Minimal change multiple system atrophy: An aggressive variant?

Minimal change multiple system atrophy: An aggressive variant?
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DOI:
10.1002/mds.26220
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发表时间:
2015-06-01
期刊:
影响因子:
8.6
通讯作者:
Holton, Janice L.
Holton, Janice L.
中科院分区:
医学1区
文献类型:
--
作者:
Ling, Helen;Asi, Yasmine T.;Holton, Janice L.

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研究背景含有β-synuclein的胶质细胞包涵体是多系统萎缩(MSA)的病理标志.最小改变(MC-MSA)是一种罕见的MSA亚型,其神经元丢失主要局限于黑质和蓝斑。方法对6例MC-MSA和8例MSA对照组进行脑区免疫组化和半定量评估。结果MC-MSA组尾状核和黑质内神经元胞浆包涵体比MSA对照组多(P=0.002),在任何区域的胶质细胞胞质包涵体负载没有任何统计学差异。在两组中,在延髓腹外侧(P=1.0)和中缝隐核(P=0.4)中发现了严重的胶质细胞胞质内含物负荷。与MSA对照组相比,3例死于意外猝死的MC-MSA病例的发病年龄较早(平均年龄:38岁vs. 57.6岁,P=0.02),疾病持续时间在数值上较短(意思是:5.3 vs. 8年,P=0.2)和更快的临床进展,大多数临床里程碑在发病后3年内达到,说明是MSA的攻击性变种另外3例MC-MSA患者死于无关的并发症,发病年龄(平均:57.7岁)和时间进程与对照组相似,内侧和背外侧黑质亚区神经元丢失和胶质增生较轻(P
BackgroundGlial cytoplasmic inclusions containing -synuclein are the pathological hallmark of multiple system atrophy (MSA). Minimal change (MC-MSA) is an unusual MSA subtype with neuronal loss largely restricted to the substantia nigra and locus coeruleus.MethodsImmunohistochemistry on selected brain regions and semiquantitative assessment were performed on six MC-MSA and eight MSA control cases.ResultsMore neuronal cytoplasmic inclusions were seen in the caudate and substantia nigra in MC-MSA than in MSA controls (P=0.002), without any statistical difference in glial cytoplasmic inclusion load in any region. Severe glial cytoplasmic inclusion load was found in the ventrolateral medulla (P=1.0) and nucleus raphe obscurus (P=0.4) in both groups. When compared with MSA controls, the three MC-MSA cases who had died of sudden unexpected death had an earlier age of onset (mean: 38 vs. 57.6 y, P=0.02), a numerically shorter disease duration (mean: 5.3 vs. 8 y, P=0.2) and a more rapid clinical progression with most of the clinical milestones reached within 3 y of presentation, suggesting an aggressive variant of MSA. Another three MC-MSA cases, who had died of unrelated concurrent diseases, had an age of onset (mean: 57.7 y) and temporal course similar to controls, had less severe neuronal loss and gliosis in the medial and dorsolateral substantia nigra subregions (P