Presentation on theme: "Unforgettable images: A multimodality pictorial review of dementia"— Presentation transcript:
1 Unforgettable images: A multimodality pictorial review of dementia Daniel Thut, DO, Alena Kreychman, MD, Susan Megas, APRN, Shan Li, MDDepartment of RadiologyBaystate Medical CenterTufts University School of MedicineeEdE-06
2 The authors have nothing to disclose. DisclosureThe authors have nothing to disclose.
3 Dementia What is dementia? Dementia refers to the deterioration in memory, thinking, language, judgment and behavior.Differentiating one type of dementia from another is a clinical challenge. What is the role of imaging in dementia?Structural imaging is used to rule out treatable causes for the patient’s symptoms or suggest the presence of comorbidities that may exacerbate dementia symptoms.As new disease-modifying agents enter clinical practice, correctly diagnosing the specific type of dementia is becoming increasingly important. Currently there is no single behavioral marker that can reliably discriminate one form of dementia from another
4 Dementia Alzheimer’s Dementia Frontotemporal Lobe Dementia Picks DementiaLewy Body DementiaParkinson’s Disease with DementiaVascular dementiaMulti-Infarct DementiaCADASILBinswanger Dementia
5 Alzheimer’s DementiaClinically characterized by progressive memory loss, as well as change in personality and thoughtAccounts for 60-70% of dementing disorders4 million patients in US100,000 deaths/year$90 billion per yearProjections are for 14 million cases in 2050Definitive diagnosis is histopathological demonstration of beta amyloid senile plaques in the cerebral cortex and tau protein neurofibrillary tangles in the nerve cells
6 Alzheimer’s Imaging: CT NECT is a helpful screening tool that can exclude potentially reversible or treatable causes of dementia such as subdural hematoma and normal pressure hydrocephalus.The earliest identifiable finding on CT is medial temporal lobe atrophy.Generalized cortical atrophy is usually a late finding.
7 Alzheimer’s Imaging: MRI MRI: Most common changes are thinned gyri, widened sulci and enlarged lateral ventriclesThere is temporal lobe predominanceparticularly the hippocampal and parahippocampal gyriPresence of deep white matter and periventricular white matter areas of high signal intensity on T2WI’s, in the absence of cardiovascular risk factors, are not seen with a statistical significance in patients with ADAxial FLAIR images in a patient with AD has severe bilateral hippocampal atrophy (arrows).
8 Alzheimer’s Disease: MR spectroscopy Reduced levels of NAA (N-acetyl aspartate) and Increased levels of myoinositol especially in the frontal, temporal and occipital cortex of AD patients presumably due to neuronal lossMultivoxel MR spectroscopic imaging in (a) a 62-year-old healthy volunteer and (b) an 80-year-old patient with AD. Sample spectra are shown from right temporal lobe (bottom left), left insula (top right) and left thalamus (bottom right). Note the increase in myo-inositol (Ino) and choline (Cho) levels and the decrease in NAA level (short arrows in b) in the right temporal lobe of the patient with AD, compared with those levels in the healthy volunteer, suggesting the presence of gliosis, increased membrane turnover, and neuronal loss in AD.(P)Cre creatine and phosphocreatine.Neuroimaging and Early Diagnosis of Alzheimer’s Disease : A Look to the Future Radiology, Petrella et al, 2003; 226:315–336
9 Alzheimer’s Disease: PET and SPECT Early disease is seen as bilateral hypometabolism or hypoperfusion of the posterior cingulate and tends to involve the superior posterior parietal cortexEarly in the disease, the findings may be asymmetric.As the disease progresses, it involves the frontal cortices, but to a much lesser extent than parietal and temporal lobe involvementThe occipital visual cortex, primary somatosensory and motor cortices, basal ganglia, thalamus, and cerebellum are sparedThere is slightly higher sensitivity with F-18 FDG PET (up to 94%) than SPECT (78%-91%), with similar specificities between the 2 modalities
10 Alzheimer’s Disease: HMPAO SPECT axialsagittalcoronalSPECT imaging with Tc-99m -HMPAO demonstrate subtle reduced cerebral blood flow in the temporoparietal region (arrows)
11 Alzheimer’s Disease: FDG PET axialsagittalcoronalPETCTPET/CTFDG PET/CT demonstrating markedly decreased uptake in the temporal and parietal lobes, bilaterally. An enlarged sagittal image on the right highlights the hypometabolism in the temporoparietal lobes (arrows).
