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Clinical phenotypes of corticobasal degeneration (CBD) vary and are typically presented with four phenotypes: corticobasal syndrome (CBS), frontal behavioral-spatial syndrome (FBS), nonfluent/agrammatic variant of primary progressive aphasia, and progressive supranuclear palsy syndrome [1]. FBS is the third most common phenotype of pathologically verified CBD, accounting for approximately 14% of CBD patients [1]. Conversely, the pathological features of the clinical phenotype of behavior variant frontotemporal dementia (bvFTD) also vary, and approximately 9% of these patients have been verified pathologically CBD [2]. Here, we present an autopsy-confirmed case of CBD presenting with FBS who underwent positron emission tomography (PET) with 18F-THK5351, visualizing the predominant lesion of the frontal lobes associated with the clinical phenotype.
A 72-year-old right-handed male developed gait slowing. Three years later, he lost his way when climbing mountains and was found lying. Two months later, he lost his way again in the neighborhood, and eventually, his wife started accompanying him when he went outside. He developed urinary incontinence, masked face, decreased speech output, visual hallucination, and abnormal behaviors, such as nocturnal wandering, pica, and apraxia. His condition was evaluated at an outpatient neurology clinic, and neurological examination revealed his masked face, bradykinesia, and rigidity of his neck and left-sided upper limb. He showed no therapeutic response to levodopa for parkinsonism. His abnormal behavior increased with time and he showed stereotyped behavior, such as keeping cleaning a room or washing his body. He visited our hospital for further evaluation of his neuropsychiatric symptoms at the age of 75.
Neurological examination revealed left-sided predominant parkinsonism, apraxia, and perseveration. He showed severe cognitive impairment and scored 19/30 on the Mini-Mental State Examination and 3/18 on the Frontal Assessment Battery. Brain magnetic resonance imaging (MRI) at the age of 75 revealed right-sided and frontal lobe dominant atrophy (Fig. 1A,B), which was verified using the voxel-based specific regional analysis system for Alzheimer’s disease [3] (Fig. 1C). Dopamine transporter single-photon emission computed tomography with 123I-N-ω-fluoropropyl-2β-carboxymethoxy-3β-(4-iodophenyl)nortropane obtained 4 months before he visited us showed diffusely reduced uptake in the bilateral striata with right-sided predominance (Fig. 1D). He underwent 18F-THK5351 PET (Fig. 1E–G), 18F-fluorodeoxyglucose (18F-FDG) PET (Fig. 1H), and 11C-Pittsburgh compound B (11C-PiB) PET at the age of 75. The Z score map of 18F-THK5351 was superimposed on spatially normalized T1-weighted image (Fig. 1G). The Z scores were calculated as: (mean voxel value of 30 cognitively unimpaired subjects—patient voxel value)/standard deviation of 30 cognitively unimpaired subjects with cerebellar cortex as reference. 18F-THK5351 accumulated in the frontal lobes with right-sided predominance, as well as in the parietal lobes (Fig. 1E–G). Hypometabolism of both the frontal and parietal lobes with right-sided predominance was detected by 18F-FDG PET (Fig. 1H). Amyloid deposition was not identified by 11C-PiB PET (data not shown). He was clinically diagnosed with bvFTD underlying tau-pathology, that is, frontotemporal lobar degeneration tau, according to the prominent frontal symptoms with spatial impairment, parkinsonism, and neuroimaging findings including 18F-THK5351 PET. He died of aspiration pneumonia at the age of 76.
An autopsy was performed after consent was obtained from his family. The brain weighed 1402 g and showed cerebral atrophy, especially of the frontal and temporal lobes (Fig. 1I). There was dilation of the Sylvian fissure and mild atrophy of the frontal operculum with right-sided predominance (Fig. 1J). Microscopic assessment showed neuronal loss and an increased number of astrocytes in the cerebral cortex, especially in the frontal lobes, accompanied by abnormal rarefaction of tissue (Fig. 1K, L). Immunohistochemistry of the frontal lobes using AT8 antibody revealed phosphorylated tau-positive astrocytic plaques, pretangles, coiled bodies, and threads (Fig. 1M–O), which were presented as right-sided predominance (Fig. 1P, Q). Staining for RD4 or RD3 revealed phosphorylated 4-repeat but not 3-repeat tau-positivity (Fig. 1R, S). These tau-related pathological characteristics in the cortex were prominent in the anterior part of the frontal lobes with right-sided predominance. These were also found in the substantia nigra, subthalamic nucleus, thalamus, globus pallidus, putamen, nucleus basalis of Meynert, locus coeruleus, and inferior olivary nucleus. Western blot analysis of sarkosyl-insoluble tau from the brain showed a major doublet of 68 and 64 kDa with predominant ~ 37 kDa fragments (Fig. 1T) [4]. These pathological and biochemical findings were consistent with CBD. He was finally diagnosed with CBD-FBS [1].
Various tau PET tracers are under rapid development to visualize abnormal tau accumulation for both diagnosing tauopathy and evaluating the therapeutic effects of new drugs against tauopathy. 18F-THK5351, a first-generation tau tracer, was originally developed to detect abnormal tau-pathology [5]. However, recent studies revealed that 18F-THK5351 binds to monoamine oxidase-B (MAO-B) highly expressed in astrocytes as off-target binding [6, 7]. Using the binding affinity to MAO-B, 18F-THK5351 visualizes the astrogliosis reflecting neurodegenerative changes in various neurological diseases other than tauopathy, such as amyotrophic lateral sclerosis [8].
