Phillips Owen R, Joshi Shantanu H, Piras Fabrizio, Orfei Maria Donata, Iorio Mariangela, Narr Katherine L, Shattuck David W, Caltagirone Carlo, Spalletta Gianfranco, Di Paola Margherita
Morphology and Morphometry for NeuroImaging Lab, Clinical and Behavioural Neurology Dept. IRCCS Santa Lucia Foundation, Rome, Italy.
Neuroscience Dept. University of Rome, "Tor Vergata", Italy.
Hum Brain Mapp. 2016 Apr;37(4):1321-34. doi: 10.1002/hbm.23105. Epub 2016 Jan 23.
White matter abnormalities have been shown in the large deep fibers of Alzheimer's disease patients. However, the late myelinating superficial white matter comprised of intracortical myelin and short-range association fibers has not received much attention. To investigate this area, we extracted a surface corresponding to the superficial white matter beneath the cortex and then applied a cortical pattern-matching approach which allowed us to register and subsequently sample diffusivity along thousands of points at the interface between the gray matter and white matter in 44 patients with Alzheimer's disease (Age: 71.02 ± 5.84, 16M/28F) and 47 healthy controls (Age 69.23 ± 4.45, 19M/28F). In patients we found an overall increase in the axial and radial diffusivity across most of the superficial white matter (P < 0.001) with increases in diffusivity of more than 20% in the bilateral parahippocampal regions and the temporal and frontal lobes. Furthermore, diffusivity correlated with the cognitive deficits measured by the Mini-Mental State Examination scores (P < 0.001). The superficial white matter has a unique microstructure and is critical for the integration of multimodal information during brain maturation and aging. Here we show that there are major abnormalities in patients and the deterioration of these fibers relates to clinical symptoms in Alzheimer's disease.
阿尔茨海默病患者的大脑深部大纤维已被证实存在白质异常。然而,由皮质内髓鞘和短程联合纤维组成的晚期髓鞘形成的浅表白质却未受到太多关注。为了研究这一区域,我们提取了与皮质下浅表白质相对应的表面,然后应用了一种皮质模式匹配方法,该方法使我们能够在44例阿尔茨海默病患者(年龄:71.02±5.84,16名男性/28名女性)和47名健康对照者(年龄69.23±4.45,19名男性/28名女性)的灰质与白质界面处沿着数千个点记录并随后采样扩散率。在患者中,我们发现大部分浅表白质的轴向和径向扩散率总体增加(P<0.001),双侧海马旁区域以及颞叶和额叶的扩散率增加超过20%。此外,扩散率与简易精神状态检查评分所测量的认知缺陷相关(P<0.001)。浅表白质具有独特的微观结构,在大脑成熟和衰老过程中对多模态信息的整合至关重要。在这里,我们表明患者存在主要异常,并且这些纤维的退化与阿尔茨海默病的临床症状有关。