Cingulateislandsign temporally changes in dementia with Lewy bodies The cingulateislandsign (CIS) that reflects sparing of the posterior cingulate cortex (PCC) relative to the precuneus plus cuneus on FDG-PET and brain perfusion SPECT, has been proposed as a feature of dementia with Lewy bodies (DLB). As the CIS is influenced by concomitant Alzheimer's disease (AD)-type neurofibrillary
Validation of the cingulateislandsign with optimized ratios for discriminating dementia with Lewy bodies from Alzheimer’s disease using brain perfusion SPECT Dementia with Lewy bodies (DLB) is often cited as the second most common dementia after Alzheimer's disease (AD). It is clinically important to distinguish DLB from AD because specific side effects of antipsychotic drugs are limited to DLB. The relative preservation of cingulate glucose metabolism in the posterior cingulate gyri versus that in the precuni, known as the cingulateislandsign (CIS), in patients with DLB compared with AD is supposed to be highly specific for diagnosing DLB. In a previous study, using brain perfusion SPECT, the largest value (0.873) for the area under the receiver operating characteristic (ROC) curve
The cingulateislandsign within early Alzheimer’s disease-specific hypoperfusion volumes of interest is useful for differentiating Alzheimer’s disease from dementia with Lewy bodies In addition to occipital hypoperfusion, preserved metabolism of the posterior cingulate gyri (PCG) relative to the precunei is known as the cingulateislandsign (CIS) in the patients with dementia with Lewy
Dementia with Lewy bodies: Basis of cingulateislandsign. To investigate clinical, imaging, and pathologic associations of the cingulateislandsign (CIS) in dementia with Lewy bodies (DLB). We retrospectively identified and compared patients with a clinical diagnosis of DLB (n=39); patients with Alzheimer disease (AD) matched by age, sex, and education (n=39); and cognitively normal controls (n=78) who underwent 18F-fluorodeoxyglucose (FDG) and C11 Pittsburgh compound B (PiB)-PET scans. Among these patients, we studied those who came to autopsy and underwent Braak neurofibrillary tangle (NFT) staging (n=10). Patients with a clinical diagnosis of DLB had a higher ratio of posterior cingulate to precuneus plus cuneus metabolism, cingulateislandsign (CIS), on FDG-PET than patients
been shown to distinguish between AD and DLB. Relative preservation of posterior or midcingulate metabolism on FDG-PET/CT—the cingulateislandsign—has been described in DLB. However, most studies are hampered by small sample size, and FDG-PET/CT is a second-level examination for the evaluation of DLB. Ioflupane SPECT or SPECT/CT Brain In the present guidelines, decreased dopamine transporter
assessed striatal dopaminergic and cardiac adrenergic integrity, respectively. Clinical evaluation revealed a history of REM sleep behavior disorder and parkinsonism induced by antipsychotics. The patient's cognitive function was normal. Conventional MRI showed parieto-occipital atrophy, and posterior hypoperfusion was revealed by ASL-MRI. Of note, the "cingulateislandsign" was present. FP-CIT SPECT and I-Metaiodobenzylguanidine endorsed the suspicion of α-synucleinopathy. The patient fulfils the recently proposed key features of psychiatric-onset Prodromal DLB. Prodromal DLB is an emerging concept. Biomarkers have not been yet established. We propose that nuclear imaging and advanced MRI technics showing posterior hypoperfusion and the presence of the "cingulateislandsign" could be promising
FDG-PET hypometabolism in patients with a clinical AD presentation. Twenty-one patients with autopsy-confirmed AD ('pure-AD'), 24 with AD and LB co-pathology ('AD-LB'), and 7 with LB but no or low evidence of AD pathology ('pure-LB') were studied. Pathologic groups were compared on regional and voxel-wise FDG-PET patterns, the cingulateislandsign ratio (CISr), and neuropathological ratings
the ‘CingulateIslandSign’ and has been found to be more specific than occipital hypometabolism for DLB in a separate clinically diagnosed cohort.43 In summary, there is good evidence for occipital hypometabolism as a marker of Lewy body pathology in patients with dementia. However, studies have been small and the sensitivity and specificity inconsistent, meaning that the accuracy of this finding is unclear =ISI) 43. 43. Lim SM , Katsifis A , Villemagne VL , et al . The 18F-FDG PET cingulateislandsign and comparison to 123I-beta-CIT SPECT for diagnosis of dementia with Lewy bodies. J Nucl Med 2009;50:1638–45.[doi:10.2967/jnumed.109.065870](http://dx.doi.org/10.2967/jnumed.109.065870) [Abstract/FREE Full Text](http://ebmh.bmj.com/lookup/ijlink
, anterior and posterior cingulate, reducing the expression of the DLB-typical cingulateislandsign (CIS). Education negatively covaried with metabolism in the left inferior parietal cortex and precuneus (making the CIS more prominent). These findings point out the importance of tailoring interpretation of DLB biomarkers considering the concomitant effect of individual, non-disease-related variables
, orthostatic hypotension, urinary incontinence.Hypersomnia.Hyposmia.Hallucinations in other modalities.Systematised delusions.Apathy, anxiety and depression.Supportive biomarkers:Relative preservation of medial temporal lobe structures on CT/MRI scan.Generalised low uptake on SPECT/PET perfusion/metabolism scan with reduced occipital activity +/- the cingulateislandsign on FDG-PET imaging.Prominent
was defined in Delphi Round IV, with five panellists recommending clinical use of FDG‐PET. Besides its NPV, the presence of the posterior cingulateislandsign (i.e. relatively preserved metabolism in the posterior cingulate area) and occipital hypometabolism , at the stage of MCI support a diagnosis of DLB. However, in the first instance dopamine transporter brain single‐photon emission computed tomography % sensitivity range, 74%–100% specificity range, 72%–96% accuracy range , - , 0.77–0.91 AUC range , , - and 86% PPV, 85% NPV and 4.46 LH+ value . A similar profile of cerebral hypometabolism was observed in AD and DLB, with the exception of the marked hypometabolism in the visual cortex in DLB and the relative posterior cingulate preservation (cingulateislandsign). The consensual recommendation was defined
) values have been associated with a higher Braak neurofibrillary tangle stage in autopsied DLB. Using voxel-wise analysis, we assessed the patterns of regional cortical perfusion and metabolism, and using an atlas-based approach, we measured perfusion cingulateislandsign ratio on arterial spin labeling MRI (ASL-CISr), and its associations with FDG-CISr, uptake on tau-PET and clinical severity in DLB cingulateislandsign ratios correlate with each other in DLB. Non-invasive and radiotracer-free ASL-MRI may be further developed as a tool for the screening and diagnostic evaluation of DLB patients in a variety of clinical settings where FDG-PET is not accessible.
