» Articles » PMID: 23018627

Perfusion SPECT Studies with Mapping of Brodmann Areas in Differentiating Alzheimer's Disease from Frontotemporal Degeneration Syndromes

Overview
Journal Nucl Med Commun
Specialty Nuclear Medicine
Date 2012 Sep 29
PMID 23018627
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Objectives: The aim of this study was to evaluate the contribution of brain perfusion single-photon emission computed tomography (SPECT) studies with mapping of Brodmann areas (BAs) in the differential diagnosis between Alzheimer's disease (AD) and frontotemporal degeneration (FTLD) syndromes.

Methods: Thirty-nine patients with AD and 73 patients with FTLD syndromes [behavioural variant FTLD (bvFTLD); language variant FTLD (lvFTLD), including semantic dementia (SD) and progressive nonfluent aphasia (PNFA); and corticobasal degeneration (CBD)/progressive supranuclear palsy (PSP) syndromes] underwent brain perfusion SPECT. The NeuroGam software was used for the semiquantitative evaluation of perfusion in BAs of the left (L) and right (R) hemispheres.

Results: Compared with those in AD patients, BAs with statistically significant hypoperfusion were found in the prefrontal, orbitofrontal and cingulated cortices and Broca's areas of FTLD and bvFTLD patients; in the temporal and prefrontal cortices and Broca's areas of lvFTLD patients; in the left temporal gyrus of SD patients; in premotor and supplementary motor, prefrontal, orbitofrontal, temporal and anterior cingulated cortices and Broca's areas of PNFA patients; and in the prefrontal, temporal, posterior cingulated and primary and secondary visual cortices of CBD/PSP patients. BA 46R could differentiate AD patients from FTLD and bvFTLD patients; 21L and 25L were found to be independent predictors for lvFTLD in comparison with AD, and 25R, 21L and 23R could differentiate AD patients from PNFA, SD and CBD/PSP patients, respectively.

Conclusion: Brain perfusion SPECT with BA mapping in AD and FTLD patients could improve the definition of brain areas that are specifically implicated in these disorders, resulting in a more accurate differential diagnosis.

Citing Articles

Regional cerebral blood flow in behavioral variant of FTD: hypoperfusion patterns and clinical associations.

Konstantinopoulou E, Aretouli E, Sioka C, Douli E, Petrikis P, Iakovou I Acta Neurol Belg. 2024; 124(6):1973-1980.

PMID: 39453559 DOI: 10.1007/s13760-024-02584-z.


Added Value of NeuroGam Software Analysis in Single Photon Emission Computed Tomography Localization Diagnosis of Epilepsy in Interictal Stage.

Fu P, Wei L, Zhang F, Gao J, Jing J, Wu W Med Sci Monit. 2018; 24:1494-1501.

PMID: 29531211 PMC: 5861764. DOI: 10.12659/msm.908437.


Longitudinal Neuroimaging Analysis in Mild-Moderate Alzheimer's Disease Patients Treated with Plasma Exchange with 5% Human Albumin.

Cuberas-Borros G, Roca I, Boada M, Tarraga L, Hernandez I, Buendia M J Alzheimers Dis. 2017; 61(1):321-332.

PMID: 29154283 PMC: 5734124. DOI: 10.3233/JAD-170693.


Radiological biomarkers for diagnosis in PSP: Where are we and where do we need to be?.

Whitwell J, Hoglinger G, Antonini A, Bordelon Y, Boxer A, Colosimo C Mov Disord. 2017; 32(7):955-971.

PMID: 28500751 PMC: 5511762. DOI: 10.1002/mds.27038.


Regional cerebral blood flow single photon emission computed tomography for detection of Frontotemporal dementia in people with suspected dementia.

Archer H, Smailagic N, John C, Holmes R, Takwoingi Y, Coulthard E Cochrane Database Syst Rev. 2015; (6):CD010896.

PMID: 26102272 PMC: 6464981. DOI: 10.1002/14651858.CD010896.pub2.