Steen R G, Ogg R J, Reddick W E, Kingsley P B
Department of Diagnostic Imaging, St Jude Children's Research Hospital, University of Tennessee School of Medicine, Memphis 38105-2794, USA.
AJNR Am J Neuroradiol. 1997 May;18(5):819-28.
To determine whether a quantitative MR imaging method to map spin-lattice relaxation time (T1) can be used to characterize maturational changes in the normal human brain.
An inversion-recovery technique was used to map T1 transversely at the level of the basal ganglia in a study population of 19 healthy children (4 to 10 years old) and 31 healthy adolescents (10 to 20 years old), and in a normative population of 20 healthy adults (20 to 30 years old).
Nonparametric analysis of variance showed that T1 decreases with age in the genu, frontal white matter, caudate, putamen, anterior thalamus, pulvinar nucleus, optic radiation, cortical gray matter (all P < .0001), and occipital white matter. There was a significant reduction in T1 between childhood (mean age, 7.1 +/- 1.4) and adolescence (mean age, 13.5 +/- 2.6) in all brain structures, but there was also a significant reduction in T1 between adolescence (mean age, 13.5 +/- 2.6) and adulthood (mean age, 26.5 +/- 3.4) in all brain structures except occipital white matter. Regression shows that T1 declines to within the range (mean +/- 2 SD) of young adult T1 values by about 2 years in the occipital white matter, by about 4 years in the genu, by 11 years in the cortical gray matter, by 11 years in the frontal white matter, and by 13 years in the thalamus.
Brain structures mature at strikingly different rates, yet the ratio of gray matter T1 to white matter T1 does not change significantly with age. Thus, conventional MR imaging methods based on inherent contrast are insensitive to these changes. Age-related changes tend to reach completion sooner in white matter than in gray matter tracts. Such normative data are essential for studies of specific pediatric disorders and may be useful for assessing brain maturation in cases of developmental delay.
确定一种用于绘制自旋晶格弛豫时间(T1)的定量磁共振成像方法是否可用于表征正常人类大脑的成熟变化。
采用反转恢复技术在19名健康儿童(4至10岁)、31名健康青少年(10至20岁)以及20名健康成年人(20至30岁)的正常人群中,于基底神经节水平横向绘制T1图。
非参数方差分析显示,在胼胝体、额叶白质、尾状核、壳核、丘脑前核、枕核、视辐射、皮质灰质(所有P <.0001)和枕叶白质中,T1随年龄增长而降低。在所有脑结构中,儿童期(平均年龄7.1±1.4岁)和青春期(平均年龄13.5±2.6岁)之间T1有显著降低,但除枕叶白质外,在所有脑结构中,青春期(平均年龄13.5±2.6岁)和成年期(平均年龄26.5±3.4岁)之间T1也有显著降低。回归分析表明,枕叶白质中T1下降到年轻成年人T1值范围(平均±2标准差)内约需2年,胼胝体约需4年,皮质灰质约需11年,额叶白质约需11年,丘脑约需13年。
脑结构以显著不同的速率成熟,但灰质T1与白质T1的比值不会随年龄显著变化。因此,基于固有对比度的传统磁共振成像方法对这些变化不敏感。与年龄相关的变化在白质中往往比在灰质束中更早完成。此类正常数据对于特定儿科疾病的研究至关重要,可能有助于评估发育迟缓病例中的脑成熟情况。