经退行性变方面存在大量性别特异性差异。先前的磁共振成像(MRI)研究表明,女性和男性 MS 大脑体积之间存在结构差异。本研究旨在通过在真实世界的大型 MRI 数据库中,确定整个 MS 生命期间的性别特异性全脑和组织特异性脑容量。
共有 2199 名 MS 患者(女性/男性比例为 1651/548)在 1.5T 或 3T 扫描仪上进行了结构 MRI 成像。通过利用结构图像评估正常化萎缩横断面分析(SIENAX),确定了全脑(WBV)、白质和灰质(GMV)的全脑和组织特异性体积。利用神经学软件工具进行可靠的萎缩测量(NeuroSTREAM)确定侧脑室体积(LVV)。通过一般线性模型研究了性别和年龄的相互作用,并进行了事后比较性别分析。
尽管与女性 MS 患者年龄匹配,但更多的男性 MS 患者被诊断为进展性 MS,且正常化的 WBV(P <.001)、GMV(P <.001)较低,LVV(P <.001)较大。除了显著的独立主要效应外,性别和年龄之间的相互作用对 LVV(F 统计量=4.53,P=0.033)和 GMV(F 统计量=4.59,P=0.032)也有额外的影响。当疾病亚型和疾病修正治疗(DMT)也被纳入模型时,性别和年龄的相互作用在 LVV(F 统计量=3.31,P=0.069)和 GMV(F 统计量=6.1,P=0.003)模型中仍然存在。尽管与女性相比,男性 MS 患者在早期和中期的 LVV 明显更大,GMV 明显更低(LVV 时 P <.001,GMV 时 P <.019),但在 60 岁以上患者中这些差异消失了。在入组时未接受任何 DMT 的 MS 患者的亚组分析中也观察到了类似的发现。
在 MS 生命期间,LVV 和 GMV 存在性别特异性差异。