12 Alzheimer’s Disease: Amyloid Imaging PET using amyloid-binding radiotracers such as 18F Florbetapir (Amyvid) can show early AD diagnosis.As new therapies enter clinical trials, the importance of in vivo beta amyloid (Aβ) imaging is becoming increasingly crucial.Aβ deposition occurs well before symptom onset and likely represents preclinical AD in asymptomatic individuals and prodromal AD in patients with mild cognitive impairment (MCI).The radiotracer crosses the blood–brain barrier and shows high-affinity binding for AβPositive examinations demonstrate high levels of cortical uptake in addition to nonspecific white matter binding with loss of the normal gray-white matter differentiation
13 Alzheimer’s Imaging: Amyvid Positive Amyvid scan.61 year old with clinical suspicion for AD MBq (10 mCi) of F18-Florbetapir (Amyvid) PET/CT showing intense cortical uptake in addition to the nonspecific binding of the radio-tracer in the white matterNegative Amyvid scan for comparison. The arrow points to normal preserved gray-white contrast(Amyvid website:
14 Lewy Body DementiaLewy Body Dementia (LBD) accounts for approximately 25% of dementias.On histopathology, there are Lewy body intracellular inclusions (alpha-synuclein) throughout the cortex, brainstem, and limbic system as well as loss of dopamine transporters in the striatumPatients with LBD often demonstrate a fluctuating dementia, visual hallucinations, falls, and some parkinsonian symptoms (i.e tremors).Lewy bodies were originally described in Parkinson disease, and it is likely that DLB and PD are related as part of a spectrum of disease.The clinical manifestation may be similar to that of AD or the dementia associated with PD.
15 Lewy Body Dementia: CT and MRI Deep gray matter atrophy and preservation of the medial temporal lobeMRIT1WI show only mild generalized atrophyT2/FLAIR may demonstrate nonspecific hyperintensities in the white matter that are similar to those found in normal aging patients.DTI may show increased mean diffusivity in the amygdala and decreased fractional anisotropy in the inferior longitudinal and inferior occipitofrontal fasciculi.MRS shows relatively normal NAA:Cr ratios.
16 Lewy Body Dementia: SPECT and PET SPECT or PETShow hypoperfusion or hypometabolism changes in the posterior cortical regions.The pattern tends to involve the occipital lobes and cerebellumThe involvement of the primary visual cortex can explain the clinical visual hallucinations.Hippocampus is spared
17 Lewy Body Dementia: SPECT and PET FDG PET demonstrating decreased uptake in the occipital lobes in addition to posterior temporoparietal lobes, bilaterally (arrows)Silverman et al., Semin Nucl Med 38: , 2008
18 Parkinson’s Disease with Dementia Parkinson disease is a multisystem neurodegenerative disorder, clinically manifested with resting tremor, bradykinesia, and rigidity.When PD is accompanied by dementia, it is referred to as Parkinson disease dementia (PDD).
19 Parkinson’s Disease with Dementia: CT and MRI Anatomic imaging with CT and MRI is rarely useful for PDD.CT is used primarily following deep brain stimulation (DBS) placement to evaluate for surgical complications and check electrode positioningMRI may show midbrain volume loss with a “butterfly” configuration.Other findings that may support the diagnosis of PD include thinning of the pars and loss of normal substantia nigra hyperintensity on T1WI
20 Parkinson’s Disease with Dementia: CT and MRI Axial T2WI at the midbrain level shows sulcal and ventricularenlargement and hypointensity and narrowing of the substantia nigra (arrows).
21 Parkinson’s Disease with Dementia: DaTscan Presynaptic dopamine transporter imaging with the I-123 Ioflupane (DaT scan) will show decreased uptake in the putamen and head of the caudate nucleusCannot discriminate between PDD and DLB but can be very useful in the differential diagnosis between DLB and AD and can also be of some value in the differential diagnosis between DLB and vascular dementia
22 Parkinson’s Disease with Dementia: DaTscan Positive DaTscan: Axial I-123 Ioflupane (DaT scan) SPECT and fused SPECT/CTshowing absence of uptake in bilateral putamina and slightly reduced uptake in the heads of the caudate nuclei, left greater than right.
