Research Group for Lifespan Changes in Brain and Cognition,
Research Group for Lifespan Changes in Brain and Cognition, Department of Physical Medicine and Rehabilitation, Unit of Neuropsychology, Oslo University Hospital, 0424 Oslo, Norway.
J Neurosci. 2014 Jun 18;34(25):8488-98. doi: 10.1523/JNEUROSCI.0391-14.2014.
Human cortical thickness and surface area are genetically independent, emerge through different neurobiological events during development, and are sensitive to different clinical conditions. However, the relationship between changes in the two over time is unknown. Additionally, longitudinal studies have almost invariably been restricted to older adults, precluding the delineation of adult life span trajectories of change in cortical structure. In this longitudinal study, we investigated changes in cortical thickness, surface area, and volume after an average interval of 3.6 years in 207 well screened healthy adults aged 23-87 years. We hypothesized that the relationships among metrics are dynamic across the life span, that the primary contributor to cortical volume reductions in aging is cortical thinning, and that magnitude of change varies with age and region. Changes over time were seen in cortical area (mean annual percentage change [APC], -0.19), thickness (APC, -0.35), and volume (APC, -0.51) in most regions. Volume changes were primarily explained by changes in thickness rather than area. A negative relationship between change in thickness and surface area was found across several regions, where more thinning was associated with less decrease in area, and vice versa. Accelerating changes with increasing age was seen in temporal and occipital cortices. In contrast, decelerating changes were seen in prefrontal and anterior cingulate cortices. In conclusion, a dynamic relationship between cortical thickness and surface area changes exists throughout the adult life span. The mixture of accelerating and decelerating changes further demonstrates the importance of studying these metrics across the entire adult life span.
人类皮质厚度和表面积是遗传独立的,在发育过程中通过不同的神经生物学事件出现,并且对不同的临床状况敏感。然而,两者随时间的变化关系尚不清楚。此外,纵向研究几乎无一例外地仅限于老年人,排除了在皮质结构的成年生活跨度轨迹中描述变化的可能性。在这项纵向研究中,我们在平均 3.6 年的时间内对 207 名经过严格筛选的健康成年人(年龄 23-87 岁)进行了皮质厚度、表面积和体积的变化研究。我们假设在整个生命跨度中,指标之间的关系是动态的,皮质变薄是衰老过程中皮质体积减少的主要原因,并且变化幅度随年龄和区域而变化。在大多数区域中,皮质面积(平均年百分比变化[APC],-0.19)、厚度(APC,-0.35)和体积(APC,-0.51)都随时间发生了变化。体积变化主要是由厚度变化而不是面积变化引起的。在几个区域中发现了厚度和表面积变化之间的负相关关系,其中更多的变薄与面积减少较少有关,反之亦然。在颞叶和枕叶中观察到与年龄增加相关的加速变化。相比之下,在额前叶和前扣带回皮质中观察到减速变化。总之,在整个成年生命跨度中,皮质厚度和表面积变化之间存在动态关系。加速和减速变化的混合进一步证明了在整个成年生命跨度中研究这些指标的重要性。