Quantifying iron deposition in the cerebellar subtype of multiple system atrophy and spinocerebellar ataxia type 6 by quantitative susceptibility mapping

齿状核 壳核 定量磁化率图 苍白球 红核 脊髓小脑共济失调 黑质 萎缩 病理 小脑 小脑共济失调 尾状核 医学 化学 共济失调 神经科学 核心 内科学 基底神经节 心理学 帕金森病 磁共振成像 中枢神经系统 疾病 放射科
作者
Atsuhiko Sugiyama,Noriko Sato,Yukio Kimura,Hiroyuki Fujii,Norihide Maikusa,Yoko Shigemoto,Fumio Suzuki,Emiko Morimoto,Kyosuke Koide,Yuji Takahashi,Hiroshi Matsuda,Satoshi Kuwabara
出处
期刊:Journal of the Neurological Sciences [Elsevier BV]
卷期号:407: 116525-116525 被引量:23
标识
DOI:10.1016/j.jns.2019.116525
摘要

We used quantitative susceptibility mapping (QSM) to assess the brain iron deposition in 28 patients with the cerebellar subtype of multiple system atrophy (MSA-C), nine patients with spinocerebellar ataxia type 6 (SCA6), and 23 healthy controls. Two reviewers independently measured the mean QSM values in brain structures including the putamen, globus pallidus, caudate nucleus, red nucleus, substantia nigra, and cerebellar dentate nucleus. A receiver operating characteristics (ROC) analysis was performed to assess the diagnostic usefulness of the QSM measurements. The QSM values in the substantia nigra were significantly higher in the MSA-C group compared to the HC group (p = .007). The QSM values in the cerebellar dentate nucleus were significantly higher in MSA-C than those in the SCA6 and HC groups (p < .001), and significantly lower in the SCA6 patients compared to the HCs (p = .027). The QSM values in the cerebellar dentate nucleus were correlated with disease duration in MSA-C, but inversely correlated with disease duration in SCA6. In the ROC analysis, the QSM values in the cerebellar dentate nucleus showed excellent accuracy for differentiating MSA-C from SCA6 (area under curve [AUC], 0.925), and good accuracy for differentiating MSA-C from healthy controls (AUC 0.834). QSM can identify increased susceptibility of the substantia nigra and cerebellar dentate nucleus in MSA-C patients. These results suggest that an increase in iron accumulation in the cerebellar dentate nucleus may be secondary to the neurodegeneration associated with MSA-C.

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