Infratentorial hypoperfusion in multiple sclerosis

Q4 Immunology and Microbiology
Masakazu Nakamura, Akihiro Murata, Akihiko Ogata
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Abstract

Objectives

Long-term disability in patients with multiple sclerosis (MS) results from axonal degeneration in the central nervous system, which might follow hypoperfusion in neurodegenerative diseases. This study aimed to clarify the distribution and clinical significance of brain hypoperfusion in patients with MS.

Methods

We measured brain hypoperfusion in eight patients with relapsing–remitting MS using N-isopropyl-p-iodine-123-iodoamphetamine single-photon emission computed tomography with three-dimensional stereotactic surface projection and stereotactic extraction estimation; moreover, we examined its clinical relevance.

Results

We detected marked hypoperfusion in the brainstem and cerebellum relative to that in the cerebrum. Each infratentorial segment, the midbrain, pons, and cerebellar anterior and posterior lobes, showed more severe hypoperfusion than the frontal and parietal lobes (n = 8). This was attributed mainly to oligoclonal band (OCB)-negative patients (n = 3), even when OCB-positive patients (n = 5) showed a similar trend. Consistently, OCB-negative patients had lower blood flow at the pons, and cerebellar anterior and posterior lobes than OCB-positive patients; however, both groups showed comparable hypoperfusion in the cerebral lobes. Hypoperfusion at the posterior cerebellar lobe and pons was correlated with poor performance in the Trail Making Test Part B (n = 6), indicating cognitive cerebellar dysfunction and cerebrocerebellar conductive disturbances.

Conclusions

Patients with relapsing–remitting MS had lower infratentorial perfusion, which strongly links to OCB-negativity. The distribution of brain hypoperfusion detected by N-isopropyl-p-iodine-123-iodoamphetamine single-photon emission computed tomography indicated pathological heterogeneity in relapsing–remitting MS. The infratentorial hypoperfusion is possibly associated with neurodegeneration.

多发性硬化症的幕下灌注不足
目的多发性硬化症(MS)患者的长期残疾是由中枢神经系统轴突变性引起的,这可能是神经退行性疾病的灌注不足所致。方法采用n -异丙基-对碘-123-碘安非他明单光子发射计算机断层扫描,三维立体定向表面投影和立体定向提取估计,测量8例复发缓解型多发性硬化症患者的脑灌注不足;此外,我们检查了其临床相关性。结果脑干和小脑相对于大脑明显灌注不足。每个幕下节段,中脑、脑桥和小脑前后叶的灌注不足比额叶和顶叶更严重(n = 8)。这主要归因于寡克隆带(OCB)阴性患者(n = 3),即使OCB阳性患者(n = 5)也表现出类似的趋势。与ocb阳性患者相比,ocb阴性患者脑桥、小脑前叶和后叶的血流量更低;然而,两组均表现出相当程度的脑叶灌注不足。小脑后叶和脑桥灌注不足与Trail Making Test Part B (n = 6)表现不佳相关,提示小脑认知功能障碍和脑小脑传导障碍。结论复发缓解型MS患者幕下灌注较低,与ocb阴性密切相关。n -异丙基-对碘-123-碘安非他明单光子发射计算机断层扫描检测脑灌注不足的分布显示复发缓解型ms的病理异质性,幕下灌注不足可能与神经退行性变有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical and Experimental Neuroimmunology
Clinical and Experimental Neuroimmunology Immunology and Microbiology-Immunology and Microbiology (miscellaneous)
CiteScore
1.60
自引率
0.00%
发文量
52
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