Worker Amanda, Blain Camilla, Jarosz Jozef, Chaudhuri K Ray, Barker Gareth J, Williams Steven C R, Brown Richard, Leigh P Nigel, Simmons Andrew
King's College London, Institute of Psychiatry, London, United Kingdom; National Institute for Health Research Biomedical Research Centre for Mental Health at South London and Maudsley NHS Foundation Trust and Institute of Psychiatry, King's College London, London, United Kingdom; National Institute for Health Research Biomedical Research Unit for Dementia at South London and Maudsley NHS Foundation Trust and Institute of Psychiatry, King's College London, London, United Kingdom.
King's College London, Institute of Psychiatry, London, United Kingdom; King's College Hospital, London, United Kingdom.
PLoS One. 2014 Dec 2;9(12):e114167. doi: 10.1371/journal.pone.0114167. eCollection 2014.
Parkinson's disease (PD), Multiple System Atrophy (MSA) and Progressive Supranuclear Palsy (PSP) are neurodegenerative diseases that can be difficult to distinguish clinically. The objective of the current study was to use surface-based analysis techniques to assess cortical thickness, surface area and grey matter volume to identify unique morphological patterns of cortical atrophy in PD, MSA and PSP and to relate these patterns of change to disease duration and clinical features.
High resolution 3D T1-weighted MRI volumes were acquired from 14 PD patients, 18 MSA, 14 PSP and 19 healthy control participants. Cortical thickness, surface area and volume analyses were carried out using the automated surface-based analysis package FreeSurfer (version 5.1.0). Measures of disease severity and duration were assessed for correlation with cortical morphometric changes in each clinical group.
Results show that in PSP, widespread cortical thinning and volume loss occurs within the frontal lobe, particularly the superior frontal gyrus. In addition, PSP patients also displayed increased surface area in the pericalcarine. In comparison, PD and MSA did not display significant changes in cortical morphology.
These results demonstrate that patients with clinically established PSP exhibit distinct patterns of cortical atrophy, particularly affecting the frontal lobe. These results could be used in the future to develop a useful clinical application of MRI to distinguish PSP patients from PD and MSA patients.
帕金森病(PD)、多系统萎缩(MSA)和进行性核上性麻痹(PSP)是临床上难以区分的神经退行性疾病。本研究的目的是使用基于表面的分析技术来评估皮质厚度、表面积和灰质体积,以识别PD、MSA和PSP中皮质萎缩的独特形态学模式,并将这些变化模式与疾病持续时间和临床特征相关联。
从14名PD患者、18名MSA患者、14名PSP患者和19名健康对照参与者中获取高分辨率3D T1加权MRI图像。使用基于表面的自动分析软件包FreeSurfer(版本5.1.0)进行皮质厚度、表面积和体积分析。评估疾病严重程度和持续时间的指标,以与每个临床组的皮质形态学变化进行相关性分析。
结果显示,在PSP患者中,额叶,特别是额上回出现广泛的皮质变薄和体积减少。此外,PSP患者在距状周围的表面积也增加。相比之下,PD和MSA患者的皮质形态没有显著变化。
这些结果表明,临床确诊的PSP患者表现出独特的皮质萎缩模式,尤其影响额叶。这些结果未来可用于开发一种有用的MRI临床应用,以区分PSP患者与PD和MSA患者。