Interactive Transcript
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Dr. Laser,
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This is a 68-year-old man who I know personally.
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He's a money manager.
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Things aren't going so well at work as he's having
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trouble doing math and just remembering
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things in general.
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So, he's clearly got a form of cognitive decline.
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As we scroll the coronal projection,
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we look at the size of the temporal horns.
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They're big.
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The choroidal fissures, they're big.
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And the hippocampus is a little bit lobulated
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instead of nice and generous and convex upward.
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It's starting to demonstrate this mogul-like appearance.
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Down you go into the trough,
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up you go onto the top of the mogul,
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and then down again.
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You really shouldn't have that.
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And of course,
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there are a lot of structures in here,
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like the fimbria and the subiculum
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and the hippocampus and the dentate gyrus,
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which you can sort out with high
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resolution coronal imaging.
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So he's got a medial temporal atrophic
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score of at least two.
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Correct. Yeah.
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So...
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And the number one biomarker on imaging for
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ALZ is the degree of hippocampal loss.
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Never mind that you're looking at parietal
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atrophy and temporal atrophy in general,
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and also a Sylvian atrophy.
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Now, most patients with typical Alzheimer's disease
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don't have as much frontal atrophy as
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they do temporal parietal atrophy.
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But perhaps a more specific way to go about
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including Alzheimer's disease in the diagnosis,
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besides the things we mentioned,
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namely hippocampal atrophy,
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as the number one biomarker,
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is excluding other common causes of dementia.
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One of them is vascular disease.
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So, what would you grade this according to the
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Fazekas scale for vasculopathy or white matter disease.
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So for a 68-year-old gentleman,
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he has some punctate white matter foci,
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this would be a scale of a score of 1.
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So, not much.
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Not much.
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Now, this would be normal for a patient of this age.
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Yeah, and he doesn't have any macro infarctions,
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so it'd be hard to explain his cognitive
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decline based on vascular etiology.
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So that's one we can toss aside.
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There isn't a lot of olfactory or frontal atrophy
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compared to the other distributions.
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He also doesn't have disinhibition,
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bad behavior, dysexecutive syndrome.
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So that moves us away from frontal lobar
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dementia or pick's like syndromes,
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of which there are three or four different
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diseases that have been described.
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Doesn't have visual hallucinations,
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also doesn't have tremor.
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So that takes us away from Lewy Body Dementia.
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Now, I just want to talk for a minute about the
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cingulum in the sagittal projection.
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Let's bring down the sagittal.
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We look at this cingulum and the cingulate sulcus.
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It is big. It's not huge, but it's big.
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And then the parietal occipital sulcus is big.
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Not huge, but big.
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And so that would go along with Alzheimer's disease.
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It's not pathognomonic.
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Now, one thing that is helpful in excluding
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ALZ is doing Fluorodopa PET.
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And there are a number of agents
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that are available.
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The presence of enhancement on Fluorodopa PET,
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which I don't have here,
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is not very specific.
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You can see it in aging.
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You can see it in some other disorders,
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but the complete absence of any uptake in a
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brain with Fluorodopa PET is highly specific,
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very good negative predictive value for
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the absence of Alzheimer's disease.
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So, if you got a 45-year-old with some cognitive
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decline and you want to absolutely exclude ALZ,
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that is one way to do it.
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Now, you and I have both discussed before
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that the number one biomarker for ALZ
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is the size of the hippocampus,
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and this hippocampus is pretty small.
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Unfortunately,
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this patient did go on within a year to full-blown ALZ.
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12% of cognitive impairment patients
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without strict Alzheimer's criteria
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do go on in one year and 80% by 5 years.
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Are there any other comments
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you'd like to make on this case?
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The one comment I would like to discuss would
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be the putting the whole picture together,
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looking at the global cortical atrophy scale,
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which we've talked about in a prior vignette,
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the parietal lobe atrophy.
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We talked about the temporal lobe atrophy
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and then coming up with a diagnosis.
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If this patient presents with impaired
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cognition as his first scan,
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the most important thing you can do
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is to say temporal lobe atrophy,
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suspicious for Mild Cognitive Impairment Syndrome,
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such early Alzheimer's,
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and recommend follow-up imaging to assess
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progression of disease or stability of the disease.
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Great. Pomeranz and Laser out.
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