Longitudinal MRI study of multiple system atrophy - when do the findings appear, and what is the course?

被引:96
作者
Horimoto, Y [1 ]
Aiba, I
Yasuda, T
Ohkawa, Y
Katayama, T
Yokokawa, Y
Goto, A
Ito, Y
机构
[1] Fukushimura Hosp, Choju Med Inst, Toyohashi, Aichi 4418124, Japan
[2] Higashi Nagoya Natl Hosp, Dept Neurol, Nagoya, Aichi 4658620, Japan
[3] Nagoya City Univ, Sch Med, Dept Internal Med 2, Nagoya, Aichi 4678601, Japan
关键词
multiple system atrophy; magnetic resonance imaging (MRI); pontine "cross sign;
D O I
10.1007/s00415-002-0734-0
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Several investigators have revealed features of multiple system atrophy (MSA) by magnetic resonance imaging (MRI). For use in clinical diagnosis, we determined the exact time when two main features of Pontine and putaminal intensity changes appeared. Furthermore, in order to reveal the course from when the disorder first appeared and how it spread, we also investigated the course of MRI findings and differences between clinical subtypes. The cranial MRI of 42 patients with MSA were longitudinally studied including comments on the so called "cross sign" of Pontine T2 high intensity, which was divided into 6 stages, and also on the linear T2 high intensity of the dorsolateral side of the putamen ("putaminal slit") which was divided into 4 stages. Patients were classified as 16 MSA-C, 7 autonomic dominant type (MSA-A), and 19 MSA-P. The age at onset ranged from 41 to 74 years (mean, 55 9). The duration of the disease in the MRI study ranged from 1 to 24 years. The Pontine "cross sign" was completed (shows Cross, stage IV) earlier in MSA-C mainly before 5 years, later in MSA-P and even much later in MSA-A. Regarding the "putaminal slit", MSA-P shows earlier bilateral changes (stage 11), mostly before 3 years, compared with MSA-C, which requires 4 years to reveal even a unilateral change (stage I), or MSA-A which requires even more time. MRI findings showed a tendency to relate to clinical findings, since MSA-C exhibits "cross signs" completion earlier than bilateral "putaminal slit"; however, MSA-P shows bilateral "putaminal slit" earlier than "cross sign", and MSA-A requires much more time to show both. Clinically, MSA-C, MSA-A, or MSA-P showed different M RI courses so that three subtypes could be defined also with MRI findings. Therefore these observations are useful not only for diagnosis of MSA itself, but also to distinguish clinical subtypes (MSA-C, MSA-A, or MSA-P) which have different rates of lesion progression.
引用
收藏
页码:847 / 854
页数:8
相关论文
共 50 条
  • [21] MRI of progressive supranuclear palsy, corticobasal degeneration and multiple system atrophy
    Arai, Kimihito
    JOURNAL OF NEUROLOGY, 2006, 253 (Suppl 3) : 25 - 29
  • [22] MRI of progressive supranuclear palsy, corticobasal degeneration and multiple system atrophy
    Kimihito Arai
    Journal of Neurology, 2006, 253 : iii25 - iii29
  • [23] Spatial correlation and segregation of multimodal MRI abnormalities in multiple system atrophy
    Myung Jun Lee
    Tae-Hyung Kim
    Chi-Woong Mun
    Hae Kyung Shin
    Jongsang Son
    Jae-Hyeok Lee
    Journal of Neurology, 2018, 265 : 1540 - 1547
  • [24] Spatial correlation and segregation of multimodal MRI abnormalities in multiple system atrophy
    Lee, Myung Jun
    Kim, Tae-Hyung
    Mun, Chi-Woong
    Shin, Hae Kyung
    Son, Jongsang
    Lee, Jae-Hyeok
    JOURNAL OF NEUROLOGY, 2018, 265 (07) : 1540 - 1547
  • [25] Longitudinal evolution of sleep disturbances in early multiple system atrophy: a 2‐year prospective cohort study
    Lingyu Zhang
    Yanbing Hou
    Chunyu Li
    Qianqian Wei
    Ruwei Ou
    Kuncheng Liu
    Junyu Lin
    Tianmi Yang
    Yi Xiao
    Qirui Jiang
    Bi Zhao
    Huifang Shang
    BMC Medicine, 21
  • [26] Neurofilament light chain in spinal fluid and plasma in multiple system atrophy: a prospective, longitudinal biomarker study
    Singer, Wolfgang
    Schmeichel, Ann M.
    Sletten, David M.
    Gehrking, Tonette L.
    Gehrking, Jade A.
    Trejo-Lopez, Jorge
    Suarez, Mariana D.
    Anderson, Jennifer K.
    Bass, Pamela H.
    Lesnick, Timothy G.
    Low, Phillip A.
    CLINICAL AUTONOMIC RESEARCH, 2023, 33 (06) : 635 - 645
  • [27] Neurofilament light chain in spinal fluid and plasma in multiple system atrophy: a prospective, longitudinal biomarker study
    Wolfgang Singer
    Ann M. Schmeichel
    David M. Sletten
    Tonette L. Gehrking
    Jade A. Gehrking
    Jorge Trejo-Lopez
    Mariana D. Suarez
    Jennifer K. Anderson
    Pamela H. Bass
    Timothy G. Lesnick
    Phillip A. Low
    Clinical Autonomic Research, 2023, 33 : 635 - 645
  • [28] Progression of Striatal and Extrastriatal Degeneration in Multiple System Atrophy: A Longitudinal Diffusion-Weighted MR Study
    Pellecchia, Maria Teresa
    Barone, Paolo
    Vicidomini, Caterina
    Mollica, Carmine
    Salvatore, Elena
    Ianniciello, Marta
    Liuzzi, Raffaele
    Longo, Katia
    Picillo, Marina
    De Michele, Giuseppe
    Filla, Alessandro
    Brunetti, Arturo
    Salvatore, Marco
    Pappata, Sabina
    MOVEMENT DISORDERS, 2011, 26 (07) : 1303 - 1309
  • [29] Longitudinal study on MRI intensity changes of Machado-Joseph disease: correlation between MRI findings and neuropathological changes
    Horimoto, Yoshihiko
    Matsumoto, Mitsuhiro
    Akatsu, Hiroyasu
    Kojima, Akihiro
    Yoshida, Mari
    Nokura, Kazuya
    Yuasa, Hiroyuki
    Katada, Eiichi
    Yamamoto, Takayuki
    Kosaka, Kenji
    Hashizume, Yoshio
    Yamamoto, Hiroko
    Mitake, Shigehisa
    JOURNAL OF NEUROLOGY, 2011, 258 (09) : 1657 - 1664
  • [30] Delineating the sites and progression of in vivo atrophy in multiple system atrophy using fluid-registered MRI
    Schott, JM
    Simon, JE
    Fox, NC
    King, AP
    Khan, MN
    Cipolotti, L
    Paviour, DC
    Stevens, JM
    Rossor, MN
    MOVEMENT DISORDERS, 2003, 18 (08) : 955 - 958