| Literature DB >> 22612156 |
Eric M McDade1, Bradley F Boeve, Julie A Fields, Neeraj Kumar, Rosa Rademakers, Matt C Baker, Bsc David S Knopman, Ronald C Petersen, Clifford R Jack, Kejal Kantarci.
Abstract
To evaluate the proton magnetic resonance (MR) spectroscopy ((1) H MRS) changes in carriers of a novel octapeptide repeat insertion in the prion protein gene (PRNP) and family history of frontotemporal dementia with ataxia. Four at-risk mutation carriers and 13 controls were compared using single voxel, short TE, (1) H MRS from the posterior cingulate gyrus. The mutation carriers had an increased choline/creatine, P = .003 and increased myoinositol/creatine ratio, P = .003. (1) H MRS identified differences in markers of glial activity and choline metabolism in pre- and early-symptomatic carriers of a novel PRNP gene octapeptide insertion. These findings expand the possible diagnostic utility of (1) H MRS in familial prion disorders.Entities:
Keywords: MRI; MRS; familial prion disorders; frontotemporal dementia
Mesh:
Substances:
Year: 2012 PMID: 22612156 PMCID: PMC3480551 DOI: 10.1111/j.1552-6569.2012.00717.x
Source DB: PubMed Journal: J Neuroimaging ISSN: 1051-2284 Impact factor: 2.486