Research summary
The work centers on diagnostic frameworks for late-life neurodegenerative dementias. A 2009 consensus paper on mild cognitive impairment (MCI) updated subtype definitions (amnestic vs. non-amnestic, single- vs. multi-domain) and laid out biomarker and longitudinal evidence linking MCI to Alzheimer's and other dementia trajectories [5]. The 1999 study using MRI-based hippocampal volumetry showed that smaller hippocampal volumes in older adults with MCI predicted future conversion to Alzheimer's disease, helping anchor structural imaging in early diagnosis [6]. A 2009 imaging study used serial 11C-Pittsburgh-compound-B PET together with serial MRI in normal aging, MCI, and Alzheimer's to dissociate the temporal order of amyloid accumulation from downstream neurodegeneration, supporting the now-standard sequence model of Alzheimer biomarker change [7]. In dementia with Lewy bodies (DLB), the 2005 DLB Consortium criteria revision elevated REM-sleep behavior disorder, severe neuroleptic sensitivity, and reduced striatal dopamine transporter binding to clinical features that improve diagnostic specificity [3], and a 2017 update added MIBG myocardial scintigraphy and refined the weighting of supportive features, modifying pathology criteria to incorporate Alzheimer co-pathology [4]. In frontotemporal dementia, the 2011 international revised criteria for the behavioral variant (bvFTD) showed improved sensitivity over the 1998 criteria when retrospectively applied to autopsy-confirmed cases, with a tiered "possible / probable / definite" structure [1]. The 2011 classification of primary progressive aphasia and its three variants (nonfluent/agrammatic, semantic, logopenic) standardized clinical鈥搉euroimaging definitions and improved comparability across research cohorts [2]. Together the works define the diagnostic infrastructure that distinguishes Alzheimer's, DLB, and frontotemporal syndromes during life, using a combination of clinical criteria, structural MRI, and molecular imaging.
Recent publications
- Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementiaDOI
- Classification of primary progressive aphasia and its variantsDOI
- Diagnosis and management of dementia with Lewy bodiesDOI
- Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALSDOI
- Diagnosis and management of dementia with Lewy bodiesDOI
- Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17DOI
- Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's diseaseDOI
- Mild Cognitive ImpairmentDOI
- Prediction of AD with MRI-based hippocampal volume in mild cognitive impairmentDOI
- Serial PIB and MRI in normal, mild cognitive impairment and Alzheimer's disease: implications for sequence of pathological events in Alzheimer's diseaseDOI
The lab page does not clearly state student acceptance status. Email the professor directly to confirm.
How to apply
Email Bradley F. Boeve 6-12 months before your application deadline. Read several recent papers and reference specific work in your message. Use our how to email a Japanese professor guide for the proven email structure.
For applications via MEXT scholarship: see our MEXT 2027 complete guide and university-specific University Recommendation track.
External profiles
- ORCID: https://orcid.org/0000-0002-4153-8187
- OpenAlex: openalex.org
Profile compiled from public sources (Researchmap, OpenAlex, Nagoya University faculty directory). Last refreshed 2026-05. Report incorrect information.