In vivo amyloid imaging with PET in frontotemporal dementia

Background N-methyl[11C]2-(4′methylaminophenyl)-6-hydroxy-benzothiazole (PIB) is a positron emission tomography (PET) tracer with amyloid binding properties which allows in vivo measurement of cerebral amyloid load in Alzheimer’s disease (AD). Frontotemporal dementia (FTD) is a syndrome that can be...

Full description

Saved in:
Bibliographic Details
Published inEuropean journal of nuclear medicine and molecular imaging Vol. 35; no. 1; pp. 100 - 106
Main Authors Engler, Henry, Santillo, Alexander Frizell, Wang, Shu Xia, Lindau, Maria, Savitcheva, Irina, Nordberg, Agneta, Lannfelt, Lars, Långström, Bengt, Kilander, Lena
Format Journal Article
LanguageEnglish
Published Berlin/Heidelberg Springer-Verlag 2008
Springer Nature B.V
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Background N-methyl[11C]2-(4′methylaminophenyl)-6-hydroxy-benzothiazole (PIB) is a positron emission tomography (PET) tracer with amyloid binding properties which allows in vivo measurement of cerebral amyloid load in Alzheimer’s disease (AD). Frontotemporal dementia (FTD) is a syndrome that can be clinically difficult to distinguish from AD, but in FTD amyloid deposition is not a characteristic pathological finding. Purpose The aim of this study is to investigate PIB retention in FTD. Methods Ten patients with the diagnosis of FTD participated. The diagnosis was based on clinical and neuropsychological examination, computed tomography or magnetic resonance imaging scan, and PET with 18Fluoro-2-deoxy-d-glucose (FDG). The PIB retention, measured in regions of interest, was normalised to a reference region (cerebellum). The results were compared with PIB retention data previously obtained from 17 AD patients with positive PIB retention and eight healthy controls (HC) with negative PIB retention. Statistical analysis was performed with a students t-test with significance level set to 0.00625 after Bonferroni correction. Results Eight FTD patients showed significantly lower PIB retention compared to AD in frontal ( p  < 0.0001), parietal ( p  < 0.0001), temporal ( p  = 0.0001), and occipital ( p  = 0.0003) cortices as well as in putamina ( p  < 0.0001). The PIB uptake in these FTD patients did not differ significantly from the HC in any region. However, two of the 10 FTD patients showed PIB retention similar to AD patients. Conclusion The majority of FTD patients displayed no PIB retention. Thus, PIB could potentially aid in differentiating between FTD and AD.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1619-7070
1619-7089
1619-7089
DOI:10.1007/s00259-007-0523-1