Literature DB >> 15057518

A quantitative study of the pathological changes in ten patients with multiple system atrophy (MSA).

R A Armstrong1, N J Cairns, P L Lantos.   

Abstract

The densities of the glial cytoplasmic inclusions (GCI), neuronal inclusions (NI), and abnormal neurons were studied in the frontal cortex, hippocampus, cerebellum, basal ganglia and areas of the pons and medulla in 10 cases of multiple system atrophy (MSA). GCI density was greater in the substantia nigra and globus pallidus compared with the frontal cortex and hippocampus. Abnormal neurons were most abundant in the frontal cortex, substantia nigra, and inferior olivary nucleus. NI and abnormal neuron densities were positively correlated in the globus pallidus but negatively correlated in the hippocampus. The NI and GCI were only positively correlated in the pons. GCI in the pons and inferior olivary nucleus, NI in the substantia nigra, and abnormal neurons in the frontal cortex varied significantly between cases. The MSA cases did not cluster according to disease subtype. The data suggest that: 1) the greatest densities of pathological changes occur in the substantia nigra and globus pallidus, 2) density of the GCI is unrelated to that of the NI, and 3) there is overlapping pathology between the various subtypes of MSA.

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Mesh:

Year:  2004        PMID: 15057518     DOI: 10.1007/s00702-003-0105-8

Source DB:  PubMed          Journal:  J Neural Transm (Vienna)        ISSN: 0300-9564            Impact factor:   3.575


  6 in total

1.  Comparative quantitative study of 'signature' pathological lesions in the hippocampus and adjacent gyri of 12 neurodegenerative disorders.

Authors:  Richard A Armstrong; Nigel J Cairns
Journal:  J Neural Transm (Vienna)       Date:  2015-05-01       Impact factor: 3.575

2.  Expanding the spectrum of neuronal pathology in multiple system atrophy.

Authors:  Matthew D Cykowski; Elizabeth A Coon; Suzanne Z Powell; Sarah M Jenkins; Eduardo E Benarroch; Phillip A Low; Ann M Schmeichel; Joseph E Parisi
Journal:  Brain       Date:  2015-05-16       Impact factor: 13.501

3.  Cognitive and neuropsychiatric profile of the synucleinopathies: Parkinson disease, dementia with Lewy bodies, and multiple system atrophy.

Authors:  Aimee W Kao; Caroline A Racine; Lovingly C Quitania; Joel H Kramer; Chadwick W Christine; Bruce L Miller
Journal:  Alzheimer Dis Assoc Disord       Date:  2009 Oct-Dec       Impact factor: 2.703

4.  Chronic exposure to cerebrospinal fluid of multiple system atrophy in neuroblastoma and glioblastoma cells induces cytotoxicity via ER stress and autophagy activation.

Authors:  Xuejing Wang; Mingming Ma; Junfang Teng; Jiewen Zhang; Shuang Zhou; Ying Zhang; Erxi Wu; Xuebing Ding
Journal:  Oncotarget       Date:  2015-05-30

5.  Robust α-synuclein pathology in select brainstem neuronal populations is a potential instigator of multiple system atrophy.

Authors:  Ethan W Hass; Zachary A Sorrentino; Grace M Lloyd; Nikolaus R McFarland; Stefan Prokop; Benoit I Giasson
Journal:  Acta Neuropathol Commun       Date:  2021-05-03       Impact factor: 7.801

Review 6.  Multiple System Atrophy: An Oligodendroglioneural Synucleinopathy1.

Authors:  Kurt A Jellinger
Journal:  J Alzheimers Dis       Date:  2018       Impact factor: 4.472

  6 in total

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