18F-FDG PET in Posterior Cortical Atrophy and Dementia with Lewy Bodies Posterior cortical atrophy (PCA) and dementia with Lewy bodies (DLB) have both been associated with occipital lobe hypometabolism on F-FDG PET, whereas relative sparing of posterior cingulate metabolism compared with precuneus/cuneus (i.e., cingulateislandsign) is a feature of DLB. We aimed to determine whether patterns of hypometabolism or the cingulateislandsign differed between PCA and DLB. Sixteen clinically diagnosed PCA and 13 probable DLB subjects underwent F-FDG PET. All PCA subjects showed β-amyloid deposition on PET scanning. Regional hypometabolism was assessed compared with a control cohort ( = 29) using voxel- and region-level analyses in statistical parametric mapping. A ratio of metabolism in the posterior
, Katsifis A, Villemagne VL, Best R, Jones G, Saling M, et al. The 18F-FDG PET cingulateislandsign and comparison to 123I-beta-CIT SPECT for diagnosis of dementia with Lewy bodies. J Nucl Med. 2009 Oct. 50(10):1638-45. [QxMD MEDLINE Link]. 18. Brooks DJ. Imaging amyloid in Parkinson's disease dementia and dementia with Lewy bodies with positron emission tomography. Mov Disord. 2009. 24 Suppl 2
, Katsifis A, Villemagne VL, Best R, Jones G, Saling M, et al. The 18F-FDG PET cingulateislandsign and comparison to 123I-beta-CIT SPECT for diagnosis of dementia with Lewy bodies. J Nucl Med. 2009 Oct. 50(10):1638-45. [QxMD MEDLINE Link]. 18. Brooks DJ. Imaging amyloid in Parkinson's disease dementia and dementia with Lewy bodies with positron emission tomography. Mov Disord. 2009. 24 Suppl 2
. 24 Suppl 2:S754-9. [QxMD MEDLINE Link]. 17. Lim SM, Katsifis A, Villemagne VL, Best R, Jones G, Saling M, et al. The 18F-FDG PET cingulateislandsign and comparison to 123I-beta-CIT SPECT for diagnosis of dementia with Lewy bodies. J Nucl Med. 2009 Oct. 50(10):1638-45. [QxMD MEDLINE Link]. 18. Brooks DJ. Imaging amyloid in Parkinson's disease dementia and dementia with Lewy
. 24 Suppl 2:S754-9. [QxMD MEDLINE Link]. 17. Lim SM, Katsifis A, Villemagne VL, Best R, Jones G, Saling M, et al. The 18F-FDG PET cingulateislandsign and comparison to 123I-beta-CIT SPECT for diagnosis of dementia with Lewy bodies. J Nucl Med. 2009 Oct. 50(10):1638-45. [QxMD MEDLINE Link]. 18. Brooks DJ. Imaging amyloid in Parkinson's disease dementia and dementia with Lewy
are: a. MRI/CT scans showing neuronal structural modifications with relative preservation of medial temporal lobe structures. b. Generalized low uptake on SPECT/PET perfusion/metabolism scan with reduced occipital activity +/- the cingulateislandsign on 18F-fludeoxyglucose (FDG) PET imaging. c. Prominent posterior slow wave activity on EEG with periodic fluctuations in the pre-alpha/theta
is not as severely affected as in AD.[145]Medical imaging in AD and DLBMRI of brain showing hippocampus atrophy (red rectangles), more prominent in AD than DLB, compared to normal control (NC)FDG-PET horizontal cross section of brain, with brighter areas indicating higher metabolism. The cingulateislandsign is indicated by the arrowhead.FDG-PET of brain surface, with the color red indicating areas of high with DLB often show a cingulateislandsign.[33]In East Asia, particularly Japan,123I-MIBG is used in the differential diagnosis of DLB and AD, because reduced labeling of cardiac nerves is seen only in Lewy body disorders.[114][136] Other indicative and supportive biomarkers are useful in distinguishing DLB and AD (preservation of medial temporal lobe structures, reduced occipital activity, and slow