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快速高分辨率 T1 映射作为大脑发育的标志物:关键感兴趣区域的正常范围。

Rapid high resolution T1 mapping as a marker of brain development: Normative ranges in key regions of interest.

机构信息

Department of Diagnostic and Interventional Radiology, University of Lausanne and Lausanne University Hospital (UNIL-CHUV), Lausanne, Vaud, Switzerland.

出版信息

PLoS One. 2018 Jun 14;13(6):e0198250. doi: 10.1371/journal.pone.0198250. eCollection 2018.

Abstract

OBJECTIVES

We studied in a clinical setting the age dependent T1 relaxation time as a marker of normal late brain maturation and compared it to conventional techniques, namely the apparent diffusion coefficient (ADC).

MATERIALS AND METHODS

Forty-two healthy subjects ranging from ages 1 year to 20 years were included in our study. T1 brain maps in which the intensity of each pixel corresponded to T1 relaxation times were generated based on MR imaging data acquired using a MP2RAGE sequence. During the same session, diffusion tensor imaging data was collected. T1 relaxation times and ADC in white matter and grey matter were measured in seven clinically relevant regions of interest and were correlated to subjects' age.

RESULTS

In the basal ganglia, there was a small, yet significant, decrease in T1 relaxation time (-0.45 ≤R≤-0.59, p<10-2) and ADC (-0.60≤R≤-0.65, p<10-4) as a function of age. In the frontal and parietal white matter, there was a significant decrease in T1 relaxation time (-0.62≤R≤-0.68, p<10-4) and ADC (-0.81≤R≤-0.85, p<10-4) as a function of age. T1 relaxation time changes in the corpus callosum and internal capsule were less relevant for this age range. There was no significant difference between the correlation of T1 relaxation time and ADC with respect to age (p-value = 0.39). The correlation between T1 relaxation and ADC is strong in the white matter but only moderate in basal ganglia over this age period.

CONCLUSIONS

T1 relaxation time is a marker of brain maturation or myelination during late brain development. Between the age of 1 and 20 years, T1 relaxation time decreases as a function of age in the white matter and basal ganglia. The greatest changes occur in frontal and parietal white matter. These regions are known to mature in the final stage of development and are mainly composed of association circuits. Age-correlation is not significantly different between T1 relaxation time and ADC. Therefore, T1 relaxation time does not appear to be a superior marker of brain maturation than ADC but may be considered as complementary owing the intrinsic differences in bio-physical sensitivity. This work may serve as normative ranges in clinical imaging routines.

摘要

目的

我们在临床环境中研究 T1 弛豫时间作为正常晚期脑成熟的标志物,并将其与常规技术(即表观扩散系数 ADC)进行比较。

材料和方法

本研究纳入了 42 名年龄在 1 至 20 岁的健康受试者。根据使用 MP2RAGE 序列获得的磁共振成像数据生成了 T1 脑图,其中每个像素的强度对应于 T1 弛豫时间。在同一时段,收集了扩散张量成像数据。在 7 个临床相关的感兴趣区域测量了白质和灰质中的 T1 弛豫时间和 ADC,并与受试者的年龄相关。

结果

在基底节中,T1 弛豫时间(-0.45≤R≤-0.59,p<10-2)和 ADC(-0.60≤R≤-0.65,p<10-4)随着年龄的增长呈小但显著的下降。在额顶白质中,T1 弛豫时间(-0.62≤R≤-0.68,p<10-4)和 ADC(-0.81≤R≤-0.85,p<10-4)随着年龄的增长呈显著下降。对于该年龄范围,胼胝体和内囊的 T1 弛豫时间变化不太相关。T1 弛豫时间与 ADC 随年龄的相关性无显著差异(p 值=0.39)。在该年龄段,T1 弛豫时间与 ADC 之间的相关性在白质中较强,但在基底节中仅为中度。

结论

T1 弛豫时间是晚期脑发育过程中脑成熟或髓鞘形成的标志物。在 1 至 20 岁之间,白质和基底节中的 T1 弛豫时间随年龄的变化而降低。最大的变化发生在额顶白质中。这些区域已知在发育的最后阶段成熟,主要由联络回路组成。T1 弛豫时间与 ADC 的年龄相关性无显著差异。因此,T1 弛豫时间似乎不是比 ADC 更好的脑成熟标志物,但由于其固有生物物理敏感性的差异,可被视为补充标志物。本工作可为临床成像常规提供正常范围。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e88/6002025/250cb464a410/pone.0198250.g001.jpg

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