Linked Life Data

17360763

Source:http://linkedlifedata.com/resource/pubmed/id/17360763

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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
Pt 5
pubmed:dateCreated
2007-5-2
pubmed:abstractText
Frontotemporal dementia is accompanied by motor neuron disease (FTD + MND) in approximately 10% of cases. There is accumulating evidence for a clinicopathological overlap between FTD and MND based on observations of familial aggregation and neuropathological findings of ubiquitin-positive neuronal cytoplasmatic inclusions (NCI) in lower motor neurons, hippocampus and neocortex in both conditions. Several familial forms exist with different genetic loci and defects. We investigated the familial aggregation and clinical presentation of FTD + MND cases in a large cohort of 368 FTD patients in The Netherlands. Immunohistochemistry of available brain tissue of deceased patients was investigated using a panel of antibodies including ubiquitin, p62 and TAR DNA-binding protein of 43 kDa antibodies. A total of eight patients coming from six families had a family history positive for FTD + MND (mean age at onset 53.2 +/- 8.4 years). Five patients presented with behavioural changes and cognitive changes followed by motor neuron disease, whereas symptoms of motor neuron disease were the presenting features in the remaining three patients. Other affected relatives in these families showed dementia/FTD, MND or FTD + MND reflecting the clinical interfamilial variation. No mutations were identified in any of the candidate genes, including Superoxide Dismutase 1, dynactin, angiogenin, Microtubule-Associated Protein Tau, valosin-containing protein and progranulin. Available brain tissue of five patients with familial FTD + MND showed NCI in hippocampus, neocortex and spinal cord in all, and neuronal intranuclear inclusions (NII) in two brains. TDP-43 antibody showed robust staining of neuronal inclusions similar in distribution and morphology to NCI and NII. Additionally, TDP-43 antibody also stained ubiquitin-negative glial inclusions in the basal striatum of one case. In conclusion, there exists considerable clinical variation within families with FTD + MND, which may be determined by other genetic or environmental factors. NII are also found in some cases of familial FTD + MND without Progranulin mutations. The observation of glial TDP-43 positive inclusions in one brain is very interesting, although their pathophysiological significance is yet unknown.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1460-2156
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
130
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1375-85
pubmed:dateRevised
2011-10-18
pubmed:meshHeading
pubmed-meshheading:17360763-Adult, pubmed-meshheading:17360763-Brain Chemistry, pubmed-meshheading:17360763-Cohort Studies, pubmed-meshheading:17360763-DNA-Binding Proteins, pubmed-meshheading:17360763-Female, pubmed-meshheading:17360763-Genotype, pubmed-meshheading:17360763-Hippocampus, pubmed-meshheading:17360763-Humans, pubmed-meshheading:17360763-Immunohistochemistry, pubmed-meshheading:17360763-Intercellular Signaling Peptides and Proteins, pubmed-meshheading:17360763-Male, pubmed-meshheading:17360763-Middle Aged, pubmed-meshheading:17360763-Motor Neuron Disease, pubmed-meshheading:17360763-Motor Neurons, pubmed-meshheading:17360763-Mutation, pubmed-meshheading:17360763-Neocortex, pubmed-meshheading:17360763-Pedigree, pubmed-meshheading:17360763-Pick Disease of the Brain, pubmed-meshheading:17360763-RNA-Binding Proteins, pubmed-meshheading:17360763-Ubiquitin
pubmed:year
2007
pubmed:articleTitle
TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutations.
pubmed:affiliation
Department of Neurology, Erasmus University Medical Centre, Rotterdam, The Netherlands.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't