Wallace Gregory L, Eric Schmitt J, Lenroot Rhoshel, Viding Essi, Ordaz Sarah, Rosenthal Michael A, Molloy Elizabeth A, Clasen Liv S, Kendler Kenneth S, Neale Michael C, Giedd Jay N
Child Psychiatry Branch, National Institute of Mental Health, Bethesda, MD, USA.
J Child Psychol Psychiatry. 2006 Oct;47(10):987-93. doi: 10.1111/j.1469-7610.2006.01676.x.
Longitudinal pediatric neuroimaging studies have demonstrated increasing volumes of white matter and regionally-specific inverted U shaped developmental trajectories of gray matter volumes during childhood and adolescence. Studies of monozygotic and dyzygotic twins during this developmental period allow exploration of genetic and non-genetic influences on these developmental trajectories.
Magnetic resonance imaging brain scans were acquired on a pediatric sample of 90 monozygotic twin pairs, 38 same-sex dyzygotic twin pairs, and 158 unrelated typically developing singletons. Structural equation modeling was used to estimate the additive genetic, common environment, and unique environment effects, as well as age by heritability interactions, on measures of brain volumes from these images.
Consistent with previous adult studies, additive genetic effects accounted for a substantial portion of variability in nearly all brain regions with the notable exception of the cerebellum. Significant age by heritability interactions were observed with gray matter volumes showing a reduction in heritability with increasing age, while white matter volume heritability increased with greater age.
Understanding the relative contributions of genetic and nongenetic factors on developmental brain trajectories may have implications for better understanding brain-based disorders and typical cognitive development.
纵向儿科神经影像学研究表明,在儿童期和青少年期,白质体积不断增加,灰质体积呈现区域特异性的倒U形发育轨迹。对这一发育时期的单卵双胞胎和双卵双胞胎进行研究,有助于探究遗传和非遗传因素对这些发育轨迹的影响。
对90对单卵双胞胎、38对同性双卵双胞胎以及158名发育正常的非亲属儿童进行脑部磁共振成像扫描。采用结构方程模型,估计加性遗传效应、共同环境效应和独特环境效应,以及年龄与遗传度的交互作用对这些图像中脑容量测量值的影响。
与先前的成人研究一致,除小脑外,几乎所有脑区的加性遗传效应在变异性中占很大比例。观察到显著的年龄与遗传度交互作用,灰质体积的遗传度随年龄增长而降低,而白质体积的遗传度随年龄增长而增加。
了解遗传和非遗传因素对发育中脑轨迹的相对贡献,可能有助于更好地理解基于脑的疾病和典型认知发展。