23 Frontotemporal Dementia Frontotemporal dementia (FTD) comprises a group of dementias accounting for approximately 5–10% of cases of dementia.FTD is clinically characterized by behavioral changes in personality including apathy, perseverations and inappropriate social conduct and language disturbances that may precede or overshadow memory deficits.On histopathology, there is frontal and anterior temporal neuronal degeneration.Pick bodies, a type of protein inclusion, are sometimes found, and brain and CSF are sometimes assessed for abnormalities related to tau and ubiquitin proteins.Amyloid and Lewy bodies are absent.There currently is no treatment
24 Frontotemporal Dementia Imaging CT:Asymmetric frontal and anterior temporal atrophy is a distinctive feature of FTD that distinguishes it from AD.MR:T1WI may show generalized frontotemporal volume lossPick disease is associated with strongly asymmetric atrophy involving the temporal and/or frontal regions.Gyri may be thin and “knife-like”
25 Frontotemporal Imaging: CT NECT showing the frontal lobes and anterior temporal poles are markedly atrophic with “knife-like” gyri (arrow), which is out of proportion to other lobes.
26 Frontotemporal Imaging: MRI Sagittal T1WI MRI (left) and axial T2 BLADE (right) demonstrate markedatrophy of the frontal lobe (“knife-like” gyri ) in a patient with FTD.
27 Frontotemporal Dementia Nuclear medicine PET or SPECT:hypoperfusion and hypometabolism in the frontal and temporal lobes with HMPAO SPECT and FDG PET, respectively
28 Frontotemporal Dementia: SPECT Frontotemporal Dementia. (left) Sagittal images from SPECT, (right) axial, coronal and sagittal fused SPECT/MRI (created on a separate workstation for anatomic correlation) demonstrating markedhypometabolism in the frontotemporal lobes, bilaterally
29 Vascular Dementia Accounts for about 15% of all dementias in the U.S. Distinguished from AD by its more sudden or stepwise onset and association with vascular risk factors.Vascular dementia is characterized by a stepwise course with periods of stability followed by sudden decline in cognitive function.Patients may experience focal neurologic deficits after a sudden decline, such as slurred speech or sensorimotor dysfunction.Vascular dementias can be thought of as a continuum of multi-infarct dementia, deep gray infarcts and white matter disease, severe white matter disease only, Binswanger and CADASILControl of vascular risk factors is the treatment of choice.
30 Vascular Dementia: Multi-Infarct Imaging with CT NECT scans often show generalized volume loss with multiple cortical, subcortical, and basal ganglia infarcts.Patchy or confluent hypodensities in the subcortical and deep periventricular white matter
31 Vascular Dementia: Multi-Infarct Imaging with MRI T1WI often shows generalized volume loss.Multiple hypointensities in the basal ganglia and deep WMFocal cortical and large territorial infarcts with encephalomalaciaT2/FLAIR scans show multifocal diffuse and confluent hyperintensities in the basal ganglia and cerebral white matterT2* sequences may show multiple “blooming” artifacts in the cortex and along the pial surface of the hemispheres.DTI may demonstrate decreased fractional anisotropy and increased ADC values in otherwise normal white matterTypically the inferior-frontal-occipital fascicles, corpus callosum, and superior longitudinal fasciculus
32 Vascular Dementia: Multi-Infarct Imaging with MRI Axial FLAIR images showing extensivehyperintensity in the periventricular andsubcortical white matter)Axial T2 BLADE images showing cysticencephalomalacia related to old infarcts in the left posterior temporal-occipital lobe and leftmedial occipital lobe.
33 Vascular Dementia: Multi-Infarct Imaging with FDG PET FDG PET shows multiple diffusely distributed areas of hypometabolism, generally without specific lobar predominancePETFDG PET/CT showing patchy areas of decreaseduptake, most notably in the right frontal lobe, corresponding to an old infract on the MRI(red arrow).PET/CTCT
34 Vascular Dementia: Multi-Infarct Imaging with FDG PET Arrows on this scan indicate decreased FDG uptake in the right parietal cortex (left), right prefrontal cortex, basal ganglia and thalamus (middle), and right temporal cortex (right). The decreased uptake of the left cerebellum (right) is consistent with cross-cerebellar diaschisis, caused by diminished afferent input from contralateral cortex.Silverman et al., Semin Nucl Med 38: , 2008
35 Vascular Dementia: Binswanger Subcortical arteriosclerotic encephalopathyAssociated with hypertension, generally affects patients >55Slowly progressiveInvolves white matter (which distinguishes it from multi-infarct dementia) and lacunar infarctsNECT scan of Binswanger's disease with diffuse hypodensity in the white matter and widening of the lateral ventricles.
