Format

Send to

Choose Destination
See comment in PubMed Commons below
Magn Reson Imaging. 2014 Dec;32(10):1330-4. doi: 10.1016/j.mri.2014.08.022. Epub 2014 Aug 28.

Spin labeling artery method perfusion MRI study of SPG4 and SCA3/MJD.

Author information

1
Department of Radiology, Xiangya Hospital, Central South University, Changsha, China.
2
Department of Radiology, Xiangya Hospital, Central South University, Changsha, China. Electronic address: doctorxing@sina.com.
3
Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.

Abstract

BACKGROUND:

Spinocerebellar ataxia type 3 (SCA3) and Machado-Joseph disease (MJD) are similar diseases that are often referred to jointly as SCA3/MJD. As the most common autosomal-dominantly inherited subtype of hereditary spastic paraplegia (HSP), HSP4 (or SPG4) has overlapping symptoms with SCA3/MJD, which hinders their diagnoses. Arterial spin labeling (ASL) is a noninvasive, contrast-agent free, magnetic resonance perfusion imaging method used to obtain maps of the cerebral blood flow (CBF). Here, we investigated the diagnostic value of ASL in SCA3/MJD and SPG4 patients.

METHODS:

A total of 13 SPG4 cases, 38 SCA3/MJD cases (22 onset patients and 16 genetic abnormality-only patients), and 27 healthy volunteers were examined by ASL. Data were processed to obtain the regional CBF (rCBF) and comparatively studied.

RESULTS:

In the pons, cerebellar dentate nucleus, and cerebellar cortex, rCBF of the onset SCA3/MJD group was significantly lower than that of the normal control group. In the cerebellar dentate nucleus and cerebellar cortex, the rCBF of the non-onset SCA3/MJD group was significantly lower than that of the control group. In the pons and cerebellar cortex, the rCBF of the onset SCA3/MJD group was significantly lower than that of the SPG4 group.

CONCLUSIONS:

SCA3/MJD lesions are mainly located in the cerebellum and brainstem. Gray matter and white matter were both involved, although the deep cerebellar nuclei may be the earliest involved region. Cerebellar and brainstem lesions of SCA3/MJD were more severe than those of SPG4. ASL can aid the diagnosis of SCA3/MJD and SPG4.

KEYWORDS:

Arterial spin labeling; Hereditary spastic paraplegia 4; Machado–Joseph disease; Spinocerebellar ataxia type 3

PMID:
25172988
DOI:
10.1016/j.mri.2014.08.022
[Indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments

    Supplemental Content

    Full text links

    Icon for Elsevier Science
    Loading ...
    Support Center