Schaer Marie, Cuadra Meritxell Bach, Schmansky Nick, Fischl Bruce, Thiran Jean-Philippe, Eliez Stephan
Department of Psychiatry, University of Geneva School of Medicine.
J Vis Exp. 2012 Jan 2(59):e3417. doi: 10.3791/3417.
Cortical folding (gyrification) is determined during the first months of life, so that adverse events occurring during this period leave traces that will be identifiable at any age. As recently reviewed by Mangin and colleagues(2), several methods exist to quantify different characteristics of gyrification. For instance, sulcal morphometry can be used to measure shape descriptors such as the depth, length or indices of inter-hemispheric asymmetry(3). These geometrical properties have the advantage of being easy to interpret. However, sulcal morphometry tightly relies on the accurate identification of a given set of sulci and hence provides a fragmented description of gyrification. A more fine-grained quantification of gyrification can be achieved with curvature-based measurements, where smoothed absolute mean curvature is typically computed at thousands of points over the cortical surface(4). The curvature is however not straightforward to comprehend, as it remains unclear if there is any direct relationship between the curvedness and a biologically meaningful correlate such as cortical volume or surface. To address the diverse issues raised by the measurement of cortical folding, we previously developed an algorithm to quantify local gyrification with an exquisite spatial resolution and of simple interpretation. Our method is inspired of the Gyrification Index(5), a method originally used in comparative neuroanatomy to evaluate the cortical folding differences across species. In our implementation, which we name local Gyrification Index (lGI(1)), we measure the amount of cortex buried within the sulcal folds as compared with the amount of visible cortex in circular regions of interest. Given that the cortex grows primarily through radial expansion(6), our method was specifically designed to identify early defects of cortical development. In this article, we detail the computation of local Gyrification Index, which is now freely distributed as a part of the FreeSurfer Software (http://surfer.nmr.mgh.harvard.edu/, Martinos Center for Biomedical Imaging, Massachusetts General Hospital). FreeSurfer provides a set of automated reconstruction tools of the brain's cortical surface from structural MRI data. The cortical surface extracted in the native space of the images with sub-millimeter accuracy is then further used for the creation of an outer surface, which will serve as a basis for the lGI calculation. A circular region of interest is then delineated on the outer surface, and its corresponding region of interest on the cortical surface is identified using a matching algorithm as described in our validation study(1). This process is repeatedly iterated with largely overlapping regions of interest, resulting in cortical maps of gyrification for subsequent statistical comparisons (Fig. 1). Of note, another measurement of local gyrification with a similar inspiration was proposed by Toro and colleagues(7), where the folding index at each point is computed as the ratio of the cortical area contained in a sphere divided by the area of a disc with the same radius. The two implementations differ in that the one by Toro et al. is based on Euclidian distances and thus considers discontinuous patches of cortical area, whereas ours uses a strict geodesic algorithm and include only the continuous patch of cortical area opening at the brain surface in a circular region of interest.
皮质折叠(脑回形成)在生命的最初几个月就已确定,因此在此期间发生的不良事件会留下痕迹,这些痕迹在任何年龄都可被识别。正如曼金及其同事最近所综述的那样(2),存在多种方法来量化脑回形成的不同特征。例如,脑沟形态测量法可用于测量诸如深度、长度或半球间不对称指数等形状描述符(3)。这些几何特性具有易于解释的优点。然而,脑沟形态测量法紧密依赖于对给定脑沟集的准确识别,因此提供了对脑回形成的碎片化描述。使用基于曲率的测量可以实现对脑回形成更精细的量化,其中通常在皮质表面的数千个点上计算平滑后的绝对平均曲率(4)。然而,曲率并不容易理解,因为目前尚不清楚曲率与诸如皮质体积或表面积等生物学上有意义的关联之间是否存在任何直接关系。为了解决皮质折叠测量所引发的各种问题,我们之前开发了一种算法,以极高的空间分辨率和简单的解释来量化局部脑回形成。我们的方法受到脑回形成指数(5)的启发,该方法最初用于比较神经解剖学中,以评估不同物种间的皮质折叠差异。在我们的实现中,我们将其命名为局部脑回形成指数(lGI(1)),我们测量脑沟褶皱内埋藏的皮质量与感兴趣圆形区域中可见皮质量的比值。鉴于皮质主要通过径向扩展生长(6),我们的方法专门设计用于识别皮质发育的早期缺陷。在本文中,我们详细介绍局部脑回形成指数的计算方法,该方法现在作为FreeSurfer软件(http://surfer.nmr.mgh.harvard.edu/,马萨诸塞州总医院马丁诺斯生物医学成像中心)的一部分免费发布。FreeSurfer提供了一套从结构MRI数据自动重建脑皮质表面的工具。然后,以亚毫米精度在图像的原始空间中提取的皮质表面被进一步用于创建一个外表面,该外表面将作为lGI计算的基础。然后在外表面上划定一个感兴趣的圆形区域,并使用我们验证研究(1)中描述的匹配算法识别其在皮质表面上的相应感兴趣区域。这个过程在大量重叠的感兴趣区域中反复迭代,从而生成脑回形成的皮质图,用于后续的统计比较(图1)。值得注意的是,托罗及其同事(7)提出了另一种具有类似灵感的局部脑回形成测量方法,其中每个点的折叠指数计算为球体中包含的皮质面积与具有相同半径的圆盘面积之比。这两种实现方式的不同之处在于,托罗等人的方法基于欧几里得距离,因此考虑的是皮质区域的不连续斑块,而我们的方法使用严格的测地线算法,并且只包括在感兴趣圆形区域中在脑表面开口的连续皮质区域斑块。