2/ fMRI is based on a principle called “neurovascular coupling.” This is the principle if there is increased neuronal activity in a region, there will be increased blood flow to that region to meet the increased demand
3/ Think of it like a baby crying because it is hungry—parents immediately rush to feed it. The increased oxygen demand of the neurons immediately brings increased fuel to feed it.
4/ However, the body actually overreacts to that demand—it is like going McDonald’s when you are starving—you are going to walk away with way more food than you need and end up feeling incredibly stuffed. The neurons end up getting way more oxygenated blood than they need.
5/ This changes the oxygenated to deoxygenated blood ratio. Initially deoxygenated blood is increased b/c activated neurons are using up oxygen, but this is soon overwhelmed by supply. So counterintuitively—oxygenated blood is more with this metabolic activity.
6/ This is important b/c deoxygenated blood⬇️fMRI signal & oxygenated blood⬆️it. Initially, a signal drop occurs as neurons use up oxygen, but the tidal wave of oxygenated blood coming in overwhelms this & you get increased signal w/neuronal activity.
7/ So if you perform an activity, say finger tapping, the regions involved in finger tapping (motor cortex) will experience increased blood flow compared to regions of the brain that are not involved in that activity.
8/ B/c of increased blood flow, oxygenated blood & fMRI signal will increase in regions involved in a task compared to those not involved. This is how we map what brain regions are associated with an activity—not just finger tapping, but language, memory, etc.
9/ fMRI images are made by subtracting images taken during baseline (no activity) from images taken during activity. All that will left after the subtraction is the increased flow/signal over baseline--and this will only be in regions activated by the task.
10/ For the baseline image, no activity is performed, and so no regions are activated, so all regions will show low signal.
11/ When a task begins, blood flow only increases to regions involved in the task, so only those regions will have increased blood flow/signal over baseline. This example is finger tapping, but we can map which regions are associated w/more complex brain activities.
12/ Here is an example w/finger tapping. At baseline, the motor cortex is not activated & has low flow. But w/finger tapping, signal increases w/increased flow. So when we subtract baseline images from activity images, the increased signal over baseline remains.
13/ On the fMRI images, we see the increased signal over baseline as the colored blobs you all recognize. These just mean there is increased blood flow in this region over baseline with a given activity, and so that specific activity maps to that region.
14/ Now let’s look at a region not activated by finger tapping. At baseline, it is not activated & has low flow. W/finger tapping, it is also not activated & flow is same as baseline. So w/subtraction, the 2 images are identical & cancel out, so signal is 0.
15/ Since signal is zero, there are no colored blobs in this region and so we know this region is not associated with the task.
16/ So those fMRI colored blobs just mean there is⬆️flow in a region w/an activity & so that region is involved in performing that task. That's how we map the different "functions" of brain regions
So next time if someone asks you if you understand fMRI you can say “F--- yeah!”
3/At its most basic, you can think of the PPF as a room with 4 doors opening to each of these regions: one posteriorly to the skullbase, one medially to the nasal cavity, one laterally to the infratemporal fossa, and one anteriorly to the orbit
1/My hardest thread yet! Are you up for the challenge?
How stroke perfusion imaging works!
Ever wonder why it’s Tmax & not Tmin?
Do you not question & let RAPID read the perfusion for you? Not anymore!
2/Perfusion imaging is based on one principle: When you inject CT or MR intravenous contrast, the contrast flows w/blood & so contrast can be a surrogate marker for blood.
This is key, b/c we can track contrast—it changes CT density or MR signal so we can see where it goes.
3/So if we can track how contrast gets to the tissue (by changes in CT density or MR signal), then we can approximate how BLOOD is getting to the tissue.
And how much blood is getting to the tissue is what perfusion imaging is all about.
1/”That’s a ninja turtle looking at me!” I exclaimed. My fellow rolled his eyes at me, “Why do I feel I’m going to see this a thread on this soon…”
He was right! A thread about one of my favorite imaging findings & pathology behind it
2/Now the ninja turtle isn’t an actual sign—yet!
But I am hoping to make it go viral as one. To understand what this ninja turtle is, you have to know the anatomy.
I have always thought the medulla looks like a 3 leaf clover in this region.
The most medial bump of the clover is the medullary pyramid (motor fibers).
Next to it is the inferior olivary nucleus (ION), & finally, the last largest leaf is the inferior cerebellar peduncle.
Now you can see that the ninja turtle eyes correspond to the ION.
3/But why are IONs large & bright in our ninja turtle?
This is hypertrophic olivary degeneration.
It is how ION degenerates when input to it is disrupted. Input to ION comes from a circuit called the triangle of Guillain & Mollaret—which sounds like a fine French wine label!