School of Psychology and Psychiatry, Faculty of Medicine Nursing & Health Sciences, Monash University, Clayton, VIC 3800, Australia.
Neurobiol Dis. 2013 Mar;51:82-92. doi: 10.1016/j.nbd.2012.10.001. Epub 2012 Oct 13.
We investigated two measures of neural integrity, T1-weighted volumetric measures and diffusion tensor imaging (DTI), and explored their combined potential to differentiate pre-diagnosis Huntington's disease (pre-HD) individuals from healthy controls. We applied quadratic discriminant analysis (QDA) to discriminate pre-HD individuals from controls and we utilised feature selection and dimension reduction to increase the robustness of the discrimination method. Thirty six symptomatic HD (symp-HD), 35 pre-HD, and 36 control individuals participated as part of the IMAGE-HD study and underwent T1-weighted MRI, and DTI using a Siemens 3 Tesla scanner. Volume and DTI measures [mean diffusivity (MD) and fractional anisotropy (FA)] were calculated for each group within five regions of interest (ROI; caudate, putamen, pallidum, accumbens and thalamus). QDA was then performed in a stepwise manner to differentiate pre-HD individuals from controls, based initially on unimodal analysis of motor or neurocognitive measures, or on volume, MD or FA measures from within the caudate, pallidum and putamen. We then tested for potential improvements to this model, by examining multi-modal MRI classifications (volume, FA and MD), and also included motor and neurocognitive measures, and additional brain regions (i.e., accumbens and thalamus). Volume, MD and FA differed across the three groups, with pre-HD characterised by significant volumetric reductions and increased FA within caudate, putamen and pallidum, relative to controls. The QDA results demonstrated that the differentiation of pre-HD from controls was highly accurate when both volumetric and diffusion data sets from basal ganglia (BG) regions were used. The highest discriminative accuracy however was achieved in a multi-modality approach and when including all available measures: motor and neurocognitive scores and multi-modal MRI measures from the BG, accumbens and thalamus. Our QDA findings provide evidence that combined multi-modal imaging measures can accurately classify individuals up to 15 years prior to onset when therapeutic intervention is likely to have maximal effects in slowing the trajectory of disease development.
我们研究了两种神经完整性的测量方法,即 T1 加权体积测量和弥散张量成像(DTI),并探索了它们联合应用于区分预诊断亨廷顿病(pre-HD)个体与健康对照者的潜力。我们应用二次判别分析(QDA)来区分 pre-HD 个体与对照组,并利用特征选择和降维来增加判别方法的稳健性。36 名有症状的 HD(symp-HD)患者、35 名 pre-HD 患者和 36 名健康对照者作为 IMAGE-HD 研究的一部分,接受了 T1 加权 MRI 和 DTI 检查,使用 Siemens 3T 扫描仪。在 5 个感兴趣区域(ROI;尾状核、壳核、苍白球、伏隔核和丘脑)内计算每个组的体积和 DTI 测量值[平均弥散度(MD)和分数各向异性(FA)]。然后,我们逐步进行 QDA,根据运动或神经认知测量的单模态分析,或基于尾状核、苍白球和壳核内的体积、MD 或 FA 测量值,来区分 pre-HD 个体与对照组。然后,我们通过检查多模态 MRI 分类(体积、FA 和 MD),以及纳入运动和神经认知测量值以及额外的脑区(即伏隔核和丘脑),来测试该模型的潜在改进。体积、MD 和 FA 在三组之间存在差异,与对照组相比,pre-HD 特征为尾状核、壳核和苍白球体积显著减少,FA 增加。QDA 结果表明,当使用基底节(BG)区域的体积和弥散数据集时,pre-HD 与对照组的区分非常准确。然而,在多模态方法中,当包括所有可用的测量值(运动和神经认知评分以及来自 BG、伏隔核和丘脑的多模态 MRI 测量值)时,实现了最高的判别准确性。我们的 QDA 结果提供了证据,表明联合多模态成像测量值可以在发病前 15 年内准确地对个体进行分类,此时治疗干预可能会最大限度地减缓疾病发展的轨迹。