Center for the Study of Human Cognition, Department of Psychology, University of Oslo, Oslo, Norway.
Neuroimage. 2010 Aug 1;52(1):172-85. doi: 10.1016/j.neuroimage.2010.03.056. Epub 2010 Mar 27.
Cortical thickness decreases from childhood throughout life, as estimated by magnetic resonance imaging (MRI). This monotone trajectory does not reflect the fundamentally different neurobiological processes underlying morphometric changes in development versus aging. We hypothesized that intracortical gray matter (GM) and subjacent white matter (WM) T1-weighted signal intensity would distinguish developmental and age-related changes in the cortex better than thickness. Intracortical GM and subjacent WM signal intensity and cortical thickness was measured across the brain surface in a healthy life span sample (n=429, 8-85 years). We also computed the relaxation rate of T2* (R2*) from multiecho sequences and mapped intracortical GM and subjacent WM values to the surface to delineate age-related variability in R2* and to adjust the T1 signal intensity for possible confounds of accumulated iron. While monotone age-related reductions in thickness were found, both intracortical GM and subcortical WM signal intensity showed inverted U patterns with peaks from eight to approximately 30 years of age. The spatial pattern of intracortical neurodevelopment followed a posterior-anterior gradient, with earliest maturation of occipital visual cortices and most protracted in superior frontal regions. From 50s and 60s, substantial signal reductions were observed in several regions, including the insula, cingulate, and inferior temporal gyrus. R2* showed similar patterns but peaked much later than the T1-weighted signal intensity measures. The results are presented as animations yielding detailed depictions of the dynamic regional variability in cortical neurodevelopment and aging and demonstrate that cortical thickness and T1-weighted signal intensity are sensitive to different cortical maturational and aging-related processes.
皮质厚度会随着磁共振成像(MRI)的发展而从儿童期贯穿整个生命期逐渐变薄。这种单调的轨迹并不能反映出形态学变化在发展和衰老过程中所涉及的根本不同的神经生物学过程。我们假设,皮质内灰质(GM)和下皮质白质(WM)的 T1 加权信号强度会比厚度更能区分发展和与年龄相关的变化。在一个健康的寿命样本中(n=429,8-85 岁),我们在大脑表面测量了皮质内 GM 和下皮质 WM 的信号强度和皮质厚度。我们还从多回波序列中计算了 T2*(R2*)弛豫率,并将皮质内 GM 和下皮质 WM 值映射到表面,以描绘 R2与年龄相关的可变性,并调整 T1 信号强度以适应可能存在的累积铁的混杂因素。虽然厚度呈现单调的与年龄相关的减少,但皮质内 GM 和下皮质 WM 的信号强度都表现出倒 U 型模式,峰值出现在 8 岁到 30 岁左右。皮质内神经发育的空间模式遵循一个从后向前的梯度,枕叶视觉皮质最早成熟,额上区域的成熟时间最长。从 50 多岁到 60 多岁,几个区域的信号明显减少,包括岛叶、扣带回和颞下回。R2也表现出类似的模式,但比 T1 加权信号强度测量的峰值出现得晚得多。结果以动画形式呈现,详细描绘了皮质神经发育和衰老的动态区域变异性,并证明皮质厚度和 T1 加权信号强度对不同的皮质成熟和与年龄相关的过程敏感。