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Glial fibrillary acidic protein

Glial fibrillary acidic protein

ProteinWikipedia

Search complete. 26 mentions across 16 episodes found for "Glial fibrillary acidic protein".

Sep 14, 2026

speaker_0NARRATOR
3:11
And that leads into biomarker science.
speaker_0NARRATOR
3:13
P tau 217, P tau 181, GFAP, neurofilament light, amyloid ratios, cerebrospinal fluid signals.
speaker_0NARRATOR
3:22
The common thread running through everything is orally intervention.
speaker_2NARRATOR
3:27
Davidson's ultimate argument is that both cardiovascular disease and Alzheimer's become much harder to stop once symptoms appear.
Heather McKenziePANELIST
10:51
So AFC is an extremely rare leukodystrophy.
Heather McKenziePANELIST
10:55
It's caused by changes in the GFAP gene that lead to its overproduction of the corresponding protein and therefore toxic accumulation in glial cells.
Heather McKenziePANELIST
11:05
So there's a scientific explanation.
Heather McKenziePANELIST
11:09
And Zanvastro is an antisense drug that binds to the RNA to decrease the body's production of this protein.
James RadkeHOST
0:50
It only affects one to three people per million.
James RadkeHOST
0:54
It's a progressive neurological disorder caused by mutations to the GFAP gene that produces a GFA protein.
James RadkeHOST
1:02
And when this protein is abnormal, it accumulates in glial cells and causes damage and severe disabilities, including seizures, loss of developmental milestones, difficulty walking, increased pressure on the brain, et cetera.
James RadkeHOST
1:19
Zanvastro is a antisense oligonucleotide that binds to the mRNA to reduce the production of that abnormal protein and thereby reduce its ability to reach toxic levels.
Richard HorowitzGUEST
77:11
Yeah.
Richard HorowitzGUEST
77:11
But the last one is called glial fibrillate acidic protein, GFAP.
Gary BreckaHOST
77:16
Okay.
Richard HorowitzGUEST
77:17
So if you are Alzheimer's ApoE44, you want to get GFAP, glial fibrillate acidic acid, because if that's positive, your 10 year risk down the line is going to be high, you're going to develop dementia.
Richard HorowitzGUEST
77:29
You don't have to do that biomarker if you're not ApoE44.
Richard HorowitzGUEST
77:31
Okay.
Henrik ZetterbergGUEST
11:14
And then, of course, one should be very careful and halt the administration of the drug and see what the reason could be.
Henrik ZetterbergGUEST
11:21
And there are also some inflammation markers that can be interesting here, GFAP and some other proteins that reflect inflammation changes in the brain.
Henrik ZetterbergGUEST
11:30
If you introduce a drug in the brain and you get a strong inflammatory reaction, that's probably not good.
Henrik ZetterbergGUEST
11:37
And then you can use biomarkers to detect this.

22 MINS LATER

Nathaniel ChinHOST
33:17
Henrik, some of the inflammatory measures that you've spoken to at presentations on this, they appear to move in different directions.
Nathaniel ChinHOST
33:25
So some went down, like the CRP in the blood went down, but then...
Nathaniel ChinHOST
33:29
the GFAP went up, and then in spinal fluid, one other one went down.
Nathaniel ChinHOST
33:33
You know, how do you make sense of something like that? And does it reflect this idea that this, quote, neuroinflammation is much more complicated than we give credit to, and one test really can't capture it?
Maya PatelHOST
4:29
It landed more than two weeks ahead of the September 22nd decision date.
Maya PatelHOST
4:33
It's an antisense drug that lowers GFAP, the protein that drives the disease.
Alex MercerHOST
4:38
We flagged that date on Tuesday's calendar.
Maya PatelHOST
4:40
And an early approval is its own signal.
Simon ThebaultHOST
41:36
I see a lot of the teething problems that we're having here is kind of smoothing the way to the next test that we hopefully can implement in this context, where we learn how to sort of speak to you guys, the laboratorians, and then also communicate these results to our patients.
Simon ThebaultHOST
41:54
And in the future, that future implementation for other biomarkers, for instance, glial fibrillary acetic protein, GFAP, which is I guess, rapidly coming behind neurofilament, in my opinion, as another useful biomarker can follow much more rapidly.
Simon ThebaultHOST
42:10
And I think we're already starting to see the utility of combining biomarkers in that way.
Simon ThebaultHOST
42:16
So we've shown data and as have many other groups that actually the combination of neurofilament and glial fibrillary acidic protein as a pair is actually greater than either one of those markers in isolation, particularly around that prognostic time point at the very beginning of the disease.
Gemma DaleyGUEST
55:41
There's amyloid beta 4240 ratio.
Gemma DaleyGUEST
55:45
There's GFAP.
Gemma DaleyGUEST
55:46
There's lots of new markers coming out.
Gemma DaleyGUEST
55:49
And there'll be more and more because it's just such a growing area of research.
Gemma DaleyGUEST
55:41
There's amyloid beta 4240 ratio.
Gemma DaleyGUEST
55:45
There's GFAP.
Gemma DaleyGUEST
55:46
There's lots of new markers coming out.
Gemma DaleyGUEST
55:49
And there'll be more and more because it's just such a growing area of research.
speaker_2HOST
17:32
Perfeito, um radar.
speaker_2HOST
17:34
E além disso, eles também usaram camundongos transgênicos repórteres, que possuem um marcador chamado GFAP.
speaker_3PANELIST
17:41
E o que isso faz?
speaker_2HOST
17:42
Nesses animais, sempre que ocorre astrocitose, que é aquela inflamação grave no cérebro...

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