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!”
If you don’t know the time of stroke onset, are you able to deduce it from imaging?
Here’s a thread to help you date a stroke on MRI!
2/Strokes evolve, or grow old, the same way people evolve or grow old.
The appearance of stroke on imaging mirrors the life stages of a person—you just have to change days for a stroke into years for a person
So 15 day old stroke has features of a 15 year old person, etc.
3/Initially (less than 4-6 hrs), the only finding is restriction (brightness) on diffusion imaging (DWI).
You can remember this bc in the first few months, a baby does nothing but be swaddled or restricted. So early/newly born stroke is like a baby, only restricted
1/”I LOVE spinal cord syndromes!” is a phrase that has NEVER, EVER been said by anyone.
Do you become paralyzed when you see cord signal abnormality?
Never fear—here is a thread on all the incomplete spinal cord syndromes to get you moving again!
2/Spinal cord anatomy can be complex. On imaging, we can see the ant & post nerve roots. We can also see the gray & white matter. Hidden w/in the white matter, however, are numerous efferent & afferent tracts—enough to make your head spin.
3/Lucky for you, for the incomplete cord syndromes, all you need to know is gray matter & 3 main tracts. Anterolaterally, spinothalamic tract (pain & temp). Posteriorly, dorsal columns (vibration, proprioception, & light touch), & next to it, corticospinal tracts—providing motor
1/Do you get a Broca’s aphasia trying remember the location of Broca's area?
Does trying to remember inferior frontal gyrus anatomy leave you speechless?
Don't be at a loss for words when it comes to Broca's area
Here’s a 🧵to help you remember the anatomy of this key region!
2/Anatomy of the inferior frontal gyrus (IFG) is best seen on the sagittal images, where it looks like the McDonald’s arches.
So, to find this area on MR, I open the sagittal images & scroll until I see the arches. When it comes to this method of finding the IFG, i’m lovin it.
3/Inferior frontal gyrus also looks like a sideways 3, if you prefer. This 3 is helpful bc the inferior frontal gyrus has 3 parts—called pars
1/Need help reading spine imaging? I’ve got your back!
It’s as easy as ABC!
A thread about an easy mnemonic you can use on every single spine study you see to increase your speed & make sure you never miss a thing!
2/A is for alignment
Look for: (1) Unstable injuries
(2) Malalignment that causes early degenerative change. Abnormal motion causes spinal elements to abnormally move against each other, like grinding teeth wears down teeth—this wears down the spine
3/B is for bones.
On CT, the most important thing to look for w/bones is fractures. You may see focal bony lesions, but you may not
On MR, it is the opposite—you can see marrow lesions easily but you may or may not see edema associated w/fractures if the fracture is subtle