36 Vascular Dementia: Binswanger on MRI (Left 2 images) Axial T2WI showing multiple old lacunar infarcts within bilateral basal ganglia (arrows) and the left centrum semiovale (arrowhead).(Right 2 images) Axial FLAIR images show innumerable small and patchy areas of hyperintensity in theperiventricular and subcortical white matters bilaterally.
37 Vascular Dementia: CADASIL CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy) is the most common heritable cause of stroke and vascular dementia.Inherited arterial disease created by mutations in the Notch 3 gene on chromosome 19Begins in young adults with TIAs and strokesTypical involvement of the temporal lobe white matter, internal capsule and subinsular (surrounding the basal ganglia) regionsClinically, it presents with nonspecific symptoms including aura- initiated migraines, early-onset TIAs or stroke, mood disturbance, and progressive cognitive decline.Imaging of patients with CADASIL commonly yields white matter hyperintensities (WMH), a nonspecific finding seen in many disorders.
38 Vascular Dementia: CADASIL on MRI This is a 32 years old male with a history of multiple strokes and a 1st degree relative who died from stroke. Axial PD, T2 and FLAIR show striking confluent deep periventricular white matter signal abnormality.The findings of such extensive white matter disease is highly unusual in a 32 year old patient. The clue to the diagnosis is seen on the FLAIR, where there is signal abnormality in both anterior temporal lobes (arrows). This is an uncommon location for typical, "small vessel vascular disease" seen in older patients. Signal abnormality in the anterior temporal lobes and external capsules, especially in a patient with a positive family history, is suggestive of CADASIL. Biopsy in this case confirmed NOTCH 3 mutation
39 Vascular Dementia: CADASIL on PET Very few functional imaging studies have been conducted on CADASIL patients.In a study by Tatsch et al. (2003), the mean regional metabolic rate of glucose was significantly reduced in all cortical and subcortical structures (especially thalamus and striatum) in CADASIL patients compared with healthy controls.
40 Vascular Dementia: CADASIL on PET FDG PET showing marked reduction in uptake in the frontal, temporal, and parietal cortices ( left > right ) as well as the left striatum and thalamus. Uptake is also reduced in the right cerebellar hemisphere ( arrows ), suggesting crossed cerebellar diaschisisTatsch et al. J of Nuc Med 44.6 (2003):
41 ConclusionOften the nonspecific structural changes depicted on CT and MRI are preceded by changes in cerebral blood flow and metabolism.Patterns of hypoperfusion and hypometabolism may be more specific for one form of dementia versus another.New molecular imaging techniques can identify specific biomarkers, such as beta amyloid plaque deposition or dopaminergic neuron deficit, which can help differentiate between dementia types.In summary, as there is an increasing reliance on neuroimaging as part of a comprehensive evaluation of dementia, it is important that the interpreting radiologist can recognize these common patterns and imaging characteristics to suggest the correct diagnosis.
42 ReferencesSilverman, Daniel HS, et al. "Positron emission tomography scans obtained for the evaluation of cognitive dysfunction." Seminars in nuclear medicine. Vol. 38. No. 4. WB Saunders, 2008.Tatsch K, Koch W, Linke R et al (2003) Cortical hypometabolism and crossed cerebellar diaschisis suggest subcortically induced disconnection in CADASIL: an 18F-FDG PET study. J Nucl Med 44:862–869Osborn, Anne G. Osborn's brain: imaging, pathology, and anatomy. Amirsys Pub., 2013.Dierckx, Rudi AJO, et al. PET and SPECT in Neurology. Springer,Neuroimaging and Early Diagnosis of Alzheimer’s Disease : A Look to the Future Radiology, Petrella et al, 2003; 226:315–336Amyvid website: pi.lilly.com/us/amyvid-uspi.pdf