Funding agencies: This study was supported by grants K23NS060949 (to J.G.G.) and P01AG09466 (to L.deT-M.) from the National Institutes of Health and from the Parkinson's Disease Foundation.
Article first published online: 12 MAR 2012
Copyright © 2012 Movement Disorder Society
Volume 27, Issue 6, pages 727–734, May 2012
How to Cite
Goldman, J. G., Stebbins, G. T., Bernard, B., Stoub, T. R., Goetz, C. G. and deToledo-Morrell, L. (2012), Entorhinal cortex atrophy differentiates Parkinson's disease patients with and without dementia. Mov. Disord., 27: 727–734. doi: 10.1002/mds.24938
Relevant conflicts of interest/financial disclosures: J.G.G. has received grant/research support from the National Institutes of Health (NIH) (K23NS060949) and the Parkinson's Disease Foundation. L.deT-M. has received grant/research support from the NIH (P01AG09466, T32AG00269, and U01AG024904).
Full financial disclosures and author roles may be found in the online version of this article.
- Issue published online: 30 MAY 2012
- Article first published online: 12 MAR 2012
- Manuscript Accepted: 6 JAN 2012
- Manuscript Revised: 23 DEC 2011
- Manuscript Received: 16 SEP 2011
- Parkinson's disease;
- magnetic resonance imaging;
- mesial temporal lobe;
- Alzheimer's disease
Volumetric measures of mesial temporal lobe structures on MRI scans recently have been explored as potential biomarkers of dementia in patients with PD, with investigations primarily focused on hippocampal volume. Both in vivo MRI and postmortem tissue studies in Alzheimer's disease, however, demonstrate that the entorhinal cortex (ERC) is involved earlier in disease-related pathology than the hippocampus. The ERC, a region integral in declarative memory function, projects multimodal sensory information to the hippocampus through the perforant path. In PD, ERC atrophy, as measured on MRI, however, has received less attention, compared to hippocampal atrophy. We compared ERC and hippocampal atrophy in 12 subjects with PD dementia including memory impairment, 14 PD subjects with normal cognition, and 14 healthy controls with normal cognition using manual segmentation methods on MRI scans. Though hippocampal volumes were similar in the two PD cognitive groups, ERC volumes were substantially smaller in the demented PD subjects, compared to cognitively normal PD subjects (P < 0.05). In addition, normalized ERC and hippocampal volumes for right and left hemispheres were significantly lower in the demented PD group, compared to healthy controls. Our findings suggest that ERC atrophy differentiates demented and cognitively normal PD subjects, in contrast to hippocampal atrophy. Thus, ERC atrophy on MRI may be a potential biomarker for dementia in PD, particularly in the setting of memory impairment. © 2012 Movement Disorder Society