The main clinical phenotypes of our case imply that the core lesions were in the frontal lobes. Conventional morphological and functional imaging modalities using brain MRI and 18F-FDG PET imaging showed both atrophy and hypometabolism with right-sided predominance, respectively. Being consistent with these results of the imaging study, 18F-THK5351 PET accumulated in similar lesions, which concurred with the previous study [9]. In addition, these abnormalities obtained from in vivo imaging studies were verified through pathological evaluation of tau-positive deposition and astrogliosis in the frontal lobes with right-sided predominance. Despite the neuropathological features of bvFTD being heterogeneous [2], previous studies on 18F-THK5351 PET with bvFTD patients lack pathological confirmation. To our knowledge, this is the first clinicopathological case report demonstrating 18F-THK5351 accumulation in the frontal lobes in a CBD-FBS patient, in which the presence of tau-related neurodegenerative change was pathologically verified. However, our study was unable to distinguish the 18F-THK5351 accumulation derived from tau accumulation, an increased number of MAO-B positive astrocytes, or both, because of the limited discriminability of 18F-THK5351 between tau and MAO-B. Thus, pathologically, radiologically, and biochemically validated MAO-B PET tracers, which can more sensitively visualize neurodegeneration consisting of astrogliosis, are required [10]. Our findings provide the use of 18F-THK5351 PET as a marker closely associated with tau-related neurodegeneration.
In conclusion, the 18F-THK5351 PET image visualizes abnormal tau-related neurodegeneration reflecting clinicopathological severities in CBD-FBS. Our case highlights that 18F-THK5351 PET can be a potent technique for visualizing the tau-related predominant lesions of CBD-FBS and for discriminating the underlying pathologies of bvFTD.
Abbreviations
- bvFTD:
-
Behavior variant frontotemporal dementia
- 11C-PiB:
-
11C-Pittsburgh compound B
- CBD:
-
Corticobasal degeneration
- DaT:
-
Dopamine transporter
- 18F-FDG:
-
18F-fluorodeoxyglucose
- FBS:
-
Frontal behavioral-spatial syndrome
- 123I-FP-CIT:
-
123I-N-ω-fluoropropyl-2β-carboxymethoxy-3β-(4-iodophenyl)nortropane
- MAO-B:
-
Monoamine oxidase-B
- MRI:
-
Magnetic resonance imaging
- PET:
-
Positron emission tomography
- PSP:
-
Progressive supranuclear palsy
- SBR:
-
Specific binding ratio
- SPECT:
-
Single-photon emission computed tomography
- SUV:
-
Standardized uptake value
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Acknowledgements
We would like to thank the patient’s family for their comments and for permitting the autopsy. We also thank all of the medical professionals engaged in the patient’s care and for technical assistance with the autopsy and pathological study. We thank Dr. Nobuyuki Okamura (Tohoku Medical and Pharmaceutical University, Tohoku University), Shozo Furumoto (Tohoku University), and Yukitsuka Kudo (Tohoku University) for providing the precursor and the reference materials for the synthesis of the tracer 18F-THK5351. We thank U-English Corporation (https://www.u-english.co.jp/) for English editing of a draft of this manuscript.
Funding
This study was partially supported by the Intramural Research Grant for Neurological and Psychiatric Disorders of the National Center of Neurology and Psychiatry under grant number 30-3 (to Y Saitoh), 30-8 (to Y Saito), and 3-3 (to Y Saitoh), by JSPS KAKENHI under Grant JP221S0003 (to Y Saito), JP15K09369 (to EI), and JP15K09981 (to HM), by the grants-in-aid from the Research Committee of CNS Degenerative Diseases, Research on Policy Planning and Evaluation for Rare and Intractable Diseases, Health, Labor and Welfare Sciences Research Grants, the Ministry of Health, Labor and Welfare, Japan, MEXT/JSPS KAKENHI Grant JP16H06277 (to Y Saito), and by AMED under grant JP18dm0107103 (to Y Saito).
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Conception and design of the study: YS; Primary patient care and analysis of data: YS, EI, MM, TT, MH, YS, HM, YT; Drafting a significant portion of the manuscript or figures/tables: YS; Reviewing and approving the final manuscript: YS, EI, MM, TT, MH, YS, HM, YT.
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The authors have no competing interests to declare that are relevant to the content of this article.
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The PET study was approved by the Institutional Review Committee of the National Center of Neurology and Psychiatry. Written informed consent was obtained from the patient or the patient’s next-of-kin for inclusion in this PET study, donation for diagnostic and research purposes, and publication as a medical report.
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Saitoh, Y., Imabayashi, E., Mizutani, M. et al. 18F-THK5351 PET for visualizing predominant lesions of pathologically confirmed corticobasal degeneration presenting with frontal behavioral-spatial syndrome. J Neurol 269, 5157–5161 (2022). https://doi.org/10.1007/s00415-022-11121-y
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DOI: https://doi.org/10.1007/s00415-022-11121-y