Arani Arvin, Murphy Matthew C, Glaser Kevin J, Manduca Armando, Lake David S, Kruse Scott A, Jack Clifford R, Ehman Richard L, Huston John
Department of Radiology, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.
Department of Radiology, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.
Neuroimage. 2015 May 1;111:59-64. doi: 10.1016/j.neuroimage.2015.02.016. Epub 2015 Feb 17.
Changes in tissue composition and cellular architecture have been associated with neurological disease, and these in turn can affect biomechanical properties. Natural biological factors such as aging and an individual's sex also affect underlying tissue biomechanics in different brain regions. Understanding the normal changes is necessary before determining the efficacy of stiffness imaging for neurological disease diagnosis and therapy monitoring. The objective of this study was to evaluate global and regional changes in brain stiffness as a function of age and sex, using improved MRE acquisition and processing that have been shown to provide median stiffness values that are typically reproducible to within 1% in global measurements and within 2% for regional measurements. Furthermore, this is the first study to report the effects of age and sex over the entire cerebrum volume and over the full frontal, occipital, parietal, temporal, deep gray matter/white matter (insula, deep gray nuclei and white matter tracts), and cerebellum volumes. In 45 volunteers, we observed a significant linear correlation between age and brain stiffness in the cerebrum (P<.0001), frontal lobes (P<.0001), occipital lobes (P=.0005), parietal lobes (P=.0002), and the temporal lobes (P<.0001) of the brain. No significant linear correlation between brain stiffness and age was observed in the cerebellum (P=.74), and the sensory-motor regions (P=.32) of the brain, and a weak linear trend was observed in the deep gray matter/white matter (P=.075). A multiple linear regression model predicted an annual decline of 0.011 ± 0.002 kPa in cerebrum stiffness with a theoretical median age value (76 years old) of 2.56 ± 0.08 kPa. Sexual dimorphism was observed in the temporal (P=.03) and occipital (P=.001) lobes of the brain, but no significant difference was observed in any of the other brain regions (P>.20 for all other regions). The model predicted female occipital and temporal lobes to be 0.23 kPa and 0.09 kPa stiffer than males of the same age, respectively. This study confirms that as the brain ages, there is softening; however, the changes are dependent on region. In addition, stiffness effects due to sex exist in the occipital and temporal lobes.
组织成分和细胞结构的变化与神经疾病相关,而这些变化反过来又会影响生物力学特性。诸如衰老和个体性别等自然生物因素也会影响不同脑区潜在的组织生物力学。在确定硬度成像对神经疾病诊断和治疗监测的有效性之前,了解正常变化是必要的。本研究的目的是利用改进的磁共振弹性成像(MRE)采集和处理方法,评估脑硬度随年龄和性别的全局和区域变化,该方法已被证明能提供中位数硬度值,在全局测量中通常可重复性在1%以内,区域测量中在2%以内。此外,这是第一项报告年龄和性别对整个大脑体积以及额叶、枕叶、顶叶、颞叶、深部灰质/白质(岛叶、深部灰质核团和白质束)和小脑体积影响的研究。在45名志愿者中,我们观察到大脑的大脑半球(P<0.0001)、额叶(P<0.0001)、枕叶(P=0.0005)、顶叶(P=0.0002)和颞叶(P<0.0001)中年龄与脑硬度之间存在显著的线性相关性。在小脑(P=0.74)和大脑的感觉运动区域(P=0.32)中未观察到脑硬度与年龄之间的显著线性相关性,而在深部灰质/白质中观察到较弱的线性趋势(P=0.075)。一个多元线性回归模型预测,大脑半球硬度每年下降0.011±0.002 kPa,理论中位数年龄值(76岁)时为2.56±0.08 kPa。在大脑的颞叶(P=0.03)和枕叶(P=0.001)中观察到性别差异,但在其他任何脑区均未观察到显著差异(所有其他区域P>0.20)。该模型预测,同龄女性的枕叶和颞叶硬度分别比男性高0.23 kPa和0.09 kPa。本研究证实,随着大脑衰老,会出现软化;然而,这些变化因区域而异。此外,枕叶和颞叶存在性别导致的硬度差异。